Colon Cancer: Gene >> OR51E2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396950
Start	4682341:4682341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.371C>T
AA Mutation	p.Ala124Val(p.A124V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396950
Start	4682047:4682047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565364663
CDS Mutation	c.665G>A
AA Mutation	p.Arg222Gln(p.R222Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396950
Start	4682245:4682245(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs779431410
CDS Mutation	c.467delT
AA Mutation	p.Phe156SerfsTer6(p.F156Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000396950
Start	4682214:4682214(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.498delC
AA Mutation	p.Phe167SerfsTer17(p.F167Sfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> OR51E2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000396950
Start	4682350:4682350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201184158
CDS Mutation	c.362G>A
AA Mutation	p.Arg121His(p.R121H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000396950
Start	4681927:4681927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143376710
CDS Mutation	c.785G>A
AA Mutation	p.Arg262His(p.R262H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript