ClinVar Miner

List of variants in gene NLGN4X reported by Ambry Genetics

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Gene type:
ClinVar version:
Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_181332.3(NLGN4X):c.933C>T (p.Thr311=) rs7049300 0.13090
NM_181332.3(NLGN4X):c.1251G>C (p.Arg417=) rs61741754 0.06453
NM_181332.3(NLGN4X):c.897A>G (p.Ile299Met) rs151073358 0.00757
NM_181332.3(NLGN4X):c.1777C>T (p.Leu593Phe) rs3747333 0.00756
NM_181332.3(NLGN4X):c.2271G>A (p.Pro757=) rs4999056 0.00609
NM_181332.3(NLGN4X):c.558C>T (p.Asp186=) rs145911431 0.00414
NM_181332.3(NLGN4X):c.2280C>T (p.Tyr760=) rs75350246 0.00384
NM_181332.3(NLGN4X):c.591C>T (p.Ile197=) rs149003627 0.00101
NM_181332.3(NLGN4X):c.1641T>C (p.Ile547=) rs371132194 0.00036
NM_181332.3(NLGN4X):c.1133A>G (p.Lys378Arg) rs144093574 0.00028
NM_181332.3(NLGN4X):c.1341C>T (p.His447=) rs9699239 0.00026
NM_181332.3(NLGN4X):c.2360C>T (p.Thr787Met) rs4995611 0.00016
NM_181332.3(NLGN4X):c.2049G>A (p.Ala683=) rs772348674 0.00013
NM_181332.3(NLGN4X):c.1284C>T (p.Ala428=) rs201588956 0.00009
NM_181332.3(NLGN4X):c.955C>A (p.Arg319=) rs199769855 0.00009
NM_181332.3(NLGN4X):c.936G>A (p.Thr312=) rs201720833 0.00008
NM_181332.3(NLGN4X):c.971A>G (p.Lys324Arg) rs750826324 0.00008
NM_181332.3(NLGN4X):c.282G>A (p.Pro94=) rs777791438 0.00007
NM_181332.3(NLGN4X):c.2178C>T (p.Asn726=) rs187221748 0.00006
NM_181332.3(NLGN4X):c.1360G>A (p.Val454Met) rs199525017 0.00005
NM_181332.3(NLGN4X):c.1144G>A (p.Gly382Ser) rs760969834 0.00003
NM_181332.3(NLGN4X):c.1470T>C (p.Gly490=) rs9785509 0.00003
NM_181332.3(NLGN4X):c.1476G>A (p.Glu492=) rs9785605 0.00003
NM_181332.3(NLGN4X):c.516C>T (p.Ile172=) rs182247389 0.00002
NM_181332.3(NLGN4X):c.1054G>A (p.Asp352Asn) rs1412018300 0.00001
NM_181332.3(NLGN4X):c.1197G>C (p.Val399=) rs1456373848 0.00001
NM_181332.3(NLGN4X):c.1545C>T (p.Asn515=) rs772619986 0.00001
NM_181332.3(NLGN4X):c.2223C>T (p.His741=) rs541646409 0.00001
NM_181332.3(NLGN4X):c.2284C>G (p.Leu762Val) rs764361221 0.00001
NM_181332.3(NLGN4X):c.2324C>T (p.Thr775Met) rs746531523 0.00001
NM_181332.3(NLGN4X):c.105G>T (p.Lys35Asn)
NM_181332.3(NLGN4X):c.115A>G (p.Ile39Val) rs201534650
NM_181332.3(NLGN4X):c.1206C>T (p.Phe402=)
NM_181332.3(NLGN4X):c.1235G>A (p.Gly412Glu)
NM_181332.3(NLGN4X):c.1267A>G (p.Met423Val)
NM_181332.3(NLGN4X):c.1301A>G (p.Glu434Gly)
NM_181332.3(NLGN4X):c.1371C>T (p.Ala457=)
NM_181332.3(NLGN4X):c.1386G>A (p.Gln462=)
NM_181332.3(NLGN4X):c.1477G>C (p.Val493Leu)
NM_181332.3(NLGN4X):c.1480C>G (p.Pro494Ala) rs1569118116
NM_181332.3(NLGN4X):c.1658G>A (p.Arg553His)
NM_181332.3(NLGN4X):c.1747C>T (p.Arg583Trp) rs1555913640
NM_181332.3(NLGN4X):c.1779C>G (p.Leu593=) rs3747334
NM_181332.3(NLGN4X):c.1796A>G (p.Asn599Ser) rs2031314764
NM_181332.3(NLGN4X):c.1874C>A (p.Thr625Asn)
NM_181332.3(NLGN4X):c.1879C>T (p.Arg627Ter) rs1226379186
NM_181332.3(NLGN4X):c.1880G>A (p.Arg627Gln) rs1569110556
NM_181332.3(NLGN4X):c.1897T>C (p.Trp633Arg)
NM_181332.3(NLGN4X):c.191A>G (p.Asn64Ser)
NM_181332.3(NLGN4X):c.1984A>G (p.Thr662Ala)
NM_181332.3(NLGN4X):c.2020G>A (p.Glu674Lys)
NM_181332.3(NLGN4X):c.2288C>T (p.Thr763Met)
NM_181332.3(NLGN4X):c.2325G>A (p.Thr775=)
NM_181332.3(NLGN4X):c.2390C>A (p.Thr797Asn)
NM_181332.3(NLGN4X):c.2405A>G (p.Gln802Arg)
NM_181332.3(NLGN4X):c.24A>G (p.Leu8=)
NM_181332.3(NLGN4X):c.268C>G (p.Pro90Ala)
NM_181332.3(NLGN4X):c.292A>G (p.Thr98Ala)
NM_181332.3(NLGN4X):c.334dup (p.Gln112fs)
NM_181332.3(NLGN4X):c.544G>A (p.Gly182Ser)
NM_181332.3(NLGN4X):c.553A>G (p.Ile185Val)
NM_181332.3(NLGN4X):c.560G>A (p.Gly187Asp) rs1569195529
NM_181332.3(NLGN4X):c.586G>A (p.Val196Ile)
NM_181332.3(NLGN4X):c.592G>A (p.Val198Met)
NM_181332.3(NLGN4X):c.59T>C (p.Met20Thr)
NM_181332.3(NLGN4X):c.847G>T (p.Ala283Ser)

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