Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M
Location

Chromosome 17:7283487 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_052503

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 11 sample genotypes.

Variant displays