Colon Cancer: Gene >> TBK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331710
Start	64460268:64460268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167T>G
AA Mutation	p.Phe56Cys(p.F56C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000331710
Start	64464368:64464368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263T>G
AA Mutation	p.Phe88Cys(p.F88C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000331710
Start	64497195:64497195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1895C>T
AA Mutation	p.Ser632Leu(p.S632L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000331710
Start	64501349:64501349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2158G>T
AA Mutation	p.Asp720Tyr(p.D720Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000331710
Start	64481853:64481853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824T>A
AA Mutation	p.Val275Asp(p.V275D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000331710
Start	64495564:64495564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199905735
CDS Mutation	c.1603G>A
AA Mutation	p.Ala535Thr(p.A535T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000331710
Start	64495775:64495775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1720A>G
AA Mutation	p.Arg574Gly(p.R574G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000331710
Start	64480097:64480097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373705051
CDS Mutation	c.787A>G
AA Mutation	p.Met263Val(p.M263V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000331710
Start	64484476:64484476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1166C>T
AA Mutation	p.Thr389Ile(p.T389I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000331710
Start	64474252:64474252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.563C>T
AA Mutation	p.Ala188Val(p.A188V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000331710
Start	64484373:64484373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1063G>A
AA Mutation	p.Glu355Lys(p.E355K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331710
Start	64497253:64497253(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1953T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331710
Start	64496985:64496985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758803587
CDS Mutation	c.1797G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000331710
Start	64484493:64484494(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1189dupA
AA Mutation	p.Ile397AsnfsTer5(p.I397Nfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000331710
Start	64466900:64466900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.359-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TBK1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000331710
Start	64484350:64484350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1040C>A
AA Mutation	p.Ser347Tyr(p.S347Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000331710
Start	64484406:64484406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529643988
CDS Mutation	c.1096C>T
Mutation Classification	Silent
Feature Type	Transcript