Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.05 (A)
Location

Chromosome 17:50199874 (forward strand)|View in location tab

Co-located variant

COSMIC COSM5019853

Most severe consequence
 
Synonymous variant
Evidence status

HGVS names

This variant has 9 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 3494 sample genotypes and is mentioned in 1 citation.

Variant displays