Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.01 (G)
Location

Chromosome 12:57765390 (forward strand) | View in location tab

Co-located

with COSMIC COSM1363437 (C/T)

Most severe consequence
Evidence status

This variation has 2 synonyms - click the plus to show

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 15 transcripts, has 3187 individual genotypes and is mentioned in 2 citations.

Variation displays