Colon Cancer: Gene >> MAOA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338702
Start	43728241:43728241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.572C>T
AA Mutation	p.Ala191Val(p.A191V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338702
Start	43744135:43744135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762042526
CDS Mutation	c.1401C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338702
Start	43731723:43731723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138703731
CDS Mutation	c.825G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338702
Start	43712776:43712776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.483T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338702
Start	43741995:43741995(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1214delG
AA Mutation	p.Gly405AlafsTer12(p.G405Afs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAOA

Mutation ID	1
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000338702
Start	43741979:43741980(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1198_1200dupGAG
AA Mutation	p.Glu400dup(p.E400dup)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript