Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> DNAJB1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000254322
Start 14516839:14516839(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.419G>A
AA Mutation p.Gly140Asp(p.G140D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000254322
Start 14518140:14518140(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.210A>C
AA Mutation p.Glu70Asp(p.E70D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000254322
Start 14516514:14516514(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.744G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence frameshift_variant
Transcription ID ENST00000254322
Start 14515980:14515981(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.982dupC
AA Mutation p.Gln328ProfsTer8(p.Q328Pfs*8)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript
Mutation ID 5
Mutation Consequence frameshift_variant
Transcription ID ENST00000254322
Start 14516676:14516677(version: GRCh38)
Mutation Type INS
dbSNP_RS novel
CDS Mutation c.581_582insCCATCTCTCTT
AA Mutation p.Lys195HisfsTer4(p.K195Hfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> DNAJB1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000254322
Start 14516815:14516815(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.443G>C
AA Mutation p.Arg148Pro(p.R148P)
Mutation Classification Missense_Mutation
Feature Type Transcript