Colon Cancer: Gene >> NONO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276079
Start	71297388:71297388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.955C>T
AA Mutation	p.Arg319Cys(p.R319C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000276079
Start	71294362:71294362(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484G>A
AA Mutation	p.Glu162Lys(p.E162K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000276079
Start	71296871:71296871(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767G>T
AA Mutation	p.Arg256Ile(p.R256I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000276079
Start	71294440:71294440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562T>C
AA Mutation	p.Ser188Pro(p.S188P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000276079
Start	71290652:71290652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.15A>C
AA Mutation	p.Lys5Asn(p.K5N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000276079
Start	71294234:71294234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356G>A
AA Mutation	p.Arg119Gln(p.R119Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000276079
Start	71294296:71294296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.418C>T
AA Mutation	p.Arg140Cys(p.R140C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000276079
Start	71297933:71297933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1126G>T
AA Mutation	p.Asp376Tyr(p.D376Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000276079
Start	71297934:71297934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1127A>T
AA Mutation	p.Asp376Val(p.D376V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000276079
Start	71297900:71297900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1093C>T
AA Mutation	p.Arg365Ter(p.R365*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> NONO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000276079
Start	71298734:71298734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199C>T
AA Mutation	p.Ala400Val(p.A400V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript