Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 4:73981270 (forward strand)|View in location tab

Co-located variant

COSMIC COSM3918128

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs1801537, rs17349795

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 1 transcript, 1 regulatory feature and has 1 sample genotype.

Variant displays