Primary Site >> Stomach Cancer

Gene >> TGFBR1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000374994
Start 99144839:99144839(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1081G>A
AA Mutation p.Ala361Thr(p.A361T)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000374994
Start 99132635:99132635(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.470G>A
AA Mutation p.Arg157Gln(p.R157Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000374994
Start 99149253:99149253(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs113605875
CDS Mutation c.1460G>A
AA Mutation p.Arg487Gln(p.R487Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000374994
Start 99128968:99128968(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.211T>G
AA Mutation p.Cys71Gly(p.C71G)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000374994
Start 99128888:99128888(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.131A>T
AA Mutation p.Asp44Val(p.D44V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000374994
Start 99144819:99144819(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1061T>C
AA Mutation p.Leu354Pro(p.L354P)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000374994
Start 99142588:99142588(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.858A>T
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000374994
Start 99144883:99144883(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1129delA
AA Mutation p.Arg377GlyfsTer12(p.R377Gfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000374994
Start 99149206:99149209(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1415_1418delGAGA
AA Mutation p.Arg472AsnfsTer74(p.R472Nfs*74)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000374994
Start 99128995:99128995(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.238C>T
AA Mutation p.Arg80Ter(p.R80*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence stop_gained
Transcription ID ENST00000374994
Start 99128860:99128860(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.103C>T
AA Mutation p.Gln35Ter(p.Q35*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 12
Mutation Consequence stop_gained
Transcription ID ENST00000374994
Start 99129075:99129075(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.318C>A
AA Mutation p.Cys106Ter(p.C106*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript