Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> FLNC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128852944:128852944(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6121G>A
AA Mutation p.Ala2041Thr(p.A2041T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128845046:128845046(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs773481064
CDS Mutation c.3581C>T
AA Mutation p.Ser1194Leu(p.S1194L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128848842:128848842(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4787G>A
AA Mutation p.Gly1596Asp(p.G1596D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128849562:128849562(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5183G>T
AA Mutation p.Ser1728Ile(p.S1728I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128856606:128856606(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7340C>G
AA Mutation p.Pro2447Arg(p.P2447R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 6
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128843458:128843458(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777692031
CDS Mutation c.2692G>A
AA Mutation p.Gly898Ser(p.G898S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 7
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128845205:128845205(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775496136
CDS Mutation c.3740C>T
AA Mutation p.Ala1247Val(p.A1247V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 8
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128841491:128841491(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs756904288
CDS Mutation c.2045G>A
AA Mutation p.Cys682Tyr(p.C682Y)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 9
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128846893:128846893(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763218103
CDS Mutation c.4276C>T
AA Mutation p.Arg1426Trp(p.R1426W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 10
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128848910:128848910(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4855G>A
AA Mutation p.Asp1619Asn(p.D1619N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 11
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128837705:128837705(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763968152
CDS Mutation c.919G>A
AA Mutation p.Val307Met(p.V307M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 12
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128854015:128854015(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs376885778
CDS Mutation c.6526C>T
AA Mutation p.Arg2176Cys(p.R2176C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 13
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128844166:128844166(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs372467579
CDS Mutation c.3092C>T
AA Mutation p.Pro1031Leu(p.P1031L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 14
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128843872:128843872(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2888C>A
AA Mutation p.Pro963Gln(p.P963Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 15
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128838701:128838701(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374847180
CDS Mutation c.1309C>T
AA Mutation p.Arg437Cys(p.R437C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 16
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128854885:128854885(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs201917318
CDS Mutation c.7108G>A
AA Mutation p.Gly2370Ser(p.G2370S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 17
Mutation Consequence missense_variant;splice_region_variant
Transcription ID ENST00000325888
Start 128838427:128838427(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777199447
CDS Mutation c.1208C>T
AA Mutation p.Ala403Val(p.A403V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 18
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128852744:128852744(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5996G>A
AA Mutation p.Arg1999Gln(p.R1999Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 19
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128837536:128837536(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778751919
CDS Mutation c.838G>A
AA Mutation p.Ala280Thr(p.A280T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 20
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128851265:128851265(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5573A>T
AA Mutation p.Asn1858Ile(p.N1858I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 21
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128844057:128844057(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs752053093
CDS Mutation c.2983G>A
AA Mutation p.Gly995Ser(p.G995S)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 22
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128846065:128846065(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs755896234
CDS Mutation c.3866C>T
AA Mutation p.Thr1289Met(p.T1289M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 23
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128842917:128842917(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs775085661
CDS Mutation c.2513C>T
AA Mutation p.Ala838Val(p.A838V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 24
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128858148:128858148(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs750629528
CDS Mutation c.7921C>T
AA Mutation p.Arg2641Trp(p.R2641W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 25
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128844760:128844760(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs759452636
CDS Mutation c.3295G>A
AA Mutation p.Val1099Ile(p.V1099I)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 26
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128840671:128840671(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs776881635
CDS Mutation c.1673G>A
AA Mutation p.Arg558His(p.R558H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 27
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128844887:128844887(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3422C>T
AA Mutation p.Pro1141Leu(p.P1141L)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 28
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128852872:128852872(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6049G>A
AA Mutation p.Val2017Met(p.V2017M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 29
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128837439:128837439(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.741G>T
AA Mutation p.Glu247Asp(p.E247D)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 30
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128843566:128843566(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs763954095
CDS Mutation c.2800G>A
AA Mutation p.Ala934Thr(p.A934T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 31
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128852891:128852891(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6068A>G
AA Mutation p.His2023Arg(p.H2023R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 32
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128838650:128838650(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766755439
CDS Mutation c.1258C>T
AA Mutation p.Arg420Trp(p.R420W)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 33
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128837476:128837476(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.778G>A
AA Mutation p.Ala260Thr(p.A260T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 34
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128835550:128835550(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs387906587
CDS Mutation c.577G>A
AA Mutation p.Ala193Thr(p.A193T)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 35
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128840917:128840917(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1760G>T
AA Mutation p.Gly587Val(p.G587V)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 36
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128854867:128854867(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374973240
CDS Mutation c.7090C>T
AA Mutation p.Arg2364Cys(p.R2364C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 37
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128843314:128843314(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs367997079
CDS Mutation c.2636G>A
AA Mutation p.Arg879His(p.R879H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 38
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128830812:128830812(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.175G>A
AA Mutation p.Asp59Asn(p.D59N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 39
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128847711:128847711(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370643162
CDS Mutation c.4303G>A
AA Mutation p.Val1435Met(p.V1435M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 40
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128847853:128847853(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4445T>G
AA Mutation p.Leu1482Arg(p.L1482R)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 41
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128854514:128854514(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs761696270
CDS Mutation c.6829C>T
AA Mutation p.Arg2277Cys(p.R2277C)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 42
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128837749:128837749(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs749769428
CDS Mutation c.963C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 43
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128847704:128847704(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs370827536
CDS Mutation c.4296G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 44
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128843273:128843273(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs778744785
CDS Mutation c.2595C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 45
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128849539:128849539(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs562101000
CDS Mutation c.5160C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 46
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128851552:128851552(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs58914363
CDS Mutation c.5766G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 47
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128858493:128858493(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8148T>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 48
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128854492:128854492(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs777337698
CDS Mutation c.6807C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 49
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128842589:128842589(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.2280G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 50
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128838736:128838736(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1344T>C
Mutation Classification Silent
Feature Type Transcript
Mutation ID 51
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128842619:128842619(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374087953
CDS Mutation c.2310C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 52
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128857137:128857137(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7581C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 53
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128850446:128850446(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.5361G>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 54
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128846066:128846066(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.3867G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 55
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128853479:128853479(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6219C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 56
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128853722:128853722(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6369C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 57
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128858088:128858088(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7861C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 58
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128845023:128845023(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs774467047
CDS Mutation c.3558G>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 59
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128854893:128854893(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.7116C>A
Mutation Classification Silent
Feature Type Transcript
Mutation ID 60
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128837469:128837469(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.771C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 61
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128846344:128846344(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.4008C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 62
Mutation Consequence frameshift_variant
Transcription ID ENST00000325888
Start 128844701:128844701(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.3240delC
AA Mutation p.Ala1081ArgfsTer17(p.A1081Rfs*17)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 63
Mutation Consequence frameshift_variant;splice_region_variant
Transcription ID ENST00000325888
Start 128848795:128848795(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4743delC
AA Mutation p.Glu1582ArgfsTer25(p.E1582Rfs*25)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 64
Mutation Consequence frameshift_variant
Transcription ID ENST00000325888
Start 128846887:128846887(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.4275delG
AA Mutation p.Arg1426GlyfsTer12(p.R1426Gfs*12)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 65
Mutation Consequence frameshift_variant
Transcription ID ENST00000325888
Start 128856767:128856767(version: GRCh38)
Mutation Type DEL
dbSNP_RS null
CDS Mutation c.7411delC
AA Mutation p.His2471ThrfsTer58(p.H2471Tfs*58)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 66
Mutation Consequence frameshift_variant
Transcription ID ENST00000325888
Start 128851472:128851472(version: GRCh38)
Mutation Type DEL
dbSNP_RS novel
CDS Mutation c.5686delG
AA Mutation p.Val1896TrpfsTer57(p.V1896Wfs*57)
Mutation Classification Frame_Shift_Del
Feature Type Transcript
Mutation ID 67
Mutation Consequence stop_gained
Transcription ID ENST00000325888
Start 128858474:128858474(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.8129G>A
AA Mutation p.Trp2710Ter(p.W2710*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 68
Mutation Consequence stop_gained
Transcription ID ENST00000325888
Start 128854054:128854054(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.6565G>T
AA Mutation p.Glu2189Ter(p.E2189*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 69
Mutation Consequence stop_gained
Transcription ID ENST00000325888
Start 128846839:128846839(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4222G>T
AA Mutation p.Glu1408Ter(p.E1408*)
Mutation Classification Nonsense_Mutation
Feature Type Transcript
Mutation ID 70
Mutation Consequence splice_donor_variant
Transcription ID ENST00000325888
Start 128837549:128837549(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.850+1G>T
Mutation Classification Splice_Site
Feature Type Transcript
Mutation ID 71
Mutation Consequence splice_donor_variant
Transcription ID ENST00000325888
Start 128840676:128840676(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.1676+2T>C
Mutation Classification Splice_Site
Feature Type Transcript

Rectum Cancer: Gene >> FLNC

Mutation ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128854563:128854563(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.6878G>A
AA Mutation p.Arg2293His(p.R2293H)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128837171:128837171(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs767740333
CDS Mutation c.613G>A
AA Mutation p.Asp205Asn(p.D205N)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 3
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128848029:128848029(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.4541C>T
AA Mutation p.Thr1514Met(p.T1514M)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 4
Mutation Consequence missense_variant
Transcription ID ENST00000325888
Start 128849349:128849349(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs374294752
CDS Mutation c.4970G>A
AA Mutation p.Arg1657Gln(p.R1657Q)
Mutation Classification Missense_Mutation
Feature Type Transcript
Mutation ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128844759:128844759(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs753772262
CDS Mutation c.3294C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 6
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128849521:128849521(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs573362121
CDS Mutation c.5142C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 7
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128843502:128843502(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs768894698
CDS Mutation c.2736C>T
Mutation Classification Silent
Feature Type Transcript
Mutation ID 8
Mutation Consequence synonymous_variant
Transcription ID ENST00000325888
Start 128852743:128852743(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.5995C>A
Mutation Classification Silent
Feature Type Transcript