ClinVar Miner

List of variants in gene NRP1 reported as uncertain significance for NRP1-related disorder

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Gene type:
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Total variants: 110
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HGVS dbSNP gnomAD frequency
NM_003873.7(NRP1):c.1459A>G (p.Ile487Val) rs182437025 0.00019
NM_003873.7(NRP1):c.44T>C (p.Val15Ala) rs374322029 0.00017
NM_003873.7(NRP1):c.620G>A (p.Arg207His) rs148308681 0.00015
NM_003873.7(NRP1):c.2571C>G (p.Ile857Met) rs144845322 0.00014
NM_003873.7(NRP1):c.1009A>G (p.Thr337Ala) rs367928513 0.00011
NM_003873.7(NRP1):c.194A>G (p.Gln65Arg) rs371886197 0.00008
NM_003873.7(NRP1):c.2262G>A (p.Met754Ile) rs780027653 0.00008
NM_003873.7(NRP1):c.1760C>T (p.Ala587Val) rs754732280 0.00005
NM_003873.7(NRP1):c.1898C>T (p.Thr633Met) rs201288994 0.00005
NM_003873.7(NRP1):c.2222G>A (p.Arg741His) rs554872876 0.00005
NM_003873.7(NRP1):c.1000C>T (p.Arg334Cys) rs747418517 0.00004
NM_003873.7(NRP1):c.1517G>A (p.Arg506Gln) rs554892989 0.00004
NM_003873.7(NRP1):c.1676C>T (p.Thr559Met) rs143124682 0.00004
NM_003873.7(NRP1):c.1096G>A (p.Gly366Arg) rs370551432 0.00003
NM_003873.7(NRP1):c.1214G>A (p.Arg405Gln) rs752043800 0.00003
NM_003873.7(NRP1):c.1483G>A (p.Val495Met) rs749575467 0.00003
NM_003873.7(NRP1):c.2632G>A (p.Val878Met) rs200330871 0.00003
NM_003873.7(NRP1):c.271G>A (p.Asp91Asn) rs533652148 0.00003
NM_003873.7(NRP1):c.92T>C (p.Ile31Thr) rs867341914 0.00003
NM_003873.7(NRP1):c.1654C>T (p.Arg552Trp) rs779745790 0.00002
NM_003873.7(NRP1):c.365A>C (p.Lys122Thr) rs753645404 0.00002
NM_003873.7(NRP1):c.605G>C (p.Gly202Ala) rs941004239 0.00002
NM_003873.7(NRP1):c.1445A>G (p.Asn482Ser) rs1042934113 0.00001
NM_003873.7(NRP1):c.1552G>A (p.Gly518Arg) rs769982693 0.00001
NM_003873.7(NRP1):c.1626C>T (p.Gly542=) rs762826442 0.00001
NM_003873.7(NRP1):c.1717G>A (p.Gly573Arg) rs778160256 0.00001
NM_003873.7(NRP1):c.1925-3A>C rs371729403 0.00001
NM_003873.7(NRP1):c.2192C>T (p.Ser731Phe) rs757977129 0.00001
NM_003873.7(NRP1):c.221A>T (p.His74Leu) rs750237365 0.00001
NM_003873.7(NRP1):c.227A>G (p.Asp76Gly) rs1285825996 0.00001
NM_003873.7(NRP1):c.2502A>T (p.Glu834Asp) rs936099600 0.00001
NM_003873.7(NRP1):c.2689G>C (p.Glu897Gln) rs777261396 0.00001
NM_003873.7(NRP1):c.2696A>G (p.Tyr899Cys) rs769226149 0.00001
NM_003873.7(NRP1):c.602C>T (p.Pro201Leu) rs200265591 0.00001
NM_003873.7(NRP1):c.733A>G (p.Met245Val) rs375021532 0.00001
NM_003873.7(NRP1):c.755C>T (p.Ala252Val) rs780290010 0.00001
NM_003873.7(NRP1):c.914G>A (p.Arg305His) rs1174102640 0.00001
NM_003873.7(NRP1):c.1000C>A (p.Arg334Ser)
NM_003873.7(NRP1):c.1001G>A (p.Arg334His)
NM_003873.7(NRP1):c.1010C>T (p.Thr337Met) rs142121081
NM_003873.7(NRP1):c.1070C>A (p.Thr357Asn)
NM_003873.7(NRP1):c.1089C>A (p.Ser363Arg)
NM_003873.7(NRP1):c.1162A>T (p.Thr388Ser)
NM_003873.7(NRP1):c.127G>A (p.Gly43Ser) rs2493473679
NM_003873.7(NRP1):c.1283-5C>A
NM_003873.7(NRP1):c.1357G>C (p.Gly453Arg)
NM_003873.7(NRP1):c.1365A>C (p.Arg455Ser)
NM_003873.7(NRP1):c.1403G>A (p.Arg468His) rs751563527
NM_003873.7(NRP1):c.1429C>T (p.Pro477Ser)
NM_003873.7(NRP1):c.1461A>G (p.Ile487Met)
NM_003873.7(NRP1):c.1483G>T (p.Val495Leu)
NM_003873.7(NRP1):c.1504G>A (p.Gly502Ser)
NM_003873.7(NRP1):c.1507G>T (p.Gly503Trp)
NM_003873.7(NRP1):c.1559G>C (p.Ser520Thr)
NM_003873.7(NRP1):c.1609G>A (p.Ala537Thr) rs1330019086
NM_003873.7(NRP1):c.1621G>C (p.Glu541Gln)
NM_003873.7(NRP1):c.1627AAC[2] (p.Asn545del)
NM_003873.7(NRP1):c.1658C>T (p.Thr553Ile)
NM_003873.7(NRP1):c.1712A>T (p.His571Leu)
NM_003873.7(NRP1):c.1775C>T (p.Pro592Leu)
NM_003873.7(NRP1):c.1789G>A (p.Gly597Arg) rs141633354
NM_003873.7(NRP1):c.1789G>C (p.Gly597Arg)
NM_003873.7(NRP1):c.1809T>G (p.Cys603Trp)
NM_003873.7(NRP1):c.1819C>G (p.Gln607Glu)
NM_003873.7(NRP1):c.1854C>G (p.Phe618Leu)
NM_003873.7(NRP1):c.1865-1G>T
NM_003873.7(NRP1):c.1906G>A (p.Asp636Asn)
NM_003873.7(NRP1):c.1924+6A>G
NM_003873.7(NRP1):c.1952A>C (p.Glu651Ala)
NM_003873.7(NRP1):c.2017T>G (p.Trp673Gly)
NM_003873.7(NRP1):c.202A>G (p.Met68Val)
NM_003873.7(NRP1):c.2039C>T (p.Thr680Met)
NM_003873.7(NRP1):c.204G>C (p.Met68Ile)
NM_003873.7(NRP1):c.2106G>T (p.Lys702Asn)
NM_003873.7(NRP1):c.2196C>A (p.His732Gln) rs376053165
NM_003873.7(NRP1):c.2267T>C (p.Ile756Thr)
NM_003873.7(NRP1):c.2300G>A (p.Arg767His)
NM_003873.7(NRP1):c.2458C>T (p.Pro820Ser)
NM_003873.7(NRP1):c.248+3_248+6del rs2493471077
NM_003873.7(NRP1):c.2495G>C (p.Gly832Ala)
NM_003873.7(NRP1):c.249G>T (p.Lys83Asn)
NM_003873.7(NRP1):c.2539C>G (p.Pro847Ala)
NM_003873.7(NRP1):c.2566C>A (p.Pro856Thr)
NM_003873.7(NRP1):c.2575A>C (p.Ile859Leu)
NM_003873.7(NRP1):c.259G>A (p.Val87Met)
NM_003873.7(NRP1):c.270C>T (p.Phe90=)
NM_003873.7(NRP1):c.2745T>A (p.Asn915Lys)
NM_003873.7(NRP1):c.2752A>C (p.Ser918Arg)
NM_003873.7(NRP1):c.29C>T (p.Ala10Val) rs2493508921
NM_003873.7(NRP1):c.356T>C (p.Leu119Pro)
NM_003873.7(NRP1):c.406A>G (p.Ile136Val)
NM_003873.7(NRP1):c.409C>G (p.Arg137Gly)
NM_003873.7(NRP1):c.409C>T (p.Arg137Cys)
NM_003873.7(NRP1):c.49G>T (p.Ala17Ser) rs2493508273
NM_003873.7(NRP1):c.55G>A (p.Ala19Thr)
NM_003873.7(NRP1):c.608G>C (p.Gly203Ala)
NM_003873.7(NRP1):c.622T>C (p.Tyr208His)
NM_003873.7(NRP1):c.629G>A (p.Arg210Gln)
NM_003873.7(NRP1):c.664C>A (p.Pro222Thr)
NM_003873.7(NRP1):c.664C>T (p.Pro222Ser) rs143227333
NM_003873.7(NRP1):c.677G>A (p.Arg226His)
NM_003873.7(NRP1):c.689A>G (p.Gln230Arg)
NM_003873.7(NRP1):c.73+5G>A
NM_003873.7(NRP1):c.826A>T (p.Met276Leu)
NM_003873.7(NRP1):c.896C>T (p.Thr299Ile)
NM_003873.7(NRP1):c.8G>C (p.Arg3Thr)
NM_003873.7(NRP1):c.920G>T (p.Arg307Leu) rs749859903
NM_003873.7(NRP1):c.928T>C (p.Tyr310His)
NM_003873.7(NRP1):c.936G>C (p.Glu312Asp) rs2492589423
NM_003873.7(NRP1):c.955G>C (p.Glu319Gln)

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