Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.21 (G)
Location

Chromosome 11:61341502 (forward strand) | View in location tab

Co-located

with COSMIC COSM4145966 (G/A)

Most severe consequence
 
Missense variant
Evidence status

This variant has 2 synonyms - click the plus to show

This variant has 8 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 22 transcripts and has 2604 sample genotypes.

Variant displays