Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.38 (A)
Location

Chromosome 7:10982603 (forward strand) | View in location tab

Co-located

with COSMIC COSM3723031 (A/G), COSM3723030 (A/G)

Most severe consequence
 
Missense variant
Evidence status

This variant has 7 synonyms - click the plus to show

This variant has 7 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 5 transcripts and has 3693 sample genotypes.

Variant displays