Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> LSR

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35262627:35262627(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.857C>T
AA Mutation p.Pro286Leu(p.P286L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35267405:35267405(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1585C>A
AA Mutation p.Arg529Ser(p.R529S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35259058:35259058(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775741599
CDS Mutation c.712G>A
AA Mutation p.Val238Ile(p.V238I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35267726:35267726(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1906C>G
AA Mutation p.Leu636Val(p.L636V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35266436:35266436(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755436260
CDS Mutation c.1000G>A
AA Mutation p.Ala334Thr(p.A334T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35266506:35266506(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1070C>A
AA Mutation p.Pro357His(p.P357H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35266925:35266925(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372794690
CDS Mutation c.1246G>A
AA Mutation p.Asp416Asn(p.D416N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000361790
Start 35262556:35262556(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.786C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence frameshift_variant
Transcription ID ENST00000361790
Start 35261959:35261959(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.756delT
AA Mutation p.Gln253ArgfsTer5(p.Q253Rfs*5)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 10
Mutation Consequence frameshift_variant
Transcription ID ENST00000361790
Start 35266941:35266942(version: GRCh38)
Mutation Type INS
dbSNP_RS rs771235856
CDS Mutation c.1269dupC
AA Mutation p.Ser424GlnfsTer10(p.S424Qfs*10)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 11
Mutation Consequence inframe_deletion
Transcription ID ENST00000361790
Start 35266905:35266907(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1228_1230delAAG
AA Mutation p.Lys410del(p.K410del)
Mutation Classification In_Frame_Del
Feature Type Transcript

Rectum Cancer: Gene >> LSR

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35267459:35267459(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1639C>T
AA Mutation p.Arg547Trp(p.R547W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35262597:35262597(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.827T>G
AA Mutation p.Leu276Arg(p.L276R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35250464:35250464(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.403C>A
AA Mutation p.Arg135Ser(p.R135S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35262656:35262656(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.886C>A
AA Mutation p.Pro296Thr(p.P296T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35250458:35250458(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.397C>T
AA Mutation p.Arg133Trp(p.R133W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000361790
Start 35262690:35262690(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.920C>G
AA Mutation p.Ala307Gly(p.A307G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000361790
Start 35266367:35266367(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755518851
CDS Mutation c.931G>A
AA Mutation p.Ala311Thr(p.A311T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000361790
Start 35267732:35267732(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1912A>C
AA Mutation p.Lys638Gln(p.K638Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000361790
Start 35250508:35250508(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.447C>T
Mutation Classification Silent
Feature Type Transcript