Colon Cancer: Gene >> TNC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115035283:115035283(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5708C>A
AA Mutation	p.Ala1903Asp(p.A1903D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115086581:115086581(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573699675
CDS Mutation	c.1150C>T
AA Mutation	p.Arg384Cys(p.R384C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115041058:115041058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113892305
CDS Mutation	c.5275G>A
AA Mutation	p.Gly1759Arg(p.G1759R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115090936:115090936(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.83T>A
AA Mutation	p.Val28Asp(p.V28D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115084427:115084427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370926474
CDS Mutation	c.1913C>T
AA Mutation	p.Thr638Met(p.T638M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115073695:115073695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761076779
CDS Mutation	c.3122G>A
AA Mutation	p.Arg1041Lys(p.R1041K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115086568:115086568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1163T>C
AA Mutation	p.Val388Ala(p.V388A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115062988:115062988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3962C>A
AA Mutation	p.Pro1321His(p.P1321H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115062999:115062999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3951G>T
AA Mutation	p.Arg1317Ser(p.R1317S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115046626:115046626(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4909C>T
AA Mutation	p.Arg1637Cys(p.R1637C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115082700:115082700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2239C>T
AA Mutation	p.Arg747Trp(p.R747W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115090783:115090783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770789816
CDS Mutation	c.236C>T
AA Mutation	p.Pro79Leu(p.P79L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115090840:115090840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.179T>C
AA Mutation	p.Val60Ala(p.V60A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115046613:115046613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4922C>A
AA Mutation	p.Thr1641Lys(p.T1641K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115064787:115064787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3347C>T
AA Mutation	p.Ala1116Val(p.A1116V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115064790:115064790(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3344A>T
AA Mutation	p.Glu1115Val(p.E1115V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115064009:115064009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3547C>A
AA Mutation	p.Leu1183Ile(p.L1183I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115086419:115086419(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771475685
CDS Mutation	c.1312C>T
AA Mutation	p.Arg438Trp(p.R438W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115076066:115076066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2916G>T
AA Mutation	p.Lys972Asn(p.K972N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115046422:115046422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5113A>G
AA Mutation	p.Ile1705Val(p.I1705V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115073785:115073785(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3032A>G
AA Mutation	p.Lys1011Arg(p.K1011R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115086902:115086902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145121881
CDS Mutation	c.829G>A
AA Mutation	p.Asp277Asn(p.D277N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115063078:115063078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779335819
CDS Mutation	c.3872A>G
AA Mutation	p.Gln1291Arg(p.Q1291R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115086794:115086794(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.937C>A
AA Mutation	p.Leu313Ile(p.L313I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115073777:115073777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373842890
CDS Mutation	c.3040C>T
AA Mutation	p.Arg1014Cys(p.R1014C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115048324:115048324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4788G>T
AA Mutation	p.Glu1596Asp(p.E1596D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115036149:115036149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5605G>A
AA Mutation	p.Ala1869Thr(p.A1869T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115036150:115036150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5604T>A
AA Mutation	p.Phe1868Leu(p.F1868L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115086853:115086853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878G>A
AA Mutation	p.Arg293Gln(p.R293Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115026635:115026635(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371541652
CDS Mutation	c.6230G>A
AA Mutation	p.Arg2077Gln(p.R2077Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115062992:115062992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs745899976
CDS Mutation	c.3958A>C
AA Mutation	p.Thr1320Pro(p.T1320P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115046625:115046625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4910G>A
AA Mutation	p.Arg1637His(p.R1637H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115087135:115087135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596G>A
AA Mutation	p.Arg199Gln(p.R199Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115048497:115048497(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770213784
CDS Mutation	c.4615G>A
AA Mutation	p.Asp1539Asn(p.D1539N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115064652:115064652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3482C>T
AA Mutation	p.Ser1161Phe(p.S1161F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115064848:115064848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138406927
CDS Mutation	c.3286G>A
AA Mutation	p.Ala1096Thr(p.A1096T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000350763
Start	115026534:115026534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6331G>T
AA Mutation	p.Gly2111Cys(p.G2111C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115086634:115086634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762128715
CDS Mutation	c.1097G>T
AA Mutation	p.Gly366Val(p.G366V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115026605:115026605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6260A>G
AA Mutation	p.Tyr2087Cys(p.Y2087C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115046477:115046477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5058C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115086090:115086090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149491853
CDS Mutation	c.1641C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115062969:115062969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750137926
CDS Mutation	c.3981C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115086156:115086156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1575T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115064891:115064891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373432241
CDS Mutation	c.3243C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	45
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115076526:115076526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2724C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	46
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115076550:115076550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2700A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	47
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115090782:115090782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149512169
CDS Mutation	c.237G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	48
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115026592:115026592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142272539
CDS Mutation	c.6273C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	49
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115076571:115076571(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760256103
CDS Mutation	c.2679C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	50
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115046594:115046594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201689087
CDS Mutation	c.4941C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115086489:115086489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746496814
CDS Mutation	c.1242C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115062966:115062966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs554908600
CDS Mutation	c.3984C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	53
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115024129:115024129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	54
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115063959:115063959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764479295
CDS Mutation	c.3597G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	55
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115021163:115021163(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6600G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	56
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115087038:115087038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769090541
CDS Mutation	c.693C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	57
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115057361:115057361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4371C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	58
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115086381:115086381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759590939
CDS Mutation	c.1350C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	59
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115078127:115078127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145321605
CDS Mutation	c.2490C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	60
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115087167:115087167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.564C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	61
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115036183:115036183(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764363683
CDS Mutation	c.5571C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	62
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115090893:115090893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.126A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	63
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350763
Start	115035260:115035260(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.5731delC
AA Mutation	p.Arg1911GlyfsTer35(p.R1911Gfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	64
Mutation Consequence	stop_gained
Transcription ID	ENST00000350763
Start	115087142:115087142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.589C>T
AA Mutation	p.Arg197Ter(p.R197*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	65
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000350763
Start	115063796:115063796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3760G>T
AA Mutation	p.Glu1254Ter(p.E1254*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	66
Mutation Consequence	stop_gained
Transcription ID	ENST00000350763
Start	115086839:115086839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.892G>T
AA Mutation	p.Glu298Ter(p.E298*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	67
Mutation Consequence	stop_gained
Transcription ID	ENST00000350763
Start	115064831:115064831(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3303T>A
AA Mutation	p.Tyr1101Ter(p.Y1101*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	68
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350763
Start	115086454:115086455(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1275_1276dupTG
AA Mutation	p.Asp426ValfsTer44(p.D426Vfs*44)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	69
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000350763
Start	115087274:115087274(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.458-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	70
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000350763
Start	115057426:115057426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4307-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TNC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115086560:115086560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs45481099
CDS Mutation	c.1171C>T
AA Mutation	p.Arg391Trp(p.R391W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115087166:115087166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757206565
CDS Mutation	c.565G>A
AA Mutation	p.Glu189Lys(p.E189K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115086418:115086418(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763289734
CDS Mutation	c.1313G>A
AA Mutation	p.Arg438Gln(p.R438Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115057327:115057327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4405A>G
AA Mutation	p.Thr1469Ala(p.T1469A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000350763
Start	115048415:115048415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4697C>A
AA Mutation	p.Ser1566Tyr(p.S1566Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115084378:115084378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113110161
CDS Mutation	c.1962C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115036222:115036222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200409463
CDS Mutation	c.5532G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115076451:115076451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2799G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115046594:115046594(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201689087
CDS Mutation	c.4941C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115078159:115078159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2458T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115087029:115087029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.702A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115078190:115078190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2427C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115087014:115087014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115031584:115031584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5889G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115084336:115084336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2004C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350763
Start	115046465:115046465(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5070C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000350763
Start	115076552:115076552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2698C>T
AA Mutation	p.Arg900Ter(p.R900*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000350763
Start	115035223:115035223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5768C>A
AA Mutation	p.Ser1923Ter(p.S1923*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript