Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 12:6845700 (forward strand) | View in location tab

Co-located

with COSMIC COSM3736074 (G/A)

Most severe consequence
Evidence status

This variation has 7 synonyms - click the plus to show

This variation has 12 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 21 transcripts, has 781 individual genotypes and is mentioned in 2 citations.

Variation displays