Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

G/A/T | Ancestral: G | Ambiguity code: D

Chromosome 19:1220488 (forward strand) | View in location tab


with COSMIC COSM20944 (G/T), COSM25847 (G/A) ; HGMD-PUBLIC CM991156 ; PhenCode KinMutBase_STK11_DNA:g.14575G>A (G/A), KinMutBase_STK11_DNA:g.14575G>T (G/T)

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB Cosmic:25847, 10855

This variant has 26 HGVS names - click the plus to show

About this variant

This variant overlaps 20 transcripts, 1 regulatory feature and is associated with 3 phenotypes.

Variant displays