Colon Cancer: Gene >> SFRP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266066
Start	97771650:97771650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.184C>A
AA Mutation	p.Leu62Ile(p.L62I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000266066
Start	97767849:97767849(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.619C>T
AA Mutation	p.Arg207Cys(p.R207C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000266066
Start	97771495:97771495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.339G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000266066
Start	97767518:97767519(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.949dupC
AA Mutation	p.His317ProfsTer55(p.H317Pfs*55)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SFRP5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000266066
Start	97767551:97767551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.917A>G
AA Mutation	p.Tyr306Cys(p.Y306C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript