Original source

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

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

Chromosome 16:46663005 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_054046

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 4 transcripts and has 36 sample genotypes.

Variant displays