Original source

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

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

Chromosome 15:44574997 (forward strand) | View in location tab

Most severe consequence
 
Missense variant

This variant has 11 HGVS names - click the plus to show

About this variant

This variant overlaps 11 transcripts.

Variant displays