Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.48 (A)
Location

Chromosome 17:7078078 (forward strand) | View in location tab

Co-located

with COSMIC COSM4130542 (A/G), COSM4130543 (A/G)

Most severe consequence
 
Missense variant
Evidence status

This variant has 7 synonyms - click the plus to show

This variant has 9 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 3797 sample genotypes.

Variant displays