Colon Cancer: Gene >> CBX8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269385
Start	79794639:79794639(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166G>T
AA Mutation	p.Arg389Ile(p.R389I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000269385
Start	79794867:79794867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.938C>A
AA Mutation	p.Pro313His(p.P313H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000269385
Start	79795146:79795146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757406974
CDS Mutation	c.659C>T
AA Mutation	p.Ala220Val(p.A220V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000269385
Start	79796089:79796089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214C>T
AA Mutation	p.Arg72Cys(p.R72C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000269385
Start	79794852:79794852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.953G>A
AA Mutation	p.Gly318Glu(p.G318E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000269385
Start	79796088:79796088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.215G>A
AA Mutation	p.Arg72His(p.R72H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000269385
Start	79796085:79796085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.218G>T
AA Mutation	p.Gly73Val(p.G73V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000269385
Start	79794856:79794856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.949G>A
AA Mutation	p.Gly317Arg(p.G317R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000269385
Start	79794993:79794993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812C>A
AA Mutation	p.Ala271Asp(p.A271D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269385
Start	79796939:79796939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.60C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269385
Start	79794728:79794728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1077G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000269385
Start	79795148:79795148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150395239
CDS Mutation	c.657C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269385
Start	79794819:79794819(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.986delG
AA Mutation	p.Gly329GlufsTer27(p.G329Efs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269385
Start	79794863:79794863(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.942delC
AA Mutation	p.Ser315AlafsTer41(p.S315Afs*41)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269385
Start	79794849:79794849(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.956delG
AA Mutation	p.Gly319AlafsTer37(p.G319Afs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000269385
Start	79794650:79794650(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1155delT
AA Mutation	p.Phe385LeufsTer26(p.F385Lfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CBX8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000269385
Start	79796536:79796536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.74G>A
AA Mutation	p.Arg25His(p.R25H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript