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SARS2 p.Val351=

c.1053G>A · rs2513526772 · VCV2834061

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Absent
absent from gnomAD v4.1

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation/SpliceAI carries the signal.
Splicing
SpliceAIΔ0.35acceptor gain · deltas
PangolinΔ0.44gain · loss 0.14 · agrees with SpliceAI · independent
Constraint at this position
ConservationphyloP 0.97GERP -0.63, phastCons 1
Overall
CADD17.43PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Absent from gnomAD v4.1. Not observed in any sequenced alleles — a rarity signal (ACMG PM2-supporting), not evidence of pathogenicity on its own.

Variant & gene context

Gene
SARS2
Protein
p.Val351=
Coding
c.1053G>A
MANE Select
NM_017827
dbSNP
rs2513526772
Type
single nucleotide variant
Location
chr19:38917831 (GRCh38)
Gene constraint
LOEUF 1.02 · pLI <0.01 (gnomAD)
Structure
AlphaFold pLDDT 90.58 · 6 PDB
Residue 351
a β-strand
Full SARS2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

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/sars2-p-val351 (accessed [today's date]).

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