Colon Cancer: Gene >> OPN1SW

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128775480:128775480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775018062
CDS Mutation	c.311G>A
AA Mutation	p.Arg104His(p.R104H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128773659:128773659(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.917T>C
AA Mutation	p.Met306Thr(p.M306T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128775468:128775468(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.323C>G
AA Mutation	p.Ala108Gly(p.A108G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128773719:128773719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.857C>A
AA Mutation	p.Thr286Asn(p.T286N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128772605:128772605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545093905
CDS Mutation	c.982G>A
AA Mutation	p.Asp328Asn(p.D328N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128775481:128775481(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149847165
CDS Mutation	c.310C>T
AA Mutation	p.Arg104Cys(p.R104C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128775052:128775052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769004186
CDS Mutation	c.455C>T
AA Mutation	p.Thr152Met(p.T152M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128775083:128775083(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.424A>C
AA Mutation	p.Asn142His(p.N142H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128775016:128775016(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.491T>C
AA Mutation	p.Val164Ala(p.V164A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128775490:128775490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144524727
CDS Mutation	c.301G>A
AA Mutation	p.Val101Ile(p.V101I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128773789:128773789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751647679
CDS Mutation	c.787G>A
AA Mutation	p.Val263Met(p.V263M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249389
Start	128775479:128775479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.312C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OPN1SW

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000249389
Start	128775459:128775459(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.332G>C
AA Mutation	p.Gly111Ala(p.G111A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000249389
Start	128775497:128775497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294A>T
Mutation Classification	Silent
Feature Type	Transcript