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 19:1220503 (forward strand) | View in location tab

Co-located

with COSMIC COSM21359 (G/A), COSM27280 (G/C), COSM25229 (G/T) ; PhenCode KinMutBase_STK11_DNA:g.14590G>A (G/A)

Most severe consequence

This variation has 3 synonyms - click the plus to show

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

Variation displays