Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> RNMT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262173
Start	13731678:13731678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161A>G
AA Mutation	p.Asp54Gly(p.D54G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262173
Start	13742626:13742626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1113C>A
AA Mutation	p.Phe371Leu(p.F371L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262173
Start	13742580:13742580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1067G>A
AA Mutation	p.Cys356Tyr(p.C356Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262173
Start	13741531:13741531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779338611
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Cys(p.R272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262173
Start	13737073:13737073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617G>A
AA Mutation	p.Cys206Tyr(p.C206Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262173
Start	13746254:13746254(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1180delA
AA Mutation	p.Thr394HisfsTer19(p.T394Hfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000262173
Start	13742513:13742513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1000G>T
AA Mutation	p.Glu334Ter(p.E334*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> RNMT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262173
Start	13741531:13741531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779338611
CDS Mutation	c.814C>T
AA Mutation	p.Arg272Cys(p.R272C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262173
Start	13731606:13731606(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.89T>G
AA Mutation	p.Phe30Cys(p.F30C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262173
Start	13731729:13731729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746089526
CDS Mutation	c.212C>A
AA Mutation	p.Ser71Tyr(p.S71Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262173
Start	13731817:13731817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300C>T
Mutation Classification	Silent
Feature Type	Transcript