Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CLSPN

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35764300:35764300(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.548T>A
AA Mutation p.Ile183Asn(p.I183N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35764677:35764677(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.171A>C
AA Mutation p.Lys57Asn(p.K57N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35737009:35737009(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3814C>T
AA Mutation p.His1272Tyr(p.H1272Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35748475:35748475(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2402C>A
AA Mutation p.Pro801His(p.P801H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35751396:35751396(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1882T>C
AA Mutation p.Phe628Leu(p.F628L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35739439:35739439(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3234A>T
AA Mutation p.Glu1078Asp(p.E1078D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35751455:35751455(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs748750595
CDS Mutation c.1823G>A
AA Mutation p.Arg608Gln(p.R608Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000318121
Start 35762000:35762000(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs115197921
CDS Mutation c.893G>A
AA Mutation p.Arg298Gln(p.R298Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35763197:35763197(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.707T>C
AA Mutation p.Ile236Thr(p.I236T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35736528:35736528(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3988A>G
AA Mutation p.Thr1330Ala(p.T1330A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35748494:35748494(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2383C>G
AA Mutation p.Arg795Gly(p.R795G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35764459:35764459(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.389C>A
AA Mutation p.Pro130His(p.P130H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence stop_gained
Transcription ID ENST00000318121
Start 35764487:35764487(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.361C>T
AA Mutation p.Gln121Ter(p.Q121*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence stop_gained
Transcription ID ENST00000318121
Start 35739151:35739151(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3415C>T
AA Mutation p.Arg1139Ter(p.R1139*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence stop_gained;splice_region_variant
Transcription ID ENST00000318121
Start 35761097:35761097(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1003A>T
AA Mutation p.Lys335Ter(p.K335*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence frameshift_variant
Transcription ID ENST00000318121
Start 35764557:35764558(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.290dupA
AA Mutation p.Asn97LysfsTer15(p.N97Kfs*15)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 17
Mutation Consequence frameshift_variant
Transcription ID ENST00000318121
Start 35763178:35763179(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.725dupA
AA Mutation p.Asn242LysfsTer21(p.N242Kfs*21)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> CLSPN

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35739150:35739150(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375345515
CDS Mutation c.3416G>A
AA Mutation p.Arg1139Gln(p.R1139Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35749514:35749514(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2225A>G
AA Mutation p.Glu742Gly(p.E742G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35743496:35743496(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3001T>A
AA Mutation p.Phe1001Ile(p.F1001I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35737388:35737388(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3698C>A
AA Mutation p.Ser1233Tyr(p.S1233Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35764478:35764478(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.370C>A
AA Mutation p.Leu124Ile(p.L124I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000318121
Start 35748001:35748001(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2533G>C
AA Mutation p.Ala845Pro(p.A845P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000318121
Start 35763229:35763229(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777818827
CDS Mutation c.675T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000318121
Start 35760880:35760880(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1041C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000318121
Start 35739452:35739453(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.3220dupG
AA Mutation p.Glu1074GlyfsTer4(p.E1074Gfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript