Colon Cancer: Gene >> COPS5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357849
Start	67061911:67061911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.86A>G
AA Mutation	p.Tyr29Cys(p.Y29C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357849
Start	67051297:67051297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138638780
CDS Mutation	c.704G>A
AA Mutation	p.Arg235His(p.R235H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357849
Start	67057401:67057401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570152372
CDS Mutation	c.552C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000357849
Start	67051291:67051291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.710T>A
AA Mutation	p.Leu237Ter(p.L237*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> COPS5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357849
Start	67045851:67045851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881G>A
AA Mutation	p.Arg294Gln(p.R294Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357849
Start	67045860:67045860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143525514
CDS Mutation	c.872C>T
AA Mutation	p.Thr291Met(p.T291M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript