Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S
Location

Chromosome 4:110621259 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
HGVS names

This variant has 22 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and 1 regulatory feature.

Variant displays