Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SLITRK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83879786:83879786(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763494516
CDS Mutation c.1722T>A
AA Mutation p.Asn574Lys(p.N574K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880642:83880642(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.866C>A
AA Mutation p.Pro289His(p.P289H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83881216:83881216(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.292G>A
AA Mutation p.Val98Ile(p.V98I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880414:83880414(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1094G>A
AA Mutation p.Ser365Asn(p.S365N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83879643:83879643(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1865C>A
AA Mutation p.Pro622Gln(p.P622Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880198:83880198(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1310C>A
AA Mutation p.Thr437Lys(p.T437K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83881353:83881353(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.155G>A
AA Mutation p.Arg52His(p.R52H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83881163:83881163(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.345C>A
AA Mutation p.Asn115Lys(p.N115K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880531:83880531(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.977C>T
AA Mutation p.Ala326Val(p.A326V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880409:83880409(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1099T>G
AA Mutation p.Leu367Val(p.L367V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83879746:83879746(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1762A>G
AA Mutation p.Thr588Ala(p.T588A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83879432:83879432(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2076C>A
AA Mutation p.His692Gln(p.H692Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880784:83880784(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.724G>A
AA Mutation p.Glu242Lys(p.E242K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880460:83880460(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1048A>T
AA Mutation p.Ile350Phe(p.I350F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880579:83880579(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.929A>T
AA Mutation p.Lys310Met(p.K310M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83879530:83879530(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1978G>A
AA Mutation p.Glu660Lys(p.E660K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83879736:83879736(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1772C>T
AA Mutation p.Ser591Leu(p.S591L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880597:83880597(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.911C>A
AA Mutation p.Ala304Asp(p.A304D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83881240:83881240(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.268G>A
AA Mutation p.Glu90Lys(p.E90K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880435:83880435(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1073A>G
AA Mutation p.Asn358Ser(p.N358S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880274:83880274(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1234G>A
AA Mutation p.Ala412Thr(p.A412T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880961:83880961(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.547G>A
AA Mutation p.Asp183Asn(p.D183N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence synonymous_variant
Transcription ID ENST00000377084
Start 83880935:83880935(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370310778
CDS Mutation c.573G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 24
Mutation Consequence synonymous_variant
Transcription ID ENST00000377084
Start 83881118:83881118(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370805552
CDS Mutation c.390C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 25
Mutation Consequence synonymous_variant
Transcription ID ENST00000377084
Start 83879468:83879468(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2040A>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 26
Mutation Consequence synonymous_variant
Transcription ID ENST00000377084
Start 83880461:83880461(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1047C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 27
Mutation Consequence synonymous_variant
Transcription ID ENST00000377084
Start 83880179:83880179(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1329C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 28
Mutation Consequence synonymous_variant
Transcription ID ENST00000377084
Start 83881274:83881274(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.234C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 29
Mutation Consequence synonymous_variant
Transcription ID ENST00000377084
Start 83879429:83879429(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2079G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 30
Mutation Consequence frameshift_variant
Transcription ID ENST00000377084
Start 83881374:83881374(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.134delA
AA Mutation p.Lys45ArgfsTer64(p.K45Rfs*64)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 31
Mutation Consequence stop_gained
Transcription ID ENST00000377084
Start 83880748:83880748(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.760G>T
AA Mutation p.Glu254Ter(p.E254*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence stop_gained
Transcription ID ENST00000377084
Start 83881294:83881294(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.214C>T
AA Mutation p.Arg72Ter(p.R72*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence frameshift_variant
Transcription ID ENST00000377084
Start 83881373:83881374(version: GRCh38)
Mutation Type INS
dbSNP_RS rs763682501
CDS Mutation c.134dupA
AA Mutation p.Phe47LeufsTer30(p.F47Lfs*30)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> SLITRK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83879913:83879913(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1595A>T
AA Mutation p.Glu532Val(p.E532V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880198:83880198(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1310C>T
AA Mutation p.Thr437Met(p.T437M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880495:83880495(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1013G>A
AA Mutation p.Ser338Asn(p.S338N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880799:83880799(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.709G>A
AA Mutation p.Gly237Ser(p.G237S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880810:83880810(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.698A>G
AA Mutation p.Asn233Ser(p.N233S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880333:83880333(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1175A>C
AA Mutation p.Lys392Thr(p.K392T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83881055:83881055(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.453G>T
AA Mutation p.Gln151His(p.Q151H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880877:83880877(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.631G>T
AA Mutation p.Asp211Tyr(p.D211Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000377084
Start 83880330:83880330(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1178C>T
AA Mutation p.Ser393Leu(p.S393L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000377084
Start 83880035:83880035(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1473C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 11
Mutation Consequence synonymous_variant
Transcription ID ENST00000377084
Start 83881088:83881088(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.420T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 12
Mutation Consequence synonymous_variant
Transcription ID ENST00000377084
Start 83880467:83880467(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1041C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 13
Mutation Consequence frameshift_variant
Transcription ID ENST00000377084
Start 83881374:83881374(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.134delA
AA Mutation p.Lys45ArgfsTer64(p.K45Rfs*64)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 14
Mutation Consequence frameshift_variant
Transcription ID ENST00000377084
Start 83880776:83880777(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.731_732delCC
AA Mutation p.Pro244HisfsTer6(p.P244Hfs*6)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 15
Mutation Consequence stop_gained
Transcription ID ENST00000377084
Start 83879984:83879984(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1524C>A
AA Mutation p.Tyr508Ter(p.Y508*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript