TRPC5 p.Asn62=
c.186C>T · rs762529573 · VCV3054050
Likely benign
No assertion criteria
Classification
Likely benign
ClinVar
Review
No assertion criteria ☆☆☆☆
ClinVar · 1 submitter
gnomAD v4.1
Rare
rare (popmax 0.366%, mid)
Conditions
1
TRPC5-related disorder
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 2.6 | GERP 1, phastCons 1 |
| Overall | ||
| CADD | 6.922 | PHRED · no single calibrated threshold — expert panels disagree |
Population frequency
gnomAD v4.1 · exomes + genomes
Grpmax group
0.366%
Middle Eastern · 16/4,377 alleles
Filtering AF
0.229%
ClinGen BA1/BS1 input
FAF95, joint · FAF99 0.187%
Overall
0.00273%
33/1,210,437 alleles · rare
| Ancestry group | Frequency | 1 in |
|---|---|---|
| Middle Easterngrpmax | 0.366% | 274 |
| South Asian | 0.00352% | 28,415 |
| European (non-Finnish) | 0.00168% | 59,693 |
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
- TRPC5
- Protein
- p.Asn62=
- Coding
- c.186C>T
- MANE Select
- NM_012471
- dbSNP
- rs762529573
- Type
- single nucleotide variant
- Location
- chrX:111952235 (GRCh38)
- Structure
- AlphaFold pLDDT 73.82 · 30 PDB
Disease context
TRPC5-related disorder
Similar variants
- TRPC5 p.Arg222Cys Uncertain significance ★ ⚠ same condition
- TRPC5 p.Gln914Glu Uncertain significance ★ ⚠ same condition
- TRPC5 p.Lys7Gln Uncertain significance ★ ⚠ same condition
- TRPC5 p.Ala912Thr Uncertain significance ⚠ same condition
- TRPC5 p.Arg120Trp Uncertain significance ⚠ same condition
- TRPC5 p.Arg191His Uncertain significance ⚠ same condition
- TRPC5 p.Arg260Trp Uncertain significance ⚠ same condition
- TRPC5 p.Arg324Gln 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/trpc5-p-asn62 (accessed [today's date]).
Preprint & method: sugi.bio/variant/method Machine-readable: this page as Markdown