Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> XPO1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61488232:61488232(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2246G>A
AA Mutation p.Arg749Gln(p.R749Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61495558:61495558(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.944A>G
AA Mutation p.Glu315Gly(p.E315G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61478876:61478876(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3160A>C
AA Mutation p.Met1054Leu(p.M1054L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61481225:61481225(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3029C>A
AA Mutation p.Ala1010Asp(p.A1010D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61485863:61485863(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2413G>A
AA Mutation p.Ala805Thr(p.A805T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61499765:61499765(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.538G>T
AA Mutation p.Asp180Tyr(p.D180Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000401558
Start 61483939:61483939(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755621083
CDS Mutation c.2675C>T
AA Mutation p.Thr892Met(p.T892M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000401558
Start 61482475:61482475(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2877T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000401558
Start 61493030:61493030(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1269A>G
Mutation Classification Silent
Feature Type Transcript
Mutation ID 10
Mutation Consequence synonymous_variant
Transcription ID ENST00000401558
Start 61482421:61482421(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2931T>C
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> XPO1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61478892:61478892(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3144G>T
AA Mutation p.Glu1048Asp(p.E1048D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61492337:61492337(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1711G>A
AA Mutation p.Glu571Lys(p.E571K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61485949:61485949(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2327T>G
AA Mutation p.Phe776Cys(p.F776C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61499822:61499822(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.481G>A
AA Mutation p.Glu161Lys(p.E161K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61488756:61488756(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2038A>C
AA Mutation p.Lys680Gln(p.K680Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000401558
Start 61495544:61495544(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.958C>A
AA Mutation p.Gln320Lys(p.Q320K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000401558
Start 61498790:61498790(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.642A>C
AA Mutation p.Glu214Asp(p.E214D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000401558
Start 61494044:61494044(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs770682729
CDS Mutation c.1095C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 9
Mutation Consequence synonymous_variant
Transcription ID ENST00000401558
Start 61499727:61499727(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.576G>A
Mutation Classification Silent
Feature Type Transcript