Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: < 0.01 (T)
Location

Chromosome 12:110919160 (forward strand) | View in location tab

Co-located

with COSMIC COSM4038694 (C/T) ; HGMD-PUBLIC CM961004 ; PhenCode FHC0201 (C/T)

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

This variant has 9 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 2504 sample genotypes, is associated with 6 phenotypes and is mentioned in 3 citations.

Variant displays