T22M (p.Thr22Met) variant of TRPM4 (Q8TD43)
T22M (p.Thr22Met) in TRPM4 (Q8TD43) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Progressive familial heart block type IB. The available variant effect predictions contribute to a CATVariant prioritization score of 0.51 / 1. The record also includes population frequency data and structural context.
T22M (p.Thr22Met) variant details
- p.Thr22Met
- rs1600379607
- ClinGen CA406788043
- cosmic curated COSV53258
- ClinVar RCV001043152
- Uncertain significance
- Progressive familial heart block type IB
- Missense
- Variant Prioritization Score for Impact Estimate 0.505
- REVEL 0.43
- ESM-1b 0.00
- AlphaMissense 0.13
- CADD 26.90
- PolyPhen-2 0.98
- SIFT 0.00
- ClinVar: Uncertain significance (Progressive familial heart block type IB)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Most common in the East Asian population (allele frequency 0.0002)
- Structural context available