ClinVar Miner

List of variants in gene SCN1A reported as not provided for brain disorder

Included ClinVar conditions (1834):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 91
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001165963.4(SCN1A):c.1625G>A (p.Arg542Gln) rs121918817 0.00154
NM_001165963.4(SCN1A):c.1811G>A (p.Arg604His) rs121918769 0.00087
NM_001165963.4(SCN1A):c.80G>C (p.Arg27Thr) rs121917906 0.00006
NM_001165963.4(SCN1A):c.890C>T (p.Thr297Ile) rs121918771 0.00003
NM_001165963.4(SCN1A):c.187T>C (p.Phe63Leu) rs121917907 0.00001
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.1130G>A (p.Arg377Gln) rs121917957
NM_001165963.4(SCN1A):c.1149C>G (p.Phe383Leu) rs121917939
NM_001165963.4(SCN1A):c.1162T>C (p.Tyr388His) rs121918781
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.1183G>C (p.Ala395Pro) rs121917988
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.1265T>A (p.Val422Glu) rs121917989
NM_001165963.4(SCN1A):c.1276T>A (p.Tyr426Asn) rs121917940
NM_001165963.4(SCN1A):c.1876A>G (p.Ser626Gly) rs121917990
NM_001165963.4(SCN1A):c.220T>C (p.Ser74Pro) rs121917931
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.2369A>G (p.Tyr790Cys) rs121918782
NM_001165963.4(SCN1A):c.238dup (p.Leu80fs) rs1684663586
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.2508C>A (p.Asp836Glu)
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.2575C>T (p.Arg859Cys) rs121918784
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.2624C>T (p.Thr875Met) 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>A (p.Arg931Ser) rs121918788
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.2917A>G (p.Met973Val) rs121917991
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.345T>A (p.Asn115Lys) rs61741123
NM_001165963.4(SCN1A):c.354G>C (p.Arg118Ser) rs121917959
NM_001165963.4(SCN1A):c.371T>A (p.Ile124Asn) rs121918761
NM_001165963.4(SCN1A):c.434T>C (p.Met145Thr) rs121918631
NM_001165963.4(SCN1A):c.484A>C (p.Thr162Pro) rs121917934
NM_001165963.4(SCN1A):c.512T>A (p.Ile171Lys) rs121918766
NM_001165963.4(SCN1A):c.523G>A (p.Ala175Thr) rs121918767
NM_001165963.4(SCN1A):c.530G>A (p.Gly177Glu) rs121918770
NM_001165963.4(SCN1A):c.563A>T (p.Asp188Val) rs121917953
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.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.787C>G (p.Leu263Val) rs2105890052
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.965G>T (p.Arg322Ile) rs121917928

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.