Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.166277284A>CCA349078037SCN1A-AS1,SCN9Ac.2573T>G (p.Ile858Ser)
c.2540T>G (p.Ile847Ser)
c.230T>G (p.Ile77Ser)
c.1575T>G
n.1029+37A>C
c.2186T>G (p.Ile729Ser)
c.1829T>G (p.Ile610Ser)
n.2887T>G
2g.166277284A>GCA349078038SCN1A-AS1,SCN9Ac.2573T>C (p.Ile858Thr)
c.2540T>C (p.Ile847Thr)
c.230T>C (p.Ile77Thr)
c.1575T>C
n.1029+37A>G
c.2186T>C (p.Ile729Thr)
c.1829T>C (p.Ile610Thr)
n.2887T>C
2g.166277284A>TCA349078039SCN1A-AS1,SCN9Ac.2573T>A (p.Ile858Asn)
c.2540T>A (p.Ile847Asn)
c.230T>A (p.Ile77Asn)
c.1575T>A
n.1029+37A>T
c.2186T>A (p.Ile729Asn)
c.1829T>A (p.Ile610Asn)
n.2887T>A
2g.166277285T>ACA349078041SCN1A-AS1,SCN9Ac.2572A>T (p.Ile858Phe)
c.2539A>T (p.Ile847Phe)
c.229A>T (p.Ile77Phe)
c.1574A>T
n.1029+38T>A
c.2185A>T (p.Ile729Phe)
c.1828A>T (p.Ile610Phe)
n.2886A>T
2g.166277285T>CCA59794805SCN1A-AS1,SCN9Ac.2572A>G (p.Ile858Val)
c.2539A>G (p.Ile847Val)
c.229A>G (p.Ile77Val)
c.1574A>G
n.1029+38T>C
c.2185A>G (p.Ile729Val)
c.1828A>G (p.Ile610Val)
n.2886A>G
 dbSNP
2g.166277285T>GCA349078040SCN1A-AS1,SCN9Ac.2572A>C (p.Ile858Leu)
c.2539A>C (p.Ile847Leu)
c.229A>C (p.Ile77Leu)
c.1574A>C
n.1029+38T>G
c.2185A>C (p.Ile729Leu)
c.1828A>C (p.Ile610Leu)
n.2886A>C
2g.166277285T=CA1304965498SCN1A-AS1,SCN9Ac.2572A= (p.Ile858=)
c.2539A= (p.Ile847=)
c.229A= (p.Ile77=)
c.1574A=
n.1029+38T=
c.2185A= (p.Ile729=)
c.1828A= (p.Ile610=)
n.2886A=
2g.166277286C>ACA349078042SCN1A-AS1,SCN9Ac.2571G>T (p.Lys857Asn)
c.2538G>T (p.Lys846Asn)
c.228G>T (p.Lys76Asn)
c.1573G>T
n.1029+39C>A
c.2184G>T (p.Lys728Asn)
c.1827G>T (p.Lys609Asn)
n.2885G>T
2g.166277286C>GCA349078043SCN1A-AS1,SCN9Ac.2571G>C (p.Lys857Asn)
c.2538G>C (p.Lys846Asn)
c.228G>C (p.Lys76Asn)
c.1573G>C
n.1029+39C>G
c.2184G>C (p.Lys728Asn)
c.1827G>C (p.Lys609Asn)
n.2885G>C
2g.166277286C>TCA429978223SCN1A-AS1,SCN9Ac.2571G>A (p.Lys857=)
c.2538G>A (p.Lys846=)
c.228G>A (p.Lys76=)
c.1573G>A
n.1029+39C>T
c.2184G>A (p.Lys728=)
c.1827G>A (p.Lys609=)
n.2885G>A
2g.166277287T>ACA349078044SCN1A-AS1,SCN9Ac.2570A>T (p.Lys857Met)
c.2537A>T (p.Lys846Met)
c.227A>T (p.Lys76Met)
c.1572A>T
n.1029+40T>A
c.2183A>T (p.Lys728Met)
c.1826A>T (p.Lys609Met)
n.2884A>T
2g.166277287T>CCA349078045SCN1A-AS1,SCN9Ac.2570A>G (p.Lys857Arg)
c.2537A>G (p.Lys846Arg)
c.227A>G (p.Lys76Arg)
c.1572A>G
n.1029+40T>C
c.2183A>G (p.Lys728Arg)
c.1826A>G (p.Lys609Arg)
n.2884A>G
2g.166277287T>GCA349078046SCN1A-AS1,SCN9Ac.2570A>C (p.Lys857Thr)
c.2537A>C (p.Lys846Thr)
c.227A>C (p.Lys76Thr)
c.1572A>C
n.1029+40T>G
c.2183A>C (p.Lys728Thr)
c.1826A>C (p.Lys609Thr)
n.2884A>C
2g.166277288T>ACA349078047SCN1A-AS1,SCN9Ac.2569A>T (p.Lys857Ter)
c.2536A>T (p.Lys846Ter)
c.226A>T (p.Lys76Ter)
c.1571A>T
n.1029+41T>A
c.2182A>T (p.Lys728Ter)
c.1825A>T (p.Lys609Ter)
n.2883A>T
 dbSNP
2g.166277288T>CCA349078048SCN1A-AS1,SCN9Ac.2569A>G (p.Lys857Glu)
c.2536A>G (p.Lys846Glu)
c.226A>G (p.Lys76Glu)
c.1571A>G
n.1029+41T>C
c.2182A>G (p.Lys728Glu)
c.1825A>G (p.Lys609Glu)
n.2883A>G
2g.166277288T>GCA349078049SCN1A-AS1,SCN9Ac.2569A>C (p.Lys857Gln)
c.2536A>C (p.Lys846Gln)
c.226A>C (p.Lys76Gln)
c.1571A>C
n.1029+41T>G
c.2182A>C (p.Lys728Gln)
c.1825A>C (p.Lys609Gln)
n.2883A>C
2g.166277288T=CA1304965506SCN1A-AS1,SCN9Ac.2569A= (p.Lys857=)
c.2536A= (p.Lys846=)
c.226A= (p.Lys76=)
c.1571A=
n.1029+41T=
c.2182A= (p.Lys728=)
c.1825A= (p.Lys609=)
n.2883A=
2g.166277289A=CA1304965512SCN1A-AS1,SCN9Ac.2568T= (p.Ile856=)
c.2535T= (p.Ile845=)
c.225T= (p.Ile75=)
c.1570T=
n.1029+42A=
c.2181T= (p.Ile727=)
c.1824T= (p.Ile608=)
n.2882T=
2g.166277289A>CCA349078050SCN1A-AS1,SCN9Ac.2568T>G (p.Ile856Met)
c.2535T>G (p.Ile845Met)
c.225T>G (p.Ile75Met)
c.1570T>G
n.1029+42A>C
c.2181T>G (p.Ile727Met)
c.1824T>G (p.Ile608Met)
n.2882T>G
 dbSNP gnomAD v3 gnomAD v4
2g.166277289A>GCA429978224SCN1A-AS1,SCN9Ac.2568T>C (p.Ile856=)
c.2535T>C (p.Ile845=)
c.225T>C (p.Ile75=)
c.1570T>C
n.1029+42A>G
c.2181T>C (p.Ile727=)
c.1824T>C (p.Ile608=)
n.2882T>C
2g.166277289A>TCA429978225SCN1A-AS1,SCN9Ac.2568T>A (p.Ile856=)
c.2535T>A (p.Ile845=)
c.225T>A (p.Ile75=)
c.1570T>A
n.1029+42A>T
c.2181T>A (p.Ile727=)
c.1824T>A (p.Ile608=)
n.2882T>A
2g.166277290A=CA1304965518SCN1A-AS1,SCN9Ac.2567T= (p.Ile856=)
c.2534T= (p.Ile845=)
c.224T= (p.Ile75=)
c.1569T=
n.1029+43A=
c.2180T= (p.Ile727=)
c.1823T= (p.Ile608=)
n.2881T=
2g.166277290A>CCA349078051SCN1A-AS1,SCN9Ac.2567T>G (p.Ile856Ser)
c.2534T>G (p.Ile845Ser)
c.224T>G (p.Ile75Ser)
c.1569T>G
n.1029+43A>C
c.2180T>G (p.Ile727Ser)
c.1823T>G (p.Ile608Ser)
n.2881T>G
2g.166277290A>GCA59794809SCN1A-AS1,SCN9Ac.2567T>C (p.Ile856Thr)
c.2534T>C (p.Ile845Thr)
c.224T>C (p.Ile75Thr)
c.1569T>C
n.1029+43A>G
c.2180T>C (p.Ile727Thr)
c.1823T>C (p.Ile608Thr)
n.2881T>C
 dbSNP gnomAD v4
2g.166277290A>TCA349078052SCN1A-AS1,SCN9Ac.2567T>A (p.Ile856Asn)
c.2534T>A (p.Ile845Asn)
c.224T>A (p.Ile75Asn)
c.1569T>A
n.1029+43A>T
c.2180T>A (p.Ile727Asn)
c.1823T>A (p.Ile608Asn)
n.2881T>A
2g.166277291T>ACA349078054SCN1A-AS1,SCN9Ac.2566A>T (p.Ile856Phe)
c.2533A>T (p.Ile845Phe)
c.223A>T (p.Ile75Phe)
c.1568A>T
n.1029+44T>A
c.2179A>T (p.Ile727Phe)
c.1822A>T (p.Ile608Phe)
n.2880A>T
2g.166277291T>CCA349078055SCN1A-AS1,SCN9Ac.2566A>G (p.Ile856Val)
c.2533A>G (p.Ile845Val)
c.223A>G (p.Ile75Val)
c.1568A>G
n.1029+44T>C
c.2179A>G (p.Ile727Val)
c.1822A>G (p.Ile608Val)
n.2880A>G
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.166277291T>GCA349078053SCN1A-AS1,SCN9Ac.2566A>C (p.Ile856Leu)
c.2533A>C (p.Ile845Leu)
c.223A>C (p.Ile75Leu)
c.1568A>C
n.1029+44T>G
c.2179A>C (p.Ile727Leu)
c.1822A>C (p.Ile608Leu)
n.2880A>C
2g.166277291T=CA1304965527SCN1A-AS1,SCN9Ac.2566A= (p.Ile856=)
c.2533A= (p.Ile845=)
c.223A= (p.Ile75=)
c.1568A=
n.1029+44T=
c.2179A= (p.Ile727=)
c.1822A= (p.Ile608=)
n.2880A=
2g.166277292C>ACA429978226SCN1A-AS1,SCN9Ac.2565G>T (p.Leu855=)
c.2532G>T (p.Leu844=)
c.222G>T (p.Leu74=)
c.1567G>T
n.1029+45C>A
c.2178G>T (p.Leu726=)
c.1821G>T (p.Leu607=)
n.2879G>T
2g.166277292C=CA1304965535SCN1A-AS1,SCN9Ac.2565G= (p.Leu855=)
c.2532G= (p.Leu844=)
c.222G= (p.Leu74=)
c.1567G=
n.1029+45C=
c.2178G= (p.Leu726=)
c.1821G= (p.Leu607=)
n.2879G=
2g.166277292C>GCA429978227SCN1A-AS1,SCN9Ac.2565G>C (p.Leu855=)
c.2532G>C (p.Leu844=)
c.222G>C (p.Leu74=)
c.1567G>C
n.1029+45C>G
c.2178G>C (p.Leu726=)
c.1821G>C (p.Leu607=)
n.2879G>C
 gnomAD v4
2g.166277292C>TCA429978228SCN1A-AS1,SCN9Ac.2565G>A (p.Leu855=)
c.2532G>A (p.Leu844=)
c.222G>A (p.Leu74=)
c.1567G>A
n.1029+45C>T
c.2178G>A (p.Leu726=)
c.1821G>A (p.Leu607=)
n.2879G>A
 dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
2g.166277293A>CCA349078058SCN1A-AS1,SCN9Ac.2564T>G (p.Leu855Arg)
c.2531T>G (p.Leu844Arg)
c.221T>G (p.Leu74Arg)
c.1566T>G
n.1029+46A>C
c.2177T>G (p.Leu726Arg)
c.1820T>G (p.Leu607Arg)
n.2878T>G
2g.166277293A>GCA349078056SCN1A-AS1,SCN9Ac.2564T>C (p.Leu855Pro)
c.2531T>C (p.Leu844Pro)
c.221T>C (p.Leu74Pro)
c.1566T>C
n.1029+46A>G
c.2177T>C (p.Leu726Pro)
c.1820T>C (p.Leu607Pro)
n.2878T>C
2g.166277293A>TCA349078057SCN1A-AS1,SCN9Ac.2564T>A (p.Leu855Gln)
c.2531T>A (p.Leu844Gln)
c.221T>A (p.Leu74Gln)
c.1566T>A
n.1029+46A>T
c.2177T>A (p.Leu726Gln)
c.1820T>A (p.Leu607Gln)
n.2878T>A
2g.166277294G>ACA429978229SCN1A-AS1,SCN9Ac.2563C>T (p.Leu855=)
c.2530C>T (p.Leu844=)
c.220C>T (p.Leu74=)
c.1565C>T
n.1029+47G>A
c.2176C>T (p.Leu726=)
c.1819C>T (p.Leu607=)
n.2877C>T
 gnomAD v4
2g.166277294G>CCA349078059SCN1A-AS1,SCN9Ac.2563C>G (p.Leu855Val)
c.2530C>G (p.Leu844Val)
c.220C>G (p.Leu74Val)
c.1565C>G
n.1029+47G>C
c.2176C>G (p.Leu726Val)
c.1819C>G (p.Leu607Val)
n.2877C>G
2g.166277294G>TCA349078060SCN1A-AS1,SCN9Ac.2563C>A (p.Leu855Met)
c.2530C>A (p.Leu844Met)
c.220C>A (p.Leu74Met)
c.1565C>A
n.1029+47G>T
c.2176C>A (p.Leu726Met)
c.1819C>A (p.Leu607Met)
n.2877C>A
2g.166277295C>ACA349078061SCN1A-AS1,SCN9Ac.2562G>T (p.Met854Ile)
c.2529G>T (p.Met843Ile)
c.219G>T (p.Met73Ile)
c.1564G>T
n.1029+48C>A
c.2175G>T (p.Met725Ile)
c.1818G>T (p.Met606Ile)
n.2876G>T
2g.166277295C=CA1304965541SCN1A-AS1,SCN9Ac.2562G= (p.Met854=)
c.2529G= (p.Met843=)
c.219G= (p.Met73=)
c.1564G=
n.1029+48C=
c.2175G= (p.Met725=)
c.1818G= (p.Met606=)
n.2876G=
2g.166277295C>GCA349078062SCN1A-AS1,SCN9Ac.2562G>C (p.Met854Ile)
c.2529G>C (p.Met843Ile)
c.219G>C (p.Met73Ile)
c.1564G>C
n.1029+48C>G
c.2175G>C (p.Met725Ile)
c.1818G>C (p.Met606Ile)
n.2876G>C
2g.166277295C>TCA349078063SCN1A-AS1,SCN9Ac.2562G>A (p.Met854Ile)
c.2529G>A (p.Met843Ile)
c.219G>A (p.Met73Ile)
c.1564G>A
n.1029+48C>T
c.2175G>A (p.Met725Ile)
c.1818G>A (p.Met606Ile)
n.2876G>A
 dbSNP gnomAD v4
2g.166277296A=CA1304965543SCN1A-AS1,SCN9Ac.2561T= (p.Met854=)
c.2528T= (p.Met843=)
c.218T= (p.Met73=)
c.1563T=
n.1029+49A=
c.2174T= (p.Met725=)
c.1817T= (p.Met606=)
n.2875T=
2g.166277296A>CCA349078064SCN1A-AS1,SCN9Ac.2561T>G (p.Met854Arg)
c.2528T>G (p.Met843Arg)
c.218T>G (p.Met73Arg)
c.1563T>G
n.1029+49A>C
c.2174T>G (p.Met725Arg)
c.1817T>G (p.Met606Arg)
n.2875T>G
2g.166277296A>GCA59794827SCN1A-AS1,SCN9Ac.2561T>C (p.Met854Thr)
c.2528T>C (p.Met843Thr)
c.218T>C (p.Met73Thr)
c.1563T>C
n.1029+49A>G
c.2174T>C (p.Met725Thr)
c.1817T>C (p.Met606Thr)
n.2875T>C
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.166277296A>TCA349078065SCN1A-AS1,SCN9Ac.2561T>A (p.Met854Lys)
c.2528T>A (p.Met843Lys)
c.218T>A (p.Met73Lys)
c.1563T>A
n.1029+49A>T
c.2174T>A (p.Met725Lys)
c.1817T>A (p.Met606Lys)
n.2875T>A
2g.166277297T>ACA349078066SCN1A-AS1,SCN9Ac.2560A>T (p.Met854Leu)
c.2527A>T (p.Met843Leu)
c.217A>T (p.Met73Leu)
c.1562A>T
n.1029+50T>A
c.2173A>T (p.Met725Leu)
c.1816A>T (p.Met606Leu)
n.2874A>T
2g.166277297T>CCA349078067SCN1A-AS1,SCN9Ac.2560A>G (p.Met854Val)
c.2527A>G (p.Met843Val)
c.217A>G (p.Met73Val)
c.1562A>G
n.1029+50T>C
c.2173A>G (p.Met725Val)
c.1816A>G (p.Met606Val)
n.2874A>G
2g.166277297T>GCA349078068SCN1A-AS1,SCN9Ac.2560A>C (p.Met854Leu)
c.2527A>C (p.Met843Leu)
c.217A>C (p.Met73Leu)
c.1562A>C
n.1029+50T>G
c.2173A>C (p.Met725Leu)
c.1816A>C (p.Met606Leu)
n.2874A>C

Number of alleles fetched