Primary Site >> Stomach Cancer

Gene >> TCOF1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000377797
Start 150374755:150374755(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1222G>A
AA Mutation p.Glu408Lys(p.E408K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000377797
Start 150376520:150376520(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201352878
CDS Mutation c.2240C>T
AA Mutation p.Thr747Met(p.T747M)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000377797
Start 150375505:150375505(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1655C>T
AA Mutation p.Ser552Leu(p.S552L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000377797
Start 150368756:150368756(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.419C>T
AA Mutation p.Pro140Leu(p.P140L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000377797
Start 150389982:150389982(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs764924499
CDS Mutation c.3142C>T
AA Mutation p.Arg1048Trp(p.R1048W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000377797
Start 150396369:150396369(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201368732
CDS Mutation c.3869C>T
AA Mutation p.Ala1290Val(p.A1290V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000377797
Start 150396760:150396760(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs779693329
CDS Mutation c.4260G>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000377797
Start 150372080:150372080(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs147186583
CDS Mutation c.714G>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000377797
Start 150388066:150388066(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3024C>T
Mutation Classification Silent
Feature Type Transcript
ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000377797
Start 150375849:150375849(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1833C>T
Mutation Classification Silent
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000377797
Start 150376120:150376120(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1932C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000377797
Start 150375448:150375448(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1602delC
AA Mutation p.Ser535GlnfsTer61(p.S535Qfs*61)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000377797
Start 150367878:150367878(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.343delG
AA Mutation p.Ala115ArgfsTer7(p.A115Rfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000377797
Start 150398394:150398394(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.4388delA
AA Mutation p.Lys1463ArgfsTer112(p.K1463Rfs*112)
Mutation Classification Frame_Shift_Del
Feature Type Transcript