Colon Cancer: Gene >> SIRT7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328666
Start	81913784:81913784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190336639
CDS Mutation	c.994G>A
AA Mutation	p.Ala332Thr(p.A332T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328666
Start	81912577:81912577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781471662
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Cys(p.R348C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328666
Start	81912434:81912434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1185A>C
AA Mutation	p.Lys395Asn(p.K395N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000328666
Start	81913826:81913826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200982525
CDS Mutation	c.952G>A
AA Mutation	p.Val318Ile(p.V318I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328666
Start	81915497:81915497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199778686
CDS Mutation	c.423C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SIRT7

No Mutation Annotation!