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 2:104856710 (forward strand)|View in location tab

Co-located variant

COSMIC COSM3425060

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts.

Variant displays