P13A (p.Pro13Ala) variant of RASA1 (Ras GTPase-activating protein 1)
P13A (p.Pro13Ala) in RASA1 (Ras GTPase-activating protein 1) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Capillary malformation-arteriovenous malformation syndrome. The available variant effect predictions contribute to a CATVariant prioritization score of 0.33 / 1. The record also includes population frequency data, experimental measurements, and structural context.
P13A (p.Pro13Ala) variant details
- p.Pro13Ala
- TOPMed rs1191737466
- gnomAD rs1191737466
- Uncertain significance
- Capillary malformation-arteriovenous malformation syndrome
- Missense
- Variant Prioritization Score for Impact Estimate 0.33
- REVEL 0.19
- CADD 21.30
- PolyPhen-2 0.01
- SIFT 0.09
- ClinVar: Uncertain significance (Capillary malformation-arteriovenous malformation syndrome)
- UniProt: Uncertain significance
- Most common in the Non-Finnish European population (allele frequency 3e-05)
- Structural context available
- RASA1 SH3 domain domainome 1.0: score -0.137