Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.06 (A)
Location

Chromosome 9:712766 (forward strand) | View in location tab

Co-located

with COSMIC COSM1462722 (G/A), COSM1462721 (G/A)

Most severe consequence
 
Missense variant
Evidence status

This variant has 3 synonyms - click the plus to show

This variant has 11 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts and has 3434 sample genotypes.

Variant displays