Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

with COSMIC COSM3918128 (C/T)

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

Archive dbSNP rs1801537, rs17349795

This variant has 2 HGVS names - click the plus to show

About this variant

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

Variant displays