Colon Cancer: Gene >> NNMT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299964
Start	114312385:114312385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703T>G
AA Mutation	p.Phe235Val(p.F235V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299964
Start	114312298:114312298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.616A>C
AA Mutation	p.Ile206Leu(p.I206L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299964
Start	114312378:114312378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536229777
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299964
Start	114297968:114297968(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.172C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299964
Start	114298051:114298051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.255C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000299964
Start	114298096:114298097(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.302_303delAG
AA Mutation	p.Glu101AlafsTer5(p.E101Afs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> NNMT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299964
Start	114312379:114312379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750805211
CDS Mutation	c.697G>A
AA Mutation	p.Glu233Lys(p.E233K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000299964
Start	114296620:114296620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.64G>T
AA Mutation	p.Glu22Ter(p.E22*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript