Original source

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

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

Chromosome 4:54274869 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1430077, COSM739 ; HGMD-PUBLIC CM074406

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:739, 4744

HGVS names

This variant has 10 HGVS names - Show

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature and is associated with 3 phenotypes.

Variant displays