Original source

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

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

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

Most severe consequence
Missense variant
Evidence status


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