Colon Cancer: Gene >> PPARD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311565
Start	35424113:35424113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.592C>T
AA Mutation	p.Arg198Cys(p.R198C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311565
Start	35425889:35425889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752963884
CDS Mutation	c.1136G>A
AA Mutation	p.Arg379His(p.R379H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311565
Start	35424576:35424576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.875C>T
AA Mutation	p.Ala292Val(p.A292V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311565
Start	35423952:35423952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.431G>A
AA Mutation	p.Arg144His(p.R144H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311565
Start	35425859:35425859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772150465
CDS Mutation	c.1106G>A
AA Mutation	p.Arg369Gln(p.R369Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000311565
Start	35424663:35424663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.962G>A
AA Mutation	p.Arg321His(p.R321H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000311565
Start	35424653:35424653(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750529579
CDS Mutation	c.952C>T
AA Mutation	p.Arg318Cys(p.R318C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311565
Start	35421837:35421837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.303G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311565
Start	35425836:35425836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1083G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311565
Start	35424529:35424529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751619761
CDS Mutation	c.828C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> PPARD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311565
Start	35423951:35423951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430C>T
AA Mutation	p.Arg144Cys(p.R144C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311565
Start	35425961:35425961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1208T>C
AA Mutation	p.Met403Thr(p.M403T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript