Colon Cancer: Gene >> SIRT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000337491
Start	4174729:4174729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.956C>T
AA Mutation	p.Pro319Leu(p.P319L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000337491
Start	4174879:4174879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.806T>A
AA Mutation	p.Leu269Gln(p.L269Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000337491
Start	4180882:4180882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.94C>T
AA Mutation	p.Arg32Trp(p.R32W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337491
Start	4180829:4180829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.147C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000337491
Start	4175892:4175892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SIRT6

No Mutation Annotation!