Is ANK1 p.Val905Met (c.2713G>A) pathogenic?

ANK1 p.Val905Met (c.2713G>A) is classified Uncertain significance in ANK1 (ClinVar, Multiple submitters, 3 submitters; last evaluated 2025-12-11). AlphaMissense: ambiguous (0.4008); Ultra-rare (popmax 0.045%, nfe); Associated with hereditary spherocytosis type 1.

What condition is associated with ANK1 p.Val905Met (c.2713G>A)?

ANK1 p.Val905Met (c.2713G>A) is associated with hereditary spherocytosis type 1 (ClinVar).

How common is ANK1 p.Val905Met (c.2713G>A) in the general population?

ANK1 p.Val905Met (c.2713G>A) is ultra-rare (popmax 0.045%, nfe) (gnomAD).

How is Hereditary spherocytosis inherited?

Typically Autosomal dominant, Autosomal recessive (Orphanet). A genetic counselor can assess individual risk for a family.

What do computational predictors say about ANK1 p.Val905Met (c.2713G>A)?

AlphaMissense predicts ambiguous (score 0.4008) — an in-silico prediction, not a clinical call.

ANK1 p.Val905Met

c.2713G>A · rs141069023 · VCV910879

Uncertain significance Multiple submitters

Classification

Uncertain significance

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 3 submitters

AlphaMissense

ambiguous

0.4008 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.045%, nfe)

Missense predictors

0/2 damaging

REVEL, SaProt · AlphaMissense no call

Conditions

hereditary spherocytosis type 1

Computational evidence

Protein change
AlphaMissense	0.4008	ambiguous
REVEL	0.29	benign-leaning
SaProt	LLR -6.47	tolerated
⇒ REVEL and SaProt both call this tolerated; AlphaMissense makes no call.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 7.6	GERP 2, phastCons 1
Regional constraint	o/e 0.83	unconstrained · MANE · 38 kb · p 1e-12 · regional, not allelic
Overall
CADD	25.3	PHRED · 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

Grpmax group 0.045% European (non-Finnish) · 531/1,179,928 alleles

Filtering AF 0.0418% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0405%

Overall 0.0352% 564/1,603,386 alleles · ultra-rare

Ancestry group	Frequency	1 in
European (non-Finnish)grpmax	0.045%	2,222
Remaining individualsnot grpmax-eligible	0.0336%	2,972
Admixed American	0.0117%	8,572
African / African-American	0.00668%	14,974

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: ANK1
Protein: p.Val905Met
Coding: c.2713G>A
MANE Select: NM_000037
dbSNP: rs141069023
Type: single nucleotide variant
Location: chr8:41696698 (GRCh38)
Gene constraint: LOEUF 0.299 · pLI 1.00 (gnomAD)
Structure: AlphaFold pLDDT 69.64 · 21 PDB

Full ANK1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

hereditary spherocytosis type 1 — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Hereditary spherocytosis (Orphanet):

Inheritance: Autosomal dominant, Autosomal recessive
Onset: All ages
Prevalence: 1-5 / 10 000 (Germany)

Similar variants

ANK1 c.1305+1G>A Pathogenic ★★ same condition
ANK1 c.1405-9G>A Pathogenic/Likely pathogenic ★★ same condition
ANK1 c.1702-2A>G Pathogenic/Likely pathogenic ★★ same condition
ANK1 c.1801-17G>A Pathogenic/Likely pathogenic ★★ same condition
ANK1 c.2296-1G>A Likely pathogenic ★★ same condition
ANK1 c.2296-2A>G Pathogenic/Likely pathogenic ★★ same condition
ANK1 c.2389-2A>G Likely pathogenic ★★ same condition
ANK1 c.2462-2A>G Pathogenic ★★ 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/ank1-p-val905met (accessed [today's date]).

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