Colon Cancer: Gene >> CRY2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000616080
Start	45861018:45861018(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638C>T
AA Mutation	p.Ser213Phe(p.S213F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000616080
Start	45872185:45872185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1736G>A
AA Mutation	p.Arg579Gln(p.R579Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000616080
Start	45869558:45869558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.935G>A
AA Mutation	p.Arg312Gln(p.R312Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000616080
Start	45870174:45870174(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767177340
CDS Mutation	c.1316G>A
AA Mutation	p.Arg439His(p.R439H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000616080
Start	45870917:45870917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1625G>T
AA Mutation	p.Gly542Val(p.G542V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000616080
Start	45860995:45860995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377682679
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000616080
Start	45870505:45870505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1522C>T
AA Mutation	p.Gln508Ter(p.Q508*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CRY2

No Mutation Annotation!