Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 19:1220415 (forward strand) | View in location tab

Co-located

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

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB Cosmic:20943, 10860

This variation has 12 HGVS names - click the plus to show

Variation displays