C349G (p.Cys349Gly) variant of GATA2 (P23769)
C349G (p.Cys349Gly) in GATA2 (P23769) is a missense change. Clinical records from ClinVar, EBI, and UniProt describe it as likely pathogenic in the context of Deafness-lymphedema-leukemia syndrome; GATA2 deficiency with susceptibility to M. The available variant effect predictions contribute to a CATVariant prioritization score of 0.99 / 1. The record also includes structural context.
C349G (p.Cys349Gly) variant details
- p.Cys349Gly
- rs1576745260
- ClinGen CA354413658
- ClinVar RCV001542203
- Ensembl rs1576745260
- Likely pathogenic
- Deafness-lymphedema-leukemia syndrome; GATA2 deficiency with susceptibility to M
- Missense
- Variant Prioritization Score for Impact Estimate 0.989
- AlphaMissense 1.00
- MetaLR 1.00
- MetaSVM 1.46
- PolyPhen-2 1.00
- SIFT 0.00
- EVE 1.00
- ClinVar: Likely pathogenic (Deafness-lymphedema-leukemia syndrome; GATA2 deficiency with sus)
- EBI: Pathogenic
- UniProt: Pathogenic
- Structural context available