Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

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

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:25847, 10855

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

Variation displays