Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/T|Ancestral: A|Ambiguity code: W
Location

Chromosome 4:54285926 (forward strand)|View in location tab

Co-located variant

COSMIC COSM736

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB 4741, Cosmic:736

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and is associated with 2 phenotypes.

Variant displays