ClinVar Miner

List of variants in gene SCN9A studied for not provided

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Total variants: 55
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HGVS dbSNP gnomAD frequency
NM_001365536.1(SCN9A):c.444A>G (p.Pro148=) rs9646771 0.70187
NM_001365536.1(SCN9A):c.174G>A (p.Gln58=) rs6432901 0.64588
NM_001365536.1(SCN9A):c.554G>A (p.Arg185His) rs73969684 0.00574
NM_001365536.1(SCN9A):c.684C>G (p.Ile228Met) rs71428908 0.00081
NM_001365536.1(SCN9A):c.688+9T>C rs188814235 0.00076
NM_001365536.1(SCN9A):c.129T>C (p.Asp43=) rs200826539 0.00019
NM_001365536.1(SCN9A):c.689-6T>C rs201905108 0.00010
NM_001365536.1(SCN9A):c.361A>C (p.Lys121Gln) rs200486515 0.00009
NM_001365536.1(SCN9A):c.213G>A (p.Val71=) rs200240989 0.00008
NM_001365536.1(SCN9A):c.393C>T (p.Leu131=) rs199756028 0.00007
NM_001365536.1(SCN9A):c.561G>A (p.Pro187=) rs200182914 0.00006
NM_001365536.1(SCN9A):c.641G>A (p.Arg214Gln) rs201741634 0.00006
NM_001365536.1(SCN9A):c.642A>G (p.Arg214=) rs376908183 0.00006
NM_001365536.1(SCN9A):c.390G>T (p.Met130Ile) rs376036522 0.00005
NM_001365536.1(SCN9A):c.764G>A (p.Cys255Tyr) rs755139637 0.00005
NM_001365536.1(SCN9A):c.76C>T (p.Arg26Cys) rs199933920 0.00005
NM_001365536.1(SCN9A):c.184A>G (p.Ile62Val) rs121908920 0.00004
NM_001365536.1(SCN9A):c.118A>G (p.Lys40Glu) rs371565974 0.00003
NM_001365536.1(SCN9A):c.136G>A (p.Ala46Thr) rs779344629 0.00002
NM_001365536.1(SCN9A):c.294C>A (p.Phe98Leu) rs199824489 0.00002
NM_001365536.1(SCN9A):c.576T>C (p.Asp192=) rs762966087 0.00002
NM_001365536.1(SCN9A):c.20C>T (p.Pro7Leu) rs773012423 0.00001
NM_001365536.1(SCN9A):c.258+1G>A rs755067851 0.00001
NM_001365536.1(SCN9A):c.262T>C (p.Phe88Leu) rs1012999498 0.00001
NM_001365536.1(SCN9A):c.304G>T (p.Ala102Ser) rs201343843 0.00001
NM_001365536.1(SCN9A):c.377+5C>T rs200972952 0.00001
NM_001365536.1(SCN9A):c.507A>G (p.Val169=) rs778674007 0.00001
NM_001365536.1(SCN9A):c.560C>T (p.Pro187Leu) rs771227297 0.00001
NM_001365536.1(SCN9A):c.628G>A (p.Val210Ile) rs200619065 0.00001
NM_001365536.1(SCN9A):c.892G>A (p.Asp298Asn) rs1057518384 0.00001
GRCh37/hg19 2q24.3(chr2:167149203-167158736)x1
GRCh37/hg19 2q24.3(chr2:167153789-167158736)x1
GRCh37/hg19 2q24.3(chr2:167155131-167158685)x1
GRCh37/hg19 2q24.3(chr2:167156282-167158736)x1
GRCh37/hg19 2q24.3(chr2:167163942-167250612)x3
NM_001365536.1(SCN9A):c.113A>G (p.Glu38Gly) rs974242226
NM_001365536.1(SCN9A):c.131AAG[1] (p.Glu45del) rs1198936365
NM_001365536.1(SCN9A):c.20C>G (p.Pro7Arg) rs773012423
NM_001365536.1(SCN9A):c.223C>G (p.Leu75Val) rs201563763
NM_001365536.1(SCN9A):c.267A>C (p.Ile89=) rs200809157
NM_001365536.1(SCN9A):c.378-1C>T rs1309621904
NM_001365536.1(SCN9A):c.428_444delinsG (p.Met143fs) rs1574906521
NM_001365536.1(SCN9A):c.431C>T (p.Thr144Ile) rs748032198
NM_001365536.1(SCN9A):c.488A>G (p.Tyr163Cys) rs876661294
NM_001365536.1(SCN9A):c.523G>C (p.Gly175Arg) rs1213397059
NM_001365536.1(SCN9A):c.559C>A (p.Pro187Thr) rs774694132
NM_001365536.1(SCN9A):c.59T>G (p.Leu20Arg) rs757627939
NM_001365536.1(SCN9A):c.611_612dup (p.Val205fs) rs1574903287
NM_001365536.1(SCN9A):c.660A>C (p.Arg220Ser)
NM_001365536.1(SCN9A):c.689-20C>G rs112644902
NM_001365536.1(SCN9A):c.695A>G (p.Lys232Arg) rs879253936
NM_001365536.1(SCN9A):c.713T>C (p.Leu238Ser) rs1553495258
NM_001365536.1(SCN9A):c.817C>T (p.His273Tyr)
NM_001365536.1(SCN9A):c.847A>T (p.Asn283Tyr) rs1553495127
NM_001365536.1(SCN9A):c.861A>G (p.Glu287=) rs1553495104

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