Original source

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

Alleles
A/-|Ancestral: A
Location

Chromosome 12:90978266 (forward strand)|View in location tab

Co-located variant

COSMIC COSM1735994

Most severe consequence
 
Splice region variant
Evidence status

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts, 1 regulatory feature and has 6 sample genotypes.

Variant displays