ClinVar Miner

List of variants studied for Dravet syndrome by UniProtKB/Swiss-Prot

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 150
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HGVS dbSNP
NM_001165963.4(SCN1A):c.1028G>A (p.Gly343Asp) rs121918753
NM_001165963.4(SCN1A):c.1066A>G (p.Arg356Gly) rs121917920
NM_001165963.4(SCN1A):c.1072C>A (p.Pro358Thr) rs121917923
NM_001165963.4(SCN1A):c.1098T>A (p.Asp366Glu) rs121917958
NM_001165963.4(SCN1A):c.1149C>G (p.Phe383Leu) rs121917939
NM_001165963.4(SCN1A):c.1177C>A (p.Arg393Ser) rs121917929
NM_001165963.4(SCN1A):c.1177C>T (p.Arg393Cys) rs121917929
NM_001165963.4(SCN1A):c.1178G>A (p.Arg393His) rs121917927
NM_001165963.4(SCN1A):c.1207T>C (p.Phe403Leu) rs121917966
NM_001165963.4(SCN1A):c.1216G>T (p.Val406Phe) rs121918768
NM_001165963.4(SCN1A):c.1237T>A (p.Tyr413Asn) rs121917967
NM_001165963.4(SCN1A):c.1276T>A (p.Tyr426Asn) rs121917940
NM_001165963.4(SCN1A):c.1811G>A (p.Arg604His) rs121918769
NM_001165963.4(SCN1A):c.187T>C (p.Phe63Leu) rs121917907
NM_001165963.4(SCN1A):c.2348T>C (p.Leu783Pro) rs121917968
NM_001165963.4(SCN1A):c.234G>T (p.Glu78Asp) rs121917933
NM_001165963.4(SCN1A):c.235G>C (p.Asp79His) rs121917982
NM_001165963.4(SCN1A):c.2422A>T (p.Thr808Ser) rs121918758
NM_001165963.4(SCN1A):c.2435C>G (p.Thr812Arg) rs121917941
NM_001165963.4(SCN1A):c.251A>G (p.Tyr84Cys) rs121917964
NM_001165963.4(SCN1A):c.2536G>A (p.Glu846Lys) rs121917942
NM_001165963.4(SCN1A):c.2585G>A (p.Arg862Gln) rs121918785
NM_001165963.4(SCN1A):c.2624C>A (p.Thr875Lys) rs121918623
NM_001165963.4(SCN1A):c.269T>C (p.Phe90Ser) rs121918733
NM_001165963.4(SCN1A):c.2705T>G (p.Phe902Cys) rs121918787
NM_001165963.4(SCN1A):c.272T>C (p.Ile91Thr) rs121918734
NM_001165963.4(SCN1A):c.2791C>T (p.Arg931Cys) rs121918788
NM_001165963.4(SCN1A):c.2802G>C (p.Met934Ile) rs121918774
NM_001165963.4(SCN1A):c.2815C>T (p.His939Tyr) rs121918736
NM_001165963.4(SCN1A):c.2817C>G (p.His939Gln) rs121918795
NM_001165963.4(SCN1A):c.2825T>C (p.Leu942Pro) rs121917943
NM_001165963.4(SCN1A):c.2831T>C (p.Val944Ala) rs121917969
NM_001165963.4(SCN1A):c.2833T>C (p.Phe945Leu) rs121917970
NM_001165963.4(SCN1A):c.2836C>A (p.Arg946Ser) rs121918775
NM_001165963.4(SCN1A):c.2836C>T (p.Arg946Cys) rs121918775
NM_001165963.4(SCN1A):c.2837G>A (p.Arg946His)
NM_001165963.4(SCN1A):c.2849G>A (p.Gly950Glu) rs121917972
NM_001165963.4(SCN1A):c.2854T>G (p.Trp952Gly) rs121918737
NM_001165963.4(SCN1A):c.2860G>A (p.Glu954Lys) rs121918786
NM_001165963.4(SCN1A):c.2870G>T (p.Trp957Leu) rs121917917
NM_001165963.4(SCN1A):c.2875T>C (p.Cys959Arg) rs121918796
NM_001165963.4(SCN1A):c.2878A>G (p.Met960Val) rs121918750
NM_001165963.4(SCN1A):c.2935G>A (p.Gly979Arg) rs121918754
NM_001165963.4(SCN1A):c.2948T>C (p.Val983Ala) rs121918756
NM_001165963.4(SCN1A):c.2954A>T (p.Asn985Ile) rs121918747
NM_001165963.4(SCN1A):c.2956C>T (p.Leu986Phe) rs121918625
NM_001165963.4(SCN1A):c.301C>T (p.Arg101Trp) rs121917965
NM_001165963.4(SCN1A):c.302G>A (p.Arg101Gln) rs121917918
NM_001165963.4(SCN1A):c.3032A>T (p.Asn1011Ile) rs121918759
NM_001165963.4(SCN1A):c.307A>G (p.Ser103Gly) rs121918743
NM_001165963.4(SCN1A):c.335C>T (p.Thr112Ile) rs121918745
NM_001165963.4(SCN1A):c.354G>C (p.Arg118Ser) rs121917959
NM_001165963.4(SCN1A):c.3620T>C (p.Leu1207Pro) rs121917963
NM_001165963.4(SCN1A):c.3629C>A (p.Thr1210Lys) rs121918738
NM_001165963.4(SCN1A):c.3692G>C (p.Ser1231Thr) rs121918800
NM_001165963.4(SCN1A):c.3693T>A (p.Ser1231Arg) rs121918746
NM_001165963.4(SCN1A):c.3697G>C (p.Gly1233Arg) rs121917911
NM_001165963.4(SCN1A):c.3714A>C (p.Glu1238Asp) rs121917973
NM_001165963.4(SCN1A):c.371T>A (p.Ile124Asn) rs121918761
NM_001165963.4(SCN1A):c.3734G>A (p.Arg1245Gln) rs121917912
NM_001165963.4(SCN1A):c.3778A>C (p.Thr1260Pro) rs121918739
NM_001165963.4(SCN1A):c.3789C>G (p.Phe1263Leu) rs121918752
NM_001165963.4(SCN1A):c.3794T>C (p.Leu1265Pro) rs121918794
NM_001165963.4(SCN1A):c.3860T>C (p.Leu1287Pro) rs121918740
NM_001165963.4(SCN1A):c.3924A>T (p.Glu1308Asp) rs121917910
NM_001165963.4(SCN1A):c.3976G>C (p.Ala1326Pro) rs121918803
NM_001165963.4(SCN1A):c.4003G>A (p.Val1335Met) rs121917960
NM_001165963.4(SCN1A):c.4064T>C (p.Leu1355Pro) rs121918776
NM_001165963.4(SCN1A):c.4073G>C (p.Trp1358Ser) rs121917961
NM_001165963.4(SCN1A):c.4101T>A (p.Asn1367Lys) rs121918760
NM_001165963.4(SCN1A):c.4168G>A (p.Val1390Met) rs121917986
NM_001165963.4(SCN1A):c.4186T>G (p.Cys1396Gly) rs121917987
NM_001165963.4(SCN1A):c.4240A>T (p.Asn1414Tyr) rs121917925
NM_001165963.4(SCN1A):c.4265A>G (p.Tyr1422Cys) rs121917913
NM_001165963.4(SCN1A):c.4277T>G (p.Leu1426Arg) rs121917944
NM_001165963.4(SCN1A):c.4297G>A (p.Gly1433Arg) rs121917908
NM_001165963.4(SCN1A):c.4298G>A (p.Gly1433Glu) rs121918741
NM_001165963.4(SCN1A):c.4300T>C (p.Trp1434Arg) rs121918789
NM_001165963.4(SCN1A):c.4321G>C (p.Ala1441Pro) rs121917974
NM_001165963.4(SCN1A):c.4348C>A (p.Gln1450Lys) rs121918806
NM_001165963.4(SCN1A):c.4349A>G (p.Gln1450Arg) rs121918790
NM_001165963.4(SCN1A):c.4352C>T (p.Pro1451Leu) rs121917945
NM_001165963.4(SCN1A):c.4381C>A (p.Leu1461Ile) rs121918772
NM_001165963.4(SCN1A):c.4385A>G (p.Tyr1462Cys) rs121917962
NM_001165963.4(SCN1A):c.4388T>C (p.Phe1463Ser) rs121917946
NM_001165963.4(SCN1A):c.4408G>T (p.Gly1470Trp) rs121917924
NM_001165963.4(SCN1A):c.4424T>C (p.Leu1475Ser) rs121917947
NM_001165963.4(SCN1A):c.4541T>C (p.Leu1514Ser) rs121918764
NM_001165963.4(SCN1A):c.4633A>G (p.Ile1545Val) rs121917975
NM_001165963.4(SCN1A):c.4757G>A (p.Gly1586Glu) rs121918742
NM_001165963.4(SCN1A):c.4762T>C (p.Cys1588Arg) rs121917919
NM_001165963.4(SCN1A):c.4822G>T (p.Asp1608Tyr) rs121917915
NM_001165963.4(SCN1A):c.4831G>T (p.Val1611Phe) rs121918630
NM_001165963.4(SCN1A):c.4834G>A (p.Val1612Ile) rs121918808
NM_001165963.4(SCN1A):c.484A>C (p.Thr162Pro) rs121917934
NM_001165963.4(SCN1A):c.4888G>A (p.Val1630Met) rs121917914
NM_001165963.4(SCN1A):c.4894C>T (p.Pro1632Ser) rs121918755
NM_001165963.4(SCN1A):c.4934G>A (p.Arg1645Gln) rs121917976
NM_001165963.4(SCN1A):c.4942C>T (p.Arg1648Cys) rs121918791
NM_001165963.4(SCN1A):c.4943G>A (p.Arg1648His) rs121918622
NM_001165963.4(SCN1A):c.4973C>G (p.Thr1658Arg) rs121917922
NM_001165963.4(SCN1A):c.4973C>T (p.Thr1658Met) rs121917922
NM_001165963.4(SCN1A):c.4982T>C (p.Phe1661Ser) rs121918797
NM_001165963.4(SCN1A):c.4991T>A (p.Met1664Lys) rs121918765
NM_001165963.4(SCN1A):c.5002C>G (p.Pro1668Ala) rs121917948
NM_001165963.4(SCN1A):c.5020G>C (p.Gly1674Arg) rs121918792
NM_001165963.4(SCN1A):c.5054C>A (p.Ala1685Asp) rs121918744
NM_001165963.4(SCN1A):c.5075T>C (p.Phe1692Ser) rs121918778
NM_001165963.4(SCN1A):c.5081A>G (p.Tyr1694Cys) rs121918777
NM_001165963.4(SCN1A):c.5119T>G (p.Phe1707Val) rs121917977
NM_001165963.4(SCN1A):c.5126C>T (p.Thr1709Ile) rs121918629
NM_001165963.4(SCN1A):c.512T>A (p.Ile171Lys) rs121918766
NM_001165963.4(SCN1A):c.5138G>A (p.Ser1713Asn) rs121918816
NM_001165963.4(SCN1A):c.5141T>G (p.Met1714Arg) rs121917949
NM_001165963.4(SCN1A):c.5146T>C (p.Cys1716Arg) rs121917926
NM_001165963.4(SCN1A):c.5162C>G (p.Thr1721Arg) rs121917978
NM_001165963.4(SCN1A):c.5176T>C (p.Trp1726Arg) rs121917979
NM_001165963.4(SCN1A):c.523G>A (p.Ala175Thr) rs121918767
NM_001165963.4(SCN1A):c.5246G>A (p.Gly1749Glu) rs121918798
NM_001165963.4(SCN1A):c.5266T>G (p.Cys1756Gly) rs121918809
NM_001165963.4(SCN1A):c.5285G>A (p.Gly1762Glu) rs121917950
NM_001165963.4(SCN1A):c.530G>A (p.Gly177Glu) rs121918770
NM_001165963.4(SCN1A):c.5318C>T (p.Ser1773Phe) rs121917951
NM_001165963.4(SCN1A):c.5339T>C (p.Met1780Thr) rs121917952
NM_001165963.4(SCN1A):c.5342A>G (p.Tyr1781Cys) rs121918779
NM_001165963.4(SCN1A):c.5346C>G (p.Ile1782Met) rs121918763
NM_001165963.4(SCN1A):c.5347G>A (p.Ala1783Thr)
NM_001165963.4(SCN1A):c.5348C>T (p.Ala1783Val) rs121917921
NM_001165963.4(SCN1A):c.5359G>A (p.Glu1787Lys) rs121917916
NM_001165963.4(SCN1A):c.5422T>C (p.Phe1808Leu) rs121918757
NM_001165963.4(SCN1A):c.5434T>G (p.Trp1812Gly) rs121918751
NM_001165963.4(SCN1A):c.5492T>C (p.Phe1831Ser) rs121918748
NM_001165963.4(SCN1A):c.5643G>C (p.Glu1881Asp) rs121918804
NM_001165963.4(SCN1A):c.568T>C (p.Trp190Arg) rs121918773
NM_001165963.4(SCN1A):c.571A>T (p.Asn191Tyr) rs121918762
NM_001165963.4(SCN1A):c.5726C>T (p.Thr1909Ile) rs121918793
NM_001165963.4(SCN1A):c.5765T>C (p.Ile1922Thr) rs121917981
NM_001165963.4(SCN1A):c.580G>A (p.Asp194Asn) rs121917935
NM_001165963.4(SCN1A):c.596C>G (p.Thr199Arg) rs121917983
NM_001165963.4(SCN1A):c.650C>A (p.Thr217Lys) rs121917936
NM_001165963.4(SCN1A):c.677C>T (p.Thr226Met) rs121917984
NM_001165963.4(SCN1A):c.680T>G (p.Ile227Ser) rs121917937
NM_001165963.4(SCN1A):c.715G>A (p.Ala239Thr) rs121917985
NM_001165963.4(SCN1A):c.716C>T (p.Ala239Val) rs121917909
NM_001165963.4(SCN1A):c.755T>A (p.Ile252Asn) rs121918780
NM_001165963.4(SCN1A):c.777C>A (p.Ser259Arg) rs121918735
NM_001165963.4(SCN1A):c.793G>T (p.Gly265Trp) rs121918749
NM_001165963.4(SCN1A):c.838T>C (p.Trp280Arg) rs121917938
NM_001165963.4(SCN1A):c.890C>T (p.Thr297Ile) rs121918771
NM_001165963.4(SCN1A):c.965G>T (p.Arg322Ile) rs121917928

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