Is ANKRD1 p.Ser62= (c.186C>T) pathogenic?

ANKRD1 p.Ser62= (c.186C>T) is classified Likely benign in ANKRD1 (ClinVar, Single submitter, 1 submitter; last evaluated 2021-02-04). Very rare (popmax 0.00769%, sas); Associated with Cardiovascular phenotype.

What condition is associated with ANKRD1 p.Ser62= (c.186C>T)?

ANKRD1 p.Ser62= (c.186C>T) is associated with Cardiovascular phenotype (ClinVar).

How common is ANKRD1 p.Ser62= (c.186C>T) in the general population?

ANKRD1 p.Ser62= (c.186C>T) is very rare (popmax 0.00769%, sas) (gnomAD).

ANKRD1 p.Ser62=

c.186C>T · rs766962252 · VCV1781649

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 0.00769%, sas)

Conditions

Cardiovascular phenotype

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
Conservation	phyloP -0.75	GERP -4.8
Overall
CADD	6.31	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00769% South Asian · 7/91,046 alleles

Filtering AF 0.00359% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00255%

Overall 0.00093% 15/1,613,690 alleles · very rare exomes 14/1,461,674 · genomes 1/152,016 · joint denominator

Ancestry group	Frequency	1 in
South Asiangrpmax	0.00769%	13,007
Admixed American	0.005%	19,995
European (non-Finnish)	0.000424%	235,999

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: ANKRD1
Protein: p.Ser62=
Coding: c.186C>T
MANE Select: NM_014391
dbSNP: rs766962252
Type: single nucleotide variant
Location: chr10:90920190 (GRCh38)
Gene constraint: LOEUF 1.038 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 82.64

Full ANKRD1 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Cardiovascular phenotype — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

ANKRD1 c.207+1G>T Uncertain significance ★★ same condition
ANKRD1 c.27+1G>T Uncertain significance ★★ same condition
ANKRD1 c.28-3T>C Uncertain significance ★★ same condition
ANKRD1 c.651+4T>A Uncertain significance ★★ same condition
ANKRD1 c.750+2T>C Uncertain significance ★★ same condition
ANKRD1 c.750+4A>G Uncertain significance ★★ same condition
ANKRD1 c.751-3T>C Uncertain significance ★★ same condition
ANKRD1 p.Ala156Pro 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/ankrd1-p-ser62 (accessed [today's date]).

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