Colon Cancer: Gene >> OR7A17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327462
Start	14880517:14880517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.839T>G
AA Mutation	p.Val280Gly(p.V280G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000327462
Start	14881112:14881112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244C>T
AA Mutation	p.Leu82Phe(p.L82F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000327462
Start	14880745:14880745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.611G>T
AA Mutation	p.Gly204Val(p.G204V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000327462
Start	14880713:14880713(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643C>A
AA Mutation	p.Leu215Ile(p.L215I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000327462
Start	14881268:14881268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OR7A17

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000327462
Start	14880988:14880988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.368T>C
AA Mutation	p.Phe123Ser(p.F123S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript