M1I (p.Met1Ile) variant of CSRP3 (P50461)
M1I (p.Met1Ile) in CSRP3 (P50461) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as uncertain significance in the context of Cardiovascular phenotype. The record also includes structural context.
M1I (p.Met1Ile) variant details
- p.Met1Ile
- rs2494229293
- ClinGen CA379888704
- ClinVar RCV003296750
- Uncertain significance
- Cardiovascular phenotype
- Missense
- ClinVar: Uncertain significance (Cardiovascular phenotype)
- EBI: Variant of uncertain significance
- UniProt: Uncertain significance
- Structural context available