Colon Cancer: Gene >> OR8D2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357438
Start	124319447:124319447(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.751T>C
AA Mutation	p.Phe251Leu(p.F251L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357438
Start	124319816:124319816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770093735
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Cys(p.R128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357438
Start	124319543:124319543(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.655G>A
AA Mutation	p.Ala219Thr(p.A219T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357438
Start	124319836:124319836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362A>G
AA Mutation	p.Asp121Gly(p.D121G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357438
Start	124319302:124319302(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.896delA
AA Mutation	p.Asn299MetfsTer3(p.N299Mfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_lost
Transcription ID	ENST00000357438
Start	124319264:124319264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934T>C
AA Mutation	p.Ter312ArgextTer?(p.*312Rext*?)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OR8D2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357438
Start	124319437:124319437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761C>T
AA Mutation	p.Ser254Phe(p.S254F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357438
Start	124320012:124320012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.186T>C
Mutation Classification	Silent
Feature Type	Transcript