Colon Cancer: Gene >> MOXD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132328516:132328516(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768904208
CDS Mutation	c.742G>A
AA Mutation	p.Asp248Asn(p.D248N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132297908:132297908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1556C>A
AA Mutation	p.Ser519Tyr(p.S519Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132297230:132297230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1765C>A
AA Mutation	p.Leu589Met(p.L589M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132322708:132322708(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1276T>C
AA Mutation	p.Tyr426His(p.Y426H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132297887:132297887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1577A>C
AA Mutation	p.Lys526Thr(p.K526T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132322746:132322746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750766213
CDS Mutation	c.1238A>G
AA Mutation	p.Tyr413Cys(p.Y413C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132328438:132328438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820T>G
AA Mutation	p.Phe274Val(p.F274V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132328058:132328058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.901T>C
AA Mutation	p.Tyr301His(p.Y301H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MOXD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132322776:132322776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201058024
CDS Mutation	c.1208G>A
AA Mutation	p.Arg403Gln(p.R403Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132322785:132322785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369720103
CDS Mutation	c.1199G>A
AA Mutation	p.Arg400His(p.R400H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132297216:132297216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1779C>A
AA Mutation	p.Phe593Leu(p.F593L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000367963
Start	132297788:132297788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748046713
CDS Mutation	c.1676C>T
AA Mutation	p.Ser559Leu(p.S559L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132320664:132320664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138817081
CDS Mutation	c.1330C>T
AA Mutation	p.Arg444Cys(p.R444C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367963
Start	132374761:132374761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146200701
CDS Mutation	c.281C>T
AA Mutation	p.Ala94Val(p.A94V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript