Colon Cancer: Gene >> SIRT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249396
Start	38893837:38893837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.94G>A
AA Mutation	p.Ala32Thr(p.A32T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249396
Start	38889738:38889738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199856206
CDS Mutation	c.383C>T
AA Mutation	p.Pro128Leu(p.P128L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249396
Start	38883672:38883672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200616294
CDS Mutation	c.586G>A
AA Mutation	p.Val196Ile(p.V196I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249396
Start	38879182:38879182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1143G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249396
Start	38879251:38879251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142522547
CDS Mutation	c.1074G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SIRT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249396
Start	38883690:38883690(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.568T>G
AA Mutation	p.Phe190Val(p.F190V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249396
Start	38879161:38879161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1164C>A
Mutation Classification	Silent
Feature Type	Transcript