Primary Site >> Stomach Cancer

Gene >> DLK1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000341267
Start 100734489:100734489(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs138651182
CDS Mutation c.745G>A
AA Mutation p.Ala249Thr(p.A249T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000341267
Start 100727094:100727094(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.26G>A
AA Mutation p.Arg9His(p.R9H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000341267
Start 100728979:100728979(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.175A>G
AA Mutation p.Thr59Ala(p.T59A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000341267
Start 100732182:100732182(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs191731751
CDS Mutation c.403G>A
AA Mutation p.Gly135Ser(p.G135S)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000341267
Start 100727098:100727098(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.30C>T
Mutation Classification Silent
Feature Type Transcript
ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000341267
Start 100727110:100727110(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.42G>A
Mutation Classification Silent
Feature Type Transcript
ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000341267
Start 100734218:100734218(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.479delC
AA Mutation p.Pro160LeufsTer50(p.P160Lfs*50)
Mutation Classification Frame_Shift_Del
Feature Type Transcript