Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NTNG1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107324846:107324846(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.811G>A
AA Mutation p.Val271Ile(p.V271I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107436769:107436769(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1360C>T
AA Mutation p.Pro454Ser(p.P454S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107324634:107324634(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773062054
CDS Mutation c.599C>T
AA Mutation p.Thr200Met(p.T200M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107148711:107148711(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.118G>A
AA Mutation p.Glu40Lys(p.E40K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107324741:107324741(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.706C>A
AA Mutation p.Arg236Ser(p.R236S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107430765:107430765(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1103G>A
AA Mutation p.Gly368Asp(p.G368D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107324747:107324747(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.712C>T
AA Mutation p.Arg238Cys(p.R238C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107324298:107324298(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.263G>T
AA Mutation p.Cys88Phe(p.C88F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107480767:107480767(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1547C>T
AA Mutation p.Ala516Val(p.A516V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107480637:107480637(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1417C>T
AA Mutation p.His473Tyr(p.H473Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107324883:107324883(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.848G>A
AA Mutation p.Arg283His(p.R283H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107148830:107148830(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.237C>A
AA Mutation p.Phe79Leu(p.F79L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107148654:107148654(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.61C>G
AA Mutation p.Gln21Glu(p.Q21E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000370068
Start 107480621:107480621(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1401C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000370068
Start 107480807:107480807(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1587G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000370068
Start 107324413:107324413(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.378T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000370068
Start 107324548:107324548(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.513A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000370068
Start 107148749:107148749(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774773683
CDS Mutation c.156G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000370068
Start 107148617:107148617(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs557686809
CDS Mutation c.24G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000370068
Start 107324533:107324533(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs267597900
CDS Mutation c.498C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence frameshift_variant
Transcription ID ENST00000370068
Start 107324726:107324726(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.696delT
AA Mutation p.Phe232LeufsTer31(p.F232Lfs*31)
Mutation Classification Frame_Shift_Del
Feature Type Transcript

Rectum Cancer: Gene >> NTNG1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107324846:107324846(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.811G>A
AA Mutation p.Val271Ile(p.V271I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107324724:107324724(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs386352339
CDS Mutation c.689C>T
AA Mutation p.Ala230Val(p.A230V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107436700:107436700(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1291C>T
AA Mutation p.Arg431Cys(p.R431C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000370068
Start 107324729:107324729(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.694T>G
AA Mutation p.Phe232Val(p.F232V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000370068
Start 107407686:107407686(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1065C>T
Mutation Classification Silent
Feature Type Transcript