Colon Cancer: Gene >> PPARA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262735
Start	46215244:46215244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.280C>T
AA Mutation	p.Pro94Ser(p.P94S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262735
Start	46231930:46231930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.850G>A
AA Mutation	p.Val284Ile(p.V284I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262735
Start	46218279:46218279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747200358
CDS Mutation	c.386C>T
AA Mutation	p.Thr129Met(p.T129M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262735
Start	46215232:46215232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs559996245
CDS Mutation	c.268G>A
AA Mutation	p.Val90Met(p.V90M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262735
Start	46215317:46215317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.353C>T
AA Mutation	p.Ala118Val(p.A118V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262735
Start	46198589:46198589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561580529
CDS Mutation	c.206C>T
AA Mutation	p.Thr69Met(p.T69M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262735
Start	46218276:46218276(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>A
AA Mutation	p.Arg128Gln(p.R128Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262735
Start	46215192:46215192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774377701
CDS Mutation	c.228G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262735
Start	46219886:46219887(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.584_585delTA
AA Mutation	p.Ile195ArgfsTer4(p.I195Rfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262735
Start	46235256:46235256(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1288delA
AA Mutation	p.Met430TrpfsTer8(p.M430Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> PPARA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262735
Start	46215265:46215265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301G>A
AA Mutation	p.Glu101Lys(p.E101K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262735
Start	46231972:46231972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.892G>A
AA Mutation	p.Ala298Thr(p.A298T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262735
Start	46232205:46232205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1125C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000262735
Start	46198471:46198471(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88G>T
AA Mutation	p.Glu30Ter(p.E30*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript