Original source

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

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

Chromosome 11:17075167 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 14 transcripts.

Variant displays