V17I (p.Val17Ile) variant of TGFB2 (P61812)
V17I (p.Val17Ile) in TGFB2 (P61812) is a missense change. Clinical records from ClinVar and UniProt describe it as uncertain significance in the context of Familial thoracic aortic aneurysm and aortic dissection. The available variant effect predictions contribute to a CATVariant prioritization score of 0.43 / 1. The record also includes population frequency data and structural context.
V17I (p.Val17Ile) variant details
- p.Val17Ile
- gnomAD rs1334873734
- Uncertain significance
- Familial thoracic aortic aneurysm and aortic dissection
- Missense
- Variant Prioritization Score for Impact Estimate 0.425
- REVEL 0.20
- CADD 23.00
- PolyPhen-2 0.01
- SIFT 0.15
- ClinVar: Uncertain significance (Familial thoracic aortic aneurysm and aortic dissection)
- UniProt: Uncertain significance
- Most common in the East Asian population (allele frequency 2.5e-05)
- Structural context available