A37V (p.Ala37Val) variant of FHL1 (Q13642)
A37V (p.Ala37Val) in FHL1 (Q13642) is a missense change. Clinical records from UniProt describe it as variant assessed as somatic; moderate impact. The record also includes experimental measurements and structural context.
A37V (p.Ala37Val) variant details
- p.Ala37Val
- NCI-TCGA Cosmic COSV1006
- cosmic curated COSV10060
- Variant assessed as somatic; moderate impact.
- Missense
- UniProt: Variant assessed as somatic; moderate impact.
- Structural context available
- FHL1 Zinc finger, LIM-type domain domainome 1.0: score -0.0816