Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 17:39410534 (forward strand) | View in location tab

Co-located

with COSMIC COSM1257542 (G/T), COSM4065965 (G/A)

Most severe consequence
 
Missense variant

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

About this variant

This variant overlaps 4 transcripts.

Variant displays