Colon Cancer: Gene >> OIT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334011
Start	72898913:72898913(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311C>A
AA Mutation	p.Ala104Asp(p.A104D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334011
Start	72932430:72932430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763046737
CDS Mutation	c.1544G>A
AA Mutation	p.Arg515Gln(p.R515Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334011
Start	72906606:72906606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555A>T
AA Mutation	p.Glu185Asp(p.E185D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334011
Start	72924262:72924262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.985G>A
AA Mutation	p.Val329Met(p.V329M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334011
Start	72898799:72898799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141122150
CDS Mutation	c.197C>T
AA Mutation	p.Ala66Val(p.A66V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334011
Start	72924432:72924432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334011
Start	72913318:72913318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.801G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334011
Start	72898932:72898932(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334011
Start	72924558:72924558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536250413
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> OIT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334011
Start	72924512:72924512(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1235T>G
AA Mutation	p.Leu412Arg(p.L412R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000334011
Start	72899038:72899038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs535158135
CDS Mutation	c.436C>T
AA Mutation	p.His146Tyr(p.H146Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334011
Start	72924346:72924346(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367570425
CDS Mutation	c.1069G>A
AA Mutation	p.Glu357Lys(p.E357K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334011
Start	72913465:72913465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759790374
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334011
Start	72900390:72900390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.450C>A
Mutation Classification	Silent
Feature Type	Transcript