Colon Cancer: Gene >> IKBKE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000581977
Start	206480464:206480464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1358C>T
AA Mutation	p.Thr453Ile(p.T453I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000581977
Start	206478191:206478191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.844G>T
AA Mutation	p.Ala282Ser(p.A282S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000581977
Start	206485263:206485263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781867739
CDS Mutation	c.1573C>T
AA Mutation	p.Arg525Trp(p.R525W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000581977
Start	206474405:206474405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.162G>T
AA Mutation	p.Arg54Ser(p.R54S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000581977
Start	206474985:206474985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782549877
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Cys(p.R117C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000581977
Start	206485298:206485298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1608G>T
AA Mutation	p.Glu536Asp(p.E536D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000581977
Start	206479068:206479068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781909564
CDS Mutation	c.1118C>T
AA Mutation	p.Thr373Met(p.T373M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581977
Start	206476704:206476704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.567G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581977
Start	206480033:206480033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374782915
CDS Mutation	c.1260C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581977
Start	206479880:206479880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1194C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581977
Start	206476224:206476224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782809498
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581977
Start	206485009:206485009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1440G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581977
Start	206476338:206476338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs41296030
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000581977
Start	206478987:206478987(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1042delC
AA Mutation	p.Arg348AspfsTer32(p.R348Dfs*32)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000581977
Start	206476720:206476721(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.588dupA
AA Mutation	p.Ala197SerfsTer108(p.A197Sfs*108)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IKBKE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000581977
Start	206485067:206485067(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781938435
CDS Mutation	c.1498C>T
AA Mutation	p.Arg500Trp(p.R500W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000581977
Start	206491712:206491712(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1798T>G
AA Mutation	p.Tyr600Asp(p.Y600D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000581977
Start	206474947:206474947(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.311C>T
AA Mutation	p.Ala104Val(p.A104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000581977
Start	206480094:206480094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1321C>T
AA Mutation	p.Arg441Trp(p.R441W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581977
Start	206476731:206476731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368978181
CDS Mutation	c.594C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000581977
Start	206478232:206478232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144754298
CDS Mutation	c.885C>T
Mutation Classification	Silent
Feature Type	Transcript