Colon Cancer: Gene >> NT5C3A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000242210
Start	33015837:33015837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.742C>A
AA Mutation	p.His248Asn(p.H248N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000242210
Start	33015792:33015792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.787T>G
AA Mutation	p.Phe263Val(p.F263V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000242210
Start	33014828:33014828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.913G>A
AA Mutation	p.Asp305Asn(p.D305N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000242210
Start	33021330:33021330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772942875
CDS Mutation	c.397G>A
AA Mutation	p.Ala133Thr(p.A133T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000242210
Start	33022066:33022066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.356A>G
AA Mutation	p.Glu119Gly(p.E119G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000242210
Start	33015748:33015748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831C>A
AA Mutation	p.Asp277Glu(p.D277E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000242210
Start	33017457:33017457(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.690delT
AA Mutation	p.Phe230LeufsTer17(p.F230Lfs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000242210
Start	33015870:33015871(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.709-1_709insATTTTGATGAAACT
AA Mutation	p.Gly237IlefsTer15(p.G237Ifs*15)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000242210
Start	33015872:33015872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.709-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> NT5C3A

No Mutation Annotation!