Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TGFBR3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91719430:91719430(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1448T>G
AA Mutation p.Leu483Trp(p.L483W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91712405:91712405(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2004C>A
AA Mutation p.Phe668Leu(p.F668L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91719900:91719900(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1406C>A
AA Mutation p.Ser469Tyr(p.S469Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91734850:91734850(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs148843052
CDS Mutation c.494G>A
AA Mutation p.Arg165Gln(p.R165Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91695723:91695723(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2386G>C
AA Mutation p.Val796Leu(p.V796L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91716689:91716689(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1586C>T
AA Mutation p.Ala529Val(p.A529V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91861509:91861509(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.23C>T
AA Mutation p.Ala8Val(p.A8V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91727672:91727672(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.872G>A
AA Mutation p.Ser291Asn(p.S291N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91719359:91719359(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1519A>G
AA Mutation p.Thr507Ala(p.T507A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91797439:91797439(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767943888
CDS Mutation c.94C>T
AA Mutation p.Pro32Ser(p.P32S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91712475:91712475(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773736382
CDS Mutation c.1934C>T
AA Mutation p.Ser645Leu(p.S645L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91698098:91698098(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2320A>T
AA Mutation p.Ile774Phe(p.I774F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91797344:91797344(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.189G>T
AA Mutation p.Glu63Asp(p.E63D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000212355
Start 91716589:91716589(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1686C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000212355
Start 91708748:91708748(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs143550507
CDS Mutation c.2202C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000212355
Start 91727714:91727714(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.830delA
AA Mutation p.Lys277SerfsTer6(p.K277Sfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> TGFBR3

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91758741:91758741(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.256C>T
AA Mutation p.His86Tyr(p.H86Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91734953:91734953(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.391G>A
AA Mutation p.Glu131Lys(p.E131K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91721970:91721970(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs41305630
CDS Mutation c.1060C>T
AA Mutation p.Arg354Trp(p.R354W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91727690:91727690(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.854C>A
AA Mutation p.Ser285Tyr(p.S285Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91729858:91729858(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.684G>T
AA Mutation p.Gln228His(p.Q228H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000212355
Start 91721981:91721981(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1049G>T
AA Mutation p.Arg350Ile(p.R350I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000212355
Start 91683832:91683832(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2463C>T
Mutation Classification Silent
Feature Type Transcript