Original source

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

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

Chromosome 14:100834673 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 24 transcripts.

Variant displays