Colon Cancer: Gene >> CYP2J2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371204
Start	59907901:59907901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.888C>A
AA Mutation	p.Phe296Leu(p.F296L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371204
Start	59904925:59904925(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528475456
CDS Mutation	c.1137C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371204
Start	59904934:59904934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1128C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371204
Start	59904997:59904997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1065C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371204
Start	59893739:59893739(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1421delC
AA Mutation	p.Pro474GlnfsTer6(p.P474Qfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000371204
Start	59912195:59912195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.490C>T
AA Mutation	p.Gln164Ter(p.Q164*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CYP2J2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371204
Start	59904999:59904999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144856672
CDS Mutation	c.1063G>A
AA Mutation	p.Ala355Thr(p.A355T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371204
Start	59912250:59912250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs111798172
CDS Mutation	c.435A>G
Mutation Classification	Silent
Feature Type	Transcript