Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KHDRBS1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000327300
Start 32031554:32031554(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.538C>A
AA Mutation p.Gln180Lys(p.Q180K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000327300
Start 32033200:32033200(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.637C>T
AA Mutation p.Arg213Cys(p.R213C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000327300
Start 32014303:32014303(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.308A>G
AA Mutation p.Tyr103Cys(p.Y103C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000327300
Start 32038035:32038035(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1106A>G
AA Mutation p.Tyr369Cys(p.Y369C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000327300
Start 32033269:32033269(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.710delC
AA Mutation p.Pro237HisfsTer19(p.P237Hfs*19)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000327300
Start 32037932:32037932(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1007delC
AA Mutation p.Pro336HisfsTer4(p.P336Hfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 7
Mutation Consequence frameshift_variant
Transcription ID ENST00000327300
Start 32037857:32037858(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.934dupG
AA Mutation p.Ala312GlyfsTer56(p.A312Gfs*56)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 8
Mutation Consequence frameshift_variant
Transcription ID ENST00000327300
Start 32014256:32014257(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.267dupC
AA Mutation p.Ser90LeufsTer41(p.S90Lfs*41)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> KHDRBS1

Mutation ID 1
Mutation Consequence frameshift_variant
Transcription ID ENST00000327300
Start 32037858:32037858(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.934delG
AA Mutation p.Ala312LeufsTer8(p.A312Lfs*8)
Mutation Classification Frame_Shift_Del
Feature Type Transcript