Primary Site >> Stomach Cancer

Gene >> CDKN2D

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000335766
Start 10567284:10567284(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.275T>C
AA Mutation p.Val92Ala(p.V92A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000335766
Start 10567158:10567158(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.401G>A
AA Mutation p.Arg134His(p.R134H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000335766
Start 10567396:10567396(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs577358923
CDS Mutation c.163G>A
AA Mutation p.Ala55Thr(p.A55T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000335766
Start 10567151:10567151(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs554620640
CDS Mutation c.408C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence stop_gained
Transcription ID ENST00000335766
Start 10567117:10567117(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs765322862
CDS Mutation c.442C>T
AA Mutation p.Gln148Ter(p.Q148*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript