Colon Cancer: Gene >> SIRT4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000202967
Start	120312716:120312716(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.758C>T
AA Mutation	p.Ala253Val(p.A253V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000202967
Start	120312614:120312614(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.656C>T
AA Mutation	p.Thr219Ile(p.T219I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000202967
Start	120303820:120303820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.259C>A
AA Mutation	p.Arg87Ser(p.R87S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000202967
Start	120312491:120312491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs546233791
CDS Mutation	c.533G>A
AA Mutation	p.Arg178Gln(p.R178Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000202967
Start	120312978:120312978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371968487
CDS Mutation	c.887C>T
AA Mutation	p.Ala296Val(p.A296V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202967
Start	120312967:120312967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746858573
CDS Mutation	c.876G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202967
Start	120303603:120303603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000202967
Start	120312491:120312491(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.538delG
AA Mutation	p.Val180CysfsTer9(p.V180Cfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000202967
Start	120312505:120312505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.547G>T
AA Mutation	p.Glu183Ter(p.E183*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000202967
Start	120303988:120303989(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.431dupA
AA Mutation	p.Asn144LysfsTer52(p.N144Kfs*52)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SIRT4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000202967
Start	120303821:120303821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762295806
CDS Mutation	c.260G>A
AA Mutation	p.Arg87His(p.R87H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000202967
Start	120312570:120312570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150373559
CDS Mutation	c.612C>T
Mutation Classification	Silent
Feature Type	Transcript