Colon Cancer: Gene >> RXFP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368318
Start	155942229:155942229(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520G>C
AA Mutation	p.Val174Leu(p.V174L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368318
Start	155941748:155941748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777267179
CDS Mutation	c.39C>A
AA Mutation	p.Phe13Leu(p.F13L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368318
Start	155941810:155941810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.101A>T
AA Mutation	p.Lys34Ile(p.K34I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368318
Start	155942542:155942542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.833C>G
AA Mutation	p.Pro278Arg(p.P278R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368318
Start	155941876:155941876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167G>T
AA Mutation	p.Gly56Val(p.G56V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368318
Start	155942331:155942331(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622A>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RXFP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368318
Start	155942233:155942233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524C>A
AA Mutation	p.Pro175His(p.P175H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript