ClinVar Miner

List of variants in gene combination SCN1A, SCN9A reported as uncertain significance for Indifference to pain, congenital, autosomal recessive

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Gene type:
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Total variants: 92
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HGVS dbSNP
NM_001365536.1(SCN9A):c.*1014G>A rs200393413
NM_001365536.1(SCN9A):c.*124A>G rs201137748
NM_001365536.1(SCN9A):c.*1357C>T rs200338267
NM_001365536.1(SCN9A):c.*1383G>T
NM_001365536.1(SCN9A):c.*1417A>G
NM_001365536.1(SCN9A):c.*1422T>C
NM_001365536.1(SCN9A):c.*159T>C
NM_001365536.1(SCN9A):c.*1605T>C rs199848927
NM_001365536.1(SCN9A):c.*1643T>C
NM_001365536.1(SCN9A):c.*164G>A
NM_001365536.1(SCN9A):c.*1735C>A
NM_001365536.1(SCN9A):c.*1770A>C rs200353065
NM_001365536.1(SCN9A):c.*1815T>C
NM_001365536.1(SCN9A):c.*2078C>T rs548072061
NM_001365536.1(SCN9A):c.*217G>A rs200625860
NM_001365536.1(SCN9A):c.*2191G>A rs201184093
NM_001365536.1(SCN9A):c.*2222T>C rs199958892
NM_001365536.1(SCN9A):c.*2226T>G rs141310425
NM_001365536.1(SCN9A):c.*2228G>T rs200790957
NM_001365536.1(SCN9A):c.*226A>C rs886055048
NM_001365536.1(SCN9A):c.*2344C>T rs200962814
NM_001365536.1(SCN9A):c.*237C>T
NM_001365536.1(SCN9A):c.*2677T>C
NM_001365536.1(SCN9A):c.*2729C>A
NM_001365536.1(SCN9A):c.*2860C>T rs200963393
NM_001365536.1(SCN9A):c.*2928G>A rs199559478
NM_001365536.1(SCN9A):c.*2945C>A
NM_001365536.1(SCN9A):c.*2986T>G rs201730339
NM_001365536.1(SCN9A):c.*3053G>A
NM_001365536.1(SCN9A):c.*3094A>G
NM_001365536.1(SCN9A):c.*3102C>T rs182687583
NM_001365536.1(SCN9A):c.*3202T>C
NM_001365536.1(SCN9A):c.*3204G>A
NM_001365536.1(SCN9A):c.*3282A>C rs139483482
NM_001365536.1(SCN9A):c.*3426A>T rs186838828
NM_001365536.1(SCN9A):c.*408A>G
NM_001365536.1(SCN9A):c.*410A>T
NM_001365536.1(SCN9A):c.*669A>G rs538508619
NM_001365536.1(SCN9A):c.*785C>T rs181229506
NM_001365536.1(SCN9A):c.*835C>A
NM_001365536.1(SCN9A):c.*887T>C
NM_001365536.1(SCN9A):c.*900T>C
NM_001365536.1(SCN9A):c.*948G>A rs201415802
NM_001365536.1(SCN9A):c.1014T>G (p.Asp338Glu) rs886055056
NM_001365536.1(SCN9A):c.1094A>G (p.Asn365Ser) rs886055055
NM_001365536.1(SCN9A):c.1110G>A (p.Thr370=) rs202002028
NM_001365536.1(SCN9A):c.1139T>A (p.Ile380Asn) rs188798505
NM_001365536.1(SCN9A):c.1207A>C (p.Met403Leu) rs746956041
NM_001365536.1(SCN9A):c.1208T>C (p.Met403Thr) rs199986805
NM_001365536.1(SCN9A):c.1285C>T (p.Arg429Cys) rs763256222
NM_001365536.1(SCN9A):c.1347T>C (p.Ser449=) rs201990547
NM_001365536.1(SCN9A):c.1464C>T (p.Leu488=) rs200682458
NM_001365536.1(SCN9A):c.1482G>T (p.Lys494Asn) rs777699798
NM_001365536.1(SCN9A):c.1619G>A (p.Arg540His) rs199748300
NM_001365536.1(SCN9A):c.1713C>T (p.Ala571=) rs200876333
NM_001365536.1(SCN9A):c.1793G>A (p.Arg598His) rs201318927
NM_001365536.1(SCN9A):c.1980G>A (p.Thr660=) rs200014315
NM_001365536.1(SCN9A):c.1998G>C (p.Lys666Asn) rs369989247
NM_001365536.1(SCN9A):c.2239G>C (p.Asp747His)
NM_001365536.1(SCN9A):c.2240A>T (p.Asp747Val)
NM_001365536.1(SCN9A):c.2461G>A (p.Val821Met) rs41268671
NM_001365536.1(SCN9A):c.2496A>C (p.Ser832=) rs200185692
NM_001365536.1(SCN9A):c.2852T>C (p.Val951Ala) rs201890077
NM_001365536.1(SCN9A):c.2916T>C (p.Ser972=) rs886055054
NM_001365536.1(SCN9A):c.3002A>G (p.Tyr1001Cys) rs199692186
NM_001365536.1(SCN9A):c.3020G>A (p.Arg1007His) rs188145203
NM_001365536.1(SCN9A):c.3125C>T (p.Thr1042Ile) rs757989638
NM_001365536.1(SCN9A):c.3167A>G (p.Lys1056Arg) rs200560768
NM_001365536.1(SCN9A):c.3265G>A (p.Val1089Met) rs886055053
NM_001365536.1(SCN9A):c.3272T>C (p.Ile1091Thr)
NM_001365536.1(SCN9A):c.3343A>G (p.Ser1115Gly) rs201984007
NM_001365536.1(SCN9A):c.3368G>A (p.Ser1123Asn) rs141040985
NM_001365536.1(SCN9A):c.3388G>A (p.Val1130Ile) rs765384427
NM_001365536.1(SCN9A):c.3402G>T (p.Leu1134Phe) rs200160858
NM_001365536.1(SCN9A):c.3476G>A (p.Cys1159Tyr)
NM_001365536.1(SCN9A):c.3684T>C (p.Tyr1228=) rs144941725
NM_001365536.1(SCN9A):c.3754A>G (p.Thr1252Ala) rs886055052
NM_001365536.1(SCN9A):c.3801T>C (p.Asp1267=) rs202047865
NM_001365536.1(SCN9A):c.3925-13T>C rs886055051
NM_001365536.1(SCN9A):c.3944T>C (p.Ile1315Thr) rs202235611
NM_001365536.1(SCN9A):c.4099C>T (p.Arg1367Cys)
NM_001365536.1(SCN9A):c.4143A>G (p.Arg1381=) rs200610689
NM_001365536.1(SCN9A):c.4314C>T (p.Val1438=) rs188336294
NM_001365536.1(SCN9A):c.4441T>C (p.Tyr1481His)
NM_001365536.1(SCN9A):c.4923T>C (p.Leu1641=) rs199550149
NM_001365536.1(SCN9A):c.5247G>C (p.Leu1749=)
NM_001365536.1(SCN9A):c.5379G>A (p.Ala1793=) rs201875421
NM_001365536.1(SCN9A):c.5543G>A (p.Arg1848His)
NM_001365536.1(SCN9A):c.5586G>A (p.Gln1862=) rs199572382
NM_001365536.1(SCN9A):c.5945A>T (p.Asp1982Val) rs199822303
NM_001365536.1(SCN9A):c.965+13T>C rs772337722
NM_001365536.1(SCN9A):c.980G>A (p.Gly327Glu)

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