Colon Cancer: Gene >> OR1F1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304646
Start	3205152:3205152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.906A>C
AA Mutation	p.Lys302Asn(p.K302N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304646
Start	3204840:3204840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.594A>G
AA Mutation	p.Ile198Met(p.I198M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000304646
Start	3205151:3205151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.905A>C
AA Mutation	p.Lys302Thr(p.K302T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000304646
Start	3204784:3204784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746066317
CDS Mutation	c.538G>A
AA Mutation	p.Asp180Asn(p.D180N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000304646
Start	3204672:3204672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.426C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000304646
Start	3204832:3204832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.586G>T
AA Mutation	p.Glu196Ter(p.E196*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OR1F1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000304646
Start	3204253:3204253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751283450
CDS Mutation	c.7G>A
AA Mutation	p.Gly3Arg(p.G3R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000304646
Start	3205004:3205004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.758G>T
AA Mutation	p.Ser253Ile(p.S253I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript