Colon Cancer: Gene >> PTGDR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306051
Start	52274901:52274901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1017C>A
AA Mutation	p.Phe339Leu(p.F339L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306051
Start	52274799:52274799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.915C>A
AA Mutation	p.Asp305Glu(p.D305E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306051
Start	52268613:52268613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.799C>A
AA Mutation	p.Leu267Met(p.L267M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PTGDR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306051
Start	52274813:52274813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143143539
CDS Mutation	c.929G>A
AA Mutation	p.Arg310Gln(p.R310Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript