Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.46 (A)
Location

Chromosome 6:39357302 (forward strand) | View in location tab

Co-located

with COSMIC COSM150088 (A/G) ; HGMD-PUBLIC CM074911

Most severe consequence
 
Missense variant
Evidence status

This variant has 4 synonyms - click the plus to show

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

This variant has assays on 13 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, has 2511 sample genotypes and is mentioned in 38 citations.

Variant displays