A65D (p.Ala65Asp) variant of TTR (Transthyretin)
A65D (p.Ala65Asp) in TTR (Transthyretin) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as pathogenic/likely pathogenic in the context of not provided; Amyloidosis, hereditary systemic 1. The available variant effect predictions contribute to a CATVariant prioritization score of 0.68 / 1. The record also includes published literature and structural context.
A65D (p.Ala65Asp) variant details
- p.Ala65Asp
- rs730881169
- ClinGen CA297540
- ClinVar RCV000159436
- ClinVar RCV001228889
- Pathogenic/Likely pathogenic
- not provided; Amyloidosis, hereditary systemic 1
- Missense
- Variant Prioritization Score for Impact Estimate 0.676
- AlphaMissense 0.20
- MetaLR 0.95
- MetaSVM 1.08
- PolyPhen-2 1.00
- SIFT 0.01
- EVE 0.25
- ClinVar: Pathogenic/Likely pathogenic (not provided; Amyloidosis, hereditary systemic 1)
- EBI: Pathogenic (in AMYLD1)
- UniProt: Pathogenic (in AMYLD1)
- Structural context available
- Cited in: Transthyretin mutations in health and disease. (PMID 7599630)
- Cited in: Hereditary Transthyretin Amyloidosis. (PMID 20301373)