Original source

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

T/C | Ancestral: T | Ambiguity code: Y

Chromosome 4:154604968 (forward strand) | View in location tab

Most severe consequence
Missense variant
Evidence status


Uniprot VAR_014171

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 270 sample genotypes.

Variant displays