Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 variant

COSMIC COSM1363437

Most severe consequence
 
Missense variant
Evidence status

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 14 transcripts, 1 regulatory feature, has 3187 sample genotypes and is mentioned in 2 citations.

Variant displays