Primary Site >> Stomach Cancer

Gene >> SEPT6

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000343984
Start 119663546:119663546(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.277G>A
AA Mutation p.Val93Met(p.V93M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000343984
Start 119633410:119633410(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1039G>A
AA Mutation p.Val347Ile(p.V347I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000343984
Start 119629490:119629490(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs150468538
CDS Mutation c.1108C>T
AA Mutation p.Arg370Cys(p.R370C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000343984
Start 119633489:119633489(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.960A>G
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000343984
Start 119633435:119633435(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1014delA
AA Mutation p.Glu339LysfsTer4(p.E339Kfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 6
Mutation Consequence stop_gained
Transcription ID ENST00000343984
Start 119629409:119629409(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1189A>T
AA Mutation p.Lys397Ter(p.K397*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence splice_acceptor_variant
Transcription ID ENST00000343984
Start 119633493:119633493(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.957-1G>C
Mutation Classification Splice_Site
Feature Type Transcript