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 13:113118491 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_013936

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 15 transcripts and has 180 sample genotypes.

Variant displays