Is SAMD9L p.Phe762= (c.2286C>T) pathogenic?

SAMD9L p.Phe762= (c.2286C>T) is classified Likely benign in SAMD9L (ClinVar, Multiple submitters, 2 submitters; last evaluated 2025-05-27). Ultra-rare (popmax 0.0209%, sas); Associated with Inborn genetic diseases.

What condition is associated with SAMD9L p.Phe762= (c.2286C>T)?

SAMD9L p.Phe762= (c.2286C>T) is associated with Inborn genetic diseases (ClinVar).

How common is SAMD9L p.Phe762= (c.2286C>T) in the general population?

SAMD9L p.Phe762= (c.2286C>T) is ultra-rare (popmax 0.0209%, sas) (gnomAD).

SAMD9L p.Phe762=

c.2286C>T · rs746907720 · VCV2963569

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0209%, sas)

Conditions

Inborn genetic diseases

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 3.7	phastCons 1
Overall
CADD	4.689	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0209% South Asian · 19/91,010 alleles

Filtering AF 0.0136% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0114%

Overall 0.0013% 21/1,613,422 alleles · ultra-rare exomes 20/1,461,330 · genomes 1/152,092 · joint denominator

Ancestry group	Frequency	1 in
South Asiangrpmax	0.0209%	4,790
Middle Eastern	0.0164%	6,080
European (non-Finnish)	8.48e-05%	1,179,842

Rarity supports pathogenicity (ACMG PM2); frequency above a disease-specific BA1/BS1 threshold argues against it. A variant frequent in one ancestry group can be near-absent in others, so a single global figure can mislead.

Variant & gene context

Gene: SAMD9L
Protein: p.Phe762=
Coding: c.2286C>T
MANE Select: NM_152703
dbSNP: rs746907720
Type: single nucleotide variant
Location: chr7:93133686 (GRCh38)
Gene constraint: LOEUF 0.876 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 83.85

Full SAMD9L gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

SAMD9L p.Ala1073Thr Uncertain significance ★★ ⚠ same condition
SAMD9L p.Ala1087Asp Uncertain significance ★★ ⚠ same condition
SAMD9L p.Ala1106Thr Uncertain significance ★★ ⚠ same condition
SAMD9L p.Ala1106Val Uncertain significance ★★ ⚠ same condition
SAMD9L p.Ala1109Pro Uncertain significance ★★ ⚠ same condition
SAMD9L p.Ala1156Glu Uncertain significance ★★ ⚠ same condition
SAMD9L p.Ala1156Ser Uncertain significance ★★ ⚠ same condition
SAMD9L p.Ala1159Pro Uncertain significance ★★ ⚠ same condition

Built on 18 open, versioned datasets — ClinVar, gnomAD, AlphaMissense, REVEL, ClinGen & more — plus Sugi Variant's own cross-source analysis. Source data 2026-01–2026-10, ClinVar 2026-10. Full sources & versions →

Cite Sugi Variant

Gür T. Sugi Variant: A Deterministic Per-Variant Germline Reference from a Knowledge Graph for Humans and AI Agents. 2026. doi:10.5281/zenodo.21509445. This variant: https://sugi.bio/variant/samd9l-p-phe762 (accessed [today's date]).

Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown