Colon Cancer: Gene >> CDK20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325303
Start	87974029:87974029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.82G>A
AA Mutation	p.Glu28Lys(p.E28K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325303
Start	87967485:87967485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759457795
CDS Mutation	c.1018C>T
AA Mutation	p.Arg340Trp(p.R340W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325303
Start	87970823:87970823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325303
Start	87970615:87970615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142841498
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325303
Start	87971249:87971249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.276G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000325303
Start	87967548:87967548(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs67862915
CDS Mutation	c.955delC
AA Mutation	p.His319ThrfsTer16(p.H319Tfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000325303
Start	87969920:87969920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.564-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CDK20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325303
Start	87971210:87971210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315G>C
AA Mutation	p.Lys105Asn(p.K105N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325303
Start	87967589:87967589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376253655
CDS Mutation	c.914G>A
AA Mutation	p.Arg305His(p.R305H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript