Original source

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

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

Chromosome 5:139325464 (forward strand)|View in location tab

Most severe consequence
 
Stop gained
HGVS names

This variant has 26 HGVS names - Show

About this variant

This variant overlaps 19 transcripts.

Variant displays