Original source

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

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

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

Most severe consequence
 
Missense variant
Evidence status

Synonyms

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