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AMER1 p.Ser715=

c.2145T>C · rs1569191703 · VCV2981422

Likely benign Single submitter
Classification
Likely benign
ClinVar
Review
Single submitter ★☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
very rare (popmax 0.000112%, nfe)

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
ConservationphyloP 3.3GERP 1.9, phastCons 1
Overall
CADD7.969PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes
Grpmax group 0.000112% European (non-Finnish) · 1/895,645 alleles
Overall 9.11e-05% 1/1,098,261 alleles · very rare

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
AMER1
Protein
p.Ser715=
Coding
c.2145T>C
MANE Select
NM_152424
dbSNP
rs1569191703
Type
single nucleotide variant
Location
chrX:64191142 (GRCh38)
Structure
AlphaFold pLDDT 48.88 · 3 PDB
Full AMER1 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/amer1-p-ser715 (accessed [today's date]).

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