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C7 p.Trp443Cys

c.1329G>C · VCV4772442

Uncertain significance Single submitter
Classification
Uncertain significance
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
AlphaMissense
ambiguous
0.4523 · ACMG-weighted
gnomAD v4.1
Absent
absent from gnomAD v4.1

Computational evidence

Protein change
AlphaMissense0.4523ambiguous
REVEL0.342indeterminate
SaProtLLR -9.29tolerated
Splicing
SpliceAI—not assessed · no allele here is in the release
Constraint at this position
ConservationphyloP 0.39GERP -0.45, phastCons 0.97
Overall
CADD21.4PHRED · no single calibrated threshold — expert panels disagree

AlphaMissense carries the ACMG weight for missense; REVEL and SaProt are independent agreement signals.

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
C7
Protein
p.Trp443Cys
Coding
c.1329G>C
MANE Select
NM_001565 · reported on NM_000587
Type
single nucleotide variant
Location
chr5:40958101 (GRCh38)
Structure
AlphaFold pLDDT 89.67 · 6 PDB
Full C7 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/c7-p-trp443cys (accessed [today's date]).

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