ClinVar Miner

List of variants in gene NEDD4L reported as benign by Invitae

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Gene type:
ClinVar version:
Total variants: 105
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HGVS dbSNP gnomAD frequency
NM_001144967.3(NEDD4L):c.49-16229G>A rs4149601 0.32848
NM_001144967.3(NEDD4L):c.2655+9G>A rs112196694 0.02540
NM_001144967.3(NEDD4L):c.513+14G>A rs77259956 0.02368
NM_001144967.3(NEDD4L):c.514-4G>A rs78005374 0.01389
NM_001144967.3(NEDD4L):c.2752+6C>T rs12964776 0.01046
NM_001144967.3(NEDD4L):c.297+17A>G rs115799375 0.00846
NM_001144967.3(NEDD4L):c.2753-4C>T rs116251315 0.00571
NM_001144967.3(NEDD4L):c.2802G>A (p.Glu934=) rs115364125 0.00521
NM_001144967.3(NEDD4L):c.698C>T (p.Ser233Leu) rs202231187 0.00354
NM_001144967.3(NEDD4L):c.2426+14T>C rs114391081 0.00205
NM_001144967.3(NEDD4L):c.2613C>T (p.Asn871=) rs141136641 0.00163
NM_001144967.3(NEDD4L):c.122+9G>C rs115907798 0.00128
NM_001144967.3(NEDD4L):c.2542C>T (p.Leu848=) rs370069597 0.00099
NM_001144967.3(NEDD4L):c.2487+14G>A rs199851734 0.00095
NM_001144967.3(NEDD4L):c.1980T>C (p.Tyr660=) rs202013710 0.00075
NM_001144967.3(NEDD4L):c.1708+11G>A rs114908156 0.00056
NM_001144967.3(NEDD4L):c.1911C>T (p.Ser637=) rs371612571 0.00054
NM_001144967.3(NEDD4L):c.49-6T>C rs375043092 0.00052
NM_001144967.3(NEDD4L):c.639C>T (p.Asn213=) rs202008394 0.00049
NM_001144967.3(NEDD4L):c.1833+17T>C rs189511948 0.00039
NM_001144967.3(NEDD4L):c.1197G>A (p.Gly399=) rs368597288 0.00031
NM_001144967.3(NEDD4L):c.580C>T (p.Pro194Ser) rs375316659 0.00026
NM_001144967.3(NEDD4L):c.937A>C (p.Arg313=) rs140550335 0.00026
NM_001144967.3(NEDD4L):c.2715A>C (p.Thr905=) rs374600334 0.00022
NM_001144967.3(NEDD4L):c.163A>G (p.Asn55Asp) rs200025824 0.00014
NM_001144967.3(NEDD4L):c.2488-20del rs752322832 0.00012
NM_001144967.3(NEDD4L):c.1530C>T (p.Asn510=) rs199582650 0.00011
NM_001144967.3(NEDD4L):c.2161G>A (p.Val721Ile) rs764634193 0.00010
NM_001144967.3(NEDD4L):c.58C>T (p.Arg20Cys) rs373553230 0.00009
NM_001144967.3(NEDD4L):c.2565C>T (p.Leu855=) rs375065890 0.00008
NM_001144967.3(NEDD4L):c.2063+6T>C rs751818108 0.00007
NM_001144967.3(NEDD4L):c.815C>T (p.Pro272Leu) rs371954364 0.00007
NM_001144967.3(NEDD4L):c.1036G>A (p.Ala346Thr) rs545427970 0.00006
NM_001144967.3(NEDD4L):c.1279G>A (p.Gly427Arg) rs141078303 0.00006
NM_001144967.3(NEDD4L):c.2892C>T (p.Ala964=) rs372898637 0.00006
NM_001144967.3(NEDD4L):c.547G>A (p.Ala183Thr) rs372009925 0.00006
NM_001144967.3(NEDD4L):c.2635G>A (p.Val879Ile) rs907217983 0.00005
NM_001144967.3(NEDD4L):c.1064C>T (p.Pro355Leu) rs767136811 0.00004
NM_001144967.3(NEDD4L):c.1329G>A (p.Arg443=) rs185018054 0.00004
NM_001144967.3(NEDD4L):c.781C>T (p.Pro261Ser) rs764280225 0.00004
NM_001144967.3(NEDD4L):c.902G>A (p.Arg301Gln) rs372196719 0.00004
NM_001144967.3(NEDD4L):c.1353A>G (p.Thr451=) rs375061430 0.00003
NM_001144967.3(NEDD4L):c.1634A>G (p.Asn545Ser) rs773924900 0.00003
NM_001144967.3(NEDD4L):c.1654-10C>G rs373387102 0.00003
NM_001144967.3(NEDD4L):c.2093A>G (p.Asn698Ser) rs377143286 0.00003
NM_001144967.3(NEDD4L):c.2240A>G (p.Asn747Ser) rs751509135 0.00003
NM_001144967.3(NEDD4L):c.2614G>A (p.Gly872Ser) rs746532070 0.00003
NM_001144967.3(NEDD4L):c.411-6G>A rs765977807 0.00003
NM_001144967.3(NEDD4L):c.885G>A (p.Pro295=) rs765699158 0.00003
NM_001144967.3(NEDD4L):c.1370C>T (p.Pro457Leu) rs766146854 0.00002
NM_001144967.3(NEDD4L):c.1027G>A (p.Val343Ile) rs1388246823 0.00001
NM_001144967.3(NEDD4L):c.1052G>C (p.Gly351Ala) rs1270448589 0.00001
NM_001144967.3(NEDD4L):c.1274C>T (p.Ala425Val) rs748170219 0.00001
NM_001144967.3(NEDD4L):c.2062A>G (p.Thr688Ala) rs565332359 0.00001
NM_001144967.3(NEDD4L):c.2186-4T>G rs1299947228 0.00001
NM_001144967.3(NEDD4L):c.546G>A (p.Ser182=) rs776098051 0.00001
NM_001144967.3(NEDD4L):c.568C>T (p.Leu190Phe) rs764101138 0.00001
NM_001144967.3(NEDD4L):c.704A>G (p.Asn235Ser) rs375921587 0.00001
NM_001144967.3(NEDD4L):c.743G>A (p.Arg248His) rs948274978 0.00001
NM_001144967.3(NEDD4L):c.768C>T (p.Ser256=) rs183766749 0.00001
NM_001144967.3(NEDD4L):c.811G>A (p.Glu271Lys) rs373720887 0.00001
NM_001144967.3(NEDD4L):c.847G>A (p.Ala283Thr) rs1408580789 0.00001
NM_001144967.3(NEDD4L):c.1045G>C (p.Glu349Gln) rs2041364455
NM_001144967.3(NEDD4L):c.1139A>T (p.Tyr380Phe) rs753954381
NM_001144967.3(NEDD4L):c.1151C>G (p.Thr384Arg) rs370254467
NM_001144967.3(NEDD4L):c.122+17T>A
NM_001144967.3(NEDD4L):c.1249A>G (p.Ile417Val) rs1057524052
NM_001144967.3(NEDD4L):c.1258-6A>G
NM_001144967.3(NEDD4L):c.1297A>G (p.Asn433Asp) rs1245506692
NM_001144967.3(NEDD4L):c.1378-3T>C rs1002322308
NM_001144967.3(NEDD4L):c.137A>G (p.Lys46Arg) rs2047139560
NM_001144967.3(NEDD4L):c.1396G>A (p.Val466Ile) rs757173296
NM_001144967.3(NEDD4L):c.157G>A (p.Asp53Asn)
NM_001144967.3(NEDD4L):c.1607T>C (p.Met536Thr) rs369952868
NM_001144967.3(NEDD4L):c.1721C>G (p.Thr574Ser) rs2044795067
NM_001144967.3(NEDD4L):c.1749C>G (p.Asn583Lys)
NM_001144967.3(NEDD4L):c.1756A>G (p.Ile586Val)
NM_001144967.3(NEDD4L):c.194C>A (p.Thr65Lys)
NM_001144967.3(NEDD4L):c.1952A>G (p.Glu651Gly)
NM_001144967.3(NEDD4L):c.2087A>G (p.Asn696Ser)
NM_001144967.3(NEDD4L):c.2186-3T>C
NM_001144967.3(NEDD4L):c.2256+15G>A
NM_001144967.3(NEDD4L):c.2342A>C (p.Asn781Thr) rs2047127716
NM_001144967.3(NEDD4L):c.2402A>G (p.Asn801Ser) rs2048580915
NM_001144967.3(NEDD4L):c.2426+4T>C rs1601943711
NM_001144967.3(NEDD4L):c.2471T>G (p.Met824Arg)
NM_001144967.3(NEDD4L):c.2488-8del rs751368482
NM_001144967.3(NEDD4L):c.2488-8dup rs751368482
NM_001144967.3(NEDD4L):c.2488-9_2488-8del rs751368482
NM_001144967.3(NEDD4L):c.2509A>G (p.Ile837Val) rs2146867720
NM_001144967.3(NEDD4L):c.2770C>A (p.Leu924Met) rs2146993102
NM_001144967.3(NEDD4L):c.349-9del rs748936457
NM_001144967.3(NEDD4L):c.349-9dup rs748936457
NM_001144967.3(NEDD4L):c.431G>A (p.Gly144Glu)
NM_001144967.3(NEDD4L):c.450G>T (p.Met150Ile) rs2059009305
NM_001144967.3(NEDD4L):c.526G>A (p.Val176Ile) rs2059187873
NM_001144967.3(NEDD4L):c.698C>G (p.Ser233Trp) rs202231187
NM_001144967.3(NEDD4L):c.791C>T (p.Ser264Leu) rs200330105
NM_001144967.3(NEDD4L):c.812A>C (p.Glu271Ala) rs1404724194
NM_001144967.3(NEDD4L):c.813+13del rs764470079
NM_001144967.3(NEDD4L):c.845T>G (p.Ile282Ser) rs2144697526
NM_001144967.3(NEDD4L):c.868G>T (p.Ala290Ser)
NM_001144967.3(NEDD4L):c.935G>A (p.Ser312Asn) rs2059732245
NM_001144967.3(NEDD4L):c.989T>C (p.Ile330Thr) rs1601342676
NM_001144967.3(NEDD4L):c.991-14dup

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