Colon Cancer: Gene >> ONECUT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000305901
Start	52789473:52789473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.412C>T
AA Mutation	p.His138Tyr(p.H138Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000305901
Start	52757728:52757728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776002886
CDS Mutation	c.1225C>T
AA Mutation	p.Arg409Cys(p.R409C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000305901
Start	52788969:52788969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916A>G
AA Mutation	p.Lys306Glu(p.K306E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000305901
Start	52788842:52788842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1043G>A
AA Mutation	p.Arg348Gln(p.R348Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000305901
Start	52788992:52788992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.893C>T
AA Mutation	p.Ala298Val(p.A298V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000305901
Start	52789058:52789058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.827C>T
AA Mutation	p.Thr276Ile(p.T276I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000305901
Start	52789236:52789236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.649G>T
AA Mutation	p.Gly217Cys(p.G217C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305901
Start	52789051:52789051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746244397
CDS Mutation	c.834G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305901
Start	52789693:52789693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748705076
CDS Mutation	c.192C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305901
Start	52789642:52789642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.243C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305901
Start	52757648:52757648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780170577
CDS Mutation	c.1305C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305901
Start	52789231:52789231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305901
Start	52789294:52789294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.591C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000305901
Start	52788822:52788822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1063C>T
AA Mutation	p.Gln355Ter(p.Q355*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ONECUT1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000305901
Start	52757648:52757648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780170577
CDS Mutation	c.1305C>T
Mutation Classification	Silent
Feature Type	Transcript