Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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


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

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

About this variant

This variant overlaps 6 transcripts, has 1092 individual genotypes, is associated with 4 phenotypes and is mentioned in 3 citations.

Variation displays