Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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 COSM21355 (C/T), COSM12924 (C/-) ; HGMD-PUBLIC CD982961, CX075747 ; PhenCode KinMutBase_STK11_DNA:g.15407C>T (C/T), KinMutBase_STK11_DNA:g.15407delC (C/-) ; 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: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 11 transcripts and has 2504 individual genotypes.

Variation displays