Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TEX11

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70623965:70623965(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770614604
CDS Mutation c.1781C>T
AA Mutation p.Pro594Leu(p.P594L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70529977:70529977(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2588T>C
AA Mutation p.Ile863Thr(p.I863T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70833539:70833539(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.625G>T
AA Mutation p.Asp209Tyr(p.D209Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70740756:70740756(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.833G>T
AA Mutation p.Trp278Leu(p.W278L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70529132:70529132(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2786T>G
AA Mutation p.Val929Gly(p.V929G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70591798:70591798(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2138A>C
AA Mutation p.Glu713Ala(p.E713A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70853135:70853135(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773083176
CDS Mutation c.469G>A
AA Mutation p.Val157Ile(p.V157I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70873244:70873244(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.268A>C
AA Mutation p.Asn90His(p.N90H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70670456:70670456(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1346C>G
AA Mutation p.Thr449Ser(p.T449S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000344304
Start 70610507:70610507(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1833T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000344304
Start 70853136:70853136(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.468C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence frameshift_variant
Transcription ID ENST00000344304
Start 70853284:70853284(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.414delT
AA Mutation p.Leu139Ter(p.L139*)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> TEX11

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70529166:70529166(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2752C>A
AA Mutation p.Leu918Ile(p.L918I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70624852:70624852(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1726C>A
AA Mutation p.Leu576Ile(p.L576I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70682760:70682760(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1115G>A
AA Mutation p.Gly372Glu(p.G372E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70529975:70529975(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2590C>A
AA Mutation p.Leu864Ile(p.L864I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70806740:70806740(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.702G>T
AA Mutation p.Lys234Asn(p.K234N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000344304
Start 70740787:70740787(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.802C>A
AA Mutation p.Leu268Ile(p.L268I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000344304
Start 70682681:70682681(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1194C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000344304
Start 70740758:70740758(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.831T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence stop_gained
Transcription ID ENST00000344304
Start 70610536:70610536(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1804G>T
AA Mutation p.Glu602Ter(p.E602*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence splice_donor_variant
Transcription ID ENST00000344304
Start 70833512:70833512(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.651+1G>A
Mutation Classification Splice_Site
Feature Type Transcript