Colon Cancer: Gene >> BCL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000164227
Start	44758390:44758390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1036C>T
AA Mutation	p.Leu346Phe(p.L346F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000164227
Start	44757144:44757144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.647G>A
AA Mutation	p.Arg216His(p.R216H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000164227
Start	44757132:44757132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.635C>T
AA Mutation	p.Ala212Val(p.A212V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000164227
Start	44758373:44758373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1019G>A
AA Mutation	p.Cys340Tyr(p.C340Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000164227
Start	44757117:44757117(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.620C>T
AA Mutation	p.Thr207Met(p.T207M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000164227
Start	44758312:44758312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199807623
CDS Mutation	c.958G>A
AA Mutation	p.Gly320Arg(p.G320R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000164227
Start	44759537:44759537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200468364
CDS Mutation	c.1287C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000164227
Start	44757145:44757145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.648C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000164227
Start	44757178:44757178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757076905
CDS Mutation	c.681C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000164227
Start	44758302:44758302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.948G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000164227
Start	44759480:44759480(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1235delC
AA Mutation	p.Pro412LeufsTer70(p.P412Lfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BCL3

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000164227
Start	44759474:44759474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224C>A
Mutation Classification	Silent
Feature Type	Transcript