Is DCAF13 p.Asp372His (c.1114G>C) pathogenic?

DCAF13 p.Asp372His (c.1114G>C) is classified Uncertain significance in DCAF13 (ClinVar, Single submitter, 1 submitter; last evaluated 2021-09-14). AlphaMissense: likely benign (0.1259); Ultra-rare (popmax 0.0371%, amr).

How common is DCAF13 p.Asp372His (c.1114G>C) in the general population?

DCAF13 p.Asp372His (c.1114G>C) is ultra-rare (popmax 0.0371%, amr) (gnomAD).

What do computational predictors say about DCAF13 p.Asp372His (c.1114G>C)?

AlphaMissense predicts likely benign (score 0.1259) — an in-silico prediction, not a clinical call.

DCAF13 p.Asp372His

c.1114G>C · rs924457710 · VCV2210601

Uncertain significance Single submitter

Classification

Uncertain significance

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

AlphaMissense

likely benign

0.1259 · ACMG-weighted

gnomAD v4.1

Rare

ultra-rare (popmax 0.0371%, amr)

Missense predictors

1/2 damaging

AlphaMissense, SaProt · REVEL no call

Computational evidence

Protein change
AlphaMissense	0.1259	likely benign
REVEL	0.358	indeterminate
SaProt	LLR -10.31	damaging
⇒ SaProt calls this damaging; AlphaMissense does not; REVEL makes no call.
Splicing
SpliceAI	—	not assessed · no allele here is in the release
Constraint at this position
Conservation	phyloP 5.7	GERP 1.1, phastCons 1
Regional constraint	o/e 0.45	unconstrained · MANE · 1,349 bp · p 6e-06 · regional, not allelic
Overall
CADD	23.0	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 0.0371% Admixed American · 20/53,882 alleles

Filtering AF 0.0245% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.0205%

Overall 0.00175% 28/1,595,932 alleles · ultra-rare

Ancestry group	Frequency	1 in
Admixed Americangrpmax	0.0371%	2,694
Remaining individualsnot grpmax-eligible	0.00324%	30,900
African / African-American	0.00136%	73,414
European (non-Finnish)	0.000425%	235,091

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: DCAF13
Protein: p.Asp372His
Coding: c.1114G>C
MANE Select: NM_015420
dbSNP: rs924457710
Type: single nucleotide variant
Location: chr8:103441482 (GRCh38)
Gene constraint: LOEUF 0.848 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 92.84 · 3 PDB
Residue 372: an α-helix; the 'required for nucleolar location' region

Full DCAF13 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Similar variants

DCAF13 p.His327Arg Uncertain significance ★★ ⚠ same type
DCAF13 p.Phe381Cys Uncertain significance ★★ ⚠ same type
DCAF13 p.Ala109Gly Benign ★★ same type
DCAF13 p.Ala70= Benign ★★ same type
DCAF13 c.-20C>T Uncertain significance ★ same type
DCAF13 c.-30T>C Uncertain significance ★ same type
DCAF13 c.-33A>G Uncertain significance ★ same type
DCAF13 c.-38C>A Uncertain significance ★ same type

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/dcaf13-p-asp372his (accessed [today's date]).

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