Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.02 (A)
Location

Chromosome 1:12193005 (forward strand) | View in location tab

Co-located

with COSMIC COSM3747515 (G/A)

Most severe consequence
Evidence status

This variation has 6 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

This variation has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 3830 individual genotypes and is mentioned in 5 citations.

Variation displays