Original source

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

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

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

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_013936

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 180 sample genotypes.

Variant displays