Colon Cancer: Gene >> CBX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225603
Start	48076905:48076905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100G>A
AA Mutation	p.Gly34Ser(p.G34S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225603
Start	48071449:48071449(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>T
AA Mutation	p.Asp182Tyr(p.D182Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000225603
Start	48076154:48076154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.165A>T
AA Mutation	p.Glu55Asp(p.E55D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000225603
Start	48077001:48077001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4G>T
AA Mutation	p.Gly2Trp(p.G2W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000225603
Start	48076135:48076135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.184G>A
AA Mutation	p.Asp62Asn(p.D62N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225603
Start	48076993:48076993(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.12delA
AA Mutation	p.Lys4AsnfsTer11(p.K4Nfs*11)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000225603
Start	48071450:48071450(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.543delA
AA Mutation	p.Asp182MetfsTer30(p.D182Mfs*30)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CBX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000225603
Start	48071438:48071438(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555C>A
AA Mutation	p.Asn185Lys(p.N185K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000225603
Start	48076926:48076926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.79C>A
AA Mutation	p.Leu27Ile(p.L27I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript