Colon Cancer: Gene >> CASP9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333868
Start	15518191:15518191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337C>T
AA Mutation	p.Pro113Ser(p.P113S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333868
Start	15506951:15506951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748271106
CDS Mutation	c.578G>A
AA Mutation	p.Arg193His(p.R193H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333868
Start	15506997:15506997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145588217
CDS Mutation	c.532C>T
AA Mutation	p.Arg178Cys(p.R178C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333868
Start	15506958:15506958(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771197055
CDS Mutation	c.571C>T
AA Mutation	p.Arg191Trp(p.R191W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333868
Start	15504699:15504699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.780C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CASP9

No Mutation Annotation!