Is TXNRD2 p.Ala234= (c.702T>C) pathogenic?

TXNRD2 p.Ala234= (c.702T>C) is classified Likely benign in TXNRD2 (ClinVar, Single submitter, 1 submitter; last evaluated 2021-12-02). Very rare (popmax 8.66e-05%, nfe); Associated with dilated cardiomyopathy.

What condition is associated with TXNRD2 p.Ala234= (c.702T>C)?

TXNRD2 p.Ala234= (c.702T>C) is associated with dilated cardiomyopathy (ClinVar).

How common is TXNRD2 p.Ala234= (c.702T>C) in the general population?

TXNRD2 p.Ala234= (c.702T>C) is very rare (popmax 8.66e-05%, nfe) (gnomAD).

TXNRD2 p.Ala234=

c.702T>C · rs1165554583 · VCV2183249

Likely benign Single submitter

Classification

Likely benign

ClinVar

Review

Single submitter ★☆☆☆

ClinVar · 1 submitter

gnomAD v4.1

Rare

very rare (popmax 8.66e-05%, nfe)

Conditions

dilated cardiomyopathy

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 -5.3	GERP -3.5
Overall
CADD	5.19	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 8.66e-05% European (non-Finnish) · 1/1,154,770 alleles

Overall 6.39e-05% 1/1,564,662 alleles · very rare exomes 1/1,412,308 · genomes 0/152,354 · joint denominator

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: TXNRD2
Protein: p.Ala234=
Coding: c.702T>C
MANE Select: NM_006440
dbSNP: rs1165554583
Type: single nucleotide variant
Location: chr22:19898111 (GRCh38)
Gene constraint: LOEUF 1.18 · pLI <0.01 (gnomAD)

Full TXNRD2 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

dilated cardiomyopathy — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

Similar variants

TXNRD2 c.104-1G>A Uncertain significance ★★ same condition
TXNRD2 c.104-3C>G Uncertain significance ★★ same condition
TXNRD2 c.1086+4C>T Uncertain significance ★★ same condition
TXNRD2 c.1087-2A>G Uncertain significance ★★ same condition
TXNRD2 c.1348-2A>G Uncertain significance ★★ same condition
TXNRD2 c.1348-9G>A Uncertain significance ★★ same condition
TXNRD2 c.1445+5G>C Uncertain significance ★★ same condition
TXNRD2 c.172+3A>G 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/txnrd2-p-ala234 (accessed [today's date]).

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