Colon Cancer: Gene >> ONECUT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000491143
Start	57436165:57436165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449C>T
AA Mutation	p.Thr150Met(p.T150M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000491143
Start	57476515:57476515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1307T>C
AA Mutation	p.Leu436Pro(p.L436P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000491143
Start	57436268:57436268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186386413
CDS Mutation	c.552C>G
AA Mutation	p.His184Gln(p.H184Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000491143
Start	57476556:57476556(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755413489
CDS Mutation	c.1348C>T
AA Mutation	p.Arg450Cys(p.R450C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000491143
Start	57436321:57436321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.605G>A
AA Mutation	p.Arg202His(p.R202H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000491143
Start	57436919:57436919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1203G>C
AA Mutation	p.Gln401His(p.Q401H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ONECUT2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000491143
Start	57436502:57436502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749300131
CDS Mutation	c.786C>T
Mutation Classification	Silent
Feature Type	Transcript