M27T (p.Met27Thr) variant of MYD88 (Q99836)
M27T (p.Met27Thr) in MYD88 (Q99836) is a missense change. Clinical records from EBI and UniProt describe it as benign. The available variant effect predictions contribute to a CATVariant prioritization score of 0.58 / 1. The record also includes population frequency data and structural context.
M27T (p.Met27Thr) variant details
- p.Met27Thr
- rs201871349
- ClinGen CA160960
- cosmic curated COSV57182
- ClinVar RCV000121611
- Benign
- Missense
- Variant Prioritization Score for Impact Estimate 0.578
- CADD 22.50
- PolyPhen-2 0.04
- SIFT 0.34
- EBI: Benign
- UniProt: Benign
- Most common in the 1KG:IBS population (allele frequency 0.017)
- Structural context available