Colon Cancer: Gene >> CDK9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373264
Start	127789217:127789217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793C>G
AA Mutation	p.Leu265Val(p.L265V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000373264
Start	127788385:127788385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770506343
CDS Mutation	c.604G>A
AA Mutation	p.Gly202Arg(p.G202R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000373264
Start	127789275:127789275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851G>A
AA Mutation	p.Arg284His(p.R284H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000373264
Start	127789274:127789274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370938433
CDS Mutation	c.850C>T
AA Mutation	p.Arg284Cys(p.R284C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373264
Start	127789205:127789205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000373264
Start	127789423:127789423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150060991
CDS Mutation	c.999G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CDK9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000373264
Start	127789301:127789301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877G>T
AA Mutation	p.Asp293Tyr(p.D293Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000373264
Start	127789497:127789497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753758776
CDS Mutation	c.1073G>A
AA Mutation	p.Arg358His(p.R358H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript