Primary Site >> Stomach Cancer

Gene >> MMP8

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000236826
Start 102722504:102722504(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.272G>T
AA Mutation p.Cys91Phe(p.C91F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000236826
Start 102715423:102715423(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.917G>T
AA Mutation p.Arg306Met(p.R306M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000236826
Start 102722559:102722559(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753882335
CDS Mutation c.217A>C
AA Mutation p.Asn73His(p.N73H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000236826
Start 102722508:102722508(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs546201458
CDS Mutation c.268C>T
AA Mutation p.Arg90Cys(p.R90C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000236826
Start 102721430:102721430(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.593C>T
AA Mutation p.Ala198Val(p.A198V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000236826
Start 102722552:102722552(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779074177
CDS Mutation c.224C>T
AA Mutation p.Thr75Met(p.T75M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000236826
Start 102713447:102713447(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1305T>A
AA Mutation p.His435Gln(p.H435Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000236826
Start 102714626:102714626(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs149306045
CDS Mutation c.1120G>A
AA Mutation p.Val374Ile(p.V374I)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000236826
Start 102714705:102714705(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1041C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000236826
Start 102718436:102718436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750688454
CDS Mutation c.762C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000236826
Start 102722566:102722566(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.210delT
AA Mutation p.Phe70LeufsTer3(p.F70Lfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000236826
Start 102713424:102713425(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1327dupT
AA Mutation p.Tyr443LeufsTer4(p.Y443Lfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 13
Mutation Consequence inframe_insertion;splice_region_variant
Transcription ID ENST00000236826
Start 102716417:102716418(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.786_787insATATTTCAATTTTATACCTGT
AA Mutation p.Gly262_Leu263insIlePheGlnPheTyrThrCys(p.G262_L263insIFQFYTC)
Mutation Classification In_Frame_Ins
Feature Type Transcript