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 19:1221320 (forward strand) | View in location tab


with COSMIC COSM12924 (C/-), COSM21355 (C/T) ; HGMD-PUBLIC CX075747, CD982961 ; PhenCode KinMutBase_STK11_DNA:g.15407delC (C/-), KinMutBase_STK11_DNA:g.15407C>T (C/T) ; dbSNP rs121913321 (C/-)

Most severe consequence
Evidence status

Clinical significance


LSDB Cosmic:21355

This variation has 11 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

About this variant

This variant overlaps 11 transcripts, has 1092 individual genotypes and is associated with 1 phenotype.

Variation displays