Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> CDK10

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000353379
Start 89691530:89691530(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.320G>A
AA Mutation p.Gly107Glu(p.G107E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000353379
Start 89689294:89689294(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.130C>A
AA Mutation p.Arg44Ser(p.R44S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000353379
Start 89690600:89690600(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.208G>T
AA Mutation p.Val70Leu(p.V70L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000353379
Start 89689265:89689265(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755952324
CDS Mutation c.101G>A
AA Mutation p.Arg34Gln(p.R34Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000353379
Start 89690582:89690582(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.190A>G
AA Mutation p.Ile64Val(p.I64V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000353379
Start 89691498:89691498(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs772182758
CDS Mutation c.288G>A
Mutation Classification Silent
Feature Type Transcript

Rectum Cancer: Gene >> CDK10

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000353379
Start 89694689:89694689(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750772459
CDS Mutation c.693G>C
AA Mutation p.Glu231Asp(p.E231D)
Mutation Classification Missense_Mutation
Feature Type Transcript