Is ANKRD11 p.Ser614= (c.1842C>T) pathogenic?

ANKRD11 p.Ser614= (c.1842C>T) is classified Benign/Likely benign in ANKRD11 (ClinVar, Multiple submitters, 5 submitters; last evaluated 2024-11-18). Rare (popmax 0.227%, amr); Associated with Inborn genetic diseases.

What condition is associated with ANKRD11 p.Ser614= (c.1842C>T)?

ANKRD11 p.Ser614= (c.1842C>T) is associated with Inborn genetic diseases, KBG syndrome (ClinVar).

How common is ANKRD11 p.Ser614= (c.1842C>T) in the general population?

ANKRD11 p.Ser614= (c.1842C>T) is rare (popmax 0.227%, amr) (gnomAD).

ANKRD11 p.Ser614=

c.1842C>T · rs764479350 · VCV588770

Benign/Likely benign Multiple submitters

Classification

Benign/Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 5 submitters

gnomAD v4.1

Rare

rare (popmax 0.227%, amr)

Conditions

Inborn genetic diseases

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 -3.9	GERP -3.7
Overall
CADD	0.539	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.227% Admixed American · 136/60,002 alleles

Filtering AF 0.196% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.184%

Overall 0.0107% 172/1,613,758 alleles · rare

Ancestry group	Frequency	1 in
Admixed Americangrpmax	0.227%	441
South Asian	0.0154%	6,506
Finnishnot grpmax-eligible	0.011%	9,115
Remaining individualsnot grpmax-eligible	0.0016%	62,484
African / African-American	0.00134%	74,892
European (non-Finnish)	0.0011%	90,771

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: ANKRD11
Protein: p.Ser614=
Coding: c.1842C>T
MANE Select: NM_013275
dbSNP: rs764479350
Type: single nucleotide variant
Location: chr16:89284700 (GRCh38)
Gene constraint: LOEUF 0.132 · pLI 1.00 · ClinGen HI 3/3 (gnomAD)
Structure: AlphaFold pLDDT 39.44
Residue 614: the 'disordered' region

Full ANKRD11 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

Inborn genetic diseases — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Also linked: KBG syndrome

Similar variants

ANKRD11 c.744+1G>T Pathogenic ★★ same condition
ANKRD11 c.745-2A>G Likely pathogenic ★★ same condition
ANKRD11 c.7470+1G>C Pathogenic ★★ same condition
ANKRD11 c.7569+1G>A Pathogenic ★★ same condition
ANKRD11 c.7569+1G>C Likely pathogenic ★★ same condition
ANKRD11 c.7570-1G>A Pathogenic ★★ same condition
ANKRD11 c.892+1G>A Likely pathogenic ★★ same condition
ANKRD11 p.Arg1007Ter Pathogenic/Likely 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/ankrd11-p-ser614 (accessed [today's date]).

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