Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome 8:127415632 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant

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

About this variant

This variant overlaps 4 transcripts.

Variant displays