Colon Cancer: Gene >> TENM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182754694:182754694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776390399
CDS Mutation	c.4327G>A
AA Mutation	p.Gly1443Arg(p.G1443R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182737072:182737072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3232G>T
AA Mutation	p.Val1078Phe(p.V1078F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182754841:182754841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4474A>G
AA Mutation	p.Asn1492Asp(p.N1492D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182714186:182714186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2321A>G
AA Mutation	p.Asp774Gly(p.D774G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182743376:182743376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3586C>T
AA Mutation	p.Arg1196Trp(p.R1196W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182800073:182800073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7822C>T
AA Mutation	p.Arg2608Cys(p.R2608C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182793759:182793759(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757494710
CDS Mutation	c.7087C>T
AA Mutation	p.Arg2363Trp(p.R2363W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182653778:182653778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.996T>A
AA Mutation	p.His332Gln(p.H332Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182681832:182681832(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1853G>T
AA Mutation	p.Gly618Val(p.G618V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182800020:182800020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7769C>T
AA Mutation	p.Thr2590Met(p.T2590M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182628779:182628779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.878G>T
AA Mutation	p.Arg293Ile(p.R293I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182755166:182755166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4799C>T
AA Mutation	p.Ala1600Val(p.A1600V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182792425:182792425(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5753C>T
AA Mutation	p.Pro1918Leu(p.P1918L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182751872:182751872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3702C>G
AA Mutation	p.Asn1234Lys(p.N1234K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182773582:182773582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5003G>T
AA Mutation	p.Arg1668Leu(p.R1668L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182799869:182799869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7618A>G
AA Mutation	p.Thr2540Ala(p.T2540A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182793355:182793355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201200379
CDS Mutation	c.6683G>A
AA Mutation	p.Arg2228His(p.R2228H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182793193:182793193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751169755
CDS Mutation	c.6521G>A
AA Mutation	p.Arg2174His(p.R2174H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000511685
Start	182682014:182682014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2035G>A
AA Mutation	p.Glu679Lys(p.E679K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182754482:182754482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs543878787
CDS Mutation	c.4115G>A
AA Mutation	p.Arg1372His(p.R1372H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182792905:182792905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767821436
CDS Mutation	c.6233C>T
AA Mutation	p.Thr2078Met(p.T2078M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182793277:182793277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146065963
CDS Mutation	c.6605C>T
AA Mutation	p.Thr2202Met(p.T2202M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182346681:182346681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.263T>C
AA Mutation	p.Val88Ala(p.V88A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182792410:182792410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5738A>G
AA Mutation	p.Asn1913Ser(p.N1913S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182792706:182792706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6034A>G
AA Mutation	p.Met2012Val(p.M2012V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182792934:182792934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6262A>G
AA Mutation	p.Lys2088Glu(p.K2088E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182792677:182792677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6005G>T
AA Mutation	p.Arg2002Met(p.R2002M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182628725:182628725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.824C>T
AA Mutation	p.Ser275Phe(p.S275F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182679762:182679762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182946886
CDS Mutation	c.1423G>A
AA Mutation	p.Val475Ile(p.V475I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182743320:182743320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3530C>T
AA Mutation	p.Ala1177Val(p.A1177V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	31
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182754886:182754886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4519T>G
AA Mutation	p.Ser1507Ala(p.S1507A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	32
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182789378:182789378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5590T>A
AA Mutation	p.Tyr1864Asn(p.Y1864N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	33
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182736908:182736908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3068C>G
AA Mutation	p.Thr1023Ser(p.T1023S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	34
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182792688:182792688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6016C>T
AA Mutation	p.Arg2006Cys(p.R2006C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	35
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182754547:182754547(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4180G>A
AA Mutation	p.Gly1394Arg(p.G1394R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	36
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182800037:182800037(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7786G>A
AA Mutation	p.Val2596Met(p.V2596M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	37
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182751877:182751877(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367732296
CDS Mutation	c.3707G>A
AA Mutation	p.Arg1236His(p.R1236H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	38
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182346893:182346893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.475G>A
AA Mutation	p.Asp159Asn(p.D159N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	39
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182731119:182731119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2947C>T
AA Mutation	p.Pro983Ser(p.P983S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	40
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182743373:182743373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376147382
CDS Mutation	c.3583C>T
AA Mutation	p.Arg1195Trp(p.R1195W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	41
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182754574:182754574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4207G>A
AA Mutation	p.Glu1403Lys(p.E1403K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	42
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182793451:182793451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.6779C>T
AA Mutation	p.Thr2260Ile(p.T2260I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	43
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182681976:182681976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374213747
CDS Mutation	c.1997C>T
AA Mutation	p.Thr666Met(p.T666M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	44
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182793519:182793519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6847G>T
AA Mutation	p.Ala2283Ser(p.A2283S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	45
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182754698:182754698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4331T>C
AA Mutation	p.Ile1444Thr(p.I1444T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	46
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182775038:182775038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572530565
CDS Mutation	c.5189C>T
AA Mutation	p.Thr1730Met(p.T1730M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	47
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182754763:182754763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371087410
CDS Mutation	c.4396G>A
AA Mutation	p.Ala1466Thr(p.A1466T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	48
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182773488:182773488(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4909C>T
AA Mutation	p.Arg1637Cys(p.R1637C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	49
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182793175:182793175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371406834
CDS Mutation	c.6503C>T
AA Mutation	p.Ala2168Val(p.A2168V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	50
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182324073:182324073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.53A>G
AA Mutation	p.Glu18Gly(p.E18G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	51
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182681836:182681836(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1857T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	52
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182793131:182793131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61732939
CDS Mutation	c.6459C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	53
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182324197:182324197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758643488
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	54
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182680685:182680685(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1782C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	55
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182793518:182793518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6846T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	56
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182799949:182799949(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7698C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	57
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182751974:182751974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369770052
CDS Mutation	c.3804C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	58
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182800012:182800012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7761C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	59
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182731079:182731079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2907A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	60
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182789266:182789266(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.5478A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	61
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182680715:182680715(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1812C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	62
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182799859:182799859(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7608C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	63
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182729014:182729014(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2418C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	64
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182754762:182754762(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201867735
CDS Mutation	c.4395C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	65
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182792906:182792906(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61746883
CDS Mutation	c.6234G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	66
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182799805:182799805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763203300
CDS Mutation	c.7554C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	67
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182774973:182774973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145946924
CDS Mutation	c.5124C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	68
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000511685
Start	182688206:182688206(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2082delG
AA Mutation	p.Thr695ArgfsTer81(p.T695Rfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	69
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000511685
Start	182793414:182793414(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.6748delT
AA Mutation	p.Tyr2250MetfsTer4(p.Y2250Mfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	70
Mutation Consequence	stop_gained
Transcription ID	ENST00000511685
Start	182681935:182681935(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1956C>A
AA Mutation	p.Cys652Ter(p.C652*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	71
Mutation Consequence	stop_gained
Transcription ID	ENST00000511685
Start	182792388:182792388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5716C>T
AA Mutation	p.Arg1906Ter(p.R1906*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	72
Mutation Consequence	stop_gained
Transcription ID	ENST00000511685
Start	182792748:182792748(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753144702
CDS Mutation	c.6076C>T
AA Mutation	p.Arg2026Ter(p.R2026*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	73
Mutation Consequence	stop_gained
Transcription ID	ENST00000511685
Start	182755093:182755093(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4726C>T
AA Mutation	p.Arg1576Ter(p.R1576*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	74
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000511685
Start	182792628:182792629(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.5956_5957insATGGA
AA Mutation	p.Gly1986AspfsTer16(p.G1986Dfs*16)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TENM3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182729115:182729115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377429153
CDS Mutation	c.2519G>A
AA Mutation	p.Arg840Gln(p.R840Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182754908:182754908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs192269513
CDS Mutation	c.4541C>T
AA Mutation	p.Ala1514Val(p.A1514V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182792316:182792316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775010852
CDS Mutation	c.5644G>A
AA Mutation	p.Glu1882Lys(p.E1882K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182796732:182796732(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.7309G>A
AA Mutation	p.Glu2437Lys(p.E2437K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182792905:182792905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767821436
CDS Mutation	c.6233C>T
AA Mutation	p.Thr2078Met(p.T2078M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182793033:182793033(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.6361C>T
AA Mutation	p.Pro2121Ser(p.P2121S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182681838:182681838(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1859C>A
AA Mutation	p.Ser620Tyr(p.S620Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182792489:182792489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5817C>A
AA Mutation	p.Phe1939Leu(p.F1939L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182754458:182754458(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.4091T>C
AA Mutation	p.Val1364Ala(p.V1364A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182346897:182346897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479C>T
AA Mutation	p.Thr160Met(p.T160M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182673049:182673049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750160895
CDS Mutation	c.1156G>A
AA Mutation	p.Gly386Arg(p.G386R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182754490:182754490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763920847
CDS Mutation	c.4123C>T
AA Mutation	p.Arg1375Cys(p.R1375C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182789340:182789340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770088513
CDS Mutation	c.5552C>T
AA Mutation	p.Ser1851Phe(p.S1851F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000511685
Start	182792503:182792503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5831G>A
AA Mutation	p.Arg1944Gln(p.R1944Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000511685
Start	182796765:182796765(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.7342C>T
AA Mutation	p.Pro2448Ser(p.P2448S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182774952:182774952(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369200143
CDS Mutation	c.5103C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182743357:182743357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs189480567
CDS Mutation	c.3567C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182792315:182792315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5643C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182774973:182774973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145946924
CDS Mutation	c.5124C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000511685
Start	182792963:182792963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776630968
CDS Mutation	c.6291G>A
Mutation Classification	Silent
Feature Type	Transcript