Colon Cancer: Gene >> CNN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263097
Start	1037787:1037787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.817T>G
AA Mutation	p.Tyr273Asp(p.Y273D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000263097
Start	1037658:1037658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.688A>G
AA Mutation	p.Ile230Val(p.I230V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000263097
Start	1037662:1037662(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757933615
CDS Mutation	c.692A>G
AA Mutation	p.Tyr231Cys(p.Y231C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000263097
Start	1036170:1036170(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431T>C
AA Mutation	p.Val144Ala(p.V144A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000263097
Start	1037864:1037864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.894A>C
AA Mutation	p.Glu298Asp(p.E298D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000263097
Start	1037679:1037679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.709A>G
AA Mutation	p.Thr237Ala(p.T237A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000263097
Start	1037815:1037815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.845G>T
AA Mutation	p.Gly282Val(p.G282V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000263097
Start	1037849:1037849(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.883delG
AA Mutation	p.Glu295ArgfsTer45(p.E295Rfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000263097
Start	1032390:1032390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.186-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> CNN2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000263097
Start	1036490:1036490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582G>T
AA Mutation	p.Lys194Asn(p.K194N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript