Original source

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

Alleles
C/A/T|Ancestral: C|Ambiguity code: H
Location

Chromosome 4:47403391 (forward strand)|View in location tab

Co-located variant

COSMIC COSM3604134

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 270 sample genotypes.

Variant displays