Colon Cancer: Gene >> BCL11B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99174162:99174162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2674G>A
AA Mutation	p.Glu892Lys(p.E892K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99174204:99174204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758918107
CDS Mutation	c.2632G>A
AA Mutation	p.Gly878Ser(p.G878S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99174314:99174314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2522G>A
AA Mutation	p.Arg841His(p.R841H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99176057:99176057(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756798054
CDS Mutation	c.779C>T
AA Mutation	p.Thr260Met(p.T260M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99174450:99174450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2386G>A
AA Mutation	p.Asp796Asn(p.D796N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99174272:99174272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749262405
CDS Mutation	c.2564G>A
AA Mutation	p.Arg855His(p.R855H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99176075:99176075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.761C>T
AA Mutation	p.Pro254Leu(p.P254L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99174735:99174735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2101C>T
AA Mutation	p.Leu701Phe(p.L701F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99231392:99231392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.593G>A
AA Mutation	p.Gly198Asp(p.G198D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99174335:99174335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2501C>T
AA Mutation	p.Ala834Val(p.A834V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99174624:99174624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2212G>A
AA Mutation	p.Ala738Thr(p.A738T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357195
Start	99174445:99174445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2391G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357195
Start	99174784:99174784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2052C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357195
Start	99231415:99231415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760038299
CDS Mutation	c.570G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357195
Start	99175129:99175129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748442142
CDS Mutation	c.1707C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357195
Start	99231361:99231361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357195
Start	99231505:99231505(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.480C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357195
Start	99176122:99176122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000357195
Start	99175577:99175577(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1259delC
AA Mutation	p.Pro420ArgfsTer55(p.P420Rfs*55)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> BCL11B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357195
Start	99257531:99257531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.367G>A
AA Mutation	p.Glu123Lys(p.E123K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357195
Start	99176140:99176140(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357195
Start	99231460:99231460(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372881820
CDS Mutation	c.525C>T
Mutation Classification	Silent
Feature Type	Transcript