Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.07 (G)
Location

Chromosome 8:127416506 (forward strand) | View in location tab

Co-located

with COSMIC COSM3982390 (A/G), COSM3982391 (A/G) ; HGMD-PUBLIC CM073273

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 6 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 4 transcripts and has 2505 individual genotypes.

Variation displays