Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome 2:236166256 (forward strand) | View in location tab

Co-located

with COSMIC COSM1253122 (G/A)

Most severe consequence
 
Missense variant

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts.

Variant displays