Colon Cancer: Gene >> BCL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000232014
Start	187725557:187725557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1781G>A
AA Mutation	p.Arg594Gln(p.R594Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000232014
Start	187722496:187722496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2083G>A
AA Mutation	p.Ala695Thr(p.A695T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000232014
Start	187729107:187729107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1298C>T
AA Mutation	p.Ala433Val(p.A433V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000232014
Start	187725000:187725000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1918C>T
AA Mutation	p.Arg640Trp(p.R640W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000232014
Start	187729842:187729842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563T>C
AA Mutation	p.Leu188Pro(p.L188P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000232014
Start	187726889:187726889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776993725
CDS Mutation	c.1550C>T
AA Mutation	p.Ala517Val(p.A517V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000232014
Start	187729596:187729596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780987785
CDS Mutation	c.809G>A
AA Mutation	p.Arg270Gln(p.R270Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000232014
Start	187729131:187729131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1274T>G
AA Mutation	p.Leu425Arg(p.L425R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000232014
Start	187729986:187729986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.419G>A
AA Mutation	p.Arg140His(p.R140H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232014
Start	187726828:187726828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142294621
CDS Mutation	c.1611G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232014
Start	187726852:187726852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1587G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232014
Start	187728482:187728482(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1418delC
AA Mutation	p.Pro473ArgfsTer117(p.P473Rfs*117)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000232014
Start	187729447:187729448(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.957dupC
AA Mutation	p.Asn320GlnfsTer11(p.N320Qfs*11)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BCL6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000232014
Start	187724969:187724969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1949G>A
AA Mutation	p.Arg650Gln(p.R650Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000232014
Start	187729400:187729400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005G>T
AA Mutation	p.Gln335His(p.Q335H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000232014
Start	187729178:187729178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750915742
CDS Mutation	c.1227G>A
Mutation Classification	Silent
Feature Type	Transcript