Original source

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

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

Chromosome 5:136046407 (forward strand)|View in location tab

Co-located variants

COSMIC COSM3138534 ; HGMD-PUBLIC CM981909, CM971472, CP05317

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and is associated with 4 phenotypes.

Variant displays