Colon Cancer: Gene >> SLC25A16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000609923
Start	68488584:68488584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656C>T
AA Mutation	p.Ser219Phe(p.S219F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000609923
Start	68483464:68483464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747313620
CDS Mutation	c.967G>A
AA Mutation	p.Glu323Lys(p.E323K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000609923
Start	68487205:68487205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.781T>A
AA Mutation	p.Phe261Ile(p.F261I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000609923
Start	68483542:68483542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139107749
CDS Mutation	c.889C>T
AA Mutation	p.Arg297Ter(p.R297*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SLC25A16

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000609923
Start	68516830:68516830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144C>A
AA Mutation	p.Cys48Ter(p.C48*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000609923
Start	68483542:68483542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139107749
CDS Mutation	c.889C>T
AA Mutation	p.Arg297Ter(p.R297*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript