Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.15 (A)
Location

Chromosome 11:6394233 (forward strand) | View in location tab

Co-located

with COSMIC COSM3752609 (G/A), COSM3752608 (G/A)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 7 synonyms - click the plus to show

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

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 27 transcripts, has 2621 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays