Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> BHLHE41

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000242728
Start 26123160:26123160(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.355T>C
AA Mutation p.Ser119Pro(p.S119P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence synonymous_variant
Transcription ID ENST00000242728
Start 26124774:26124774(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000242728
Start 26123643:26123643(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.333T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000242728
Start 26124738:26124738(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.42G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000242728
Start 26123676:26123676(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.300C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence frameshift_variant
Transcription ID ENST00000242728
Start 26122985:26122985(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.530delC
AA Mutation p.Pro177ArgfsTer4(p.P177Rfs*4)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 7
Mutation Consequence stop_gained
Transcription ID ENST00000242728
Start 26124149:26124149(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.157G>T
AA Mutation p.Glu53Ter(p.E53*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence stop_gained
Transcription ID ENST00000242728
Start 26124533:26124533(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.112C>T
AA Mutation p.Arg38Ter(p.R38*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> BHLHE41

Mutation ID 1
Mutation Consequence stop_gained
Transcription ID ENST00000242728
Start 26123094:26123094(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.421G>T
AA Mutation p.Glu141Ter(p.E141*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript