RRAS2 — 83 ClinVar variants
All ClinVar germline RRAS2 variants across every classification, each assembled from ClinVar, gnomAD, AlphaMissense, conservation and more. 35 flagged for review →
1 Pathogenic · 2 Likely pathogenic · 9 Benign · 2 Benign/Likely benign · 23 Likely benign · 46 Uncertain significance
Full RRAS2 gene report on Sugi Atlas → Gene function, pathways, protein structure, constraint & interactions⚑ Evidence disagreements 35
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 lean, ClinVar uncertain 32
ClinVar classifies these uncertain (VUS), but the independent predictors unanimously lean one way — a triage signal for review, not a reclassification.
-
RRAS2 p.Arg147Gln
Uncertain significance
Multiple submitters
Noonan syndrome
-
RRAS2 p.Arg191Trp
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
RRAS2 p.Lys150Thr
Uncertain significance
Multiple submitters
RRAS2-related disorder
-
RRAS2 p.Pro45Ala
Uncertain significance
Multiple submitters
Inborn genetic diseases
-
RRAS2 p.Tyr105Cys
Uncertain significance
Multiple submitters
Inborn genetic diseases
- RRAS2 p.Arg117Cys Uncertain significance Single submitter
-
RRAS2 p.Arg117Gly
Uncertain significance
Single submitter
RRAS2-related disorder
-
RRAS2 p.Arg117His
Uncertain significance
Single submitter
Inborn genetic diseases
-
RRAS2 p.Arg147Trp
Uncertain significance
Single submitter
noonan syndrome 12
- RRAS2 p.Arg173Trp Uncertain significance Single submitter
- RRAS2 p.Asn163Lys Uncertain significance Single submitter
- RRAS2 p.Asp44Tyr Uncertain significance Single submitter
-
RRAS2 p.Cys201Trp
Uncertain significance
Single submitter
Inborn genetic diseases
-
RRAS2 p.Gln110His
Uncertain significance
Single submitter
RRAS2-related disorder
- RRAS2 p.Gln33Arg Uncertain significance Single submitter
-
RRAS2 p.Gln33His
Uncertain significance
Single submitter
RRAS2-related disorder
- RRAS2 p.Gly88Ala Uncertain significance Single submitter
-
RRAS2 p.Ile125Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
RRAS2 p.Ile175Val
Uncertain significance
Single submitter
Inborn genetic diseases
-
RRAS2 p.Ile47Val
Uncertain significance
Single submitter
noonan syndrome 12
- RRAS2 p.Leu145Phe Uncertain significance Single submitter
- RRAS2 p.Leu64Pro Uncertain significance Single submitter
- RRAS2 p.Leu91Met Uncertain significance Single submitter
-
RRAS2 p.Lys194Arg
Uncertain significance
Single submitter
Inborn genetic diseases
-
RRAS2 p.Met162Val
Uncertain significance
Single submitter
Inborn genetic diseases
- RRAS2 p.Met78Leu Uncertain significance Single submitter
- RRAS2 p.Met83Leu Uncertain significance Single submitter
-
RRAS2 p.Pro187Arg
Uncertain significance
Single submitter
noonan syndrome 12
- RRAS2 p.Thr96Ile Uncertain significance Single submitter
- RRAS2 p.Tyr82Cys Uncertain significance Single submitter
- RRAS2 p.Val151Ile Uncertain significance Single submitter
-
RRAS2 p.Val92Ile
Uncertain significance
Single submitter
Inborn genetic diseases
Predictors split 3
The independent predictors disagree with each other — read with care.
All RRAS2 variants
Pathogenic 1
- p.Gln72Leu Expert panel Noonan syndrome
Likely pathogenic 2
- p.Ala70Thr Expert panel RASopathy
- p.Gly71Glu Single submitter
Benign 9
- c.409-16A>T Expert panel RASopathy
- c.299+19T>C Multiple submitters
- c.300-4del Multiple submitters
- c.408+102G>A Multiple submitters
- c.-2C>T Multiple submitters
- c.*124G>C Multiple submitters
- c.300-4dup Single submitter
- c.408+98dup Single submitter
- p.Thr138Ser Single submitter
Likely benign 23
- p.Arg173= Multiple submitters
- c.108+5C>T Single submitter
- c.109-7C>A Single submitter
- c.197-7T>A Single submitter
- c.299+12A>C Single submitter
- c.300-4T>G Single submitter
- c.408+17C>T Single submitter
- c.528-18G>T Single submitter
- c.-1C>A Single submitter
- p.Ala70= Single submitter
- p.Asp195Glu Single submitter
- p.Gln134= Single submitter
- p.Gly86= Single submitter
- p.Ile203= Single submitter
- p.Leu112= Single submitter
- p.Phe204= Single submitter
- p.Phe39= Single submitter
- p.Pro45= Single submitter
- p.Thr41= Single submitter
- p.Val151= Single submitter
- p.Val202= Single submitter
- p.Val92= Single submitter
- p.Thr46= No assertion criteria RRAS2-related disorder
Uncertain significance 46
- p.Arg147Gln Multiple submitters Noonan syndrome ⚠
- p.Arg191Trp Multiple submitters Inborn genetic diseases ⚠
- p.Lys150Thr Multiple submitters RRAS2-related disorder ⚠
- p.Pro45Ala Multiple submitters Inborn genetic diseases ⚠
- p.Thr41Met Multiple submitters RRAS2-related disorder
- p.Tyr105Cys Multiple submitters Inborn genetic diseases ⚠
- c.108+509A>G Single submitter
- c.196+9A>G Single submitter
- c.528-2A>C Single submitter
- p.Arg117Cys Single submitter ⚠
- p.Arg117Gly Single submitter RRAS2-related disorder ⚠
- p.Arg117His Single submitter Inborn genetic diseases ⚠
- p.Arg147Trp Single submitter noonan syndrome 12 ⚠
- p.Arg173Trp Single submitter ⚠
- p.Arg63Gln Single submitter
- p.Asn163Lys Single submitter ⚠
- p.Asp44Tyr Single submitter ⚠
- p.Asp65= Single submitter
- p.Cys199Ser Single submitter ⚠
- p.Cys201Trp Single submitter Inborn genetic diseases ⚠
- p.Gln110His Single submitter RRAS2-related disorder ⚠
- p.Gln33Arg Single submitter ⚠
- p.Gln33His Single submitter RRAS2-related disorder ⚠
- p.Glu182Asp Single submitter ⚠
- p.Gly88Ala Single submitter ⚠
- p.Ile125Val Single submitter Inborn genetic diseases ⚠
- p.Ile175Val Single submitter Inborn genetic diseases ⚠
- p.Ile47Val Single submitter noonan syndrome 12 ⚠
- p.Ile66Val Single submitter Inborn genetic diseases
- p.Leu145Phe Single submitter ⚠
- p.Leu64Pro Single submitter ⚠
- p.Leu91Met Single submitter ⚠
- p.Lys106Asn Single submitter ⚠
- p.Lys194Arg Single submitter Inborn genetic diseases ⚠
- p.Lys197Ter Single submitter
- p.Met122Leu Single submitter
- p.Met162Val Single submitter Inborn genetic diseases ⚠
- p.Met1Thr Single submitter
- p.Met78Leu Single submitter ⚠
- p.Met83Leu Single submitter ⚠
- p.Pro187Arg Single submitter noonan syndrome 12 ⚠
- p.Thr96Ile Single submitter ⚠
- p.Tyr82Cys Single submitter ⚠
- p.Val151Ile Single submitter ⚠
- p.Val164Ile Single submitter noonan syndrome 12
- p.Val92Ile Single submitter Inborn genetic diseases ⚠