Colon Cancer: Gene >> OPN5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371211
Start	47795345:47795345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.538G>A
AA Mutation	p.Gly180Arg(p.G180R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371211
Start	47795330:47795330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780695747
CDS Mutation	c.523G>A
AA Mutation	p.Val175Ile(p.V175I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371211
Start	47791870:47791870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.319C>T
AA Mutation	p.Arg107Cys(p.R107C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371211
Start	47808294:47808294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200073746
CDS Mutation	c.897G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000371211
Start	47791973:47791973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> OPN5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371211
Start	47795379:47795379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572A>G
AA Mutation	p.Gln191Arg(p.Q191R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371211
Start	47808344:47808344(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.947G>T
AA Mutation	p.Cys316Phe(p.C316F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript