Is TRPM4 p.Val787= (c.2361G>A) pathogenic?

TRPM4 p.Val787= (c.2361G>A) is classified Likely benign in TRPM4 (ClinVar, Multiple submitters, 2 submitters; last evaluated 2025-12-29). Very rare (popmax 0.00573%, amr); Associated with progressive familial heart block type IB.

What condition is associated with TRPM4 p.Val787= (c.2361G>A)?

TRPM4 p.Val787= (c.2361G>A) is associated with progressive familial heart block type IB (ClinVar).

How common is TRPM4 p.Val787= (c.2361G>A) in the general population?

TRPM4 p.Val787= (c.2361G>A) is very rare (popmax 0.00573%, amr) (gnomAD).

TRPM4 p.Val787=

Q: How is Hereditary progressive cardiac conduction defect inherited?

Typically Autosomal dominant (Orphanet). A genetic counselor can assess individual risk for a family.

c.2361G>A · rs367649770 · VCV698271

Likely benign Multiple submitters

Classification

Likely benign

ClinVar

Review

Multiple submitters ★★☆☆

ClinVar · 2 submitters

gnomAD v4.1

Rare

very rare (popmax 0.00573%, amr)

Conditions

progressive familial heart block type IB

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 8	phastCons 1
Overall
CADD	14.08	PHRED · no single calibrated threshold — expert panels disagree

Population frequency

gnomAD v4.1 · exomes + genomes

Grpmax group 0.00573% Admixed American · 3/52,358 alleles

Filtering AF 0.00289% ClinGen BA1/BS1 input FAF95, joint · FAF99 0.00257%

Overall 0.00321% 50/1,557,342 alleles · very rare exomes 40/1,405,136 · genomes 10/152,206 · joint denominator

Ancestry group	Frequency	1 in
Admixed Americangrpmax	0.00573%	17,453
European (non-Finnish)	0.00381%	26,225
Remaining individualsnot grpmax-eligible	0.00331%	30,247
South Asian	0.00118%	84,998

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: TRPM4
Protein: p.Val787=
Coding: c.2361G>A
MANE Select: NM_017636
dbSNP: rs367649770
Type: single nucleotide variant
Location: chr19:49196590 (GRCh38)
Gene constraint: LOEUF 1.084 · pLI <0.01 (gnomAD)
Structure: AlphaFold pLDDT 78.51 · 42 PDB
Residue 787: an α-helix

Full TRPM4 gene report on Sugi Atlas → Gene function, pathways, protein structure, interactions & more

Disease context

progressive familial heart block type IB — disease report on Sugi Atlas → Associated genes, phenotypes, clinical trials & treatments

For Hereditary progressive cardiac conduction defect (Orphanet):

Inheritance: Autosomal dominant
Onset: Adult

Similar variants

TRPM4 p.Val787Ala Uncertain significance ★ ⚠ same residue
TRPM4 p.Val787Glu Uncertain significance ★ ⚠ same residue
TRPM4 p.Ile1040Thr Pathogenic/Likely pathogenic ★★ same condition
TRPM4 p.Ile376Thr Pathogenic/Likely pathogenic ★★ ⚠ same condition
TRPM4 c.1050+1G>A Uncertain significance ★★ same condition
TRPM4 c.1150+5A>T Uncertain significance ★★ same condition
TRPM4 c.1150+6A>G Uncertain significance ★★ same condition
TRPM4 c.1263+1G>A 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/trpm4-p-val787 (accessed [today's date]).

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