Is ANK2 p.Asp3051= (c.9153C>T) pathogenic?

ANK2 p.Asp3051= (c.9153C>T) is classified Likely benign in ANK2 (ClinVar, Multiple submitters, 4 submitters; last evaluated 2025-05-11). Ultra-rare (popmax 0.0461%, sas); Associated with long QT syndrome.

What condition is associated with ANK2 p.Asp3051= (c.9153C>T)?

ANK2 p.Asp3051= (c.9153C>T) is associated with long QT syndrome (ClinVar).

How common is ANK2 p.Asp3051= (c.9153C>T) in the general population?

ANK2 p.Asp3051= (c.9153C>T) is ultra-rare (popmax 0.0461%, sas) (gnomAD).

ANK2 p.Asp3051=

c.9153C>T · rs144397802 · VCV704309

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 4 submitters

gnomAD v4.1

Rare

ultra-rare (popmax 0.0461%, sas)

Conditions

long QT syndrome

Computational evidence

Protein change
Missense predictors do not apply to this variant type; conservation carries the signal.
Splicing
SpliceAI	<0.2	no splice effect predicted · four deltas, not one · how we know
Constraint at this position
Conservation	phyloP -4.8	GERP -5.7
Overall
CADD	1.299	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.0461% South Asian · 42/91,072 alleles

Filtering AF 0.035% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0311%

Overall 0.00514% 83/1,613,914 alleles · ultra-rare exomes 76/1,461,736 · genomes 7/152,178 · joint denominator

Ancestry group	Frequency	1 in
South Asiangrpmax	0.0461%	2,168
African / African-American	0.00534%	18,743
Remaining individualsnot grpmax-eligible	0.0048%	20,834
European (non-Finnish)	0.0028%	35,756
East Asian	0.00223%	44,870

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: ANK2
Protein: p.Asp3051=
Coding: c.9153C>T
MANE Select: NM_001148
dbSNP: rs144397802
Type: single nucleotide variant
Location: chr4:113357771 (GRCh38)
Gene constraint: LOEUF 0.271 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)

Full ANK2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

long QT syndrome — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

ANK2 p.Arg3113Ter Pathogenic ★★ same condition
ANK2 c.11611-3T>A Uncertain significance ★★ same condition
ANK2 c.1783-3C>T Uncertain significance ★★ same condition
ANK2 c.2079+5T>G Uncertain significance ★★ same condition
ANK2 c.2278-3C>T Uncertain significance ★★ same condition
ANK2 c.3125+6G>A Uncertain significance ★★ same condition
ANK2 c.693+6G>A Uncertain significance ★★ same condition
ANK2 c.85-3C>T 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/ank2-p-asp3051 (accessed [today's date]).

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