ClinVar Miner

List of variants in gene IFT74 reported as uncertain significance for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 189
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_025103.4(IFT74):c.902C>T (p.Pro301Leu) rs78753648 0.00052
NM_025103.4(IFT74):c.120+2dup rs551515830 0.00048
NM_025103.4(IFT74):c.740T>A (p.Leu247His) rs199543657 0.00016
NM_025103.4(IFT74):c.11A>G (p.Asn4Ser) rs202023493 0.00011
NM_025103.4(IFT74):c.1589A>G (p.Lys530Arg) rs375621987 0.00011
NM_025103.4(IFT74):c.1635G>A (p.Leu545=) rs750049292 0.00010
NM_025103.4(IFT74):c.968A>G (p.Glu323Gly) rs202139740 0.00010
NM_025103.4(IFT74):c.793A>G (p.Ile265Val) rs370062629 0.00009
NM_025103.4(IFT74):c.1573G>A (p.Glu525Lys) rs1008648266 0.00006
NM_025103.4(IFT74):c.748C>G (p.Gln250Glu) rs374060021 0.00006
NM_025103.4(IFT74):c.977T>C (p.Leu326Ser) rs753977169 0.00005
NM_025103.4(IFT74):c.1623+3A>G rs775290576 0.00004
NM_025103.4(IFT74):c.1643A>G (p.Lys548Arg) rs201462617 0.00004
NM_025103.4(IFT74):c.251C>T (p.Thr84Met) rs370238286 0.00004
NM_025103.4(IFT74):c.1400A>G (p.Gln467Arg) rs746563082 0.00002
NM_025103.4(IFT74):c.1408C>G (p.Leu470Val) rs1271752655 0.00002
NM_025103.4(IFT74):c.1700G>T (p.Ser567Ile) rs1482975341 0.00002
NM_025103.4(IFT74):c.304A>C (p.Arg102=) rs761465255 0.00002
NM_025103.4(IFT74):c.863G>A (p.Arg288Gln) rs761276999 0.00002
NM_025103.4(IFT74):c.94T>C (p.Ser32Pro) rs201259858 0.00002
NM_025103.4(IFT74):c.1104G>A (p.Met368Ile) rs1288102281 0.00001
NM_025103.4(IFT74):c.1202G>C (p.Ser401Thr) rs1026606574 0.00001
NM_025103.4(IFT74):c.1217G>A (p.Arg406His) rs370969303 0.00001
NM_025103.4(IFT74):c.1261A>T (p.Met421Leu) rs768365827 0.00001
NM_025103.4(IFT74):c.1427A>G (p.Gln476Arg) rs769077886 0.00001
NM_025103.4(IFT74):c.1577A>G (p.Tyr526Cys) rs373796986 0.00001
NM_025103.4(IFT74):c.170C>T (p.Thr57Ile) rs1024826666 0.00001
NM_025103.4(IFT74):c.1771G>A (p.Val591Met) rs762276916 0.00001
NM_025103.4(IFT74):c.203C>G (p.Ala68Gly) rs768033736 0.00001
NM_025103.4(IFT74):c.259C>T (p.Pro87Ser) rs775155083 0.00001
NM_025103.4(IFT74):c.524T>C (p.Met175Thr) rs1440934591 0.00001
NM_025103.4(IFT74):c.56G>C (p.Gly19Ala) rs759834567 0.00001
NM_025103.4(IFT74):c.613G>A (p.Glu205Lys) rs756024765 0.00001
NM_025103.4(IFT74):c.933+6C>T rs372209311 0.00001
NC_000009.11:g.(?_27060569)_(27062734_?)del
NM_025103.4(IFT74):c.-20+1G>T
NM_025103.4(IFT74):c.1006T>C (p.Phe336Leu)
NM_025103.4(IFT74):c.1033A>G (p.Met345Val)
NM_025103.4(IFT74):c.1066C>G (p.Gln356Glu)
NM_025103.4(IFT74):c.1075A>G (p.Lys359Glu)
NM_025103.4(IFT74):c.1100A>T (p.His367Leu)
NM_025103.4(IFT74):c.1102A>G (p.Met368Val) rs1327165551
NM_025103.4(IFT74):c.1109-8A>G
NM_025103.4(IFT74):c.1133C>G (p.Thr378Arg)
NM_025103.4(IFT74):c.1150A>G (p.Lys384Glu)
NM_025103.4(IFT74):c.1154G>C (p.Arg385Pro) rs756441000
NM_025103.4(IFT74):c.1157A>G (p.Lys386Arg) rs2131684364
NM_025103.4(IFT74):c.1159G>A (p.Ala387Thr)
NM_025103.4(IFT74):c.1166T>C (p.Ile389Thr)
NM_025103.4(IFT74):c.1171G>C (p.Ala391Pro)
NM_025103.4(IFT74):c.1178T>C (p.Ile393Thr)
NM_025103.4(IFT74):c.1187T>A (p.Leu396His)
NM_025103.4(IFT74):c.1194G>T (p.Glu398Asp)
NM_025103.4(IFT74):c.1196A>C (p.His399Pro) rs2131684471
NM_025103.4(IFT74):c.1204C>G (p.Arg402Gly)
NM_025103.4(IFT74):c.1206+4A>G
NM_025103.4(IFT74):c.1207-3C>T
NM_025103.4(IFT74):c.1213A>C (p.Asn405His)
NM_025103.4(IFT74):c.1216C>T (p.Arg406Cys)
NM_025103.4(IFT74):c.1235C>G (p.Ser412Cys)
NM_025103.4(IFT74):c.123G>T (p.Met41Ile)
NM_025103.4(IFT74):c.1263G>A (p.Met421Ile)
NM_025103.4(IFT74):c.1268A>T (p.Asp423Val)
NM_025103.4(IFT74):c.1298A>G (p.Gln433Arg)
NM_025103.4(IFT74):c.1302A>C (p.Lys434Asn)
NM_025103.4(IFT74):c.1318C>A (p.Gln440Lys) rs533839288
NM_025103.4(IFT74):c.1319A>G (p.Gln440Arg)
NM_025103.4(IFT74):c.1320G>T (p.Gln440His)
NM_025103.4(IFT74):c.1341A>C (p.Gln447His)
NM_025103.4(IFT74):c.1342C>T (p.Arg448Cys)
NM_025103.4(IFT74):c.1343G>A (p.Arg448His)
NM_025103.4(IFT74):c.1351T>G (p.Leu451Val)
NM_025103.4(IFT74):c.1357C>A (p.Leu453Met)
NM_025103.4(IFT74):c.1367T>G (p.Met456Arg) rs1820126913
NM_025103.4(IFT74):c.1390A>G (p.Thr464Ala)
NM_025103.4(IFT74):c.1396G>A (p.Glu466Lys) rs1056984663
NM_025103.4(IFT74):c.1398A>C (p.Glu466Asp) rs202158905
NM_025103.4(IFT74):c.1432A>G (p.Thr478Ala)
NM_025103.4(IFT74):c.1435A>T (p.Thr479Ser)
NM_025103.4(IFT74):c.1445A>C (p.Glu482Ala)
NM_025103.4(IFT74):c.1445A>G (p.Glu482Gly)
NM_025103.4(IFT74):c.1447A>G (p.Ile483Val) rs2131703141
NM_025103.4(IFT74):c.1449A>G (p.Ile483Met)
NM_025103.4(IFT74):c.1450T>C (p.Tyr484His) rs2131703168
NM_025103.4(IFT74):c.1499A>C (p.Lys500Thr) rs1284257974
NM_025103.4(IFT74):c.149C>T (p.Ser50Phe)
NM_025103.4(IFT74):c.1510G>C (p.Glu504Gln)
NM_025103.4(IFT74):c.1518G>A (p.Met506Ile)
NM_025103.4(IFT74):c.1525T>C (p.Ser509Pro)
NM_025103.4(IFT74):c.1529C>T (p.Thr510Ile)
NM_025103.4(IFT74):c.152G>A (p.Arg51His) rs73436007
NM_025103.4(IFT74):c.1540G>A (p.Ala514Thr)
NM_025103.4(IFT74):c.1562A>G (p.Lys521Arg)
NM_025103.4(IFT74):c.1576T>C (p.Tyr526His)
NM_025103.4(IFT74):c.157T>C (p.Cys53Arg)
NM_025103.4(IFT74):c.15_16del (p.His5fs)
NM_025103.4(IFT74):c.1604A>T (p.Glu535Val) rs2131704919
NM_025103.4(IFT74):c.1615C>T (p.His539Tyr)
NM_025103.4(IFT74):c.161C>G (p.Pro54Arg)
NM_025103.4(IFT74):c.1627A>C (p.Thr543Pro)
NM_025103.4(IFT74):c.1671T>G (p.Phe557Leu)
NM_025103.4(IFT74):c.1673C>T (p.Ala558Val)
NM_025103.4(IFT74):c.1675A>G (p.Met559Val)
NM_025103.4(IFT74):c.1683A>G (p.Glu561=)
NM_025103.4(IFT74):c.1684+5C>G
NM_025103.4(IFT74):c.1684T>C (p.Phe562Leu)
NM_025103.4(IFT74):c.1688T>C (p.Ile563Thr)
NM_025103.4(IFT74):c.1714T>G (p.Tyr572Asp)
NM_025103.4(IFT74):c.1723A>G (p.Ile575Val)
NM_025103.4(IFT74):c.1750G>T (p.Ala584Ser)
NM_025103.4(IFT74):c.1775A>G (p.Asp592Gly)
NM_025103.4(IFT74):c.1775A>T (p.Asp592Val) rs372962980
NM_025103.4(IFT74):c.178G>T (p.Val60Phe)
NM_025103.4(IFT74):c.1790_1791delinsTT (p.Thr597Ile) rs2131720086
NM_025103.4(IFT74):c.17A>G (p.Lys6Arg)
NM_025103.4(IFT74):c.1801T>A (p.Ter601Arg)
NM_025103.4(IFT74):c.202G>T (p.Ala68Ser)
NM_025103.4(IFT74):c.205C>T (p.His69Tyr)
NM_025103.4(IFT74):c.209G>A (p.Arg70His)
NM_025103.4(IFT74):c.218C>A (p.Thr73Lys) rs779059979
NM_025103.4(IFT74):c.232A>C (p.Thr78Pro)
NM_025103.4(IFT74):c.251C>G (p.Thr84Arg)
NM_025103.4(IFT74):c.256+6T>C
NM_025103.4(IFT74):c.256G>T (p.Gly86Cys)
NM_025103.4(IFT74):c.262C>A (p.Gln88Lys)
NM_025103.4(IFT74):c.281A>T (p.Lys94Ile)
NM_025103.4(IFT74):c.283T>C (p.Ser95Pro)
NM_025103.4(IFT74):c.306-3T>C
NM_025103.4(IFT74):c.326C>A (p.Thr109Lys)
NM_025103.4(IFT74):c.32G>T (p.Arg11Leu) rs369587850
NM_025103.4(IFT74):c.3G>A (p.Met1Ile)
NM_025103.4(IFT74):c.402G>C (p.Lys134Asn)
NM_025103.4(IFT74):c.404+3_404+6del rs2131541200
NM_025103.4(IFT74):c.405G>A (p.Arg135=)
NM_025103.4(IFT74):c.40T>A (p.Ser14Thr)
NM_025103.4(IFT74):c.40T>G (p.Ser14Ala)
NM_025103.4(IFT74):c.416T>C (p.Leu139Ser)
NM_025103.4(IFT74):c.425A>G (p.Glu142Gly) rs1827549533
NM_025103.4(IFT74):c.431A>G (p.Lys144Arg)
NM_025103.4(IFT74):c.437T>G (p.Leu146Arg)
NM_025103.4(IFT74):c.441A>T (p.Gln147His)
NM_025103.4(IFT74):c.451G>A (p.Ala151Thr)
NM_025103.4(IFT74):c.454G>C (p.Asp152His)
NM_025103.4(IFT74):c.508A>C (p.Met170Leu) rs1205461850
NM_025103.4(IFT74):c.53T>C (p.Val18Ala) rs1826386837
NM_025103.4(IFT74):c.545G>A (p.Arg182Gln)
NM_025103.4(IFT74):c.587+2dup
NM_025103.4(IFT74):c.587C>A (p.Ala196Glu)
NM_025103.4(IFT74):c.587C>T (p.Ala196Val)
NM_025103.4(IFT74):c.588-16G>T
NM_025103.4(IFT74):c.593A>G (p.Glu198Gly)
NM_025103.4(IFT74):c.598C>G (p.Gln200Glu)
NM_025103.4(IFT74):c.619G>C (p.Glu207Gln)
NM_025103.4(IFT74):c.62C>T (p.Thr21Ile)
NM_025103.4(IFT74):c.643A>G (p.Thr215Ala)
NM_025103.4(IFT74):c.652A>G (p.Ile218Val)
NM_025103.4(IFT74):c.670T>G (p.Phe224Val)
NM_025103.4(IFT74):c.674A>G (p.Glu225Gly) rs1210786711
NM_025103.4(IFT74):c.679C>G (p.Gln227Glu)
NM_025103.4(IFT74):c.69G>C (p.Arg23Ser)
NM_025103.4(IFT74):c.701A>G (p.Lys234Arg)
NM_025103.4(IFT74):c.726+4A>C
NM_025103.4(IFT74):c.732A>T (p.Leu244Phe)
NM_025103.4(IFT74):c.737C>T (p.Thr246Ile)
NM_025103.4(IFT74):c.754G>T (p.Asp252Tyr)
NM_025103.4(IFT74):c.762G>C (p.Gln254His)
NM_025103.4(IFT74):c.764A>T (p.Asn255Ile)
NM_025103.4(IFT74):c.76T>G (p.Ser26Ala) rs1053474425
NM_025103.4(IFT74):c.777G>C (p.Glu259Asp)
NM_025103.4(IFT74):c.779G>T (p.Ser260Ile)
NM_025103.4(IFT74):c.789+3A>G
NM_025103.4(IFT74):c.791A>C (p.Glu264Ala)
NM_025103.4(IFT74):c.799C>G (p.His267Asp)
NM_025103.4(IFT74):c.79G>C (p.Gly27Arg)
NM_025103.4(IFT74):c.79G>T (p.Gly27Trp)
NM_025103.4(IFT74):c.813A>T (p.Lys271Asn)
NM_025103.4(IFT74):c.820G>A (p.Ala274Thr) rs1264631833
NM_025103.4(IFT74):c.851T>C (p.Leu284Ser)
NM_025103.4(IFT74):c.85C>G (p.Arg29Gly)
NM_025103.4(IFT74):c.863G>T (p.Arg288Leu)
NM_025103.4(IFT74):c.875T>C (p.Ile292Thr)
NM_025103.4(IFT74):c.892A>G (p.Ile298Val)
NM_025103.4(IFT74):c.905T>C (p.Met302Thr)
NM_025103.4(IFT74):c.916G>C (p.Glu306Gln)
NM_025103.4(IFT74):c.966G>A (p.Met322Ile)
NM_025103.4(IFT74):c.980C>A (p.Thr327Lys)
NM_025103.4(IFT74):c.985A>G (p.Thr329Ala)
NM_025103.4(IFT74):c.986C>G (p.Thr329Arg)
NM_025103.4(IFT74):c.990A>T (p.Lys330Asn)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.