ClinVar Miner

List of variants in gene FRMPD4 reported as likely benign

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Gene type:
ClinVar version:
Total variants: 105
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HGVS dbSNP gnomAD frequency
NM_001368397.1(FRMPD4):c.1401C>G (p.Val467=) rs6641078 0.11823
NM_001368397.1(FRMPD4):c.2007T>C (p.Leu669=) rs67823099 0.08669
NM_001368397.1(FRMPD4):c.1470+9C>T rs7877197 0.05067
NM_001368397.1(FRMPD4):c.741C>G (p.Leu247=) rs7049642 0.01254
NM_001368397.1(FRMPD4):c.3899C>A (p.Thr1300Asn) rs139367112 0.00175
NM_001368397.1(FRMPD4):c.4794C>T (p.Ser1598=) rs371017598 0.00141
NM_001368397.1(FRMPD4):c.3822C>G (p.Thr1274=) rs140304936 0.00108
NM_001368397.1(FRMPD4):c.388G>A (p.Ala130Thr) rs139449383 0.00099
NM_001368397.1(FRMPD4):c.4080A>G (p.Pro1360=) rs200639149 0.00070
NM_001368397.1(FRMPD4):c.3703G>A (p.Val1235Met) rs143569009 0.00053
NM_001368397.1(FRMPD4):c.1218G>A (p.Lys406=) rs140428359 0.00048
NM_001368397.1(FRMPD4):c.3438A>C (p.Gln1146His) rs139151624 0.00042
NM_001368397.1(FRMPD4):c.2878G>A (p.Ala960Thr) rs138299368 0.00039
NM_001368397.1(FRMPD4):c.1398C>T (p.His466=) rs201869535 0.00033
NM_001368397.1(FRMPD4):c.1224T>C (p.His408=) rs200736738 0.00029
NM_001368397.1(FRMPD4):c.42-3728C>T rs765188236 0.00025
NM_001368397.1(FRMPD4):c.2599A>G (p.Asn867Asp) rs144170600 0.00023
NM_001368397.1(FRMPD4):c.3260G>A (p.Arg1087His) rs769071295 0.00023
NM_001368397.1(FRMPD4):c.1736C>T (p.Thr579Met) rs149409320 0.00020
NM_001368397.1(FRMPD4):c.2072G>T (p.Gly691Val) rs200183778 0.00019
NM_001368397.1(FRMPD4):c.1452C>G (p.Leu484=) rs372073451 0.00017
NM_001368397.1(FRMPD4):c.3379G>A (p.Glu1127Lys) rs143423231 0.00017
NM_001368397.1(FRMPD4):c.1021G>A (p.Ala341Thr) rs142194011 0.00016
NM_001368397.1(FRMPD4):c.3813C>T (p.His1271=) rs376423451 0.00015
NM_001368397.1(FRMPD4):c.1479G>A (p.Thr493=) rs773949472 0.00011
NM_001368397.1(FRMPD4):c.1602G>T (p.Gln534His) rs771897369 0.00011
NM_001368397.1(FRMPD4):c.1925C>T (p.Ala642Val) rs142025193 0.00011
NM_001368397.1(FRMPD4):c.2200C>T (p.Pro734Ser) rs201325065 0.00010
NM_001368397.1(FRMPD4):c.1411G>A (p.Glu471Lys) rs747574742 0.00009
NM_001368397.1(FRMPD4):c.3566G>A (p.Arg1189His) rs751628514 0.00008
NM_001368397.1(FRMPD4):c.3567C>G (p.Arg1189=) rs146036306 0.00008
NM_001368397.1(FRMPD4):c.1636C>T (p.Leu546Phe) rs200271818 0.00007
NM_001368397.1(FRMPD4):c.1840G>A (p.Gly614Arg) rs748144907 0.00007
NM_001368397.1(FRMPD4):c.2280C>T (p.Leu760=) rs780060901 0.00007
NM_001368397.1(FRMPD4):c.3964+7C>A rs768150299 0.00007
NM_001368397.1(FRMPD4):c.2903C>T (p.Ser968Leu) rs146907470 0.00006
NM_001368397.1(FRMPD4):c.1896C>A (p.Thr632=) rs369092267 0.00005
NM_001368397.1(FRMPD4):c.2712G>A (p.Ser904=) rs145038513 0.00005
NM_001368397.1(FRMPD4):c.2820C>T (p.His940=) rs765472737 0.00005
NM_001368397.1(FRMPD4):c.3067T>C (p.Cys1023Arg) rs143929343 0.00005
NM_001368397.1(FRMPD4):c.2048A>G (p.Glu683Gly) rs760597864 0.00004
NM_001368397.1(FRMPD4):c.222G>A (p.Pro74=) rs779251615 0.00004
NM_001368397.1(FRMPD4):c.2402G>A (p.Arg801His) rs772679523 0.00004
NM_001368397.1(FRMPD4):c.2605G>A (p.Val869Ile) rs146534723 0.00004
NM_001368397.1(FRMPD4):c.3938G>A (p.Arg1313Gln) rs759503727 0.00004
NM_001368397.1(FRMPD4):c.528C>G (p.Val176=) rs777937320 0.00004
NM_001368397.1(FRMPD4):c.2003C>A (p.Thr668Asn) rs376545795 0.00003
NM_001368397.1(FRMPD4):c.2494G>A (p.Glu832Lys) rs145583343 0.00003
NM_001368397.1(FRMPD4):c.2569G>A (p.Ala857Thr) rs368784263 0.00003
NM_001368397.1(FRMPD4):c.2868C>T (p.Ser956=) rs1602373286 0.00003
NM_001368397.1(FRMPD4):c.2917G>C (p.Ala973Pro) rs200249861 0.00003
NM_001368397.1(FRMPD4):c.3766G>A (p.Val1256Met) rs1036437887 0.00003
NM_001368397.1(FRMPD4):c.868G>A (p.Val290Ile) rs779596855 0.00003
NM_001368395.3(FRMPD4):c.152+7A>G rs1333358798 0.00002
NM_001368397.1(FRMPD4):c.1068C>T (p.Ile356=) rs1040001720 0.00002
NM_001368397.1(FRMPD4):c.1596G>A (p.Ala532=) rs774001975 0.00002
NM_001368397.1(FRMPD4):c.1757C>T (p.Thr586Ile) rs779000840 0.00002
NM_001368397.1(FRMPD4):c.1790T>C (p.Ile597Thr) rs757866192 0.00002
NM_001368397.1(FRMPD4):c.3710C>T (p.Ser1237Leu) rs921183679 0.00002
NM_001368397.1(FRMPD4):c.981T>C (p.Tyr327=) rs779013797 0.00002
NM_001368397.1(FRMPD4):c.125C>T (p.Thr42Met) rs146122430 0.00001
NM_001368397.1(FRMPD4):c.1926A>G (p.Ala642=) rs887954550 0.00001
NM_001368397.1(FRMPD4):c.249G>A (p.Arg83=) rs761069076 0.00001
NM_001368397.1(FRMPD4):c.255C>T (p.Pro85=) rs769101701 0.00001
NM_001368397.1(FRMPD4):c.2784G>T (p.Gln928His) rs777248043 0.00001
NM_001368397.1(FRMPD4):c.2907C>T (p.His969=) rs776672547 0.00001
NM_001368397.1(FRMPD4):c.3097G>A (p.Asp1033Asn) rs772365939 0.00001
NM_001368397.1(FRMPD4):c.3398C>G (p.Ala1133Gly) rs747284722 0.00001
NM_001368397.1(FRMPD4):c.3420T>C (p.Asp1140=) rs1344873923 0.00001
NM_001368397.1(FRMPD4):c.3558T>C (p.Ser1186=) rs1350467659 0.00001
NM_001368397.1(FRMPD4):c.42-9C>A rs765633648 0.00001
NM_001368397.1(FRMPD4):c.4590C>T (p.Cys1530=) rs2519887446 0.00001
NM_001368397.1(FRMPD4):c.1026C>T (p.Thr342=)
NM_001368397.1(FRMPD4):c.1287+15_1287+26dup rs746601138
NM_001368397.1(FRMPD4):c.1425G>A (p.Glu475=) rs2041902858
NM_001368397.1(FRMPD4):c.1485G>A (p.Leu495=)
NM_001368397.1(FRMPD4):c.1902A>C (p.Ser634=)
NM_001368397.1(FRMPD4):c.2020C>T (p.Leu674=)
NM_001368397.1(FRMPD4):c.2022A>G (p.Leu674=)
NM_001368397.1(FRMPD4):c.2081A>G (p.Asn694Ser)
NM_001368397.1(FRMPD4):c.2182G>A (p.Ala728Thr) rs750615873
NM_001368397.1(FRMPD4):c.2184G>A (p.Ala728=)
NM_001368397.1(FRMPD4):c.221C>T (p.Pro74Leu)
NM_001368397.1(FRMPD4):c.2243C>G (p.Ala748Gly) rs370344979
NM_001368397.1(FRMPD4):c.2428C>G (p.Pro810Ala)
NM_001368397.1(FRMPD4):c.2775A>T (p.Ala925=) rs1602372902
NM_001368397.1(FRMPD4):c.2859C>T (p.Phe953=) rs1602373245
NM_001368397.1(FRMPD4):c.2892T>C (p.Pro964=) rs1602373447
NM_001368397.1(FRMPD4):c.2964G>A (p.Gln988=)
NM_001368397.1(FRMPD4):c.3161C>T (p.Thr1054Met)
NM_001368397.1(FRMPD4):c.3268A>G (p.Ser1090Gly)
NM_001368397.1(FRMPD4):c.3428G>T (p.Gly1143Val)
NM_001368397.1(FRMPD4):c.3491A>T (p.Asp1164Val) rs2147176569
NM_001368397.1(FRMPD4):c.3682G>A (p.Gly1228Ser) rs140005767
NM_001368397.1(FRMPD4):c.3814G>A (p.Gly1272Arg)
NM_001368397.1(FRMPD4):c.3880C>T (p.Leu1294=) rs1602377592
NM_001368397.1(FRMPD4):c.3937C>A (p.Arg1313=) rs41303149
NM_001368397.1(FRMPD4):c.405G>C (p.Arg135=) rs2059220073
NM_001368397.1(FRMPD4):c.4486T>C (p.Trp1496Arg)
NM_001368397.1(FRMPD4):c.4734G>A (p.Leu1578=)
NM_001368397.1(FRMPD4):c.50C>T (p.Thr17Met)
NM_001368397.1(FRMPD4):c.5124C>T (p.Ile1708=) rs968114002
NM_001368397.1(FRMPD4):c.77C>T (p.Ser26Leu)
NM_001368397.1(FRMPD4):c.867C>T (p.Phe289=) rs991451035
NM_001368397.1(FRMPD4):c.928G>A (p.Val310Ile) rs2147124913

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