Primary Site >> Stomach Cancer

Gene >> TGFBR2

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000295754
Start 30672264:30672264(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1081C>T
AA Mutation p.Leu361Phe(p.L361F)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000295754
Start 30671898:30671898(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.715A>G
AA Mutation p.Thr239Ala(p.T239A)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000295754
Start 30672051:30672051(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.868G>A
AA Mutation p.Glu290Lys(p.E290K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000295754
Start 30672249:30672249(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs199660234
CDS Mutation c.1066C>T
AA Mutation p.Arg356Trp(p.R356W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000295754
Start 30671734:30671734(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.551T>A
AA Mutation p.Ile184Asn(p.I184N)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000295754
Start 30671944:30671944(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751948498
CDS Mutation c.761G>A
AA Mutation p.Arg254His(p.R254H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000295754
Start 30672324:30672324(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1141A>G
AA Mutation p.Lys381Glu(p.K381E)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000295754
Start 30674121:30674121(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1271A>G
AA Mutation p.Tyr424Cys(p.Y424C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000295754
Start 30688431:30688431(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1444C>A
AA Mutation p.Pro482Thr(p.P482T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000295754
Start 30691478:30691478(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs104893815
CDS Mutation c.1583G>A
AA Mutation p.Arg528His(p.R528H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000295754
Start 30644871:30644871(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.219C>T
Mutation Classification Silent
Feature Type Transcript
ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000295754
Start 30672308:30672308(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs751663055
CDS Mutation c.1125C>T
Mutation Classification Silent
Feature Type Transcript
ID 13
Mutation Consequence synonymous_variant
Transcription ID ENST00000295754
Start 30606940:30606940(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.57T>C
Mutation Classification Silent
Feature Type Transcript
ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000295754
Start 30650315:30650315(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.312delC
AA Mutation p.Lys105SerfsTer19(p.K105Sfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000295754
Start 30688470:30688470(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs104893819
CDS Mutation c.1483C>T
AA Mutation p.Arg495Ter(p.R495*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000295754
Start 30688487:30688488(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.1503dupC
AA Mutation p.Ser502GlnfsTer14(p.S502Qfs*14)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
ID 17
Mutation Consequence splice_donor_variant
Transcription ID ENST00000295754
Start 30672439:30672439(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1254+2T>G
Mutation Classification Splice_Site
Feature Type Transcript
ID 18
Mutation Consequence inframe_deletion
Transcription ID ENST00000295754
Start 30672052:30672054(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.871_873delAAG
AA Mutation p.Lys291del(p.K291del)
Mutation Classification In_Frame_Del
Feature Type Transcript
ID 19
Mutation Consequence inframe_deletion
Transcription ID ENST00000295754
Start 30671689:30671694(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.508_513delATCAGC
AA Mutation p.Ile170_Ser171del(p.I170_S171del)
Mutation Classification In_Frame_Del
Feature Type Transcript