Colon Cancer: Gene >> TGIF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330513
Start	3457368:3457368(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.634T>G
AA Mutation	p.Cys212Gly(p.C212G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330513
Start	3456485:3456485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535C>A
AA Mutation	p.Leu179Ile(p.L179I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3452010:3452010(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.34delG
AA Mutation	p.Val12TrpfsTer122(p.V12Wfs*122)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3456404:3456404(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.454delA
AA Mutation	p.Ile152PhefsTer76(p.I152Ffs*76)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3457373:3457373(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.639delC
AA Mutation	p.Trp214GlyfsTer14(p.W214Gfs*14)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3456405:3456420(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.458_473delCCTTGGACCTTTCTTC
AA Mutation	p.Pro153HisfsTer70(p.P153Hfs*70)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3456552:3456552(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.604delC
AA Mutation	p.Gln202SerfsTer26(p.Q202Sfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000330513
Start	3456528:3456528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.578C>A
AA Mutation	p.Ser193Ter(p.S193*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000330513
Start	3457643:3457643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.909C>A
AA Mutation	p.Cys303Ter(p.C303*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000330513
Start	3456514:3456514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564C>A
AA Mutation	p.Tyr188Ter(p.Y188*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000330513
Start	3456479:3456479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.529C>T
AA Mutation	p.Gln177Ter(p.Q177*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000330513
Start	3456530:3456530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580G>T
AA Mutation	p.Glu194Ter(p.E194*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3457784:3457785(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1052_1053dupCT
AA Mutation	p.Gly352LeufsTer32(p.G352Lfs*32)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3456399:3456400(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.451dupG
AA Mutation	p.Asp151GlyfsTer35(p.D151Gfs*35)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3457598:3457599(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.866_869dupCGTC
AA Mutation	p.Ser291ValfsTer61(p.S291Vfs*61)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3457501:3457502(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.768_778dupGGGCATCAAAA
AA Mutation	p.Asn260ArgfsTer10(p.N260Rfs*10)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000330513
Start	3456446:3456448(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.498_500delGAG
AA Mutation	p.Arg168del(p.R168del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000330513
Start	3456406:3456408(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.456_458delTCC
AA Mutation	p.Pro153del(p.P153del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TGIF1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330513
Start	3456485:3456485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535C>A
AA Mutation	p.Leu179Ile(p.L179I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330513
Start	3457389:3457389(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.655C>G
AA Mutation	p.Arg219Gly(p.R219G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000330513
Start	3452103:3452103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.124T>C
AA Mutation	p.Phe42Leu(p.F42L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3457434:3457434(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.701delC
AA Mutation	p.Pro234GlnfsTer22(p.P234Qfs*22)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3457367:3457368(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.634dupT
AA Mutation	p.Cys212LeufsTer2(p.C212Lfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330513
Start	3456463:3456464(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.516dupC
AA Mutation	p.Lys173GlnfsTer13(p.K173Qfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000330513
Start	3457364:3457364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.631-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript