Original source

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

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

Chromosome 10:74074820 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Synonyms

Uniprot VAR_037667

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 6 transcripts.

Variant displays