Original source

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

C/T|Ancestral: C|Ambiguity code: Y

Chromosome 19:1220416 (forward strand)|View in location tab

Co-located variants

COSMIC COSM20943 ; HGMD-PUBLIC CM013293 ; PhenCode KinMutBase_STK11_DNA:g.14503C>T (C/T)

Most severe consequence
Stop gained
Evidence status

Clinical significance


LSDB Cosmic:20943, 10860

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and is associated with 2 phenotypes.

Variant displays