Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> TENM4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78701951:78701951(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4662C>A
AA Mutation p.Asp1554Glu(p.D1554E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78676160:78676160(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5488C>T
AA Mutation p.Arg1830Trp(p.R1830W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78670178:78670178(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6167G>T
AA Mutation p.Arg2056Leu(p.R2056L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78729484:78729484(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749538415
CDS Mutation c.3298C>T
AA Mutation p.Arg1100Cys(p.R1100C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78670272:78670272(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6073T>C
AA Mutation p.Tyr2025His(p.Y2025H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78854242:78854242(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1543C>T
AA Mutation p.Arg515Cys(p.R515C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669854:78669854(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6491A>G
AA Mutation p.Tyr2164Cys(p.Y2164C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78701556:78701556(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5057G>A
AA Mutation p.Ser1686Asn(p.S1686N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 79069787:79069787(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.158G>A
AA Mutation p.Arg53His(p.R53H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78712638:78712638(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3898C>T
AA Mutation p.Arg1300Trp(p.R1300W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78658407:78658407(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7961C>T
AA Mutation p.Thr2654Ile(p.T2654I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78676201:78676201(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5447G>A
AA Mutation p.Arg1816His(p.R1816H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78889794:78889794(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1075T>C
AA Mutation p.Tyr359His(p.Y359H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78676285:78676285(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5363C>T
AA Mutation p.Ala1788Val(p.A1788V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78701986:78701986(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4627G>T
AA Mutation p.Ala1543Ser(p.A1543S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78814384:78814384(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1693A>G
AA Mutation p.Asn565Asp(p.N565D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 79069771:79069771(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.174C>G
AA Mutation p.Ser58Arg(p.S58R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669167:78669167(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7178A>T
AA Mutation p.Asn2393Ile(p.N2393I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78676208:78676208(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5440C>T
AA Mutation p.Arg1814Cys(p.R1814C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669549:78669549(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs373812159
CDS Mutation c.6796G>A
AA Mutation p.Gly2266Ser(p.G2266S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000278550
Start 78786898:78786898(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761178978
CDS Mutation c.2365G>A
AA Mutation p.Ala789Thr(p.A789T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669092:78669092(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201567760
CDS Mutation c.7253G>A
AA Mutation p.Arg2418Gln(p.R2418Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78756980:78756980(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.2581C>T
AA Mutation p.Pro861Ser(p.P861S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78670458:78670458(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372515689
CDS Mutation c.5887C>T
AA Mutation p.Arg1963Trp(p.R1963W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78812172:78812172(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752573807
CDS Mutation c.1928C>T
AA Mutation p.Thr643Met(p.T643M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669194:78669194(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7151C>G
AA Mutation p.Ala2384Gly(p.A2384G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669379:78669379(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6966G>T
AA Mutation p.Lys2322Asn(p.K2322N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78903377:78903377(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.640G>A
AA Mutation p.Ala214Thr(p.A214T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 79069938:79069938(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7G>A
AA Mutation p.Val3Met(p.V3M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 79069740:79069740(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749650726
CDS Mutation c.205G>A
AA Mutation p.Glu69Lys(p.E69K)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669087:78669087(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7258G>T
AA Mutation p.Asp2420Tyr(p.D2420Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669447:78669447(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs375613256
CDS Mutation c.6898G>A
AA Mutation p.Val2300Met(p.V2300M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78672293:78672293(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5533C>T
AA Mutation p.Arg1845Cys(p.R1845C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78701937:78701937(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775610240
CDS Mutation c.4676G>A
AA Mutation p.Arg1559Gln(p.R1559Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 79069862:79069862(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.83A>G
AA Mutation p.Asp28Gly(p.D28G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669716:78669716(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6629A>G
AA Mutation p.Lys2210Arg(p.K2210R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78688078:78688078(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5236G>T
AA Mutation p.Gly1746Cys(p.G1746C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78672121:78672121(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5705C>A
AA Mutation p.Ser1902Tyr(p.S1902Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78732480:78732480(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752878204
CDS Mutation c.2974C>T
AA Mutation p.Arg992Cys(p.R992C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78712504:78712504(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4032A>T
AA Mutation p.Glu1344Asp(p.E1344D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78756993:78756993(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2568C>G
AA Mutation p.Asp856Glu(p.D856E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78658144:78658144(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs371501350
CDS Mutation c.8224G>A
AA Mutation p.Val2742Met(p.V2742M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 43
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 79064954:79064954(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs561431723
CDS Mutation c.277G>A
AA Mutation p.Gly93Arg(p.G93R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 44
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669620:78669620(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756653480
CDS Mutation c.6725G>A
AA Mutation p.Arg2242His(p.R2242H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 45
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78787045:78787045(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370272010
CDS Mutation c.2218G>A
AA Mutation p.Val740Ile(p.V740I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78670504:78670504(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752252798
CDS Mutation c.5841C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78771074:78771074(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755119868
CDS Mutation c.2457C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78688109:78688109(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5205T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78891270:78891270(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201811725
CDS Mutation c.816C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 79069813:79069813(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.132C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78672105:78672105(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768735704
CDS Mutation c.5721C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78670048:78670048(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs548460296
CDS Mutation c.6297C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78814328:78814328(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1749C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78854210:78854210(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1575C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78903435:78903435(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.582G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78688217:78688217(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5097C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 79064886:79064886(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.345C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78676245:78676245(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750937106
CDS Mutation c.5403G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 59
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78889846:78889846(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201536211
CDS Mutation c.1023C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 60
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78812306:78812306(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs551884581
CDS Mutation c.1794C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 61
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78702287:78702287(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs183078972
CDS Mutation c.4326C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 62
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78669448:78669448(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775901315
CDS Mutation c.6897C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 63
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78676362:78676362(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs542215743
CDS Mutation c.5286C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 64
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78670372:78670372(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759775617
CDS Mutation c.5973C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 65
Mutation Consequence frameshift_variant
Transcription ID ENST00000278550
Start 78658303:78658303(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.8065delC
AA Mutation p.Arg2689GlyfsTer41(p.R2689Gfs*41)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 66
Mutation Consequence frameshift_variant
Transcription ID ENST00000278550
Start 78812254:78812255(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.1845_1846delCA
AA Mutation p.His615GlnfsTer7(p.H615Qfs*7)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 67
Mutation Consequence frameshift_variant
Transcription ID ENST00000278550
Start 79064959:79064959(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.272delC
AA Mutation p.Pro91LeufsTer110(p.P91Lfs*110)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 68
Mutation Consequence frameshift_variant
Transcription ID ENST00000278550
Start 78814307:78814307(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.1770delC
AA Mutation p.Asp591ThrfsTer18(p.D591Tfs*18)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 69
Mutation Consequence stop_gained
Transcription ID ENST00000278550
Start 78863085:78863085(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1132C>T
AA Mutation p.Gln378Ter(p.Q378*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 70
Mutation Consequence stop_gained
Transcription ID ENST00000278550
Start 78658594:78658594(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7774C>T
AA Mutation p.Arg2592Ter(p.R2592*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 71
Mutation Consequence frameshift_variant
Transcription ID ENST00000278550
Start 78854215:78854216(version: GRCh38)
Mutation Type INS
dbSNP_RS null
CDS Mutation c.1569dupC
AA Mutation p.Ser524LeufsTer4(p.S524Lfs*4)
Mutation Classification Frame_Shift_Ins
Feature Type Transcript

Rectum Cancer: Gene >> TENM4

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669705:78669705(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750150227
CDS Mutation c.6640C>T
AA Mutation p.Arg2214Cys(p.R2214C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78701932:78701932(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4681C>T
AA Mutation p.Arg1561Trp(p.R1561W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78812230:78812230(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374126261
CDS Mutation c.1870G>A
AA Mutation p.Asp624Asn(p.D624N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78729489:78729489(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3293A>G
AA Mutation p.Glu1098Gly(p.E1098G)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669615:78669615(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777521844
CDS Mutation c.6730C>T
AA Mutation p.Arg2244Cys(p.R2244C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78732387:78732387(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs769818383
CDS Mutation c.3067G>A
AA Mutation p.Val1023Ile(p.V1023I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78672170:78672170(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5656A>G
AA Mutation p.Thr1886Ala(p.T1886A)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78670099:78670099(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6246C>G
AA Mutation p.Asp2082Glu(p.D2082E)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78669453:78669453(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763360287
CDS Mutation c.6892C>T
AA Mutation p.Arg2298Trp(p.R2298W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78756964:78756964(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs760415394
CDS Mutation c.2597A>G
AA Mutation p.Asn866Ser(p.N866S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 79064822:79064822(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.409C>T
AA Mutation p.Arg137Trp(p.R137W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78712533:78712533(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4003C>T
AA Mutation p.Arg1335Cys(p.R1335C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000278550
Start 78670490:78670490(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs140341040
CDS Mutation c.5855G>A
AA Mutation p.Arg1952His(p.R1952H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78669253:78669253(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7092G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 15
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78669238:78669238(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7107C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 16
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78670024:78670024(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6321C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 17
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78670504:78670504(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752252798
CDS Mutation c.5841C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 18
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78722823:78722823(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3645C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 19
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78701834:78701834(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4779C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 20
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78669256:78669256(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.7089C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 21
Mutation Consequence synonymous_variant
Transcription ID ENST00000278550
Start 78669595:78669595(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753999795
CDS Mutation c.6750C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 22
Mutation Consequence stop_gained
Transcription ID ENST00000278550
Start 78854134:78854134(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1651G>T
AA Mutation p.Glu551Ter(p.E551*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript