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: 0.08 (T)

Chromosome 6:111592059 (forward strand) | View in location tab


with COSMIC COSM3736398 (C/T) ; HGMD-PUBLIC CM107202

Most severe consequence
Evidence status

Clinical significance


Uniprot VAR_047349

This variation has 12 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 1135 individual genotypes, is associated with 5 phenotypes and is mentioned in 12 citations.

Variation displays