Primary Site >> Stomach Cancer

Gene >> TGFB3

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000238682
Start 75963383:75963383(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs757774610
CDS Mutation c.859C>T
AA Mutation p.Arg287Trp(p.R287W)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000238682
Start 75963445:75963445(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs142069844
CDS Mutation c.797G>A
AA Mutation p.Arg266His(p.R266H)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000238682
Start 75971161:75971161(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.611T>A
AA Mutation p.Val204Asp(p.V204D)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000238682
Start 75961051:75961051(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.952C>T
AA Mutation p.Arg318Cys(p.R318C)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000238682
Start 75971182:75971182(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772252884
CDS Mutation c.590C>T
AA Mutation p.Ala197Val(p.A197V)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000238682
Start 75961002:75961002(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1001A>G
AA Mutation p.His334Arg(p.H334R)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000238682
Start 75971612:75971612(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.459C>A
Mutation Classification Silent
Feature Type Transcript
ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000238682
Start 75960989:75960989(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1014C>A
Mutation Classification Silent
Feature Type Transcript
ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000238682
Start 75963358:75963358(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.884delG
AA Mutation p.Gly295ValfsTer74(p.G295Vfs*74)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
ID 10
Mutation Consequence stop_gained
Transcription ID ENST00000238682
Start 75971175:75971175(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.597G>A
AA Mutation p.Trp199Ter(p.W199*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
ID 11
Mutation Consequence splice_donor_variant
Transcription ID ENST00000238682
Start 75960922:75960922(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1080+1G>A
Mutation Classification Splice_Site
Feature Type Transcript