All transcript variants in gene NLGN3

Information The variants shown are described using the NM_018977.3 transcript reference sequence.

60 entries on 1 page. Showing entries 1 - 60.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.10C>T r.(?) p.(Arg4Trp) g.70367609C>T Copied from the Exome Variant Server NLGN3_000001 1/10354 1/6583 0/3771
?/? c.20C>T r.(?) p.(Pro7Leu) g.70367619C>T Copied from the Exome Variant Server NLGN3_000002 3/10525 3/6710 0/3815
?/? c.21G>A r.(=) p.(=) g.70367620G>A Copied from the Exome Variant Server NLGN3_000003 1/10547 1/6721 0/3826
?/? c.63C>A r.(?) p.(Ser21Arg) g.70367662C>A Copied from the Exome Variant Server NLGN3_000004 2/10563 2/6728 0/3835
?/? c.282G>A r.(=) p.(=) g.70367881G>A Copied from the Exome Variant Server NLGN3_000005 3/10563 3/6728 0/3835
?/? c.343C>A r.(?) p.(Pro115Thr) g.70367942C>A Copied from the Exome Variant Server NLGN3_000006 1/10563 1/6728 0/3835
?/? c.413A>G r.(?) p.(Asn138Ser) g.70368012A>G Copied from the Exome Variant Server NLGN3_000007 2/10563 0/6728 2/3835
?/? c.414C>T r.(=) p.(=) g.70368013C>T Copied from the Exome Variant Server NLGN3_000009 1/10563 1/6728 0/3835
?/? c.430C>T r.(=) p.(=) g.70368029C>T Copied from the Exome Variant Server NLGN3_000011 1/10563 1/6728 0/3835
?/? c.457+25G>A r.(=) p.(=) g.70368081G>A Copied from the Exome Variant Server NLGN3_000013 1/10563 1/6728 0/3835
?/? c.457+40C>T r.(=) p.(=) g.70368096C>T Copied from the Exome Variant Server NLGN3_000015 3/10563 0/6728 3/3835
?/? c.457+41G>T r.(=) p.(=) g.70368097G>T Copied from the Exome Variant Server NLGN3_000017 8/10563 8/6728 0/3835
?/? c.518-41G>A r.(=) p.(=) g.70375023G>A Copied from the Exome Variant Server NLGN3_000019 140/10561 134/6726 6/3835
?/? c.518-31C>T r.(=) p.(=) g.70375033C>T Copied from the Exome Variant Server NLGN3_000021 1/10563 1/6728 0/3835
?/? c.534T>C r.(=) p.(=) g.70375080T>C Copied from the Exome Variant Server NLGN3_000008 12/10563 10/6728 2/3835
?/? c.543C>G r.(=) p.(=) g.70375089C>G Copied from the Exome Variant Server NLGN3_000010 11/10563 0/6728 11/3835
?/? c.621T>C r.(=) p.(=) g.70375167T>C Copied from the Exome Variant Server NLGN3_000012 1/10563 0/6728 1/3835
?/? c.655G>A r.(?) p.(Val219Ile) g.70375201G>A Copied from the Exome Variant Server NLGN3_000014 1/10563 1/6728 0/3835
?/? c.667+39T>A r.(=) p.(=) g.70375252T>A Copied from the Exome Variant Server NLGN3_000016 8/10563 0/6728 8/3835
?/? c.667+47G>C r.(=) p.(=) g.70375260G>C Copied from the Exome Variant Server NLGN3_000018 6/10563 0/6728 6/3835
?/? c.668-5_668-4insCC r.spl? p.? g.70383988_70383989insCC Copied from the Exome Variant Server NLGN3_000020 4/10205 0/6484 4/3721
?/? c.737G>A r.(?) p.(Arg246His) g.70384062G>A Copied from the Exome Variant Server NLGN3_000022 1/10563 0/6728 1/3835
?/? c.747C>T r.(=) p.(=) g.70384072C>T Copied from the Exome Variant Server NLGN3_000023 4/10563 4/6728 0/3835
?/? c.775C>G r.(?) p.(Pro259Ala) g.70384100C>G Copied from the Exome Variant Server NLGN3_000024 2/10563 2/6728 0/3835
?/? c.801G>A r.(=) p.(=) g.70384126G>A Copied from the Exome Variant Server NLGN3_000025 1/10563 0/6728 1/3835
?/? c.853+11C>G r.(=) p.(=) g.70384189C>G Copied from the Exome Variant Server NLGN3_000026 2/10563 2/6728 0/3835
?/? c.854-36C>G r.(=) p.(=) g.70386825C>G Copied from the Exome Variant Server NLGN3_000027 57/10410 54/6630 3/3780
?/? c.1029G>A r.(=) p.(=) g.70387036G>A Copied from the Exome Variant Server NLGN3_000028 1/10563 1/6728 0/3835
?/? c.1053C>T r.(=) p.(=) g.70387060C>T Copied from the Exome Variant Server NLGN3_000029 1/10563 0/6728 1/3835
?/? c.1218C>T r.(=) p.(=) g.70387225C>T Copied from the Exome Variant Server NLGN3_000030 1/10563 0/6728 1/3835
?/? c.1360C>G r.(?) p.(Leu454Val) g.70387367C>G Copied from the Exome Variant Server NLGN3_000031 1/10563 0/6728 1/3835
?/? c.1362G>A r.(=) p.(=) g.70387369G>A Copied from the Exome Variant Server NLGN3_000032 1/10563 0/6728 1/3835
?/? c.1452C>T r.(=) p.(=) g.70387459C>T Copied from the Exome Variant Server NLGN3_000033 1/10563 1/6728 0/3835
?/? c.1643+17_1643+18insT r.(=) p.(=) g.70387667_70387668insT Copied from the Exome Variant Server NLGN3_000034 3/10204 1/6483 2/3721
?/? c.1644-37T>C r.(=) p.(=) g.70389067T>C Copied from the Exome Variant Server NLGN3_000035 1/10563 1/6728 0/3835
?/? c.1644-14A>T r.(=) p.(=) g.70389090A>T Copied from the Exome Variant Server NLGN3_000036 1/10563 0/6728 1/3835
?/? c.1659G>A r.(=) p.(=) g.70389119G>A Copied from the Exome Variant Server NLGN3_000037 1/10563 0/6728 1/3835
?/? c.1689C>T r.(=) p.(=) g.70389149C>T Copied from the Exome Variant Server NLGN3_000038 1/10563 0/6728 1/3835
?/? c.1722C>G r.(=) p.(=) g.70389182C>G Copied from the Exome Variant Server NLGN3_000039 1/10563 1/6728 0/3835
?/? c.1830C>A r.(?) p.(His610Gln) g.70389290C>A Copied from the Exome Variant Server NLGN3_000040 1/10562 0/6727 1/3835
?/? c.1889C>T r.(?) p.(Pro630Leu) g.70389349C>T Copied from the Exome Variant Server NLGN3_000041 1/10560 0/6727 1/3833
?/? c.1894A>G r.(?) p.(Thr632Ala) g.70389354A>G Copied from the Exome Variant Server NLGN3_000042 31/10560 27/6727 4/3833
?/? c.1918C>T r.(?) p.(Arg640Cys) g.70389378C>T Copied from the Exome Variant Server NLGN3_000043 1/10558 0/6727 1/3831
?/? c.1974C>T r.(=) p.(=) g.70389434C>T Copied from the Exome Variant Server NLGN3_000044 11/10562 0/6728 11/3834
?/? c.1980C>T r.(=) p.(=) g.70389440C>T Copied from the Exome Variant Server NLGN3_000045 3/10562 1/6728 2/3834
?/? c.1988C>T r.(?) p.(Ala663Val) g.70389448C>T Copied from the Exome Variant Server NLGN3_000046 1/10562 0/6728 1/3834
?/? c.1989C>G r.(=) p.(=) g.70389449C>G Copied from the Exome Variant Server NLGN3_000047 1/10562 0/6728 1/3834
?/? c.2004C>T r.(=) p.(=) g.70389464C>T Copied from the Exome Variant Server NLGN3_000048 1/10562 1/6728 0/3834
?/? c.2079C>T r.(=) p.(=) g.70389539C>T Copied from the Exome Variant Server NLGN3_000049 1/10563 1/6728 0/3835
?/? c.2106C>T r.(=) p.(=) g.70389566C>T Copied from the Exome Variant Server NLGN3_000050 2/10563 0/6728 2/3835
?/? c.2155G>A r.(?) p.(Glu719Lys) g.70389615G>A Copied from the Exome Variant Server NLGN3_000051 1/10561 1/6726 0/3835
?/? c.2160C>G r.(=) p.(=) g.70389620C>G Copied from the Exome Variant Server NLGN3_000052 1/10561 1/6726 0/3835
?/? c.2190C>T r.(=) p.(=) g.70389650C>T Copied from the Exome Variant Server NLGN3_000053 128/10544 0/6719 128/3825
?/? c.2199G>A r.(=) p.(=) g.70389659G>A Copied from the Exome Variant Server NLGN3_000054 1/10541 0/6715 1/3826
?/? c.2282A>G r.(?) p.(His761Arg) g.70389742A>G Copied from the Exome Variant Server NLGN3_000055 1/10553 0/6720 1/3833
?/? c.2310C>T r.(=) p.(=) g.70389770C>T Copied from the Exome Variant Server NLGN3_000056 1/10554 1/6722 0/3832
?/? c.2330G>A r.(?) p.(Arg777Gln) g.70389790G>A Copied from the Exome Variant Server NLGN3_000057 1/10559 0/6725 1/3834
?/? c.*19C>A r.(=) p.(=) g.70389966C>A Copied from the Exome Variant Server NLGN3_000058 1/10563 1/6728 0/3835
?/? c.*22A>G r.(=) p.(=) g.70389969A>G Copied from the Exome Variant Server NLGN3_000059 2/10563 2/6728 0/3835
?/? c.*50A>G r.(=) p.(=) g.70389997A>G Copied from the Exome Variant Server NLGN3_000060 1/10562 0/6727 1/3835
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