Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.19 (G)
Location

Chromosome 1:12192898 (forward strand) | View in location tab

Co-located

with COSMIC COSM146406 (T/G) ; HGMD-PUBLIC CM022071

Most severe consequence
Evidence status

This variation has 8 synonyms - click the plus to show

This variation has 5 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 5 transcripts, has 4790 individual genotypes and is mentioned in 39 citations.

Variation displays