Colon Cancer: Gene >> MPO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58272786:58272786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1754C>A
AA Mutation	p.Ala585Asp(p.A585D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58279211:58279211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.682C>T
AA Mutation	p.Arg228Cys(p.R228C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58271667:58271667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2018G>T
AA Mutation	p.Arg673Leu(p.R673L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58279931:58279931(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332C>T
AA Mutation	p.Thr111Met(p.T111M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58279207:58279207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.686C>T
AA Mutation	p.Ala229Val(p.A229V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58273534:58273534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs119469013
CDS Mutation	c.1501G>A
AA Mutation	p.Gly501Ser(p.G501S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58279551:58279551(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.520C>T
AA Mutation	p.Arg174Cys(p.R174C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58270715:58270715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2179T>G
AA Mutation	p.Phe727Val(p.F727V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58272771:58272771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753062060
CDS Mutation	c.1769G>A
AA Mutation	p.Arg590His(p.R590H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58272754:58272754(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1786C>T
AA Mutation	p.Leu596Phe(p.L596F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58280372:58280372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs565563391
CDS Mutation	c.242G>A
AA Mutation	p.Arg81Gln(p.R81Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225275
Start	58275686:58275686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1221T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000225275
Start	58272869:58272869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1671G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225275
Start	58278127:58278127(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.904delC
AA Mutation	p.Arg302AlafsTer132(p.R302Afs*132)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225275
Start	58280694:58280694(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.65delG
AA Mutation	p.Gly22ValfsTer6(p.G22Vfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000225275
Start	58275577:58275577(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1330C>T
AA Mutation	p.Gln444Ter(p.Q444*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MPO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58272771:58272771(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753062060
CDS Mutation	c.1769G>A
AA Mutation	p.Arg590His(p.R590H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58275661:58275661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1246C>A
AA Mutation	p.His416Asn(p.H416N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58277928:58277928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773687000
CDS Mutation	c.1103G>A
AA Mutation	p.Arg368His(p.R368H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58275676:58275676(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1231G>A
AA Mutation	p.Glu411Lys(p.E411K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58277856:58277856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767511612
CDS Mutation	c.1175G>A
AA Mutation	p.Arg392His(p.R392H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000225275
Start	58271832:58271832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1853G>A
AA Mutation	p.Gly618Asp(p.G618D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript