This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/A/G/T | Ancestral: C | Ambiguity code: N | 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.15407delC (C/-), KinMutBase_STK11_DNA:g.15407C>T (C/T) ; dbSNP rs121913321 (C/-)

Most severe consequence
Missense variant
Evidence status

Clinical significance


This variant has 3 synonyms - Show

HGVS names

This variant has 33 HGVS names - Show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 30 transcripts, 1 regulatory feature, has 2504 sample genotypes and is associated with 1 phenotype.

Variant displays