Colon Cancer: Gene >> MNAT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000261245
Start	60812027:60812027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.461A>T
AA Mutation	p.Glu154Val(p.E154V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000261245
Start	60798106:60798106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763740169
CDS Mutation	c.262G>T
AA Mutation	p.Asp88Tyr(p.D88Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000261245
Start	60812105:60812105(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539A>C
AA Mutation	p.Lys180Thr(p.K180T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000261245
Start	60796356:60796356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.229A>C
AA Mutation	p.Lys77Gln(p.K77Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000261245
Start	60798138:60798138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294C>A
AA Mutation	p.Phe98Leu(p.F98L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000261245
Start	60796263:60796264(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.136_137insA
AA Mutation	p.Cys46Ter(p.C46*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000261245
Start	60796264:60796265(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.137_138insTCACTTCTATTTAAAAT
AA Mutation	p.Pro47HisfsTer39(p.P47Hfs*39)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000261245
Start	60808430:60808430(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.420+2T>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MNAT1

No Mutation Annotation!