Colon Cancer: Gene >> IKBKB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000520810
Start	42316806:42316806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027G>A
AA Mutation	p.Asp343Asn(p.D343N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000520810
Start	42319273:42319273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1368G>T
AA Mutation	p.Met456Ile(p.M456I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000520810
Start	42319317:42319317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412C>T
AA Mutation	p.Ser471Phe(p.S471F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000520810
Start	42316848:42316848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069G>T
AA Mutation	p.Ala357Ser(p.A357S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000520810
Start	42314402:42314402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.773C>A
AA Mutation	p.Ser258Tyr(p.S258Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000520810
Start	42314411:42314411(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.782A>G
AA Mutation	p.Tyr261Cys(p.Y261C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000520810
Start	42316307:42316307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.898T>C
AA Mutation	p.Phe300Leu(p.F300L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520810
Start	42320824:42320824(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1673delG
AA Mutation	p.Gly558GlufsTer6(p.G558Efs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520810
Start	42317741:42317742(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1210_1211insT
AA Mutation	p.Arg404LeufsTer5(p.R404Lfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000520810
Start	42317742:42317743(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1211_1212insTTCA
AA Mutation	p.Pro405SerfsTer5(p.P405Sfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IKBKB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000520810
Start	42308967:42308967(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.634G>A
AA Mutation	p.Ala212Thr(p.A212T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000520810
Start	42319332:42319332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1427C>A
AA Mutation	p.Ser476Tyr(p.S476Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000520810
Start	42306356:42306356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491T>G
AA Mutation	p.Ile164Ser(p.I164S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript