ClinVar Miner

List of variants in gene SCN10A reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_006514.4(SCN10A):c.2441G>A (p.Arg814His) rs139861061 0.00041
NM_006514.4(SCN10A):c.472T>G (p.Tyr158Asp) rs202192818 0.00033
NM_006514.4(SCN10A):c.905G>A (p.Arg302Gln) rs201955990 0.00033
NM_006514.4(SCN10A):c.1858G>A (p.Val620Ile) rs151303346 0.00032
NM_006514.4(SCN10A):c.2428G>T (p.Gly810Trp) rs145712124 0.00030
NM_006514.4(SCN10A):c.5630C>T (p.Pro1877Leu) rs143523403 0.00021
NM_006514.4(SCN10A):c.724T>A (p.Ser242Thr) rs140288103 0.00021
NM_006514.4(SCN10A):c.5200G>A (p.Glu1734Lys) rs200645452 0.00017
NM_006514.4(SCN10A):c.4607C>G (p.Thr1536Arg) rs778754301 0.00016
NM_006514.4(SCN10A):c.4849G>T (p.Val1617Phe) rs375940680 0.00015
NM_006514.4(SCN10A):c.1315A>G (p.Thr439Ala) rs146536985 0.00014
NM_006514.4(SCN10A):c.4709C>T (p.Thr1570Met) rs772484960 0.00013
NM_006514.4(SCN10A):c.2266C>T (p.Arg756Trp) rs374341474 0.00011
NM_006514.4(SCN10A):c.4139G>A (p.Arg1380Gln) rs149155352 0.00009
NM_006514.4(SCN10A):c.4657+5G>A rs373642730 0.00007
NM_006514.4(SCN10A):c.4831G>A (p.Gly1611Arg) rs777980971 0.00007
NM_006514.4(SCN10A):c.4514C>T (p.Thr1505Met) rs184521520 0.00006
NM_006514.4(SCN10A):c.5548C>T (p.Gln1850Ter) rs149504103 0.00006
NM_006514.4(SCN10A):c.4655C>T (p.Ala1552Val) rs756133876 0.00005
NM_006514.4(SCN10A):c.1051C>T (p.Arg351Cys) rs370603046 0.00004
NM_006514.4(SCN10A):c.1093-3C>A rs373289770 0.00004
NM_006514.4(SCN10A):c.299C>A (p.Thr100Asn) rs758035498 0.00004
NM_006514.4(SCN10A):c.4726C>T (p.Arg1576Cys) rs764476034 0.00004
NM_006514.4(SCN10A):c.4780C>T (p.Arg1594Cys) rs373347787 0.00004
NM_006514.4(SCN10A):c.5539C>T (p.Arg1847Ter) rs199503439 0.00004
NM_006514.4(SCN10A):c.1196C>T (p.Ala399Val) rs371834396 0.00003
NM_006514.4(SCN10A):c.1454G>A (p.Arg485His) rs746690639 0.00003
NM_006514.4(SCN10A):c.2367C>A (p.Asn789Lys) rs770046573 0.00003
NM_006514.4(SCN10A):c.2465C>T (p.Ala822Val) rs747839312 0.00003
NM_006514.4(SCN10A):c.3943G>A (p.Asp1315Asn) rs147640811 0.00003
NM_006514.4(SCN10A):c.5694del (p.Ala1899fs) rs747321219 0.00003
NM_006514.4(SCN10A):c.1276C>T (p.Arg426Trp) rs532774213 0.00002
NM_006514.4(SCN10A):c.2195T>C (p.Phe732Ser) rs373216811 0.00002
NM_006514.4(SCN10A):c.2221C>G (p.Leu741Val) rs137906740 0.00002
NM_006514.4(SCN10A):c.2275C>G (p.Arg759Gly) rs745659019 0.00002
NM_006514.4(SCN10A):c.2579T>C (p.Val860Ala) rs781073957 0.00002
NM_006514.4(SCN10A):c.3727G>A (p.Val1243Met) rs765684724 0.00002
NM_006514.4(SCN10A):c.434T>C (p.Val145Ala) rs367751260 0.00002
NM_006514.4(SCN10A):c.46T>C (p.Phe16Leu) rs1432009058 0.00002
NM_006514.4(SCN10A):c.2158G>A (p.Asp720Asn) rs781354273 0.00001
NM_006514.4(SCN10A):c.2616G>A (p.Thr872=) rs754088416 0.00001
NM_006514.4(SCN10A):c.3802C>T (p.Arg1268Trp) rs766044301 0.00001
NM_006514.4(SCN10A):c.3890T>G (p.Ile1297Ser) rs978977328 0.00001
NM_006514.4(SCN10A):c.4763G>A (p.Arg1588Gln) rs376439863 0.00001
NM_006514.4(SCN10A):c.5177A>G (p.Asn1726Ser) rs1420941706 0.00001
NM_006514.4(SCN10A):c.5588G>A (p.Arg1863Gln) rs191869263 0.00001
NM_006514.4(SCN10A):c.883C>T (p.Pro295Ser) rs371909817 0.00001
NM_006514.4(SCN10A):c.1052G>A (p.Arg351His) rs767987787
NM_006514.4(SCN10A):c.1489C>T (p.Arg497Cys) rs370009920
NM_006514.4(SCN10A):c.158C>G (p.Pro53Arg) rs752235456
NM_006514.4(SCN10A):c.2593A>G (p.Ile865Val) rs1553617020
NM_006514.4(SCN10A):c.2677_2678del (p.Phe893fs) rs770504391
NM_006514.4(SCN10A):c.3800T>G (p.Met1267Arg) rs774337248
NM_006514.4(SCN10A):c.3910G>A (p.Ala1304Thr) rs142173735
NM_006514.4(SCN10A):c.4775_4776dup (p.Ile1593fs) rs1191414961
NM_006514.4(SCN10A):c.860C>G (p.Thr287Ser) rs779570073

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