Colon Cancer: Gene >> TTF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334270
Start	132401908:132401908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.914C>T
AA Mutation	p.Ala305Val(p.A305V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334270
Start	132390666:132390666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2153A>C
AA Mutation	p.Lys718Thr(p.K718T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334270
Start	132388143:132388143(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2308G>A
AA Mutation	p.Glu770Lys(p.E770K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334270
Start	132379094:132379094(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2429T>C
AA Mutation	p.Val810Ala(p.V810A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334270
Start	132375986:132375986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2647G>T
AA Mutation	p.Gly883Cys(p.G883C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334270
Start	132401509:132401509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200157893
CDS Mutation	c.1313G>A
AA Mutation	p.Arg438Gln(p.R438Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000334270
Start	132401461:132401461(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141255148
CDS Mutation	c.1361C>T
AA Mutation	p.Ala454Val(p.A454V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000334270
Start	132390823:132390823(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199931383
CDS Mutation	c.1996C>T
AA Mutation	p.Arg666Cys(p.R666C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000334270
Start	132401664:132401664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1158G>T
AA Mutation	p.Lys386Asn(p.K386N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000334270
Start	132400123:132400123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1503C>A
AA Mutation	p.Phe501Leu(p.F501L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334270
Start	132379111:132379111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2412T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334270
Start	132402273:132402273(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.549A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334270
Start	132400075:132400075(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778850521
CDS Mutation	c.1551C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334270
Start	132401986:132401986(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.836delA
AA Mutation	p.Lys279ArgfsTer144(p.K279Rfs*144)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334270
Start	132402322:132402322(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.500delA
AA Mutation	p.Lys167ArgfsTer101(p.K167Rfs*101)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334270
Start	132401814:132401815(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs772401251
CDS Mutation	c.1007dupA
AA Mutation	p.Lys337GlufsTer9(p.K337Efs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000334270
Start	132379146:132379146(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2379-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TTF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334270
Start	132402269:132402269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.553G>A
AA Mutation	p.Asp185Asn(p.D185N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334270
Start	132402009:132402009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.813C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334270
Start	132396456:132396456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371348195
CDS Mutation	c.1833C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000334270
Start	132376046:132376046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2587C>T
AA Mutation	p.Arg863Ter(p.R863*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript