Colon Cancer: Gene >> MAOB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378069
Start	43797233:43797233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.510C>G
AA Mutation	p.Asn170Lys(p.N170K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378069
Start	43775215:43775215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1195A>T
AA Mutation	p.Thr399Ser(p.T399S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378069
Start	43767562:43767562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1467G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378069
Start	43795871:43795871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.636C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAOB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378069
Start	43767513:43767513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1516G>A
AA Mutation	p.Ala506Thr(p.A506T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378069
Start	43769327:43769327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1327G>A
AA Mutation	p.Gly443Arg(p.G443R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000378069
Start	43803327:43803327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.357G>A
AA Mutation	p.Trp119Ter(p.W119*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript