Colon Cancer: Gene >> BCL6B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293805
Start	7024427:7024427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573289461
CDS Mutation	c.428G>A
AA Mutation	p.Arg143His(p.R143H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000293805
Start	7027077:7027077(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1313A>G
AA Mutation	p.Lys438Arg(p.K438R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000293805
Start	7025128:7025128(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817A>G
AA Mutation	p.Thr273Ala(p.T273A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000293805
Start	7024240:7024240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>T
AA Mutation	p.Ala113Ser(p.A113S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000293805
Start	7025153:7025153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.842C>A
AA Mutation	p.Ala281Asp(p.A281D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000293805
Start	7026475:7026475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.908G>A
AA Mutation	p.Cys303Tyr(p.C303Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000293805
Start	7027545:7027545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748482678
CDS Mutation	c.1366C>T
AA Mutation	p.Arg456Trp(p.R456W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293805
Start	7026982:7026982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1218C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000293805
Start	7026967:7026967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748891591
CDS Mutation	c.1203G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000293805
Start	7024539:7024539(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.546delC
AA Mutation	p.Ser183ValfsTer20(p.S183Vfs*20)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BCL6B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000293805
Start	7025188:7025188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770283128
CDS Mutation	c.877C>T
AA Mutation	p.Arg293Cys(p.R293C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript