Original source

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

Alleles
T/A/G|Ancestral: T|Ambiguity code: D
Location

Chromosome 4:54727447 (forward strand)|View in location tab

Co-located variants

COSMIC COSM1257, COSM1260, COSM36302 ; HGMD-PUBLIC CD982724, CM077194

Most severe consequence
 
Missense variant
Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 8 transcripts.

Variant displays