Colon Cancer: Gene >> BCL11A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60460819:60460819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757462932
CDS Mutation	c.2093G>A
AA Mutation	p.Arg698His(p.R698H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60545995:60545995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.361T>A
AA Mutation	p.Cys121Ser(p.C121S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60460693:60460693(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2219G>A
AA Mutation	p.Arg740His(p.R740H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60460921:60460921(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1991C>T
AA Mutation	p.Ala664Val(p.A664V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60461489:60461489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757298308
CDS Mutation	c.1423G>A
AA Mutation	p.Asp475Asn(p.D475N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60546256:60546256(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100G>A
AA Mutation	p.Gly34Ser(p.G34S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60553241:60553241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.30G>T
AA Mutation	p.Gln10His(p.Q10H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60461863:60461863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1049G>A
AA Mutation	p.Ser350Asn(p.S350N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60460807:60460807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2105C>T
AA Mutation	p.Pro702Leu(p.P702L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60460883:60460883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2029G>A
AA Mutation	p.Gly677Arg(p.G677R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60461156:60461156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1756G>A
AA Mutation	p.Asp586Asn(p.D586N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60460564:60460564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61742690
CDS Mutation	c.2348G>A
AA Mutation	p.Ser783Asn(p.S783N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60460729:60460729(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2183C>T
AA Mutation	p.Pro728Leu(p.P728L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60461923:60461923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.989C>A
AA Mutation	p.Pro330Gln(p.P330Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335712
Start	60461319:60461319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775749233
CDS Mutation	c.1593C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335712
Start	60460746:60460746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765992760
CDS Mutation	c.2166G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335712
Start	60462303:60462303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.609C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335712
Start	60460773:60460773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2139C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335712
Start	60462119:60462119(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.793delC
AA Mutation	p.Leu265CysfsTer15(p.L265Cfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335712
Start	60461834:60461834(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1078delC
AA Mutation	p.Leu360SerfsTer61(p.L360Sfs*61)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000335712
Start	60460790:60460790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2122G>T
AA Mutation	p.Gly708Ter(p.G708*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000335712
Start	60461252:60461253(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1659_1660insG
AA Mutation	p.Ser554ValfsTer18(p.S554Vfs*18)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> BCL11A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335712
Start	60460922:60460922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1990G>A
AA Mutation	p.Ala664Thr(p.A664T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335712
Start	60462309:60462309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.603C>T
Mutation Classification	Silent
Feature Type	Transcript