Original source

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

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

Chromosome 19:1220502 (forward strand) | View in location tab


with COSMIC COSM25229 (G/T), COSM27280 (G/C), COSM21359 (G/A) ; 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 24 HGVS names - click the plus to show

Variation displays