MRAS — 258 ClinVar variants
All ClinVar germline MRAS variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 93 flagged for review →
5 Likely pathogenic · 4 Conflicting · 11 Benign · 9 Benign/Likely benign · 108 Likely benign · 121 Uncertain significance
Full MRAS gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 93
Variants where the independent computational evidence doesn't line up with the clinical picture — a QC signal for a second look, not a reclassification.
Predictors agree, ClinVar conflicts 1
ClinVar submitters conflict, but the independent predictors unanimously agree — a QC review flag, not a reclassification.
-
MRAS p.Ser8Gly
Conflicting
Single submitter
Inborn genetic diseases
Predictors lean, ClinVar uncertain 71
ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.
-
MRAS p.Ala5Thr
Uncertain significance
Multiple submitters
Noonan syndrome 11
- MRAS p.Arg112His Uncertain significance Multiple submitters
-
MRAS p.Arg193Gln
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Asn10Ser
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Asn126Lys
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Asn126Ser
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Gln178Lys
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.His169Arg
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Leu111Arg
Uncertain significance
Multiple submitters
Inborn genetic diseases
- MRAS p.Leu203Arg Uncertain significance Multiple submitters
-
MRAS p.Lys189Asn
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Phe100Leu
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Pro44Ser
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Ser183Asn
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Thr200Asn
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Tyr92Ser
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Val124Met
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Val172Ile
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Val6Ile
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Ala145Glu
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Ala145Val Uncertain significance Single submitter
- MRAS p.Ala197Ser Uncertain significance Single submitter
- MRAS p.Ala98Thr Uncertain significance Single submitter
- MRAS p.Arg105His Uncertain significance Single submitter
- MRAS p.Arg112Cys Uncertain significance Single submitter
- MRAS p.Arg138Lys Uncertain significance Single submitter
-
MRAS p.Arg196Gln
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Arg78Trp Uncertain significance Single submitter
- MRAS p.Arg83His Uncertain significance Single submitter
- MRAS p.Asn10Asp Uncertain significance Single submitter
- MRAS p.Asn149Ser Uncertain significance Single submitter
- MRAS p.Asn58Ser Uncertain significance Single submitter
- MRAS p.Asp170Glu Uncertain significance Single submitter
- MRAS p.Asp170Val Uncertain significance Single submitter
-
MRAS p.Asp57Asn
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Asp9Glu Uncertain significance Single submitter
- MRAS p.Gln59His Uncertain significance Single submitter
- MRAS p.Glu117Asp Uncertain significance Single submitter
-
MRAS p.Glu55Asp
Uncertain significance
Single submitter
Inborn genetic diseases
-
MRAS p.Glu79Gln
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Gly70Arg Uncertain significance Single submitter
-
MRAS p.Gly85Glu
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.His201Arg Uncertain significance Single submitter
-
MRAS p.His201Tyr
Uncertain significance
Single submitter
Inborn genetic diseases
-
MRAS p.Ile136Val
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Ile153Leu Uncertain significance Single submitter
- MRAS p.Ile153Val Uncertain significance Single submitter
- MRAS p.Ile179Met Uncertain significance Single submitter
-
MRAS p.Ile46Phe
Uncertain significance
Single submitter
Noonan syndrome 11
- MRAS p.Ile62Val Uncertain significance Single submitter
-
MRAS p.Ile90Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
MRAS p.Leu162Val
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Leu29Arg Uncertain significance Single submitter
- MRAS p.Leu29Phe Uncertain significance Single submitter
-
MRAS p.Leu66Gln
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Lys142Gln Uncertain significance Single submitter
- MRAS p.Lys186Thr Uncertain significance Single submitter
-
MRAS p.Met131Lys
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Pro151Leu Uncertain significance Single submitter
-
MRAS p.Ser27Thr
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Ser8Thr Uncertain significance Single submitter
- MRAS p.Thr137Ile Uncertain significance Single submitter
-
MRAS p.Thr198Arg
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Thr45Ser Uncertain significance Single submitter
- MRAS p.Thr54Lys Uncertain significance Single submitter
- MRAS p.Thr54Met Uncertain significance Single submitter
- MRAS p.Tyr92Cys Uncertain significance Single submitter
- MRAS p.Val103Met Uncertain significance Single submitter
- MRAS p.Val91Ala Uncertain significance Single submitter
- MRAS p.Val91Leu Uncertain significance Single submitter
- MRAS p.Val94Ile Uncertain significance Single submitter
Predictors split 21
The independent predictors disagree with each other — read with care.
-
MRAS p.Ala167Gly
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.Arg105Cys
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
MRAS p.His102Arg
Uncertain significance
Multiple submitters
Inborn genetic diseases
- MRAS p.Ile62Thr Uncertain significance Multiple submitters
-
MRAS p.Leu66Val
Uncertain significance
Multiple submitters
Noonan syndrome 11
-
MRAS p.Thr155Ser
Uncertain significance
Multiple submitters
Noonan syndrome 11
-
MRAS p.Thr84Met
Uncertain significance
Multiple submitters
Noonan syndrome 11
-
MRAS p.Val91Ile
Uncertain significance
Multiple submitters
Inborn genetic diseases
- MRAS p.Ala98Asp Uncertain significance Single submitter
-
MRAS p.Arg105Gly
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Asn163Ser Conflicting Single submitter
- MRAS p.Asp115Glu Uncertain significance Single submitter
- MRAS p.His132Tyr Uncertain significance Single submitter
- MRAS p.Leu11Pro Uncertain significance Single submitter
- MRAS p.Lys36Thr Uncertain significance Single submitter
- MRAS p.Met121Ile Uncertain significance Single submitter
- MRAS p.Met144Thr Uncertain significance Single submitter
- MRAS p.Pro160Leu Uncertain significance Single submitter
- MRAS p.Pro180Ala Uncertain significance Single submitter
-
MRAS p.Pro180Leu
Uncertain significance
Single submitter
Inborn genetic diseases
- MRAS p.Thr137Asn Uncertain significance Single submitter
All MRAS variants
Likely pathogenic 5
- p.Gln71Arg Expert panel RASopathy
- p.Gly23Arg Expert panel RASopathy
- p.Gly23Val Expert panel RASopathy
- p.Thr68Ile Expert panel RASopathy
- p.Pro120Leu Single submitter Male infertility with azoospermia or oligozoospermia due to single gene mutation
Conflicting classifications of pathogenicity 4
- p.Asn163Ser Single submitter ⚠
- p.Asp64= Single submitter Inborn genetic diseases
- p.Lys189del Single submitter
- p.Ser8Gly Single submitter Inborn genetic diseases ⚠
Benign 11
- c.528-2del Expert panel RASopathy
- p.Gln59= Expert panel RASopathy
- p.Pro151= Expert panel RASopathy
- c.193+110G>A Multiple submitters
- c.447+154A>G Multiple submitters
- c.-18-7G>T Multiple submitters
- c.*1011C>T Multiple submitters
- c.*87C>T Multiple submitters
- c.348-162C>G Single submitter
- c.*11G>T Single submitter
- c.*8G>C Single submitter
Benign/Likely benign 9
- p.Gly22= Multiple submitters Inborn genetic diseases
- p.His102= Multiple submitters Inborn genetic diseases
- p.Ile110= Multiple submitters Inborn genetic diseases
- p.Ile175= Multiple submitters Inborn genetic diseases
- p.Leu123= Multiple submitters Inborn genetic diseases
- p.Leu66= Multiple submitters Inborn genetic diseases
- p.Lys97= Multiple submitters Inborn genetic diseases
- p.Pro180= Multiple submitters Inborn genetic diseases
- p.Thr84= Multiple submitters Inborn genetic diseases
Likely benign 108
- c.347+11A>G Multiple submitters
- c.348-17G>A Multiple submitters
- c.447+12C>T Multiple submitters
- p.Ala5= Multiple submitters Inborn genetic diseases
- p.Arg112= Multiple submitters Inborn genetic diseases
- p.Asp96= Multiple submitters Inborn genetic diseases
- p.Gly87= Multiple submitters Inborn genetic diseases
- p.His53= Multiple submitters Inborn genetic diseases
- p.Ile46= Multiple submitters Inborn genetic diseases
- p.Ile90= Multiple submitters Inborn genetic diseases
- p.Leu203= Multiple submitters Inborn genetic diseases
- p.Leu63= Multiple submitters Inborn genetic diseases
- p.Leu89= Multiple submitters Inborn genetic diseases
- p.Lys147= Multiple submitters Inborn genetic diseases
- p.Phe38= Multiple submitters Inborn genetic diseases
- p.Pro120= Multiple submitters Inborn genetic diseases
- p.Pro44= Multiple submitters Inborn genetic diseases
- p.Ser4= Multiple submitters Inborn genetic diseases
- p.Ser75= Multiple submitters Inborn genetic diseases
- p.Thr137= Multiple submitters Inborn genetic diseases
- p.Thr155= Multiple submitters Inborn genetic diseases
- p.Thr54= Multiple submitters Inborn genetic diseases
- p.Thr95= Multiple submitters Inborn genetic diseases
- p.Tyr14= Multiple submitters Inborn genetic diseases
- p.Tyr152= Multiple submitters Inborn genetic diseases
- p.Val128= Multiple submitters Inborn genetic diseases
- p.Val18= Multiple submitters Inborn genetic diseases
- c.193+18G>T Single submitter
- c.193+7C>A Single submitter
- c.193+8C>G Single submitter
- c.194-10C>T Single submitter
- c.194-16C>T Single submitter
- c.194-5C>T Single submitter
- c.347+10A>C Single submitter
- c.347+13G>A Single submitter
- c.347+18G>A Single submitter
- c.347+6C>T Single submitter
- c.347+7A>G Single submitter
- c.348-10T>C Single submitter
- c.348-13C>G Single submitter
- c.348-13C>T Single submitter
- c.348-15T>G Single submitter
- c.348-17G>C Single submitter
- c.348-19C>T Single submitter
- c.348-4C>T Single submitter
- c.348-5C>T Single submitter
- c.447+13G>A Single submitter
- c.447+15G>T Single submitter
- c.447+19G>A Single submitter
- c.448-19G>C Single submitter
- c.448-4C>T Single submitter
- c.448-7C>T Single submitter
- c.527+10G>A Single submitter
- c.527+13C>A Single submitter
- c.527+14T>C Single submitter
- c.527+14T>G Single submitter
- c.527+15C>T Single submitter
- c.527+17C>T Single submitter
- c.527+18C>T Single submitter
- c.527+7A>G Single submitter
- c.527+8C>T Single submitter
- c.527+9T>C Single submitter
- c.528-11T>C Single submitter
- c.528-13A>G Single submitter
- c.528-18C>T Single submitter
- c.528-19T>C Single submitter
- c.528-6C>A Single submitter
- c.-7G>T Single submitter
- p.Ala145= Single submitter
- p.Ala157= Single submitter
- p.Ala28= Single submitter
- p.Arg105= Single submitter
- p.Arg116= Single submitter Inborn genetic diseases
- p.Arg134= Single submitter Inborn genetic diseases
- p.Arg196= Single submitter Inborn genetic diseases
- p.Asn10= Single submitter
- p.Asn163= Single submitter
- p.Asp21= Single submitter
- p.Asp43= Single submitter
- p.Asp57= Single submitter
- p.Gln108= Single submitter
- p.Gln204= Single submitter
- p.Gln80= Single submitter
- p.Glu139= Single submitter Inborn genetic diseases
- p.Glu143= Single submitter Inborn genetic diseases
- p.Glu79= Single submitter Inborn genetic diseases
- p.Gly20= Single submitter
- p.Gly85= Single submitter Inborn genetic diseases
- p.Ile207= Single submitter
- p.Leu111= Single submitter
- p.Lys15= Single submitter Inborn genetic diseases
- p.Lys166= Single submitter
- p.Lys26= Single submitter Inborn genetic diseases
- p.Pro12= Single submitter
- p.Pro40= Single submitter Inborn genetic diseases
- p.Pro7= Single submitter Inborn genetic diseases
- p.Ser118= Single submitter
- p.Ser27= Single submitter Inborn genetic diseases
- p.Ser93= Single submitter
- p.Thr13= Single submitter
- p.Thr200= Single submitter Inborn genetic diseases
- p.Thr68= Single submitter
- p.Tyr92= Single submitter
- p.Val124= Single submitter
- p.Val19= Single submitter
- p.Val39= Single submitter
- p.Val91= Single submitter Inborn genetic diseases
- p.Val94= Single submitter
Uncertain significance 121
- c.337_347+6dup Multiple submitters
- c.347+6_347+22del Multiple submitters Noonan syndrome 11
- c.347+6_347+22dup Multiple submitters
- p.Ala167Gly Multiple submitters Inborn genetic diseases ⚠
- p.Ala5Thr Multiple submitters Noonan syndrome 11 ⚠
- p.Arg105Cys Multiple submitters Inborn genetic diseases ⚠
- p.Arg112His Multiple submitters ⚠
- p.Arg193Gln Multiple submitters Inborn genetic diseases ⚠
- p.Asn10Ser Multiple submitters Inborn genetic diseases ⚠
- p.Asn126Lys Multiple submitters Inborn genetic diseases ⚠
- p.Asn126Ser Multiple submitters Inborn genetic diseases ⚠
- p.Gln178Lys Multiple submitters Inborn genetic diseases ⚠
- p.Glu117Gly Multiple submitters Inborn genetic diseases
- p.His102Arg Multiple submitters Inborn genetic diseases ⚠
- p.His169Arg Multiple submitters Inborn genetic diseases ⚠
- p.Ile62Thr Multiple submitters ⚠
- p.Leu111Arg Multiple submitters Inborn genetic diseases ⚠
- p.Leu203Arg Multiple submitters ⚠
- p.Leu66Val Multiple submitters Noonan syndrome 11 ⚠
- p.Lys189Asn Multiple submitters Inborn genetic diseases ⚠
- p.Phe100Leu Multiple submitters Inborn genetic diseases ⚠
- p.Pro12Ser Multiple submitters Inborn genetic diseases
- p.Pro44Ser Multiple submitters Inborn genetic diseases ⚠
- p.Ser183Asn Multiple submitters Inborn genetic diseases ⚠
- p.Thr13Ile Multiple submitters
- p.Thr155Ser Multiple submitters Noonan syndrome 11 ⚠
- p.Thr200Asn Multiple submitters Inborn genetic diseases ⚠
- p.Thr84Met Multiple submitters Noonan syndrome 11 ⚠
- p.Tyr92Ser Multiple submitters Inborn genetic diseases ⚠
- p.Val124Met Multiple submitters Inborn genetic diseases ⚠
- p.Val172Ile Multiple submitters Inborn genetic diseases ⚠
- p.Val6Ile Multiple submitters Inborn genetic diseases ⚠
- p.Val91Ile Multiple submitters Inborn genetic diseases ⚠
- c.194-9C>A Single submitter
- c.347+3G>A Single submitter
- c.347+4A>G Single submitter
- c.-14G>A Single submitter
- c.-7G>A Single submitter
- c.*6C>G Single submitter
- p.Ala145Glu Single submitter Inborn genetic diseases ⚠
- p.Ala145Val Single submitter ⚠
- p.Ala197Ser Single submitter ⚠
- p.Ala61Thr Single submitter
- p.Ala61Val Single submitter Inborn genetic diseases
- p.Ala98Asp Single submitter ⚠
- p.Ala98Thr Single submitter ⚠
- p.Arg105Gly Single submitter Inborn genetic diseases ⚠
- p.Arg105His Single submitter ⚠
- p.Arg112Cys Single submitter ⚠
- p.Arg138Lys Single submitter ⚠
- p.Arg193Trp Single submitter Inborn genetic diseases
- p.Arg196Gln Single submitter Inborn genetic diseases ⚠
- p.Arg196Trp Single submitter
- p.Arg78Trp Single submitter ⚠
- p.Arg83His Single submitter ⚠
- p.Asn10Asp Single submitter ⚠
- p.Asn149Ser Single submitter ⚠
- p.Asn58Ser Single submitter ⚠
- p.Asp115Glu Single submitter ⚠
- p.Asp165Asn Single submitter
- p.Asp170Asn Single submitter
- p.Asp170Glu Single submitter ⚠
- p.Asp170Val Single submitter ⚠
- p.Asp41fs Single submitter
- p.Asp57Asn Single submitter Inborn genetic diseases ⚠
- p.Asp9Glu Single submitter ⚠
- p.Gln59His Single submitter ⚠
- p.Glu117Asp Single submitter ⚠
- p.Glu117Val Single submitter
- p.Glu55Asp Single submitter Inborn genetic diseases ⚠
- p.Glu79Gln Single submitter Inborn genetic diseases ⚠
- p.Gly70Arg Single submitter ⚠
- p.Gly85Glu Single submitter Inborn genetic diseases ⚠
- p.His132Arg Single submitter Inborn genetic diseases
- p.His132Tyr Single submitter ⚠
- p.His169_Asp170insAlaPheHis Single submitter
- p.His201Arg Single submitter ⚠
- p.His201Tyr Single submitter Inborn genetic diseases ⚠
- p.Ile136Val Single submitter Inborn genetic diseases ⚠
- p.Ile153Leu Single submitter ⚠
- p.Ile153Val Single submitter ⚠
- p.Ile179Met Single submitter ⚠
- p.Ile46Phe Single submitter Noonan syndrome 11 ⚠
- p.Ile62Val Single submitter ⚠
- p.Ile90Val Single submitter Inborn genetic diseases ⚠
- p.Leu11Pro Single submitter ⚠
- p.Leu123Val Single submitter
- p.Leu133Ser Single submitter
- p.Leu162Val Single submitter Inborn genetic diseases ⚠
- p.Leu29Arg Single submitter ⚠
- p.Leu29Phe Single submitter ⚠
- p.Leu66Gln Single submitter Inborn genetic diseases ⚠
- p.Lys142Gln Single submitter ⚠
- p.Lys186Thr Single submitter ⚠
- p.Lys189_Thr190insLys Single submitter
- p.Lys36Thr Single submitter ⚠
- p.Met121Ile Single submitter ⚠
- p.Met131Lys Single submitter Inborn genetic diseases ⚠
- p.Met144Thr Single submitter ⚠
- p.Pro12Arg Single submitter Inborn genetic diseases
- p.Pro151Leu Single submitter ⚠
- p.Pro160Leu Single submitter ⚠
- p.Pro180Ala Single submitter ⚠
- p.Pro180Leu Single submitter Inborn genetic diseases ⚠
- p.Ser183fs Single submitter
- p.Ser27Thr Single submitter Inborn genetic diseases ⚠
- p.Ser8Thr Single submitter ⚠
- p.Thr137Asn Single submitter ⚠
- p.Thr137Ile Single submitter ⚠
- p.Thr198Arg Single submitter Inborn genetic diseases ⚠
- p.Thr45Ser Single submitter ⚠
- p.Thr54fs Single submitter
- p.Thr54Lys Single submitter ⚠
- p.Thr54Met Single submitter ⚠
- p.Trp192Ter Single submitter
- p.Tyr92Cys Single submitter ⚠
- p.Val103Met Single submitter ⚠
- p.Val113Ile Single submitter Inborn genetic diseases
- p.Val91Ala Single submitter ⚠
- p.Val91Leu Single submitter ⚠
- p.Val94Ile Single submitter ⚠