Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000395284
Start 60791939:60791939(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs45540532
CDS Mutation c.539G>A
AA Mutation p.Arg180His(p.R180H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000395284
Start 60792285:60792285(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.791T>C
AA Mutation p.Leu264Pro(p.L264P)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000395284
Start 60792032:60792032(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.632A>G
AA Mutation p.Asp211Gly(p.D211G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000395284
Start 60792182:60792182(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.688G>C
AA Mutation p.Glu230Gln(p.E230Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000395284
Start 60788165:60788165(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.424A>T
AA Mutation p.Ile142Phe(p.I142F)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000395284
Start 60780191:60780191(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.26A>G
AA Mutation p.Lys9Arg(p.K9R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000395284
Start 60788114:60788114(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.373C>A
AA Mutation p.Leu125Ile(p.L125I)
Mutation Classification Missense_Mutation
Feature Type Transcript

Rectum Cancer: Gene >> CDK1

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000395284
Start 60793905:60793905(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.824G>A
AA Mutation p.Arg275Gln(p.R275Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000395284
Start 60788075:60788075(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.334A>C
AA Mutation p.Ile112Leu(p.I112L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence frameshift_variant
Transcription ID ENST00000395284
Start 60793916:60793916(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.838delA
AA Mutation p.Met280TrpfsTer3(p.M280Wfs*3)
Mutation Classification Frame_Shift_Del
Feature Type Transcript