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 7:55143357 (forward strand)|View in location tab

Co-located variant

COSMIC COSM4680390

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_019293

HGVS names

This variant has 40 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 18 transcripts, has 833 sample genotypes and is mentioned in 1 citation.

Variant displays