Primary Site >> Stomach Cancer

Gene >> MTBP

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000305949
Start 120456624:120456624(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.701A>G
AA Mutation p.Asp234Gly(p.D234G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000305949
Start 120455539:120455539(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.589T>C
AA Mutation p.Tyr197His(p.Y197H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000305949
Start 120451298:120451298(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.401G>A
AA Mutation p.Ser134Asn(p.S134N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000305949
Start 120518011:120518011(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2407G>C
AA Mutation p.Ala803Pro(p.A803P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000305949
Start 120516182:120516182(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2237C>A
AA Mutation p.Pro746His(p.P746H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000305949
Start 120451241:120451241(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs183822788
CDS Mutation c.344C>T
AA Mutation p.Thr115Met(p.T115M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000305949
Start 120516016:120516016(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2071T>C
AA Mutation p.Cys691Arg(p.C691R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000305949
Start 120451070:120451070(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.267T>G
AA Mutation p.Phe89Leu(p.F89L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000305949
Start 120451302:120451302(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.405G>A
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000305949
Start 120502577:120502577(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1695G>A
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence frameshift_variant
Transcription ID ENST00000305949
Start 120445499:120445499(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.34delG
AA Mutation p.Glu12LysfsTer39(p.E12Kfs*39)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000305949
Start 120488317:120488317(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1324G>T
AA Mutation p.Glu442Ter(p.E442*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000305949
Start 120502587:120502588(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1711dupA
AA Mutation p.Thr571AsnfsTer2(p.T571Nfs*2)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000305949
Start 120470885:120470886(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1113_1114insCACTATAAAAACT
AA Mutation p.Ser372HisfsTer5(p.S372Hfs*5)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 15
Mutation Consequence splice_donor_variant
Transcription ID ENST00000305949
Start 120453907:120453907(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.484+2T>C
Mutation Classification Splice_Site
Feature Type Transcript