Colon Cancer: Gene >> MLLT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000621332
Start	38715760:38715760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.968G>A
AA Mutation	p.Ser323Asn(p.S323N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000621332
Start	38716400:38716400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1070C>T
AA Mutation	p.Ala357Val(p.A357V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000621332
Start	38716660:38716660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1330C>T
AA Mutation	p.Arg444Trp(p.R444W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000621332
Start	38709269:38709269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.451G>A
AA Mutation	p.Val151Ile(p.V151I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000621332
Start	38716738:38716738(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1408G>A
AA Mutation	p.Ala470Thr(p.A470T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000621332
Start	38716648:38716648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1318G>T
AA Mutation	p.Gly440Cys(p.G440C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000621332
Start	38706992:38706992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.152G>A
AA Mutation	p.Cys51Tyr(p.C51Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000621332
Start	38719772:38719772(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2032G>A
AA Mutation	p.Ala678Thr(p.A678T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000621332
Start	38706959:38706959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119G>A
AA Mutation	p.Gly40Asp(p.G40D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000621332
Start	38709524:38709524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.501G>T
AA Mutation	p.Glu167Asp(p.E167D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621332
Start	38721889:38721889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2454A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621332
Start	38711912:38711912(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.618G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621332
Start	38724940:38724940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3204G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621332
Start	38709545:38709545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs186310825
CDS Mutation	c.522C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621332
Start	38716455:38716455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371737246
CDS Mutation	c.1125C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621332
Start	38715767:38715767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.975C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000621332
Start	38707848:38707848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780174315
CDS Mutation	c.330C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000621332
Start	38720452:38720452(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2240delA
AA Mutation	p.Lys747ArgfsTer45(p.K747Rfs*45)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000621332
Start	38712745:38712745(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.780delC
AA Mutation	p.Ser261AlafsTer48(p.S261Afs*48)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000621332
Start	38716682:38716682(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1355delC
AA Mutation	p.Pro452LeufsTer12(p.P452Lfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	stop_gained
Transcription ID	ENST00000621332
Start	38715681:38715681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.889G>T
AA Mutation	p.Glu297Ter(p.E297*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000621332
Start	38715783:38715785(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs759466228
CDS Mutation	c.999_1001delCTC
AA Mutation	p.Ser338del(p.S338del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MLLT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000621332
Start	38716624:38716624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377118280
CDS Mutation	c.1294G>A
AA Mutation	p.Val432Ile(p.V432I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000621332
Start	38707848:38707854(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.331_337delGTGCCTC
AA Mutation	p.Val111MetfsTer26(p.V111Mfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript