Colon Cancer: Gene >> CDK16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357227
Start	47223583:47223583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750593584
CDS Mutation	c.26G>A
AA Mutation	p.Arg9Gln(p.R9Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357227
Start	47224480:47224480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756986406
CDS Mutation	c.298C>T
AA Mutation	p.Arg100Cys(p.R100C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357227
Start	47228745:47228745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1468C>A
AA Mutation	p.Arg490Ser(p.R490S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357227
Start	47224631:47224631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350G>A
AA Mutation	p.Arg117His(p.R117H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357227
Start	47227012:47227012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1154C>T
AA Mutation	p.Thr385Met(p.T385M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357227
Start	47224502:47224502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768402965
CDS Mutation	c.320G>A
AA Mutation	p.Arg107His(p.R107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357227
Start	47227193:47227193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757032936
CDS Mutation	c.1254C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357227
Start	47225833:47225833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780573029
CDS Mutation	c.696G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000357227
Start	47226339:47226339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.853C>T
AA Mutation	p.Arg285Ter(p.R285*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CDK16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357227
Start	47224486:47224486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.304C>T
AA Mutation	p.Arg102Cys(p.R102C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357227
Start	47225030:47225030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.562G>A
AA Mutation	p.Asp188Asn(p.D188N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357227
Start	47228739:47228739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1462G>A
AA Mutation	p.Ala488Thr(p.A488T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript