T47T (p.Thr47Thr) variant of CSRP3 (P50461)
T47T (p.Thr47Thr) in CSRP3 (P50461) is a synonymous change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.15 / 1. The record also includes population frequency data, published literature, and structural context.
T47T (p.Thr47Thr) variant details
- p.Thr47Thr
- rs758842207
- gnomAD 11-19188276-C-T
- Synonymous
- Variant Prioritization Score for Impact Estimate 0.152
- CADD 4.66
- SIFT 0.01
- Most common in the South Asian population (allele frequency 5.8e-05)
- Structural context available
- Literature evidence available