Colon Cancer: Gene >> OLFM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135120104:135120104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1384T>C
AA Mutation	p.Tyr462His(p.Y462H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135120161:135120161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1441C>T
AA Mutation	p.Arg481Cys(p.R481C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135120119:135120119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774962345
CDS Mutation	c.1399G>A
AA Mutation	p.Gly467Ser(p.G467S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135119997:135119997(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1277A>G
AA Mutation	p.Tyr426Cys(p.Y426C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135119952:135119952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767622547
CDS Mutation	c.1232C>T
AA Mutation	p.Thr411Met(p.T411M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000615948
Start	135077159:135077159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.443C>A
AA Mutation	p.Thr148Lys(p.T148K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135119969:135119969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1249G>T
AA Mutation	p.Gly417Cys(p.G417C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135119948:135119948(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762305455
CDS Mutation	c.1228G>A
AA Mutation	p.Gly410Ser(p.G410S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135120140:135120140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1420G>A
AA Mutation	p.Val474Met(p.V474M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135120162:135120162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115852241
CDS Mutation	c.1442G>A
AA Mutation	p.Arg481His(p.R481H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135119721:135119721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773058353
CDS Mutation	c.1001G>A
AA Mutation	p.Arg334His(p.R334H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000615948
Start	135076857:135076857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs566603017
CDS Mutation	c.142G>A
AA Mutation	p.Glu48Lys(p.E48K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135088020:135088020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.31G>A
AA Mutation	p.Val11Met(p.V11M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135119960:135119960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766525119
CDS Mutation	c.1240G>A
AA Mutation	p.Val414Ile(p.V414I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135119535:135119535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.815G>A
AA Mutation	p.Arg272His(p.R272H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000615948
Start	135076937:135076937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.222G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371793
Start	135119737:135119737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs558323197
CDS Mutation	c.1017C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371793
Start	135095893:135095893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.330C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371793
Start	135119810:135119810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000615948
Start	135076991:135076991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.276T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000615948
Start	135076856:135076856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs190503483
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000615948
Start	135077132:135077132(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.416delA
AA Mutation	p.Gln139ArgfsTer?(p.Q139Rfs*?)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371801
Start	135076260:135076260(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.304delG
AA Mutation	p.Ala102LeufsTer44(p.A102Lfs*44)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	stop_gained
Transcription ID	ENST00000371793
Start	135090224:135090224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.180G>A
AA Mutation	p.Trp60Ter(p.W60*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> OLFM1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135119519:135119519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772311640
CDS Mutation	c.799G>A
AA Mutation	p.Gly267Ser(p.G267S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135120005:135120005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1285C>A
AA Mutation	p.Gln429Lys(p.Q429K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135119624:135119624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.904G>A
AA Mutation	p.Gly302Arg(p.G302R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135119577:135119577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372599021
CDS Mutation	c.857C>T
AA Mutation	p.Thr286Met(p.T286M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371793
Start	135098291:135098291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.462A>G
AA Mutation	p.Ile154Met(p.I154M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371793
Start	135090278:135090278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771177279
CDS Mutation	c.234C>T
Mutation Classification	Silent
Feature Type	Transcript