Colon Cancer: Gene >> OPN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366554
Start	241597792:241597792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780348058
CDS Mutation	c.899C>T
AA Mutation	p.Ser300Leu(p.S300L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000366554
Start	241604411:241604411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.542T>C
AA Mutation	p.Leu181Pro(p.L181P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000366554
Start	241640062:241640062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193C>T
AA Mutation	p.Leu65Phe(p.L65F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000366554
Start	241604529:241604529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761189513
CDS Mutation	c.424C>T
AA Mutation	p.Arg142Cys(p.R142C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000366554
Start	241604537:241604537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777101745
CDS Mutation	c.416G>A
AA Mutation	p.Arg139His(p.R139H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366554
Start	241594680:241594680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.957C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366554
Start	241604527:241604527(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs570915682
CDS Mutation	c.426C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366554
Start	241604389:241604389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000366554
Start	241604265:241604265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688C>T
AA Mutation	p.Arg230Ter(p.R230*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OPN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000366554
Start	241597810:241597810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770842729
CDS Mutation	c.881C>T
AA Mutation	p.Ser294Leu(p.S294L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000366554
Start	241604452:241604452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370046789
CDS Mutation	c.501G>A
Mutation Classification	Silent
Feature Type	Transcript