Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.2847784_2848146del | CA2825001870 | KCNQ1,KCNQ1-AS1 | c.1455_*143del (n.[c.1455_*143del;Gln485HisfsTer28]) c.1812_*143del (n.[c.1812_*143del;Gln604HisfsTer28]) c.1431_*143del (n.[c.1431_*143del;Gln477HisfsTer28]) c.216_*143del (n.[c.216_*143del;Gln72HisfsTer28]) n.319_681del n.778-7697_778-7335del | ClinVar |
11 | g.2847787G>A | CA472466075 | KCNQ1,KCNQ1-AS1 | c.1458G>A (p.Arg486=) c.1815G>A (p.Arg605=) c.1434G>A (p.Arg478=) c.219G>A (p.Arg73=) n.322G>A n.778-7345C>T | gnomAD v4 |
11 | g.2847787G>C | CA379140216 | KCNQ1,KCNQ1-AS1 | c.1458G>C (p.Arg486Ser) c.1815G>C (p.Arg605Ser) c.1434G>C (p.Arg478Ser) c.219G>C (p.Arg73Ser) n.322G>C n.778-7345C>G | |
11 | g.2847787G>T | CA379140217 | KCNQ1,KCNQ1-AS1 | c.1458G>T (p.Arg486Ser) c.1815G>T (p.Arg605Ser) c.1434G>T (p.Arg478Ser) c.219G>T (p.Arg73Ser) n.322G>T n.778-7345C>A | gnomAD v4 |
11 | g.2847788C>A | CA379140218 | KCNQ1,KCNQ1-AS1 | c.1459C>A (p.Leu487Met) c.1816C>A (p.Leu606Met) c.1435C>A (p.Leu479Met) c.220C>A (p.Leu74Met) n.323C>A n.778-7346G>T | gnomAD v4 |
11 | g.2847788C= | CA1948349594 | KCNQ1,KCNQ1-AS1 | c.1459C= (p.Leu487=) c.1816C= (p.Leu606=) c.1435C= (p.Leu479=) c.220C= (p.Leu74=) n.323C= n.778-7346G= | |
11 | g.2847788C>G | CA379140219 | KCNQ1,KCNQ1-AS1 | c.1459C>G (p.Leu487Val) c.1816C>G (p.Leu606Val) c.1435C>G (p.Leu479Val) c.220C>G (p.Leu74Val) n.323C>G n.778-7346G>C | |
11 | g.2847788C>T | CA472466079 | KCNQ1,KCNQ1-AS1 | c.1459C>T (p.Leu487=) c.1816C>T (p.Leu606=) c.1435C>T (p.Leu479=) c.220C>T (p.Leu74=) n.323C>T n.778-7346G>A | dbSNP gnomAD v2 |
11 | g.2847789T>A | CA379140220 | KCNQ1,KCNQ1-AS1 | c.1460T>A (p.Leu487Gln) c.1817T>A (p.Leu606Gln) c.1436T>A (p.Leu479Gln) c.221T>A (p.Leu74Gln) n.324T>A n.778-7347A>T | ClinVar gnomAD v4 |
11 | g.2847789T>C | CA379140221 | KCNQ1,KCNQ1-AS1 | c.1460T>C (p.Leu487Pro) c.1817T>C (p.Leu606Pro) c.1436T>C (p.Leu479Pro) c.221T>C (p.Leu74Pro) n.324T>C n.778-7347A>G | |
11 | g.2847789T>G | CA379140222 | KCNQ1,KCNQ1-AS1 | c.1460T>G (p.Leu487Arg) c.1817T>G (p.Leu606Arg) c.1436T>G (p.Leu479Arg) c.221T>G (p.Leu74Arg) n.324T>G n.778-7347A>C | |
11 | g.2847790G>A | CA472466097 | KCNQ1,KCNQ1-AS1 | c.1461G>A (p.Leu487=) c.1818G>A (p.Leu606=) c.1437G>A (p.Leu479=) c.222G>A (p.Leu74=) n.325G>A n.778-7348C>T | ClinVar dbSNP gnomAD v4 |
11 | g.2847790G>C | CA472466089 | KCNQ1,KCNQ1-AS1 | c.1461G>C (p.Leu487=) c.1818G>C (p.Leu606=) c.1437G>C (p.Leu479=) c.222G>C (p.Leu74=) n.325G>C n.778-7348C>G | |
11 | g.2847790G= | CA1948349595 | KCNQ1,KCNQ1-AS1 | c.1461G= (p.Leu487=) c.1818G= (p.Leu606=) c.1437G= (p.Leu479=) c.222G= (p.Leu74=) n.325G= n.778-7348C= | |
11 | g.2847790G>T | CA472466088 | KCNQ1,KCNQ1-AS1 | c.1461G>T (p.Leu487=) c.1818G>T (p.Leu606=) c.1437G>T (p.Leu479=) c.222G>T (p.Leu74=) n.325G>T n.778-7348C>A | gnomAD v4 |
11 | g.2847791G>A | CA379140223 | KCNQ1,KCNQ1-AS1 | c.1462G>A (p.Ala488Thr) c.1819G>A (p.Ala607Thr) c.1438G>A (p.Ala480Thr) c.223G>A (p.Ala75Thr) n.326G>A n.778-7349C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847791G>C | CA379140224 | KCNQ1,KCNQ1-AS1 | c.1462G>C (p.Ala488Pro) c.1819G>C (p.Ala607Pro) c.1438G>C (p.Ala480Pro) c.223G>C (p.Ala75Pro) n.326G>C n.778-7349C>G | dbSNP gnomAD v2 COSMIC |
11 | g.2847791G= | CA1948349596 | KCNQ1,KCNQ1-AS1 | c.1462G= (p.Ala488=) c.1819G= (p.Ala607=) c.1438G= (p.Ala480=) c.223G= (p.Ala75=) n.326G= n.778-7349C= | |
11 | g.2847791G>T | CA379140225 | KCNQ1,KCNQ1-AS1 | c.1462G>T (p.Ala488Ser) c.1819G>T (p.Ala607Ser) c.1438G>T (p.Ala480Ser) c.223G>T (p.Ala75Ser) n.326G>T n.778-7349C>A | ClinVar gnomAD v4 |
11 | g.2847792C>A | CA379140226 | KCNQ1,KCNQ1-AS1 | c.1463C>A (p.Ala488Glu) c.1820C>A (p.Ala607Glu) c.1439C>A (p.Ala480Glu) c.224C>A (p.Ala75Glu) n.327C>A n.778-7350G>T | gnomAD v4 |
11 | g.2847792C>G | CA379140227 | KCNQ1,KCNQ1-AS1 | c.1463C>G (p.Ala488Gly) c.1820C>G (p.Ala607Gly) c.1439C>G (p.Ala480Gly) c.224C>G (p.Ala75Gly) n.327C>G n.778-7350G>C | |
11 | g.2847792C>T | CA379140228 | KCNQ1,KCNQ1-AS1 | c.1463C>T (p.Ala488Val) c.1820C>T (p.Ala607Val) c.1439C>T (p.Ala480Val) c.224C>T (p.Ala75Val) n.327C>T n.778-7350G>A | gnomAD v4 |
11 | g.2847793A= | CA1948349597 | KCNQ1,KCNQ1-AS1 | c.1464A= (p.Ala488=) c.1821A= (p.Ala607=) c.1440A= (p.Ala480=) c.225A= (p.Ala75=) n.328A= n.778-7351T= | |
11 | g.2847793A>C | CA472466122 | KCNQ1,KCNQ1-AS1 | c.1464A>C (p.Ala488=) c.1821A>C (p.Ala607=) c.1440A>C (p.Ala480=) c.225A>C (p.Ala75=) n.328A>C n.778-7351T>G | |
11 | g.2847793A>G | CA472466111 | KCNQ1,KCNQ1-AS1 | c.1464A>G (p.Ala488=) c.1821A>G (p.Ala607=) c.1440A>G (p.Ala480=) c.225A>G (p.Ala75=) n.328A>G n.778-7351T>C | dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847793A>T | CA472466115 | KCNQ1,KCNQ1-AS1 | c.1464A>T (p.Ala488=) c.1821A>T (p.Ala607=) c.1440A>T (p.Ala480=) c.225A>T (p.Ala75=) n.328A>T n.778-7351T>A | |
11 | g.2847794C>A | CA379140230 | KCNQ1,KCNQ1-AS1 | c.1465C>A (p.Leu489Ile) c.1822C>A (p.Leu608Ile) c.1441C>A (p.Leu481Ile) c.226C>A (p.Leu76Ile) n.329C>A n.778-7352G>T | gnomAD v4 |
11 | g.2847794C= | CA1948349598 | KCNQ1,KCNQ1-AS1 | c.1465C= (p.Leu489=) c.1822C= (p.Leu608=) c.1441C= (p.Leu481=) c.226C= (p.Leu76=) n.329C= n.778-7352G= | |
11 | g.2847794C>G | CA379140231 | KCNQ1,KCNQ1-AS1 | c.1465C>G (p.Leu489Val) c.1822C>G (p.Leu608Val) c.1441C>G (p.Leu481Val) c.226C>G (p.Leu76Val) n.329C>G n.778-7352G>C | ClinVar dbSNP |
11 | g.2847794C>T | CA379140229 | KCNQ1,KCNQ1-AS1 | c.1465C>T (p.Leu489Phe) c.1822C>T (p.Leu608Phe) c.1441C>T (p.Leu481Phe) c.226C>T (p.Leu76Phe) n.329C>T n.778-7352G>A | ClinVar |
11 | g.2847794_2847797delinsCTCA | CA1948349599 | KCNQ1,KCNQ1-AS1 | c.1465_1468delinsCTCA (p.Leu489=) c.1822_1825delinsCTCA (p.Leu608=) c.1441_1444delinsCTCA (p.Leu481=) c.226_229delinsCTCA (p.Leu76=) n.329_332delinsCTCA n.778-7355_778-7352delinsTGAG | |
11 | g.2847795T>A | CA379140232 | KCNQ1,KCNQ1-AS1 | c.1466T>A (p.Leu489His) c.1823T>A (p.Leu608His) c.1442T>A (p.Leu481His) c.227T>A (p.Leu76His) n.330T>A n.778-7353A>T | gnomAD v4 |
11 | g.2847795T>C | CA379140233 | KCNQ1,KCNQ1-AS1 | c.1466T>C (p.Leu489Pro) c.1823T>C (p.Leu608Pro) c.1442T>C (p.Leu481Pro) c.227T>C (p.Leu76Pro) n.330T>C n.778-7353A>G | |
11 | g.2847795T>G | CA379140234 | KCNQ1,KCNQ1-AS1 | c.1466T>G (p.Leu489Arg) c.1823T>G (p.Leu608Arg) c.1442T>G (p.Leu481Arg) c.227T>G (p.Leu76Arg) n.330T>G n.778-7353A>C | |
11 | g.2847798_2847800del | CA658656098 | KCNQ1,KCNQ1-AS1 | c.1469_1471del (p.Ile490del) c.1826_1828del (p.Ile609del) c.1445_1447del (p.Ile482del) c.230_232del (p.Ile77del) n.333_335del n.778-7355_778-7353del | ClinVar dbSNP |
11 | g.2847796C>A | CA472466134 | KCNQ1,KCNQ1-AS1 | c.1467C>A (p.Leu489=) c.1824C>A (p.Leu608=) c.1443C>A (p.Leu481=) c.228C>A (p.Leu76=) n.331C>A n.778-7354G>T | gnomAD v4 |
11 | g.2847796C>G | CA472466137 | KCNQ1,KCNQ1-AS1 | c.1467C>G (p.Leu489=) c.1824C>G (p.Leu608=) c.1443C>G (p.Leu481=) c.228C>G (p.Leu76=) n.331C>G n.778-7354G>C | |
11 | g.2847796C>T | CA472466142 | KCNQ1,KCNQ1-AS1 | c.1467C>T (p.Leu489=) c.1824C>T (p.Leu608=) c.1443C>T (p.Leu481=) c.228C>T (p.Leu76=) n.331C>T n.778-7354G>A | gnomAD v4 |
11 | g.2847797A>C | CA379140235 | KCNQ1,KCNQ1-AS1 | c.1468A>C (p.Ile490Leu) c.1825A>C (p.Ile609Leu) c.1444A>C (p.Ile482Leu) c.229A>C (p.Ile77Leu) n.332A>C n.778-7355T>G | |
11 | g.2847797A>G | CA379140236 | KCNQ1,KCNQ1-AS1 | c.1468A>G (p.Ile490Val) c.1825A>G (p.Ile609Val) c.1444A>G (p.Ile482Val) c.229A>G (p.Ile77Val) n.332A>G n.778-7355T>C | |
11 | g.2847797A>T | CA379140237 | KCNQ1,KCNQ1-AS1 | c.1468A>T (p.Ile490Phe) c.1825A>T (p.Ile609Phe) c.1444A>T (p.Ile482Phe) c.229A>T (p.Ile77Phe) n.332A>T n.778-7355T>A | |
11 | g.2847798T>A | CA379140238 | KCNQ1,KCNQ1-AS1 | c.1469T>A (p.Ile490Asn) c.1826T>A (p.Ile609Asn) c.1445T>A (p.Ile482Asn) c.230T>A (p.Ile77Asn) n.333T>A n.778-7356A>T | ClinVar gnomAD v4 |
11 | g.2847798T>C | CA379140239 | KCNQ1,KCNQ1-AS1 | c.1469T>C (p.Ile490Thr) c.1826T>C (p.Ile609Thr) c.1445T>C (p.Ile482Thr) c.230T>C (p.Ile77Thr) n.333T>C n.778-7356A>G | |
11 | g.2847798T>G | CA379140240 | KCNQ1,KCNQ1-AS1 | c.1469T>G (p.Ile490Ser) c.1826T>G (p.Ile609Ser) c.1445T>G (p.Ile482Ser) c.230T>G (p.Ile77Ser) n.333T>G n.778-7356A>C | |
11 | g.2847803_2847815del | CA2612011065 | KCNQ1,KCNQ1-AS1 | c.1474_1486del (p.Asp492SerfsTer?) c.1831_1843del (p.Asp611SerfsTer?) c.1450_1462del (p.Asp484SerfsTer?) c.235_247del (p.Asp79SerfsTer?) n.338_350del n.778-7368_778-7356del | gnomAD v4 |
11 | g.2847799C>A | CA472466148 | KCNQ1,KCNQ1-AS1 | c.1470C>A (p.Ile490=) c.1827C>A (p.Ile609=) c.1446C>A (p.Ile482=) c.231C>A (p.Ile77=) n.334C>A n.778-7357G>T | gnomAD v4 |
11 | g.2847799C= | CA1948349600 | KCNQ1,KCNQ1-AS1 | c.1470C= (p.Ile490=) c.1827C= (p.Ile609=) c.1446C= (p.Ile482=) c.231C= (p.Ile77=) n.334C= n.778-7357G= | |
11 | g.2847799C>G | CA379140241 | KCNQ1,KCNQ1-AS1 | c.1470C>G (p.Ile490Met) c.1827C>G (p.Ile609Met) c.1446C>G (p.Ile482Met) c.231C>G (p.Ile77Met) n.334C>G n.778-7357G>C | |
11 | g.2847799C>T | CA033274 | KCNQ1,KCNQ1-AS1 | c.1470C>T (p.Ile490=) c.1827C>T (p.Ile609=) c.1446C>T (p.Ile482=) c.231C>T (p.Ile77=) n.334C>T n.778-7357G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847800A>C | CA379140244 | KCNQ1,KCNQ1-AS1 | c.1471A>C (p.Thr491Pro) c.1828A>C (p.Thr610Pro) c.1447A>C (p.Thr483Pro) c.232A>C (p.Thr78Pro) n.335A>C n.778-7358T>G | |
11 | g.2847800A>G | CA379140243 | KCNQ1,KCNQ1-AS1 | c.1471A>G (p.Thr491Ala) c.1828A>G (p.Thr610Ala) c.1447A>G (p.Thr483Ala) c.232A>G (p.Thr78Ala) n.335A>G n.778-7358T>C | gnomAD v4 |
11 | g.2847800A>T | CA379140242 | KCNQ1,KCNQ1-AS1 | c.1471A>T (p.Thr491Ser) c.1828A>T (p.Thr610Ser) c.1447A>T (p.Thr483Ser) c.232A>T (p.Thr78Ser) n.335A>T n.778-7358T>A | |
11 | g.2847801C>A | CA006469 | KCNQ1,KCNQ1-AS1 | c.1472C>A (p.Thr491Asn) c.1829C>A (p.Thr610Asn) c.1448C>A (p.Thr483Asn) c.233C>A (p.Thr78Asn) n.336C>A n.778-7359G>T | ClinVar dbSNP gnomAD v4 |
11 | g.2847801C= | CA1948349601 | KCNQ1,KCNQ1-AS1 | c.1472C= (p.Thr491=) c.1829C= (p.Thr610=) c.1448C= (p.Thr483=) c.233C= (p.Thr78=) n.336C= n.778-7359G= | |
11 | g.2847801C>G | CA379140245 | KCNQ1,KCNQ1-AS1 | c.1472C>G (p.Thr491Ser) c.1829C>G (p.Thr610Ser) c.1448C>G (p.Thr483Ser) c.233C>G (p.Thr78Ser) n.336C>G n.778-7359G>C | |
11 | g.2847801C>T | CA379140246 | KCNQ1,KCNQ1-AS1 | c.1472C>T (p.Thr491Ile) c.1829C>T (p.Thr610Ile) c.1448C>T (p.Thr483Ile) c.233C>T (p.Thr78Ile) n.336C>T n.778-7359G>A | gnomAD v4 |
11 | g.2847802C>A | CA472466171 | KCNQ1,KCNQ1-AS1 | c.1473C>A (p.Thr491=) c.1830C>A (p.Thr610=) c.1449C>A (p.Thr483=) c.234C>A (p.Thr78=) n.337C>A n.778-7360G>T | gnomAD v4 |
11 | g.2847802C= | CA1948349602 | KCNQ1,KCNQ1-AS1 | c.1473C= (p.Thr491=) c.1830C= (p.Thr610=) c.1449C= (p.Thr483=) c.234C= (p.Thr78=) n.337C= n.778-7360G= | |
11 | g.2847802C>G | CA472466173 | KCNQ1,KCNQ1-AS1 | c.1473C>G (p.Thr491=) c.1830C>G (p.Thr610=) c.1449C>G (p.Thr483=) c.234C>G (p.Thr78=) n.337C>G n.778-7360G>C | ClinVar gnomAD v4 COSMIC COSMIC |
11 | g.2847802C>T | CA033288 | KCNQ1,KCNQ1-AS1 | c.1473C>T (p.Thr491=) c.1830C>T (p.Thr610=) c.1449C>T (p.Thr483=) c.234C>T (p.Thr78=) n.337C>T n.778-7360G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847803G>A | CA006476 | KCNQ1,KCNQ1-AS1 | c.1474G>A (p.Asp492Asn) c.1831G>A (p.Asp611Asn) c.1450G>A (p.Asp484Asn) c.235G>A (p.Asp79Asn) n.338G>A n.778-7361C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847803G>C | CA379140247 | KCNQ1,KCNQ1-AS1 | c.1474G>C (p.Asp492His) c.1831G>C (p.Asp611His) c.1450G>C (p.Asp484His) c.235G>C (p.Asp79His) n.338G>C n.778-7361C>G | |
11 | g.2847803G= | CA1948349603 | KCNQ1,KCNQ1-AS1 | c.1474G= (p.Asp492=) c.1831G= (p.Asp611=) c.1450G= (p.Asp484=) c.235G= (p.Asp79=) n.338G= n.778-7361C= | |
11 | g.2847803G>T | CA006483 | KCNQ1,KCNQ1-AS1 | c.1474G>T (p.Asp492Tyr) c.1831G>T (p.Asp611Tyr) c.1450G>T (p.Asp484Tyr) c.235G>T (p.Asp79Tyr) n.338G>T n.778-7361C>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847803_2847806dup | CA2695213093 | KCNQ1,KCNQ1-AS1 | c.1474_1477dup (p.Met493ArgfsTer?) c.1831_1834dup (p.Met612ArgfsTer?) c.1450_1453dup (p.Met485ArgfsTer?) c.235_238dup (p.Met80ArgfsTer?) n.338_341dup n.778-7364_778-7361dup | |
11 | g.2847804A>C | CA379140248 | KCNQ1,KCNQ1-AS1 | c.1475A>C (p.Asp492Ala) c.1832A>C (p.Asp611Ala) c.1451A>C (p.Asp484Ala) c.236A>C (p.Asp79Ala) n.339A>C n.778-7362T>G | |
11 | g.2847804A>G | CA379140249 | KCNQ1,KCNQ1-AS1 | c.1475A>G (p.Asp492Gly) c.1832A>G (p.Asp611Gly) c.1451A>G (p.Asp484Gly) c.236A>G (p.Asp79Gly) n.339A>G n.778-7362T>C | |
11 | g.2847804A>T | CA379140250 | KCNQ1,KCNQ1-AS1 | c.1475A>T (p.Asp492Val) c.1832A>T (p.Asp611Val) c.1451A>T (p.Asp484Val) c.236A>T (p.Asp79Val) n.339A>T n.778-7362T>A | |
11 | g.2847805C>A | CA379140251 | KCNQ1,KCNQ1-AS1 | c.1476C>A (p.Asp492Glu) c.1833C>A (p.Asp611Glu) c.1452C>A (p.Asp484Glu) c.237C>A (p.Asp79Glu) n.340C>A n.778-7363G>T | |
11 | g.2847805C>G | CA379140252 | KCNQ1,KCNQ1-AS1 | c.1476C>G (p.Asp492Glu) c.1833C>G (p.Asp611Glu) c.1452C>G (p.Asp484Glu) c.237C>G (p.Asp79Glu) n.340C>G n.778-7363G>C | |
11 | g.2847805C>T | CA472466199 | KCNQ1,KCNQ1-AS1 | c.1476C>T (p.Asp492=) c.1833C>T (p.Asp611=) c.1452C>T (p.Asp484=) c.237C>T (p.Asp79=) n.340C>T n.778-7363G>A | gnomAD v4 |
11 | g.2847806A>C | CA379140254 | KCNQ1,KCNQ1-AS1 | c.1477A>C (p.Met493Leu) c.1834A>C (p.Met612Leu) c.1453A>C (p.Met485Leu) c.238A>C (p.Met80Leu) n.341A>C n.778-7364T>G | |
11 | g.2847806A>G | CA379140255 | KCNQ1,KCNQ1-AS1 | c.1477A>G (p.Met493Val) c.1834A>G (p.Met612Val) c.1453A>G (p.Met485Val) c.238A>G (p.Met80Val) n.341A>G n.778-7364T>C | gnomAD v4 |
11 | g.2847806A>T | CA379140253 | KCNQ1,KCNQ1-AS1 | c.1477A>T (p.Met493Leu) c.1834A>T (p.Met612Leu) c.1453A>T (p.Met485Leu) c.238A>T (p.Met80Leu) n.341A>T n.778-7364T>A | |
11 | g.2847807T>A | CA379140258 | KCNQ1,KCNQ1-AS1 | c.1478T>A (p.Met493Lys) c.1835T>A (p.Met612Lys) c.1454T>A (p.Met485Lys) c.239T>A (p.Met80Lys) n.342T>A n.778-7365A>T | |
11 | g.2847807T>C | CA379140256 | KCNQ1,KCNQ1-AS1 | c.1478T>C (p.Met493Thr) c.1835T>C (p.Met612Thr) c.1454T>C (p.Met485Thr) c.239T>C (p.Met80Thr) n.342T>C n.778-7365A>G | |
11 | g.2847807T>G | CA379140257 | KCNQ1,KCNQ1-AS1 | c.1478T>G (p.Met493Arg) c.1835T>G (p.Met612Arg) c.1454T>G (p.Met485Arg) c.239T>G (p.Met80Arg) n.342T>G n.778-7365A>C | |
11 | g.2847808G>A | CA10582887 | KCNQ1,KCNQ1-AS1 | c.1479G>A (p.Met493Ile) c.1836G>A (p.Met612Ile) c.1455G>A (p.Met485Ile) c.240G>A (p.Met80Ile) n.343G>A n.778-7366C>T | ClinVar dbSNP gnomAD v4 |
11 | g.2847808G>C | CA379140259 | KCNQ1,KCNQ1-AS1 | c.1479G>C (p.Met493Ile) c.1836G>C (p.Met612Ile) c.1455G>C (p.Met485Ile) c.240G>C (p.Met80Ile) n.343G>C n.778-7366C>G | |
11 | g.2847808G= | CA1948349604 | KCNQ1,KCNQ1-AS1 | c.1479G= (p.Met493=) c.1836G= (p.Met612=) c.1455G= (p.Met485=) c.240G= (p.Met80=) n.343G= n.778-7366C= | |
11 | g.2847808G>T | CA379140260 | KCNQ1,KCNQ1-AS1 | c.1479G>T (p.Met493Ile) c.1836G>T (p.Met612Ile) c.1455G>T (p.Met485Ile) c.240G>T (p.Met80Ile) n.343G>T n.778-7366C>A | gnomAD v4 |
11 | g.2847809C>A | CA379140262 | KCNQ1,KCNQ1-AS1 | c.1480C>A (p.Leu494Ile) c.1837C>A (p.Leu613Ile) c.1456C>A (p.Leu486Ile) c.241C>A (p.Leu81Ile) n.344C>A n.778-7367G>T | gnomAD v4 |
11 | g.2847809C= | CA1948349605 | KCNQ1,KCNQ1-AS1 | c.1480C= (p.Leu494=) c.1837C= (p.Leu613=) c.1456C= (p.Leu486=) c.241C= (p.Leu81=) n.344C= n.778-7367G= | |
11 | g.2847809C>G | CA379140261 | KCNQ1,KCNQ1-AS1 | c.1480C>G (p.Leu494Val) c.1837C>G (p.Leu613Val) c.1456C>G (p.Leu486Val) c.241C>G (p.Leu81Val) n.344C>G n.778-7367G>C | |
11 | g.2847809C>T | CA033320 | KCNQ1,KCNQ1-AS1 | c.1480C>T (p.Leu494Phe) c.1837C>T (p.Leu613Phe) c.1456C>T (p.Leu486Phe) c.241C>T (p.Leu81Phe) n.344C>T n.778-7367G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847810T>A | CA379140263 | KCNQ1,KCNQ1-AS1 | c.1481T>A (p.Leu494His) c.1838T>A (p.Leu613His) c.1457T>A (p.Leu486His) c.242T>A (p.Leu81His) n.345T>A n.778-7368A>T | gnomAD v4 |
11 | g.2847810T>C | CA379140264 | KCNQ1,KCNQ1-AS1 | c.1481T>C (p.Leu494Pro) c.1838T>C (p.Leu613Pro) c.1457T>C (p.Leu486Pro) c.242T>C (p.Leu81Pro) n.345T>C n.778-7368A>G | ClinVar dbSNP gnomAD v4 |
11 | g.2847810T>G | CA379140265 | KCNQ1,KCNQ1-AS1 | c.1481T>G (p.Leu494Arg) c.1838T>G (p.Leu613Arg) c.1457T>G (p.Leu486Arg) c.242T>G (p.Leu81Arg) n.345T>G n.778-7368A>C | |
11 | g.2847810T= | CA1948349606 | KCNQ1,KCNQ1-AS1 | c.1481T= (p.Leu494=) c.1838T= (p.Leu613=) c.1457T= (p.Leu486=) c.242T= (p.Leu81=) n.345T= n.778-7368A= | |
11 | g.2847811T>A | CA472466225 | KCNQ1,KCNQ1-AS1 | c.1482T>A (p.Leu494=) c.1839T>A (p.Leu613=) c.1458T>A (p.Leu486=) c.243T>A (p.Leu81=) n.346T>A n.778-7369A>T | ClinVar gnomAD v4 |
11 | g.2847811T>C | CA472466228 | KCNQ1,KCNQ1-AS1 | c.1482T>C (p.Leu494=) c.1839T>C (p.Leu613=) c.1458T>C (p.Leu486=) c.243T>C (p.Leu81=) n.346T>C n.778-7369A>G | gnomAD v4 |
11 | g.2847811T>G | CA472466230 | KCNQ1,KCNQ1-AS1 | c.1482T>G (p.Leu494=) c.1839T>G (p.Leu613=) c.1458T>G (p.Leu486=) c.243T>G (p.Leu81=) n.346T>G n.778-7369A>C | |
11 | g.2847811_2847814delinsTCAC | CA1948349607 | KCNQ1,KCNQ1-AS1 | c.1482_1485delinsTCAC (p.Leu494=) c.1839_1842delinsTCAC (p.Leu613=) c.1458_1461delinsTCAC (p.Leu486=) c.243_246delinsTCAC (p.Leu81=) n.346_349delinsTCAC n.778-7372_778-7369delinsGTGA | |
11 | g.2847812C>A | CA379140266 | KCNQ1,KCNQ1-AS1 | c.1483C>A (p.His495Asn) c.1840C>A (p.His614Asn) c.1459C>A (p.His487Asn) c.244C>A (p.His82Asn) n.347C>A n.778-7370G>T | gnomAD v4 |
11 | g.2847812C= | CA1948349608 | KCNQ1,KCNQ1-AS1 | c.1483C= (p.His495=) c.1840C= (p.His614=) c.1459C= (p.His487=) c.244C= (p.His82=) n.347C= n.778-7370G= | |
11 | g.2847812C>G | CA379140267 | KCNQ1,KCNQ1-AS1 | c.1483C>G (p.His495Asp) c.1840C>G (p.His614Asp) c.1459C>G (p.His487Asp) c.244C>G (p.His82Asp) n.347C>G n.778-7370G>C | |
11 | g.2847812C>T | CA379140268 | KCNQ1,KCNQ1-AS1 | c.1483C>T (p.His495Tyr) c.1840C>T (p.His614Tyr) c.1459C>T (p.His487Tyr) c.244C>T (p.His82Tyr) n.347C>T n.778-7370G>A | dbSNP |
11 | g.2847814_2847816del | CA006491 | KCNQ1,KCNQ1-AS1 | c.1485_1487del (p.His495del) c.1842_1844del (p.His614del) c.1461_1463del (p.His487del) c.246_248del (p.His82del) n.349_351del n.778-7372_778-7370del | ClinVar dbSNP |
11 | g.2847813A>C | CA379140269 | KCNQ1,KCNQ1-AS1 | c.1484A>C (p.His495Pro) c.1841A>C (p.His614Pro) c.1460A>C (p.His487Pro) c.245A>C (p.His82Pro) n.348A>C n.778-7371T>G | |
11 | g.2847813A>G | CA379140271 | KCNQ1,KCNQ1-AS1 | c.1484A>G (p.His495Arg) c.1841A>G (p.His614Arg) c.1460A>G (p.His487Arg) c.245A>G (p.His82Arg) n.348A>G n.778-7371T>C | |
11 | g.2847813A>T | CA379140270 | KCNQ1,KCNQ1-AS1 | c.1484A>T (p.His495Leu) c.1841A>T (p.His614Leu) c.1460A>T (p.His487Leu) c.245A>T (p.His82Leu) n.348A>T n.778-7371T>A | ClinVar |
11 | g.2847814C>A | CA379140272 | KCNQ1,KCNQ1-AS1 | c.1485C>A (p.His495Gln) c.1842C>A (p.His614Gln) c.1461C>A (p.His487Gln) c.246C>A (p.His82Gln) n.349C>A n.778-7372G>T | gnomAD v4 |
11 | g.2847814C>G | CA379140273 | KCNQ1,KCNQ1-AS1 | c.1485C>G (p.His495Gln) c.1842C>G (p.His614Gln) c.1461C>G (p.His487Gln) c.246C>G (p.His82Gln) n.349C>G n.778-7372G>C | |
11 | g.2847814C>T | CA472466243 | KCNQ1,KCNQ1-AS1 | c.1485C>T (p.His495=) c.1842C>T (p.His614=) c.1461C>T (p.His487=) c.246C>T (p.His82=) n.349C>T n.778-7372G>A | gnomAD v4 |
11 | g.2847815C>A | CA379140274 | KCNQ1,KCNQ1-AS1 | c.1486C>A (p.Gln496Lys) c.1843C>A (p.Gln615Lys) c.1462C>A (p.Gln488Lys) c.247C>A (p.Gln83Lys) n.350C>A n.778-7373G>T | gnomAD v4 |
11 | g.2847815C>G | CA379140275 | KCNQ1,KCNQ1-AS1 | c.1486C>G (p.Gln496Glu) c.1843C>G (p.Gln615Glu) c.1462C>G (p.Gln488Glu) c.247C>G (p.Gln83Glu) n.350C>G n.778-7373G>C | |
11 | g.2847815C>T | CA379140276 | KCNQ1,KCNQ1-AS1 | c.1486C>T (p.Gln496Ter) c.1843C>T (p.Gln615Ter) c.1462C>T (p.Gln488Ter) c.247C>T (p.Gln83Ter) n.350C>T n.778-7373G>A | |
11 | g.2847816A= | CA1948349609 | KCNQ1,KCNQ1-AS1 | c.1487A= (p.Gln496=) c.1844A= (p.Gln615=) c.1463A= (p.Gln488=) c.248A= (p.Gln83=) n.351A= n.778-7374T= | |
11 | g.2847816A>C | CA379140277 | KCNQ1,KCNQ1-AS1 | c.1487A>C (p.Gln496Pro) c.1844A>C (p.Gln615Pro) c.1463A>C (p.Gln488Pro) c.248A>C (p.Gln83Pro) n.351A>C n.778-7374T>G | ClinVar |
11 | g.2847816A>G | CA379140278 | KCNQ1,KCNQ1-AS1 | c.1487A>G (p.Gln496Arg) c.1844A>G (p.Gln615Arg) c.1463A>G (p.Gln488Arg) c.248A>G (p.Gln83Arg) n.351A>G n.778-7374T>C | ClinVar dbSNP gnomAD v4 |
11 | g.2847816A>T | CA379140279 | KCNQ1,KCNQ1-AS1 | c.1487A>T (p.Gln496Leu) c.1844A>T (p.Gln615Leu) c.1463A>T (p.Gln488Leu) c.248A>T (p.Gln83Leu) n.351A>T n.778-7374T>A | |
11 | g.2847817G>A | CA472466257 | KCNQ1,KCNQ1-AS1 | c.1488G>A (p.Gln496=) c.1845G>A (p.Gln615=) c.1464G>A (p.Gln488=) c.249G>A (p.Gln83=) n.352G>A n.778-7375C>T | gnomAD v4 |
11 | g.2847817G>C | CA379140280 | KCNQ1,KCNQ1-AS1 | c.1488G>C (p.Gln496His) c.1845G>C (p.Gln615His) c.1464G>C (p.Gln488His) c.249G>C (p.Gln83His) n.352G>C n.778-7375C>G | |
11 | g.2847817G>T | CA379140281 | KCNQ1,KCNQ1-AS1 | c.1488G>T (p.Gln496His) c.1845G>T (p.Gln615His) c.1464G>T (p.Gln488His) c.249G>T (p.Gln83His) n.352G>T n.778-7375C>A | ClinVar gnomAD v4 |
11 | g.2847820_2847822dup | CA2612011183 | KCNQ1,KCNQ1-AS1 | c.1491_1493dup (p.Leu498_Ser499insLeu) c.1848_1850dup (p.Leu617_Ser618insLeu) c.1467_1469dup (p.Leu490_Ser491insLeu) c.252_254dup (p.Leu85_Ser86insLeu) n.355_357dup n.778-7377_778-7375dup | gnomAD v4 |
11 | g.2847818C>A | CA379140283 | KCNQ1,KCNQ1-AS1 | c.1489C>A (p.Leu497Met) c.1846C>A (p.Leu616Met) c.1465C>A (p.Leu489Met) c.250C>A (p.Leu84Met) n.353C>A n.778-7376G>T | gnomAD v4 |
11 | g.2847818C>G | CA379140282 | KCNQ1,KCNQ1-AS1 | c.1489C>G (p.Leu497Val) c.1846C>G (p.Leu616Val) c.1465C>G (p.Leu489Val) c.250C>G (p.Leu84Val) n.353C>G n.778-7376G>C | |
11 | g.2847818C>T | CA472466267 | KCNQ1,KCNQ1-AS1 | c.1489C>T (p.Leu497=) c.1846C>T (p.Leu616=) c.1465C>T (p.Leu489=) c.250C>T (p.Leu84=) n.353C>T n.778-7376G>A | ClinVar gnomAD v4 |
11 | g.2847819T>A | CA379140284 | KCNQ1,KCNQ1-AS1 | c.1490T>A (p.Leu497Gln) c.1847T>A (p.Leu616Gln) c.1466T>A (p.Leu489Gln) c.251T>A (p.Leu84Gln) n.354T>A n.778-7377A>T | |
11 | g.2847819T>C | CA379140285 | KCNQ1,KCNQ1-AS1 | c.1490T>C (p.Leu497Pro) c.1847T>C (p.Leu616Pro) c.1466T>C (p.Leu489Pro) c.251T>C (p.Leu84Pro) n.354T>C n.778-7377A>G | |
11 | g.2847819T>G | CA379140286 | KCNQ1,KCNQ1-AS1 | c.1490T>G (p.Leu497Arg) c.1847T>G (p.Leu616Arg) c.1466T>G (p.Leu489Arg) c.251T>G (p.Leu84Arg) n.354T>G n.778-7377A>C | |
11 | g.2847820G>A | CA033346 | KCNQ1,KCNQ1-AS1 | c.1491G>A (p.Leu497=) c.1848G>A (p.Leu616=) c.1467G>A (p.Leu489=) c.252G>A (p.Leu84=) n.355G>A n.778-7378C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
11 | g.2847820G>C | CA472466282 | KCNQ1,KCNQ1-AS1 | c.1491G>C (p.Leu497=) c.1848G>C (p.Leu616=) c.1467G>C (p.Leu489=) c.252G>C (p.Leu84=) n.355G>C n.778-7378C>G | |
11 | g.2847820G= | CA1948349610 | KCNQ1,KCNQ1-AS1 | c.1491G= (p.Leu497=) c.1848G= (p.Leu616=) c.1467G= (p.Leu489=) c.252G= (p.Leu84=) n.355G= n.778-7378C= | |
11 | g.2847820G>T | CA472466283 | KCNQ1,KCNQ1-AS1 | c.1491G>T (p.Leu497=) c.1848G>T (p.Leu616=) c.1467G>T (p.Leu489=) c.252G>T (p.Leu84=) n.355G>T n.778-7378C>A | gnomAD v4 |
11 | g.2847821C>A | CA379140287 | KCNQ1,KCNQ1-AS1 | c.1492C>A (p.Leu498Ile) c.1849C>A (p.Leu617Ile) c.1468C>A (p.Leu490Ile) c.253C>A (p.Leu85Ile) n.356C>A n.778-7379G>T | gnomAD v4 |
11 | g.2847821C= | CA1948349611 | KCNQ1,KCNQ1-AS1 | c.1492C= (p.Leu498=) c.1849C= (p.Leu617=) c.1468C= (p.Leu490=) c.253C= (p.Leu85=) n.356C= n.778-7379G= | |
11 | g.2847821C>G | CA379140288 | KCNQ1,KCNQ1-AS1 | c.1492C>G (p.Leu498Val) c.1849C>G (p.Leu617Val) c.1468C>G (p.Leu490Val) c.253C>G (p.Leu85Val) n.356C>G n.778-7379G>C | |
11 | g.2847821C>T | CA379140289 | KCNQ1,KCNQ1-AS1 | c.1492C>T (p.Leu498Phe) c.1849C>T (p.Leu617Phe) c.1468C>T (p.Leu490Phe) c.253C>T (p.Leu85Phe) n.356C>T n.778-7379G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.2847822T>A | CA379140290 | KCNQ1,KCNQ1-AS1 | c.1493T>A (p.Leu498His) c.1850T>A (p.Leu617His) c.1469T>A (p.Leu490His) c.254T>A (p.Leu85His) n.357T>A n.778-7380A>T | |
11 | g.2847822T>C | CA379140291 | KCNQ1,KCNQ1-AS1 | c.1493T>C (p.Leu498Pro) c.1850T>C (p.Leu617Pro) c.1469T>C (p.Leu490Pro) c.254T>C (p.Leu85Pro) n.357T>C n.778-7380A>G | gnomAD v4 |
11 | g.2847822T>G | CA379140292 | KCNQ1,KCNQ1-AS1 | c.1493T>G (p.Leu498Arg) c.1850T>G (p.Leu617Arg) c.1469T>G (p.Leu490Arg) c.254T>G (p.Leu85Arg) n.357T>G n.778-7380A>C | |
11 | g.2847823C>A | CA472466315 | KCNQ1,KCNQ1-AS1 | c.1494C>A (p.Leu498=) c.1851C>A (p.Leu617=) c.1470C>A (p.Leu490=) c.255C>A (p.Leu85=) n.358C>A n.778-7381G>T | gnomAD v4 |
11 | g.2847823C= | CA1948349612 | KCNQ1,KCNQ1-AS1 | c.1494C= (p.Leu498=) c.1851C= (p.Leu617=) c.1470C= (p.Leu490=) c.255C= (p.Leu85=) n.358C= n.778-7381G= | |
11 | g.2847823C>G | CA472466317 | KCNQ1,KCNQ1-AS1 | c.1494C>G (p.Leu498=) c.1851C>G (p.Leu617=) c.1470C>G (p.Leu490=) c.255C>G (p.Leu85=) n.358C>G n.778-7381G>C | |
11 | g.2847823C>T | CA216345078 | KCNQ1,KCNQ1-AS1 | c.1494C>T (p.Leu498=) c.1851C>T (p.Leu617=) c.1470C>T (p.Leu490=) c.255C>T (p.Leu85=) n.358C>T n.778-7381G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847824del | CA645569416 | KCNQ1,KCNQ1-AS1 | c.1495del (p.Ser499ProfsTer?) c.1852del (p.Ser618ProfsTer?) c.1471del (p.Ser491ProfsTer?) c.256del (p.Ser86ProfsTer?) n.359del n.778-7382del | COSMIC COSMIC |
11 | g.2847824T>A | CA379140293 | KCNQ1,KCNQ1-AS1 | c.1495T>A (p.Ser499Thr) c.1852T>A (p.Ser618Thr) c.1471T>A (p.Ser491Thr) c.256T>A (p.Ser86Thr) n.359T>A n.778-7382A>T | |
11 | g.2847824T>C | CA379140294 | KCNQ1,KCNQ1-AS1 | c.1495T>C (p.Ser499Pro) c.1852T>C (p.Ser618Pro) c.1471T>C (p.Ser491Pro) c.256T>C (p.Ser86Pro) n.359T>C n.778-7382A>G | |
11 | g.2847824T>G | CA379140295 | KCNQ1,KCNQ1-AS1 | c.1495T>G (p.Ser499Ala) c.1852T>G (p.Ser618Ala) c.1471T>G (p.Ser491Ala) c.256T>G (p.Ser86Ala) n.359T>G n.778-7382A>C | |
11 | g.2847825C>A | CA379140297 | KCNQ1,KCNQ1-AS1 | c.1496C>A (p.Ser499Tyr) c.1853C>A (p.Ser618Tyr) c.1472C>A (p.Ser491Tyr) c.257C>A (p.Ser86Tyr) n.360C>A n.778-7383G>T | |
11 | g.2847825C= | CA1948349613 | KCNQ1,KCNQ1-AS1 | c.1496C= (p.Ser499=) c.1853C= (p.Ser618=) c.1472C= (p.Ser491=) c.257C= (p.Ser86=) n.360C= n.778-7383G= | |
11 | g.2847825C>G | CA379140298 | KCNQ1,KCNQ1-AS1 | c.1496C>G (p.Ser499Cys) c.1853C>G (p.Ser618Cys) c.1472C>G (p.Ser491Cys) c.257C>G (p.Ser86Cys) n.360C>G n.778-7383G>C | |
11 | g.2847825C>T | CA379140296 | KCNQ1,KCNQ1-AS1 | c.1496C>T (p.Ser499Phe) c.1853C>T (p.Ser618Phe) c.1472C>T (p.Ser491Phe) c.257C>T (p.Ser86Phe) n.360C>T n.778-7383G>A | dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC |
11 | g.2847826C>A | CA472466322 | KCNQ1,KCNQ1-AS1 | c.1497C>A (p.Ser499=) c.1854C>A (p.Ser618=) c.1473C>A (p.Ser491=) c.258C>A (p.Ser86=) n.361C>A n.778-7384G>T | gnomAD v4 |
11 | g.2847826C= | CA1948349614 | KCNQ1,KCNQ1-AS1 | c.1497C= (p.Ser499=) c.1854C= (p.Ser618=) c.1473C= (p.Ser491=) c.258C= (p.Ser86=) n.361C= n.778-7384G= | |
11 | g.2847826C>G | CA472466324 | KCNQ1,KCNQ1-AS1 | c.1497C>G (p.Ser499=) c.1854C>G (p.Ser618=) c.1473C>G (p.Ser491=) c.258C>G (p.Ser86=) n.361C>G n.778-7384G>C | |
11 | g.2847826C>T | CA033369 | KCNQ1,KCNQ1-AS1 | c.1497C>T (p.Ser499=) c.1854C>T (p.Ser618=) c.1473C>T (p.Ser491=) c.258C>T (p.Ser86=) n.361C>T n.778-7384G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.2847827T>A | CA006511 | KCNQ1,KCNQ1-AS1 | c.1498T>A (p.Leu500Met) c.1855T>A (p.Leu619Met) c.1474T>A (p.Leu492Met) c.259T>A (p.Leu87Met) n.362T>A n.778-7385A>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847827T>C | CA472466328 | KCNQ1,KCNQ1-AS1 | c.1498T>C (p.Leu500=) c.1855T>C (p.Leu619=) c.1474T>C (p.Leu492=) c.259T>C (p.Leu87=) n.362T>C n.778-7385A>G | gnomAD v4 |
11 | g.2847827T>G | CA379140299 | KCNQ1,KCNQ1-AS1 | c.1498T>G (p.Leu500Val) c.1855T>G (p.Leu619Val) c.1474T>G (p.Leu492Val) c.259T>G (p.Leu87Val) n.362T>G n.778-7385A>C | |
11 | g.2847827T= | CA1948349615 | KCNQ1,KCNQ1-AS1 | c.1498T= (p.Leu500=) c.1855T= (p.Leu619=) c.1474T= (p.Leu492=) c.259T= (p.Leu87=) n.362T= n.778-7385A= | |
11 | g.2847828T>A | CA379140300 | KCNQ1,KCNQ1-AS1 | c.1499T>A (p.Leu500Ter) c.1856T>A (p.Leu619Ter) c.1475T>A (p.Leu492Ter) c.260T>A (p.Leu87Ter) n.363T>A n.778-7386A>T | |
11 | g.2847828T>C | CA379140301 | KCNQ1,KCNQ1-AS1 | c.1499T>C (p.Leu500Ser) c.1856T>C (p.Leu619Ser) c.1475T>C (p.Leu492Ser) c.260T>C (p.Leu87Ser) n.363T>C n.778-7386A>G | ClinVar gnomAD v4 |
11 | g.2847828T>G | CA379140302 | KCNQ1,KCNQ1-AS1 | c.1499T>G (p.Leu500Trp) c.1856T>G (p.Leu619Trp) c.1475T>G (p.Leu492Trp) c.260T>G (p.Leu87Trp) n.363T>G n.778-7386A>C | |
11 | g.2847829G>A | CA472466342 | KCNQ1,KCNQ1-AS1 | c.1500G>A (p.Leu500=) c.1857G>A (p.Leu619=) c.1476G>A (p.Leu492=) c.261G>A (p.Leu87=) n.364G>A n.778-7387C>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847829G>C | CA379140303 | KCNQ1,KCNQ1-AS1 | c.1500G>C (p.Leu500Phe) c.1857G>C (p.Leu619Phe) c.1476G>C (p.Leu492Phe) c.261G>C (p.Leu87Phe) n.364G>C n.778-7387C>G | gnomAD v4 |
11 | g.2847829G= | CA1948349616 | KCNQ1,KCNQ1-AS1 | c.1500G= (p.Leu500=) c.1857G= (p.Leu619=) c.1476G= (p.Leu492=) c.261G= (p.Leu87=) n.364G= n.778-7387C= | |
11 | g.2847829G>T | CA379140304 | KCNQ1,KCNQ1-AS1 | c.1500G>T (p.Leu500Phe) c.1857G>T (p.Leu619Phe) c.1476G>T (p.Leu492Phe) c.261G>T (p.Leu87Phe) n.364G>T n.778-7387C>A | gnomAD v4 |
11 | g.2847830C>A | CA379140305 | KCNQ1,KCNQ1-AS1 | c.1501C>A (p.His501Asn) c.1858C>A (p.His620Asn) c.1477C>A (p.His493Asn) c.262C>A (p.His88Asn) n.365C>A n.778-7388G>T | |
11 | g.2847830C>G | CA379140306 | KCNQ1,KCNQ1-AS1 | c.1501C>G (p.His501Asp) c.1858C>G (p.His620Asp) c.1477C>G (p.His493Asp) c.262C>G (p.His88Asp) n.365C>G n.778-7388G>C | ClinVar dbSNP |
11 | g.2847830C>T | CA379140307 | KCNQ1,KCNQ1-AS1 | c.1501C>T (p.His501Tyr) c.1858C>T (p.His620Tyr) c.1477C>T (p.His493Tyr) c.262C>T (p.His88Tyr) n.365C>T n.778-7388G>A | gnomAD v4 |
11 | g.2847831A= | CA1948349617 | KCNQ1,KCNQ1-AS1 | c.1502A= (p.His501=) c.1859A= (p.His620=) c.1478A= (p.His493=) c.263A= (p.His88=) n.366A= n.778-7389T= | |
11 | g.2847831A>C | CA379140308 | KCNQ1,KCNQ1-AS1 | c.1502A>C (p.His501Pro) c.1859A>C (p.His620Pro) c.1478A>C (p.His493Pro) c.263A>C (p.His88Pro) n.366A>C n.778-7389T>G | |
11 | g.2847831A>G | CA379140309 | KCNQ1,KCNQ1-AS1 | c.1502A>G (p.His501Arg) c.1859A>G (p.His620Arg) c.1478A>G (p.His493Arg) c.263A>G (p.His88Arg) n.366A>G n.778-7389T>C | gnomAD v4 |
11 | g.2847831A>T | CA379140310 | KCNQ1,KCNQ1-AS1 | c.1502A>T (p.His501Leu) c.1859A>T (p.His620Leu) c.1478A>T (p.His493Leu) c.263A>T (p.His88Leu) n.366A>T n.778-7389T>A | |
11 | g.2847832C>A | CA379140311 | KCNQ1,KCNQ1-AS1 | c.1503C>A (p.His501Gln) c.1860C>A (p.His620Gln) c.1479C>A (p.His493Gln) c.264C>A (p.His88Gln) n.367C>A n.778-7390G>T | gnomAD v4 |
11 | g.2847832C= | CA1948349618 | KCNQ1,KCNQ1-AS1 | c.1503C= (p.His501=) c.1860C= (p.His620=) c.1479C= (p.His493=) c.264C= (p.His88=) n.367C= n.778-7390G= | |
11 | g.2847832C>G | CA379140312 | KCNQ1,KCNQ1-AS1 | c.1503C>G (p.His501Gln) c.1860C>G (p.His620Gln) c.1479C>G (p.His493Gln) c.264C>G (p.His88Gln) n.367C>G n.778-7390G>C | |
11 | g.2847832C>T | CA006519 | KCNQ1,KCNQ1-AS1 | c.1503C>T (p.His501=) c.1860C>T (p.His620=) c.1479C>T (p.His493=) c.264C>T (p.His88=) n.367C>T n.778-7390G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847835_2847849dup | CA2573053485 | KCNQ1,KCNQ1-AS1 | c.1506_1520dup (p.Gly507_Ser508insGlySerThrProGly) c.1863_1877dup (p.Gly626_Ser627insGlySerThrProGly) c.1482_1496dup (p.Gly499_Ser500insGlySerThrProGly) c.267_281dup (p.Gly94_Ser95insGlySerThrProGly) n.370_384dup n.778-7404_778-7390dup | ClinVar dbSNP |
11 | g.2847833_2847850dup | CA597432740 | KCNQ1,KCNQ1-AS1 | c.1504_1521dup (p.Gly507_Ser508insGlyGlySerThrProGly) c.1861_1878dup (p.Gly626_Ser627insGlyGlySerThrProGly) c.1480_1497dup (p.Gly499_Ser500insGlyGlySerThrProGly) c.265_282dup (p.Gly94_Ser95insGlyGlySerThrProGly) n.368_385dup n.778-7407_778-7390dup | dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847833G>A | CA006526 | KCNQ1,KCNQ1-AS1 | c.1504G>A (p.Gly502Ser) c.1861G>A (p.Gly621Ser) c.1480G>A (p.Gly494Ser) c.265G>A (p.Gly89Ser) n.368G>A n.778-7391C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847833G>C | CA379140313 | KCNQ1,KCNQ1-AS1 | c.1504G>C (p.Gly502Arg) c.1861G>C (p.Gly621Arg) c.1480G>C (p.Gly494Arg) c.265G>C (p.Gly89Arg) n.368G>C n.778-7391C>G | gnomAD v4 |
11 | g.2847833G= | CA1948349619 | KCNQ1,KCNQ1-AS1 | c.1504G= (p.Gly502=) c.1861G= (p.Gly621=) c.1480G= (p.Gly494=) c.265G= (p.Gly89=) n.368G= n.778-7391C= | |
11 | g.2847833G>T | CA379140314 | KCNQ1,KCNQ1-AS1 | c.1504G>T (p.Gly502Cys) c.1861G>T (p.Gly621Cys) c.1480G>T (p.Gly494Cys) c.265G>T (p.Gly89Cys) n.368G>T n.778-7391C>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847834dup | CA2574728562 | KCNQ1,KCNQ1-AS1 | c.1505dup (p.Gly503TrpfsTer30) c.1862dup (p.Gly622TrpfsTer30) c.1481dup (p.Gly495TrpfsTer30) c.266dup (p.Gly90TrpfsTer30) n.369dup n.778-7391dup | |
11 | g.2847834G>A | CA379140315 | KCNQ1,KCNQ1-AS1 | c.1505G>A (p.Gly502Asp) c.1862G>A (p.Gly621Asp) c.1481G>A (p.Gly494Asp) c.266G>A (p.Gly89Asp) n.369G>A n.778-7392C>T | ClinVar dbSNP gnomAD v4 |
11 | g.2847834G>C | CA379140317 | KCNQ1,KCNQ1-AS1 | c.1505G>C (p.Gly502Ala) c.1862G>C (p.Gly621Ala) c.1481G>C (p.Gly494Ala) c.266G>C (p.Gly89Ala) n.369G>C n.778-7392C>G | gnomAD v4 |
11 | g.2847834G= | CA1948349620 | KCNQ1,KCNQ1-AS1 | c.1505G= (p.Gly502=) c.1862G= (p.Gly621=) c.1481G= (p.Gly494=) c.266G= (p.Gly89=) n.369G= n.778-7392C= | |
11 | g.2847834G>T | CA379140316 | KCNQ1,KCNQ1-AS1 | c.1505G>T (p.Gly502Val) c.1862G>T (p.Gly621Val) c.1481G>T (p.Gly494Val) c.266G>T (p.Gly89Val) n.369G>T n.778-7392C>A | |
11 | g.2847834_2847845dup | CA2612011237 | KCNQ1,KCNQ1-AS1 | c.1505_1516dup (p.Thr505_Pro506insArgGlySerThr) c.1862_1873dup (p.Thr624_Pro625insArgGlySerThr) c.1481_1492dup (p.Thr497_Pro498insArgGlySerThr) c.266_277dup (p.Thr92_Pro93insArgGlySerThr) n.369_380dup n.778-7403_778-7392dup | dbSNP gnomAD v4 |
11 | g.2847835T>A | CA472466376 | KCNQ1,KCNQ1-AS1 | c.1506T>A (p.Gly502=) c.1863T>A (p.Gly621=) c.1482T>A (p.Gly494=) c.267T>A (p.Gly89=) n.370T>A n.778-7393A>T | gnomAD v4 |
11 | g.2847835T>C | CA472466378 | KCNQ1,KCNQ1-AS1 | c.1506T>C (p.Gly502=) c.1863T>C (p.Gly621=) c.1482T>C (p.Gly494=) c.267T>C (p.Gly89=) n.370T>C n.778-7393A>G | |
11 | g.2847835T>G | CA472466380 | KCNQ1,KCNQ1-AS1 | c.1506T>G (p.Gly502=) c.1863T>G (p.Gly621=) c.1482T>G (p.Gly494=) c.267T>G (p.Gly89=) n.370T>G n.778-7393A>C | |
11 | g.2847836G>A | CA379140318 | KCNQ1,KCNQ1-AS1 | c.1507G>A (p.Gly503Ser) c.1864G>A (p.Gly622Ser) c.1483G>A (p.Gly495Ser) c.268G>A (p.Gly90Ser) n.371G>A n.778-7394C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847836G>C | CA379140320 | KCNQ1,KCNQ1-AS1 | c.1507G>C (p.Gly503Arg) c.1864G>C (p.Gly622Arg) c.1483G>C (p.Gly495Arg) c.268G>C (p.Gly90Arg) n.371G>C n.778-7394C>G | |
11 | g.2847836G= | CA1948349621 | KCNQ1,KCNQ1-AS1 | c.1507G= (p.Gly503=) c.1864G= (p.Gly622=) c.1483G= (p.Gly495=) c.268G= (p.Gly90=) n.371G= n.778-7394C= | |
11 | g.2847836G>T | CA379140319 | KCNQ1,KCNQ1-AS1 | c.1507G>T (p.Gly503Cys) c.1864G>T (p.Gly622Cys) c.1483G>T (p.Gly495Cys) c.268G>T (p.Gly90Cys) n.371G>T n.778-7394C>A | gnomAD v4 |
11 | g.2847837G>A | CA379140321 | KCNQ1,KCNQ1-AS1 | c.1508G>A (p.Gly503Asp) c.1865G>A (p.Gly622Asp) c.1484G>A (p.Gly495Asp) c.269G>A (p.Gly90Asp) n.372G>A n.778-7395C>T | gnomAD v4 |
11 | g.2847837G>C | CA379140323 | KCNQ1,KCNQ1-AS1 | c.1508G>C (p.Gly503Ala) c.1865G>C (p.Gly622Ala) c.1484G>C (p.Gly495Ala) c.269G>C (p.Gly90Ala) n.372G>C n.778-7395C>G | |
11 | g.2847837G>T | CA379140322 | KCNQ1,KCNQ1-AS1 | c.1508G>T (p.Gly503Val) c.1865G>T (p.Gly622Val) c.1484G>T (p.Gly495Val) c.269G>T (p.Gly90Val) n.372G>T n.778-7395C>A | gnomAD v4 |
11 | g.2847838C>A | CA472466404 | KCNQ1,KCNQ1-AS1 | c.1509C>A (p.Gly503=) c.1866C>A (p.Gly622=) c.1485C>A (p.Gly495=) c.270C>A (p.Gly90=) n.373C>A n.778-7396G>T | gnomAD v4 |
11 | g.2847838C= | CA1948349622 | KCNQ1,KCNQ1-AS1 | c.1509C= (p.Gly503=) c.1866C= (p.Gly622=) c.1485C= (p.Gly495=) c.270C= (p.Gly90=) n.373C= n.778-7396G= | |
11 | g.2847838C>G | CA472466408 | KCNQ1,KCNQ1-AS1 | c.1509C>G (p.Gly503=) c.1866C>G (p.Gly622=) c.1485C>G (p.Gly495=) c.270C>G (p.Gly90=) n.373C>G n.778-7396G>C | |
11 | g.2847838C>T | CA472466410 | KCNQ1,KCNQ1-AS1 | c.1509C>T (p.Gly503=) c.1866C>T (p.Gly622=) c.1485C>T (p.Gly495=) c.270C>T (p.Gly90=) n.373C>T n.778-7396G>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847839A>C | CA379140324 | KCNQ1,KCNQ1-AS1 | c.1510A>C (p.Ser504Arg) c.1867A>C (p.Ser623Arg) c.1486A>C (p.Ser496Arg) c.271A>C (p.Ser91Arg) n.374A>C n.778-7397T>G | |
11 | g.2847839A>G | CA379140326 | KCNQ1,KCNQ1-AS1 | c.1510A>G (p.Ser504Gly) c.1867A>G (p.Ser623Gly) c.1486A>G (p.Ser496Gly) c.271A>G (p.Ser91Gly) n.374A>G n.778-7397T>C | ClinVar gnomAD v4 |
11 | g.2847839A>T | CA379140325 | KCNQ1,KCNQ1-AS1 | c.1510A>T (p.Ser504Cys) c.1867A>T (p.Ser623Cys) c.1486A>T (p.Ser496Cys) c.271A>T (p.Ser91Cys) n.374A>T n.778-7397T>A | |
11 | g.2847840G>A | CA379140327 | KCNQ1,KCNQ1-AS1 | c.1511G>A (p.Ser504Asn) c.1868G>A (p.Ser623Asn) c.1487G>A (p.Ser496Asn) c.272G>A (p.Ser91Asn) n.375G>A n.778-7398C>T | dbSNP gnomAD v4 |
11 | g.2847840G>C | CA379140328 | KCNQ1,KCNQ1-AS1 | c.1511G>C (p.Ser504Thr) c.1868G>C (p.Ser623Thr) c.1487G>C (p.Ser496Thr) c.272G>C (p.Ser91Thr) n.375G>C n.778-7398C>G | |
11 | g.2847840G= | CA1948349623 | KCNQ1,KCNQ1-AS1 | c.1511G= (p.Ser504=) c.1868G= (p.Ser623=) c.1487G= (p.Ser496=) c.272G= (p.Ser91=) n.375G= n.778-7398C= | |
11 | g.2847840G>T | CA033431 | KCNQ1,KCNQ1-AS1 | c.1511G>T (p.Ser504Ile) c.1868G>T (p.Ser623Ile) c.1487G>T (p.Ser496Ile) c.272G>T (p.Ser91Ile) n.375G>T n.778-7398C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847841C>A | CA379140329 | KCNQ1,KCNQ1-AS1 | c.1512C>A (p.Ser504Arg) c.1869C>A (p.Ser623Arg) c.1488C>A (p.Ser496Arg) c.273C>A (p.Ser91Arg) n.376C>A n.778-7399G>T | gnomAD v4 |
11 | g.2847841C= | CA1948349624 | KCNQ1,KCNQ1-AS1 | c.1512C= (p.Ser504=) c.1869C= (p.Ser623=) c.1488C= (p.Ser496=) c.273C= (p.Ser91=) n.376C= n.778-7399G= | |
11 | g.2847841C>G | CA379140330 | KCNQ1,KCNQ1-AS1 | c.1512C>G (p.Ser504Arg) c.1869C>G (p.Ser623Arg) c.1488C>G (p.Ser496Arg) c.273C>G (p.Ser91Arg) n.376C>G n.778-7399G>C | |
11 | g.2847841C>T | CA216345146 | KCNQ1,KCNQ1-AS1 | c.1512C>T (p.Ser504=) c.1869C>T (p.Ser623=) c.1488C>T (p.Ser496=) c.273C>T (p.Ser91=) n.376C>T n.778-7399G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847842A= | CA1948349626 | KCNQ1,KCNQ1-AS1 | c.1513A= (p.Thr505=) c.1870A= (p.Thr624=) c.1489A= (p.Thr497=) c.274A= (p.Thr92=) n.377A= n.778-7400T= | |
11 | g.2847842A>C | CA379140331 | KCNQ1,KCNQ1-AS1 | c.1513A>C (p.Thr505Pro) c.1870A>C (p.Thr624Pro) c.1489A>C (p.Thr497Pro) c.274A>C (p.Thr92Pro) n.377A>C n.778-7400T>G | dbSNP gnomAD v4 |
11 | g.2847842A>G | CA379140332 | KCNQ1,KCNQ1-AS1 | c.1513A>G (p.Thr505Ala) c.1870A>G (p.Thr624Ala) c.1489A>G (p.Thr497Ala) c.274A>G (p.Thr92Ala) n.377A>G n.778-7400T>C | ClinVar dbSNP |
11 | g.2847842A>T | CA379140333 | KCNQ1,KCNQ1-AS1 | c.1513A>T (p.Thr505Ser) c.1870A>T (p.Thr624Ser) c.1489A>T (p.Thr497Ser) c.274A>T (p.Thr92Ser) n.377A>T n.778-7400T>A | |
11 | g.2847842_2847860delinsACCCCCGGCAGCGGCGGCC | CA1948349625 | KCNQ1,KCNQ1-AS1 | c.1513_1531delinsACCCCCGGCAGCGGCGGCC (p.Thr505=) c.1870_1888delinsACCCCCGGCAGCGGCGGCC (p.Thr624=) c.1489_1507delinsACCCCCGGCAGCGGCGGCC (p.Thr497=) c.274_292delinsACCCCCGGCAGCGGCGGCC (p.Thr92=) n.377_395delinsACCCCCGGCAGCGGCGGCC n.778-7418_778-7400delinsGGCCGCCGCTGCCGGGGGT | |
11 | g.2847843C>A | CA379140334 | KCNQ1,KCNQ1-AS1 | c.1514C>A (p.Thr505Asn) c.1871C>A (p.Thr624Asn) c.1490C>A (p.Thr497Asn) c.275C>A (p.Thr92Asn) n.378C>A n.778-7401G>T | |
11 | g.2847843C= | CA1948349627 | KCNQ1,KCNQ1-AS1 | c.1514C= (p.Thr505=) c.1871C= (p.Thr624=) c.1490C= (p.Thr497=) c.275C= (p.Thr92=) n.378C= n.778-7401G= | |
11 | g.2847843C>G | CA379140335 | KCNQ1,KCNQ1-AS1 | c.1514C>G (p.Thr505Ser) c.1871C>G (p.Thr624Ser) c.1490C>G (p.Thr497Ser) c.275C>G (p.Thr92Ser) n.378C>G n.778-7401G>C | gnomAD v4 |
11 | g.2847843C>T | CA379140336 | KCNQ1,KCNQ1-AS1 | c.1514C>T (p.Thr505Ile) c.1871C>T (p.Thr624Ile) c.1490C>T (p.Thr497Ile) c.275C>T (p.Thr92Ile) n.378C>T n.778-7401G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847847dup | CA2573053486 | KCNQ1,KCNQ1-AS1 | c.1518dup (p.Gly507ArgfsTer26) c.1875dup (p.Gly626ArgfsTer26) c.1494dup (p.Gly499ArgfsTer26) c.279dup (p.Gly94ArgfsTer26) n.382dup n.778-7401dup | ClinVar dbSNP gnomAD v4 |
11 | g.2847847del | CA472466439 | KCNQ1,KCNQ1-AS1 | c.1518del (p.Gly507AlafsTer?) c.1875del (p.Gly626AlafsTer?) c.1494del (p.Gly499AlafsTer?) c.279del (p.Gly94AlafsTer?) n.382del n.778-7401del | gnomAD v4 COSMIC COSMIC |
11 | g.2847848_2847865del | CA006530 | KCNQ1,KCNQ1-AS1 | c.1519_1536del (p.Gly507_Pro512del) c.1876_1893del (p.Gly626_Pro631del) c.1495_1512del (p.Gly499_Pro504del) c.280_297del (p.Gly94_Pro99del) n.383_400del n.778-7418_778-7401del | ClinVar dbSNP gnomAD v4 |
11 | g.2847844C>A | CA472466446 | KCNQ1,KCNQ1-AS1 | c.1515C>A (p.Thr505=) c.1872C>A (p.Thr624=) c.1491C>A (p.Thr497=) c.276C>A (p.Thr92=) n.379C>A n.778-7402G>T | gnomAD v4 |
11 | g.2847844C>G | CA472466449 | KCNQ1,KCNQ1-AS1 | c.1515C>G (p.Thr505=) c.1872C>G (p.Thr624=) c.1491C>G (p.Thr497=) c.276C>G (p.Thr92=) n.379C>G n.778-7402G>C | |
11 | g.2847844C>T | CA472466450 | KCNQ1,KCNQ1-AS1 | c.1515C>T (p.Thr505=) c.1872C>T (p.Thr624=) c.1491C>T (p.Thr497=) c.276C>T (p.Thr92=) n.379C>T n.778-7402G>A | ClinVar gnomAD v4 |
11 | g.2847845C>A | CA379140339 | KCNQ1,KCNQ1-AS1 | c.1516C>A (p.Pro506Thr) c.1873C>A (p.Pro625Thr) c.1492C>A (p.Pro498Thr) c.277C>A (p.Pro93Thr) n.380C>A n.778-7403G>T | gnomAD v4 |
11 | g.2847845C>G | CA379140338 | KCNQ1,KCNQ1-AS1 | c.1516C>G (p.Pro506Ala) c.1873C>G (p.Pro625Ala) c.1492C>G (p.Pro498Ala) c.277C>G (p.Pro93Ala) n.380C>G n.778-7403G>C | |
11 | g.2847845C>T | CA379140337 | KCNQ1,KCNQ1-AS1 | c.1516C>T (p.Pro506Ser) c.1873C>T (p.Pro625Ser) c.1492C>T (p.Pro498Ser) c.277C>T (p.Pro93Ser) n.380C>T n.778-7403G>A | gnomAD v4 |
11 | g.2847846C>A | CA379140340 | KCNQ1,KCNQ1-AS1 | c.1517C>A (p.Pro506His) c.1874C>A (p.Pro625His) c.1493C>A (p.Pro498His) c.278C>A (p.Pro93His) n.381C>A n.778-7404G>T | gnomAD v4 |
11 | g.2847846C= | CA1948349628 | KCNQ1,KCNQ1-AS1 | c.1517C= (p.Pro506=) c.1874C= (p.Pro625=) c.1493C= (p.Pro498=) c.278C= (p.Pro93=) n.381C= n.778-7404G= | |
11 | g.2847846C>G | CA033459 | KCNQ1,KCNQ1-AS1 | c.1517C>G (p.Pro506Arg) c.1874C>G (p.Pro625Arg) c.1493C>G (p.Pro498Arg) c.278C>G (p.Pro93Arg) n.381C>G n.778-7404G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.2847846C>T | CA379140341 | KCNQ1,KCNQ1-AS1 | c.1517C>T (p.Pro506Leu) c.1874C>T (p.Pro625Leu) c.1493C>T (p.Pro498Leu) c.278C>T (p.Pro93Leu) n.381C>T n.778-7404G>A | gnomAD v4 COSMIC COSMIC |
11 | g.2847847C>A | CA472466471 | KCNQ1,KCNQ1-AS1 | c.1518C>A (p.Pro506=) c.1875C>A (p.Pro625=) c.1494C>A (p.Pro498=) c.279C>A (p.Pro93=) n.382C>A n.778-7405G>T | gnomAD v4 |
11 | g.2847847C= | CA1948349629 | KCNQ1,KCNQ1-AS1 | c.1518C= (p.Pro506=) c.1875C= (p.Pro625=) c.1494C= (p.Pro498=) c.279C= (p.Pro93=) n.382C= n.778-7405G= | |
11 | g.2847847C>G | CA033469 | KCNQ1,KCNQ1-AS1 | c.1518C>G (p.Pro506=) c.1875C>G (p.Pro625=) c.1494C>G (p.Pro498=) c.279C>G (p.Pro93=) n.382C>G n.778-7405G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847847C>T | CA033482 | KCNQ1,KCNQ1-AS1 | c.1518C>T (p.Pro506=) c.1875C>T (p.Pro625=) c.1494C>T (p.Pro498=) c.279C>T (p.Pro93=) n.382C>T n.778-7405G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847847_2847848delinsCG | CA1948349630 | KCNQ1,KCNQ1-AS1 | c.1518_1519delinsCG (p.Pro506=) c.1875_1876delinsCG (p.Pro625=) c.1494_1495delinsCG (p.Pro498=) c.279_280delinsCG (p.Pro93=) n.382_383delinsCG n.778-7406_778-7405delinsCG | |
11 | g.2847848G>A | CA006538 | KCNQ1,KCNQ1-AS1 | c.1519G>A (p.Gly507Ser) c.1876G>A (p.Gly626Ser) c.1495G>A (p.Gly499Ser) c.280G>A (p.Gly94Ser) n.383G>A n.778-7406C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847848G>C | CA379140342 | KCNQ1,KCNQ1-AS1 | c.1519G>C (p.Gly507Arg) c.1876G>C (p.Gly626Arg) c.1495G>C (p.Gly499Arg) c.280G>C (p.Gly94Arg) n.383G>C n.778-7406C>G | ClinVar |
11 | g.2847848G= | CA1948349632 | KCNQ1,KCNQ1-AS1 | c.1519G= (p.Gly507=) c.1876G= (p.Gly626=) c.1495G= (p.Gly499=) c.280G= (p.Gly94=) n.383G= n.778-7406C= | |
11 | g.2847848G>T | CA379140343 | KCNQ1,KCNQ1-AS1 | c.1519G>T (p.Gly507Cys) c.1876G>T (p.Gly626Cys) c.1495G>T (p.Gly499Cys) c.280G>T (p.Gly94Cys) n.383G>T n.778-7406C>A | gnomAD v4 COSMIC COSMIC |
11 | g.2847849del | CA1948349631 | KCNQ1,KCNQ1-AS1 | c.1520del (p.Gly507AlafsTer?) c.1877del (p.Gly626AlafsTer?) c.1496del (p.Gly499AlafsTer?) c.281del (p.Gly94AlafsTer?) n.384del n.778-7406del | dbSNP |
11 | g.2847849G>A | CA379140344 | KCNQ1,KCNQ1-AS1 | c.1520G>A (p.Gly507Asp) c.1877G>A (p.Gly626Asp) c.1496G>A (p.Gly499Asp) c.281G>A (p.Gly94Asp) n.384G>A n.778-7407C>T | gnomAD v4 |
11 | g.2847849G>C | CA379140345 | KCNQ1,KCNQ1-AS1 | c.1520G>C (p.Gly507Ala) c.1877G>C (p.Gly626Ala) c.1496G>C (p.Gly499Ala) c.281G>C (p.Gly94Ala) n.384G>C n.778-7407C>G | |
11 | g.2847849G= | CA1948349633 | KCNQ1,KCNQ1-AS1 | c.1520G= (p.Gly507=) c.1877G= (p.Gly626=) c.1496G= (p.Gly499=) c.281G= (p.Gly94=) n.384G= n.778-7407C= | |
11 | g.2847849G>T | CA379140346 | KCNQ1,KCNQ1-AS1 | c.1520G>T (p.Gly507Val) c.1877G>T (p.Gly626Val) c.1496G>T (p.Gly499Val) c.281G>T (p.Gly94Val) n.384G>T n.778-7407C>A | ClinVar dbSNP gnomAD v4 |
11 | g.2847850C>A | CA472466488 | KCNQ1,KCNQ1-AS1 | c.1521C>A (p.Gly507=) c.1878C>A (p.Gly626=) c.1497C>A (p.Gly499=) c.282C>A (p.Gly94=) n.385C>A n.778-7408G>T | gnomAD v4 |
11 | g.2847850C>G | CA472466489 | KCNQ1,KCNQ1-AS1 | c.1521C>G (p.Gly507=) c.1878C>G (p.Gly626=) c.1497C>G (p.Gly499=) c.282C>G (p.Gly94=) n.385C>G n.778-7408G>C | gnomAD v4 |
11 | g.2847850C>T | CA472466487 | KCNQ1,KCNQ1-AS1 | c.1521C>T (p.Gly507=) c.1878C>T (p.Gly626=) c.1497C>T (p.Gly499=) c.282C>T (p.Gly94=) n.385C>T n.778-7408G>A | |
11 | g.2847851A= | CA1948349634 | KCNQ1,KCNQ1-AS1 | c.1522A= (p.Ser508=) c.1879A= (p.Ser627=) c.1498A= (p.Ser500=) c.283A= (p.Ser95=) n.386A= n.778-7409T= | |
11 | g.2847851A>C | CA379140349 | KCNQ1,KCNQ1-AS1 | c.1522A>C (p.Ser508Arg) c.1879A>C (p.Ser627Arg) c.1498A>C (p.Ser500Arg) c.283A>C (p.Ser95Arg) n.386A>C n.778-7409T>G | |
11 | g.2847851A>G | CA379140348 | KCNQ1,KCNQ1-AS1 | c.1522A>G (p.Ser508Gly) c.1879A>G (p.Ser627Gly) c.1498A>G (p.Ser500Gly) c.283A>G (p.Ser95Gly) n.386A>G n.778-7409T>C | dbSNP |
11 | g.2847851A>T | CA379140347 | KCNQ1,KCNQ1-AS1 | c.1522A>T (p.Ser508Cys) c.1879A>T (p.Ser627Cys) c.1498A>T (p.Ser500Cys) c.283A>T (p.Ser95Cys) n.386A>T n.778-7409T>A | |
11 | g.2847852G>A | CA379140350 | KCNQ1,KCNQ1-AS1 | c.1523G>A (p.Ser508Asn) c.1880G>A (p.Ser627Asn) c.1499G>A (p.Ser500Asn) c.284G>A (p.Ser95Asn) n.387G>A n.778-7410C>T | |
11 | g.2847852G>C | CA379140351 | KCNQ1,KCNQ1-AS1 | c.1523G>C (p.Ser508Thr) c.1880G>C (p.Ser627Thr) c.1499G>C (p.Ser500Thr) c.284G>C (p.Ser95Thr) n.387G>C n.778-7410C>G | |
11 | g.2847852G>T | CA379140352 | KCNQ1,KCNQ1-AS1 | c.1523G>T (p.Ser508Ile) c.1880G>T (p.Ser627Ile) c.1499G>T (p.Ser500Ile) c.284G>T (p.Ser95Ile) n.387G>T n.778-7410C>A | gnomAD v4 |
11 | g.2847853C>A | CA379140353 | KCNQ1,KCNQ1-AS1 | c.1524C>A (p.Ser508Arg) c.1881C>A (p.Ser627Arg) c.1500C>A (p.Ser500Arg) c.285C>A (p.Ser95Arg) n.388C>A n.778-7411G>T | gnomAD v4 |
11 | g.2847853C= | CA1948349635 | KCNQ1,KCNQ1-AS1 | c.1524C= (p.Ser508=) c.1881C= (p.Ser627=) c.1500C= (p.Ser500=) c.285C= (p.Ser95=) n.388C= n.778-7411G= | |
11 | g.2847853C>G | CA379140354 | KCNQ1,KCNQ1-AS1 | c.1524C>G (p.Ser508Arg) c.1881C>G (p.Ser627Arg) c.1500C>G (p.Ser500Arg) c.285C>G (p.Ser95Arg) n.388C>G n.778-7411G>C | |
11 | g.2847853C>T | CA033494 | KCNQ1,KCNQ1-AS1 | c.1524C>T (p.Ser508=) c.1881C>T (p.Ser627=) c.1500C>T (p.Ser500=) c.285C>T (p.Ser95=) n.388C>T n.778-7411G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847854G>A | CA033512 | KCNQ1,KCNQ1-AS1 | c.1525G>A (p.Gly509Ser) c.1882G>A (p.Gly628Ser) c.1501G>A (p.Gly501Ser) c.286G>A (p.Gly96Ser) n.389G>A n.778-7412C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847854G>C | CA379140356 | KCNQ1,KCNQ1-AS1 | c.1525G>C (p.Gly509Arg) c.1882G>C (p.Gly628Arg) c.1501G>C (p.Gly501Arg) c.286G>C (p.Gly96Arg) n.389G>C n.778-7412C>G | |
11 | g.2847854G= | CA1948349636 | KCNQ1,KCNQ1-AS1 | c.1525G= (p.Gly509=) c.1882G= (p.Gly628=) c.1501G= (p.Gly501=) c.286G= (p.Gly96=) n.389G= n.778-7412C= | |
11 | g.2847854G>T | CA379140355 | KCNQ1,KCNQ1-AS1 | c.1525G>T (p.Gly509Cys) c.1882G>T (p.Gly628Cys) c.1501G>T (p.Gly501Cys) c.286G>T (p.Gly96Cys) n.389G>T n.778-7412C>A | |
11 | g.2847855G>A | CA379140357 | KCNQ1,KCNQ1-AS1 | c.1526G>A (p.Gly509Asp) c.1883G>A (p.Gly628Asp) c.1502G>A (p.Gly501Asp) c.287G>A (p.Gly96Asp) n.390G>A n.778-7413C>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847855G>C | CA379140358 | KCNQ1,KCNQ1-AS1 | c.1526G>C (p.Gly509Ala) c.1883G>C (p.Gly628Ala) c.1502G>C (p.Gly501Ala) c.287G>C (p.Gly96Ala) n.390G>C n.778-7413C>G | dbSNP gnomAD v2 |
11 | g.2847855G= | CA1948349637 | KCNQ1,KCNQ1-AS1 | c.1526G= (p.Gly509=) c.1883G= (p.Gly628=) c.1502G= (p.Gly501=) c.287G= (p.Gly96=) n.390G= n.778-7413C= | |
11 | g.2847855G>T | CA379140359 | KCNQ1,KCNQ1-AS1 | c.1526G>T (p.Gly509Val) c.1883G>T (p.Gly628Val) c.1502G>T (p.Gly501Val) c.287G>T (p.Gly96Val) n.390G>T n.778-7413C>A | gnomAD v4 |
11 | g.2847856C>A | CA472466506 | KCNQ1,KCNQ1-AS1 | c.1527C>A (p.Gly509=) c.1884C>A (p.Gly628=) c.1503C>A (p.Gly501=) c.288C>A (p.Gly96=) n.391C>A n.778-7414G>T | gnomAD v4 |
11 | g.2847856C= | CA1948349638 | KCNQ1,KCNQ1-AS1 | c.1527C= (p.Gly509=) c.1884C= (p.Gly628=) c.1503C= (p.Gly501=) c.288C= (p.Gly96=) n.391C= n.778-7414G= | |
11 | g.2847856C>G | CA472466510 | KCNQ1,KCNQ1-AS1 | c.1527C>G (p.Gly509=) c.1884C>G (p.Gly628=) c.1503C>G (p.Gly501=) c.288C>G (p.Gly96=) n.391C>G n.778-7414G>C | ClinVar dbSNP |
11 | g.2847856C>T | CA033530 | KCNQ1,KCNQ1-AS1 | c.1527C>T (p.Gly509=) c.1884C>T (p.Gly628=) c.1503C>T (p.Gly501=) c.288C>T (p.Gly96=) n.391C>T n.778-7414G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847857G>A | CA033561 | KCNQ1,KCNQ1-AS1 | c.1528G>A (p.Gly510Ser) c.1885G>A (p.Gly629Ser) c.1504G>A (p.Gly502Ser) c.289G>A (p.Gly97Ser) n.392G>A n.778-7415C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847857G>C | CA379140361 | KCNQ1,KCNQ1-AS1 | c.1528G>C (p.Gly510Arg) c.1885G>C (p.Gly629Arg) c.1504G>C (p.Gly502Arg) c.289G>C (p.Gly97Arg) n.392G>C n.778-7415C>G | gnomAD v4 |
11 | g.2847857G= | CA1948349639 | KCNQ1,KCNQ1-AS1 | c.1528G= (p.Gly510=) c.1885G= (p.Gly629=) c.1504G= (p.Gly502=) c.289G= (p.Gly97=) n.392G= n.778-7415C= | |
11 | g.2847857G>T | CA379140360 | KCNQ1,KCNQ1-AS1 | c.1528G>T (p.Gly510Cys) c.1885G>T (p.Gly629Cys) c.1504G>T (p.Gly502Cys) c.289G>T (p.Gly97Cys) n.392G>T n.778-7415C>A | gnomAD v4 |
11 | g.2847858dup | CA216345189 | KCNQ1,KCNQ1-AS1 | c.1529dup (p.Arg513GlnfsTer20) c.1886dup (p.Arg632GlnfsTer20) c.1505dup (p.Arg505GlnfsTer20) c.290dup (p.Arg100GlnfsTer20) n.393dup n.778-7415dup | dbSNP |
11 | g.2847858G>A | CA379140362 | KCNQ1,KCNQ1-AS1 | c.1529G>A (p.Gly510Asp) c.1886G>A (p.Gly629Asp) c.1505G>A (p.Gly502Asp) c.290G>A (p.Gly97Asp) n.393G>A n.778-7416C>T | gnomAD v4 |
11 | g.2847858G>C | CA379140363 | KCNQ1,KCNQ1-AS1 | c.1529G>C (p.Gly510Ala) c.1886G>C (p.Gly629Ala) c.1505G>C (p.Gly502Ala) c.290G>C (p.Gly97Ala) n.393G>C n.778-7416C>G | gnomAD v4 |
11 | g.2847858G= | CA1948349641 | KCNQ1,KCNQ1-AS1 | c.1529G= (p.Gly510=) c.1886G= (p.Gly629=) c.1505G= (p.Gly502=) c.290G= (p.Gly97=) n.393G= n.778-7416C= | |
11 | g.2847858G>T | CA379140364 | KCNQ1,KCNQ1-AS1 | c.1529G>T (p.Gly510Val) c.1886G>T (p.Gly629Val) c.1505G>T (p.Gly502Val) c.290G>T (p.Gly97Val) n.393G>T n.778-7416C>A | ClinVar dbSNP gnomAD v4 |
11 | g.2847858_2847859delinsGC | CA1948349640 | KCNQ1,KCNQ1-AS1 | c.1529_1530delinsGC (p.Gly510=) c.1886_1887delinsGC (p.Gly629=) c.1505_1506delinsGC (p.Gly502=) c.290_291delinsGC (p.Gly97=) n.393_394delinsGC n.778-7417_778-7416delinsGC | |
11 | g.2847859C>A | CA472466521 | KCNQ1,KCNQ1-AS1 | c.1530C>A (p.Gly510=) c.1887C>A (p.Gly629=) c.1506C>A (p.Gly502=) c.291C>A (p.Gly97=) n.394C>A n.778-7417G>T | gnomAD v4 |
11 | g.2847859C= | CA1948349642 | KCNQ1,KCNQ1-AS1 | c.1530C= (p.Gly510=) c.1887C= (p.Gly629=) c.1506C= (p.Gly502=) c.291C= (p.Gly97=) n.394C= n.778-7417G= | |
11 | g.2847859C>G | CA033594 | KCNQ1,KCNQ1-AS1 | c.1530C>G (p.Gly510=) c.1887C>G (p.Gly629=) c.1506C>G (p.Gly502=) c.291C>G (p.Gly97=) n.394C>G n.778-7417G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.2847859C>T | CA472466524 | KCNQ1,KCNQ1-AS1 | c.1530C>T (p.Gly510=) c.1887C>T (p.Gly629=) c.1506C>T (p.Gly502=) c.291C>T (p.Gly97=) n.394C>T n.778-7417G>A | ClinVar dbSNP gnomAD v4 |
11 | g.2847865dup | CA252591 | KCNQ1,KCNQ1-AS1 | c.1536dup (p.Arg513GlnfsTer20) c.1893dup (p.Arg632GlnfsTer20) c.1512dup (p.Arg505GlnfsTer20) c.297dup (p.Arg100GlnfsTer20) n.400dup n.778-7417dup | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
11 | g.2847863_2847865dup | CA2574728563 | KCNQ1,KCNQ1-AS1 | c.1534_1536dup (p.Pro512_Arg513insPro) c.1891_1893dup (p.Pro631_Arg632insPro) c.1510_1512dup (p.Pro504_Arg505insPro) c.295_297dup (p.Pro99_Arg100insPro) n.398_400dup n.778-7419_778-7417dup | |
11 | g.2847865del | CA006577 | KCNQ1,KCNQ1-AS1 | c.1536del (p.Arg513GlufsTer?) c.1893del (p.Arg632GlufsTer?) c.1512del (p.Arg505GlufsTer?) c.297del (p.Arg100GlufsTer?) n.400del n.778-7417del | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847860C>A | CA033609 | KCNQ1,KCNQ1-AS1 | c.1531C>A (p.Pro511Thr) c.1888C>A (p.Pro630Thr) c.1507C>A (p.Pro503Thr) c.292C>A (p.Pro98Thr) n.395C>A n.778-7418G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847860C= | CA1948349643 | KCNQ1,KCNQ1-AS1 | c.1531C= (p.Pro511=) c.1888C= (p.Pro630=) c.1507C= (p.Pro503=) c.292C= (p.Pro98=) n.395C= n.778-7418G= | |
11 | g.2847860C>G | CA006546 | KCNQ1,KCNQ1-AS1 | c.1531C>G (p.Pro511Ala) c.1888C>G (p.Pro630Ala) c.1507C>G (p.Pro503Ala) c.292C>G (p.Pro98Ala) n.395C>G n.778-7418G>C | ClinVar dbSNP gnomAD v4 |
11 | g.2847860C>T | CA216345218 | KCNQ1,KCNQ1-AS1 | c.1531C>T (p.Pro511Ser) c.1888C>T (p.Pro630Ser) c.1507C>T (p.Pro503Ser) c.292C>T (p.Pro98Ser) n.395C>T n.778-7418G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847861C>A | CA379140365 | KCNQ1,KCNQ1-AS1 | c.1532C>A (p.Pro511His) c.1889C>A (p.Pro630His) c.1508C>A (p.Pro503His) c.293C>A (p.Pro98His) n.396C>A n.778-7419G>T | gnomAD v4 |
11 | g.2847861C>G | CA379140366 | KCNQ1,KCNQ1-AS1 | c.1532C>G (p.Pro511Arg) c.1889C>G (p.Pro630Arg) c.1508C>G (p.Pro503Arg) c.293C>G (p.Pro98Arg) n.396C>G n.778-7419G>C | |
11 | g.2847861C>T | CA379140367 | KCNQ1,KCNQ1-AS1 | c.1532C>T (p.Pro511Leu) c.1889C>T (p.Pro630Leu) c.1508C>T (p.Pro503Leu) c.293C>T (p.Pro98Leu) n.396C>T n.778-7419G>A | gnomAD v4 |
11 | g.2847862C>A | CA472466540 | KCNQ1,KCNQ1-AS1 | c.1533C>A (p.Pro511=) c.1890C>A (p.Pro630=) c.1509C>A (p.Pro503=) c.294C>A (p.Pro98=) n.397C>A n.778-7420G>T | gnomAD v4 |
11 | g.2847862C= | CA1948349645 | KCNQ1,KCNQ1-AS1 | c.1533C= (p.Pro511=) c.1890C= (p.Pro630=) c.1509C= (p.Pro503=) c.294C= (p.Pro98=) n.397C= n.778-7420G= | |
11 | g.2847862C>G | CA472466543 | KCNQ1,KCNQ1-AS1 | c.1533C>G (p.Pro511=) c.1890C>G (p.Pro630=) c.1509C>G (p.Pro503=) c.294C>G (p.Pro98=) n.397C>G n.778-7420G>C | |
11 | g.2847862C>T | CA472466546 | KCNQ1,KCNQ1-AS1 | c.1533C>T (p.Pro511=) c.1890C>T (p.Pro630=) c.1509C>T (p.Pro503=) c.294C>T (p.Pro98=) n.397C>T n.778-7420G>A | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC |
11 | g.2847862_2847882delinsCCCCAGAGAGGGCGGGGCCCA | CA1948349644 | KCNQ1,KCNQ1-AS1 | c.1533_1553delinsCCCCAGAGAGGGCGGGGCCCA (p.Pro511=) c.1890_1910delinsCCCCAGAGAGGGCGGGGCCCA (p.Pro630=) c.1509_1529delinsCCCCAGAGAGGGCGGGGCCCA (p.Pro503=) c.294_314delinsCCCCAGAGAGGGCGGGGCCCA (p.Pro98=) n.397_417delinsCCCCAGAGAGGGCGGGGCCCA n.778-7440_778-7420delinsTGGGCCCCGCCCTCTCTGGGG | |
11 | g.2847863C>A | CA379140368 | KCNQ1,KCNQ1-AS1 | c.1534C>A (p.Pro512Thr) c.1891C>A (p.Pro631Thr) c.1510C>A (p.Pro504Thr) c.295C>A (p.Pro99Thr) n.398C>A n.778-7421G>T | gnomAD v4 |
11 | g.2847863C= | CA1948349646 | KCNQ1,KCNQ1-AS1 | c.1534C= (p.Pro512=) c.1891C= (p.Pro631=) c.1510C= (p.Pro504=) c.295C= (p.Pro99=) n.398C= n.778-7421G= | |
11 | g.2847863C>G | CA379140369 | KCNQ1,KCNQ1-AS1 | c.1534C>G (p.Pro512Ala) c.1891C>G (p.Pro631Ala) c.1510C>G (p.Pro504Ala) c.295C>G (p.Pro99Ala) n.398C>G n.778-7421G>C | ClinVar |
11 | g.2847863C>T | CA379140370 | KCNQ1,KCNQ1-AS1 | c.1534C>T (p.Pro512Ser) c.1891C>T (p.Pro631Ser) c.1510C>T (p.Pro504Ser) c.295C>T (p.Pro99Ser) n.398C>T n.778-7421G>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847864_2847883del | CA006551 | KCNQ1,KCNQ1-AS1 | c.1535_1554del (p.Pro512HisfsTer14) c.1892_1911del (p.Pro631HisfsTer14) c.1511_1530del (p.Pro504HisfsTer14) c.296_315del (p.Pro99HisfsTer14) n.399_418del n.778-7440_778-7421del | ClinVar dbSNP |
11 | g.2847864C>A | CA379140373 | KCNQ1,KCNQ1-AS1 | c.1535C>A (p.Pro512His) c.1892C>A (p.Pro631His) c.1511C>A (p.Pro504His) c.296C>A (p.Pro99His) n.399C>A n.778-7422G>T | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847864C= | CA1948349647 | KCNQ1,KCNQ1-AS1 | c.1535C= (p.Pro512=) c.1892C= (p.Pro631=) c.1511C= (p.Pro504=) c.296C= (p.Pro99=) n.399C= n.778-7422G= | |
11 | g.2847864C>G | CA379140372 | KCNQ1,KCNQ1-AS1 | c.1535C>G (p.Pro512Arg) c.1892C>G (p.Pro631Arg) c.1511C>G (p.Pro504Arg) c.296C>G (p.Pro99Arg) n.399C>G n.778-7422G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847864C>T | CA379140371 | KCNQ1,KCNQ1-AS1 | c.1535C>T (p.Pro512Leu) c.1892C>T (p.Pro631Leu) c.1511C>T (p.Pro504Leu) c.296C>T (p.Pro99Leu) n.399C>T n.778-7422G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
11 | g.2847865C>A | CA472466557 | KCNQ1,KCNQ1-AS1 | c.1536C>A (p.Pro512=) c.1893C>A (p.Pro631=) c.1512C>A (p.Pro504=) c.297C>A (p.Pro99=) n.400C>A n.778-7423G>T | ClinVar gnomAD v4 |
11 | g.2847865C= | CA1948349648 | KCNQ1,KCNQ1-AS1 | c.1536C= (p.Pro512=) c.1893C= (p.Pro631=) c.1512C= (p.Pro504=) c.297C= (p.Pro99=) n.400C= n.778-7423G= | |
11 | g.2847865C>G | CA472466554 | KCNQ1,KCNQ1-AS1 | c.1536C>G (p.Pro512=) c.1893C>G (p.Pro631=) c.1512C>G (p.Pro504=) c.297C>G (p.Pro99=) n.400C>G n.778-7423G>C | |
11 | g.2847865C>T | CA216345225 | KCNQ1,KCNQ1-AS1 | c.1536C>T (p.Pro512=) c.1893C>T (p.Pro631=) c.1512C>T (p.Pro504=) c.297C>T (p.Pro99=) n.400C>T n.778-7423G>A | dbSNP gnomAD v3 gnomAD v4 |
11 | g.2847867_2847884del | CA2612011342 | KCNQ1,KCNQ1-AS1 | c.1538_1555del (p.Arg513_His518del) c.1895_1912del (p.Arg632_His637del) c.1514_1531del (p.Arg505_His510del) c.299_316del (p.Arg100_His105del) n.402_419del n.778-7440_778-7423del | gnomAD v4 |
11 | g.2847866A= | CA2580983519 | KCNQ1,KCNQ1-AS1 | c.1537A= (p.Arg513=) c.1894A= (p.Arg632=) c.1513A= (p.Arg505=) c.298A= (p.Arg100=) n.401A= n.778-7424T= | |
11 | g.2847866A>C | CA472466562 | KCNQ1,KCNQ1-AS1 | c.1537A>C (p.Arg513=) c.1894A>C (p.Arg632=) c.1513A>C (p.Arg505=) c.298A>C (p.Arg100=) n.401A>C n.778-7424T>G | |
11 | g.2847866A>G | CA379140374 | KCNQ1,KCNQ1-AS1 | c.1537A>G (p.Arg513Gly) c.1894A>G (p.Arg632Gly) c.1513A>G (p.Arg505Gly) c.298A>G (p.Arg100Gly) n.401A>G n.778-7424T>C | gnomAD v4 |
11 | g.2847866A>T | CA379140375 | KCNQ1,KCNQ1-AS1 | c.1537A>T (p.Arg513Ter) c.1894A>T (p.Arg632Ter) c.1513A>T (p.Arg505Ter) c.298A>T (p.Arg100Ter) n.401A>T n.778-7424T>A | |
11 | g.2847866dup | CA006566 | KCNQ1,KCNQ1-AS1 | c.1537dup (p.Arg513LysfsTer20) c.1894dup (p.Arg632LysfsTer20) c.1513dup (p.Arg505LysfsTer20) c.298dup (p.Arg100LysfsTer20) n.401dup n.778-7424dup | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.2847867G>A | CA379140376 | KCNQ1,KCNQ1-AS1 | c.1538G>A (p.Arg513Lys) c.1895G>A (p.Arg632Lys) c.1514G>A (p.Arg505Lys) c.299G>A (p.Arg100Lys) n.402G>A n.778-7425C>T | ClinVar dbSNP gnomAD v4 COSMIC COSMIC |
11 | g.2847867G>C | CA379140377 | KCNQ1,KCNQ1-AS1 | c.1538G>C (p.Arg513Thr) c.1895G>C (p.Arg632Thr) c.1514G>C (p.Arg505Thr) c.299G>C (p.Arg100Thr) n.402G>C n.778-7425C>G | gnomAD v4 COSMIC COSMIC |
11 | g.2847867G= | CA1948349649 | KCNQ1,KCNQ1-AS1 | c.1538G= (p.Arg513=) c.1895G= (p.Arg632=) c.1514G= (p.Arg505=) c.299G= (p.Arg100=) n.402G= n.778-7425C= | |
11 | g.2847867G>T | CA379140378 | KCNQ1,KCNQ1-AS1 | c.1538G>T (p.Arg513Ile) c.1895G>T (p.Arg632Ile) c.1514G>T (p.Arg505Ile) c.299G>T (p.Arg100Ile) n.402G>T n.778-7425C>A | gnomAD v4 |
11 | g.2847868A= | CA1948349650 | KCNQ1,KCNQ1-AS1 | c.1539A= (p.Arg513=) c.1896A= (p.Arg632=) c.1515A= (p.Arg505=) c.300A= (p.Arg100=) n.403A= n.778-7426T= | |
11 | g.2847868A>C | CA379140379 | KCNQ1,KCNQ1-AS1 | c.1539A>C (p.Arg513Ser) c.1896A>C (p.Arg632Ser) c.1515A>C (p.Arg505Ser) c.300A>C (p.Arg100Ser) n.403A>C n.778-7426T>G | gnomAD v4 |
11 | g.2847868A>G | CA472466588 | KCNQ1,KCNQ1-AS1 | c.1539A>G (p.Arg513=) c.1896A>G (p.Arg632=) c.1515A>G (p.Arg505=) c.300A>G (p.Arg100=) n.403A>G n.778-7426T>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847868A>T | CA379140380 | KCNQ1,KCNQ1-AS1 | c.1539A>T (p.Arg513Ser) c.1896A>T (p.Arg632Ser) c.1515A>T (p.Arg505Ser) c.300A>T (p.Arg100Ser) n.403A>T n.778-7426T>A | |
11 | g.2847869G>A | CA379140381 | KCNQ1,KCNQ1-AS1 | c.1540G>A (p.Glu514Lys) c.1897G>A (p.Glu633Lys) c.1516G>A (p.Glu506Lys) c.301G>A (p.Glu101Lys) n.404G>A n.778-7427C>T | gnomAD v4 |
11 | g.2847869G>C | CA379140382 | KCNQ1,KCNQ1-AS1 | c.1540G>C (p.Glu514Gln) c.1897G>C (p.Glu633Gln) c.1516G>C (p.Glu506Gln) c.301G>C (p.Glu101Gln) n.404G>C n.778-7427C>G | dbSNP gnomAD v3 gnomAD v4 |
11 | g.2847869G= | CA1948349651 | KCNQ1,KCNQ1-AS1 | c.1540G= (p.Glu514=) c.1897G= (p.Glu633=) c.1516G= (p.Glu506=) c.301G= (p.Glu101=) n.404G= n.778-7427C= | |
11 | g.2847869G>T | CA379140383 | KCNQ1,KCNQ1-AS1 | c.1540G>T (p.Glu514Ter) c.1897G>T (p.Glu633Ter) c.1516G>T (p.Glu506Ter) c.301G>T (p.Glu101Ter) n.404G>T n.778-7427C>A | gnomAD v4 |
11 | g.2847870A>C | CA379140386 | KCNQ1,KCNQ1-AS1 | c.1541A>C (p.Glu514Ala) c.1898A>C (p.Glu633Ala) c.1517A>C (p.Glu506Ala) c.302A>C (p.Glu101Ala) n.405A>C n.778-7428T>G | |
11 | g.2847870A>G | CA379140384 | KCNQ1,KCNQ1-AS1 | c.1541A>G (p.Glu514Gly) c.1898A>G (p.Glu633Gly) c.1517A>G (p.Glu506Gly) c.302A>G (p.Glu101Gly) n.405A>G n.778-7428T>C | |
11 | g.2847870A>T | CA379140385 | KCNQ1,KCNQ1-AS1 | c.1541A>T (p.Glu514Val) c.1898A>T (p.Glu633Val) c.1517A>T (p.Glu506Val) c.302A>T (p.Glu101Val) n.405A>T n.778-7428T>A | |
11 | g.2847871G>A | CA472466601 | KCNQ1,KCNQ1-AS1 | c.1542G>A (p.Glu514=) c.1899G>A (p.Glu633=) c.1518G>A (p.Glu506=) c.303G>A (p.Glu101=) n.406G>A n.778-7429C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847871G>C | CA379140387 | KCNQ1,KCNQ1-AS1 | c.1542G>C (p.Glu514Asp) c.1899G>C (p.Glu633Asp) c.1518G>C (p.Glu506Asp) c.303G>C (p.Glu101Asp) n.406G>C n.778-7429C>G | |
11 | g.2847871G= | CA1948349652 | KCNQ1,KCNQ1-AS1 | c.1542G= (p.Glu514=) c.1899G= (p.Glu633=) c.1518G= (p.Glu506=) c.303G= (p.Glu101=) n.406G= n.778-7429C= | |
11 | g.2847871G>T | CA379140388 | KCNQ1,KCNQ1-AS1 | c.1542G>T (p.Glu514Asp) c.1899G>T (p.Glu633Asp) c.1518G>T (p.Glu506Asp) c.303G>T (p.Glu101Asp) n.406G>T n.778-7429C>A | gnomAD v4 |
11 | g.2847872G>A | CA379140389 | KCNQ1,KCNQ1-AS1 | c.1543G>A (p.Gly515Ser) c.1900G>A (p.Gly634Ser) c.1519G>A (p.Gly507Ser) c.304G>A (p.Gly102Ser) n.407G>A n.778-7430C>T | gnomAD v4 |
11 | g.2847872G>C | CA379140390 | KCNQ1,KCNQ1-AS1 | c.1543G>C (p.Gly515Arg) c.1900G>C (p.Gly634Arg) c.1519G>C (p.Gly507Arg) c.304G>C (p.Gly102Arg) n.407G>C n.778-7430C>G | |
11 | g.2847872G>T | CA379140391 | KCNQ1,KCNQ1-AS1 | c.1543G>T (p.Gly515Cys) c.1900G>T (p.Gly634Cys) c.1519G>T (p.Gly507Cys) c.304G>T (p.Gly102Cys) n.407G>T n.778-7430C>A | gnomAD v4 |
11 | g.2847873G>A | CA379140392 | KCNQ1,KCNQ1-AS1 | c.1544G>A (p.Gly515Asp) c.1901G>A (p.Gly634Asp) c.1520G>A (p.Gly507Asp) c.305G>A (p.Gly102Asp) n.408G>A n.778-7431C>T | gnomAD v4 |
11 | g.2847873G>C | CA379140393 | KCNQ1,KCNQ1-AS1 | c.1544G>C (p.Gly515Ala) c.1901G>C (p.Gly634Ala) c.1520G>C (p.Gly507Ala) c.305G>C (p.Gly102Ala) n.408G>C n.778-7431C>G | |
11 | g.2847873G>T | CA379140394 | KCNQ1,KCNQ1-AS1 | c.1544G>T (p.Gly515Val) c.1901G>T (p.Gly634Val) c.1520G>T (p.Gly507Val) c.305G>T (p.Gly102Val) n.408G>T n.778-7431C>A | gnomAD v4 |
11 | g.2847874C>A | CA472466638 | KCNQ1,KCNQ1-AS1 | c.1545C>A (p.Gly515=) c.1902C>A (p.Gly634=) c.1521C>A (p.Gly507=) c.306C>A (p.Gly102=) n.409C>A n.778-7432G>T | dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847874C= | CA1948349653 | KCNQ1,KCNQ1-AS1 | c.1545C= (p.Gly515=) c.1902C= (p.Gly634=) c.1521C= (p.Gly507=) c.306C= (p.Gly102=) n.409C= n.778-7432G= | |
11 | g.2847874C>G | CA472466641 | KCNQ1,KCNQ1-AS1 | c.1545C>G (p.Gly515=) c.1902C>G (p.Gly634=) c.1521C>G (p.Gly507=) c.306C>G (p.Gly102=) n.409C>G n.778-7432G>C | |
11 | g.2847874C>T | CA033650 | KCNQ1,KCNQ1-AS1 | c.1545C>T (p.Gly515=) c.1902C>T (p.Gly634=) c.1521C>T (p.Gly507=) c.306C>T (p.Gly102=) n.409C>T n.778-7432G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
11 | g.2847875G>A | CA006589 | KCNQ1,KCNQ1-AS1 | c.1546G>A (p.Gly516Arg) c.1903G>A (p.Gly635Arg) c.1522G>A (p.Gly508Arg) c.307G>A (p.Gly103Arg) n.410G>A n.778-7433C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
11 | g.2847875G>C | CA379140396 | KCNQ1,KCNQ1-AS1 | c.1546G>C (p.Gly516Arg) c.1903G>C (p.Gly635Arg) c.1522G>C (p.Gly508Arg) c.307G>C (p.Gly103Arg) n.410G>C n.778-7433C>G | |
11 | g.2847875G= | CA1948349654 | KCNQ1,KCNQ1-AS1 | c.1546G= (p.Gly516=) c.1903G= (p.Gly635=) c.1522G= (p.Gly508=) c.307G= (p.Gly103=) n.410G= n.778-7433C= | |
11 | g.2847875G>T | CA379140395 | KCNQ1,KCNQ1-AS1 | c.1546G>T (p.Gly516Trp) c.1903G>T (p.Gly635Trp) c.1522G>T (p.Gly508Trp) c.307G>T (p.Gly103Trp) n.410G>T n.778-7433C>A | gnomAD v4 |
11 | g.2847878dup | CA658656103 | KCNQ1,KCNQ1-AS1 | c.1549dup (p.Ala517GlyfsTer16) c.1906dup (p.Ala636GlyfsTer16) c.1525dup (p.Ala509GlyfsTer16) c.310dup (p.Ala104GlyfsTer16) n.413dup n.778-7433dup | ClinVar dbSNP gnomAD v4 |
11 | g.2847878del | CA2612011410 | KCNQ1,KCNQ1-AS1 | c.1549del (p.Ala517ProfsTer30) c.1906del (p.Ala636ProfsTer30) c.1525del (p.Ala509ProfsTer30) c.310del (p.Ala104ProfsTer30) n.413del n.778-7433del | gnomAD v4 |
11 | g.2847876G>A | CA216345239 | KCNQ1,KCNQ1-AS1 | c.1547G>A (p.Gly516Glu) c.1904G>A (p.Gly635Glu) c.1523G>A (p.Gly508Glu) c.308G>A (p.Gly103Glu) n.411G>A n.778-7434C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847876G>C | CA379140397 | KCNQ1,KCNQ1-AS1 | c.1547G>C (p.Gly516Ala) c.1904G>C (p.Gly635Ala) c.1523G>C (p.Gly508Ala) c.308G>C (p.Gly103Ala) n.411G>C n.778-7434C>G | |
11 | g.2847876G= | CA1948349655 | KCNQ1,KCNQ1-AS1 | c.1547G= (p.Gly516=) c.1904G= (p.Gly635=) c.1523G= (p.Gly508=) c.308G= (p.Gly103=) n.411G= n.778-7434C= | |
11 | g.2847876G>T | CA379140398 | KCNQ1,KCNQ1-AS1 | c.1547G>T (p.Gly516Val) c.1904G>T (p.Gly635Val) c.1523G>T (p.Gly508Val) c.308G>T (p.Gly103Val) n.411G>T n.778-7434C>A | gnomAD v4 |
11 | g.2847877G>A | CA216345249 | KCNQ1,KCNQ1-AS1 | c.1548G>A (p.Gly516=) c.1905G>A (p.Gly635=) c.1524G>A (p.Gly508=) c.309G>A (p.Gly103=) n.412G>A n.778-7435C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.2847877G>C | CA472466647 | KCNQ1,KCNQ1-AS1 | c.1548G>C (p.Gly516=) c.1905G>C (p.Gly635=) c.1524G>C (p.Gly508=) c.309G>C (p.Gly103=) n.412G>C n.778-7435C>G | |
11 | g.2847877G= | CA1948349656 | KCNQ1,KCNQ1-AS1 | c.1548G= (p.Gly516=) c.1905G= (p.Gly635=) c.1524G= (p.Gly508=) c.309G= (p.Gly103=) n.412G= n.778-7435C= | |
11 | g.2847877G>T | CA472466650 | KCNQ1,KCNQ1-AS1 | c.1548G>T (p.Gly516=) c.1905G>T (p.Gly635=) c.1524G>T (p.Gly508=) c.309G>T (p.Gly103=) n.412G>T n.778-7435C>A | gnomAD v4 |
11 | g.2847878G>A | CA379140399 | KCNQ1,KCNQ1-AS1 | c.1549G>A (p.Ala517Thr) c.1906G>A (p.Ala636Thr) c.1525G>A (p.Ala509Thr) c.310G>A (p.Ala104Thr) n.413G>A n.778-7436C>T | gnomAD v4 |
11 | g.2847878G>C | CA379140400 | KCNQ1,KCNQ1-AS1 | c.1549G>C (p.Ala517Pro) c.1906G>C (p.Ala636Pro) c.1525G>C (p.Ala509Pro) c.310G>C (p.Ala104Pro) n.413G>C n.778-7436C>G | |
11 | g.2847878G>T | CA379140401 | KCNQ1,KCNQ1-AS1 | c.1549G>T (p.Ala517Ser) c.1906G>T (p.Ala636Ser) c.1525G>T (p.Ala509Ser) c.310G>T (p.Ala104Ser) n.413G>T n.778-7436C>A | |
11 | g.2847878_2847879delinsGC | CA1948349657 | KCNQ1,KCNQ1-AS1 | c.1549_1550delinsGC (p.Ala517=) c.1906_1907delinsGC (p.Ala636=) c.1525_1526delinsGC (p.Ala509=) c.310_311delinsGC (p.Ala104=) n.413_414delinsGC n.778-7437_778-7436delinsGC | |
11 | g.2847879C>A | CA379140402 | KCNQ1,KCNQ1-AS1 | c.1550C>A (p.Ala517Asp) c.1907C>A (p.Ala636Asp) c.1526C>A (p.Ala509Asp) c.311C>A (p.Ala104Asp) n.414C>A n.778-7437G>T | gnomAD v4 |
11 | g.2847879C>G | CA379140403 | KCNQ1,KCNQ1-AS1 | c.1550C>G (p.Ala517Gly) c.1907C>G (p.Ala636Gly) c.1526C>G (p.Ala509Gly) c.311C>G (p.Ala104Gly) n.414C>G n.778-7437G>C | |
11 | g.2847879C>T | CA379140404 | KCNQ1,KCNQ1-AS1 | c.1550C>T (p.Ala517Val) c.1907C>T (p.Ala636Val) c.1526C>T (p.Ala509Val) c.311C>T (p.Ala104Val) n.414C>T n.778-7437G>A | gnomAD v4 |
11 | g.2847881del | CA658761312 | KCNQ1,KCNQ1-AS1 | c.1552del (p.His518ThrfsTer29) c.1909del (p.His637ThrfsTer29) c.1528del (p.His510ThrfsTer29) c.313del (p.His105ThrfsTer29) n.416del n.778-7437del | dbSNP gnomAD v3 gnomAD v4 |
11 | g.2847880C>A | CA472466665 | KCNQ1,KCNQ1-AS1 | c.1551C>A (p.Ala517=) c.1908C>A (p.Ala636=) c.1527C>A (p.Ala509=) c.312C>A (p.Ala104=) n.415C>A n.778-7438G>T | gnomAD v4 |
11 | g.2847880C= | CA1948349658 | KCNQ1,KCNQ1-AS1 | c.1551C= (p.Ala517=) c.1908C= (p.Ala636=) c.1527C= (p.Ala509=) c.312C= (p.Ala104=) n.415C= n.778-7438G= | |
11 | g.2847880C>G | CA472466664 | KCNQ1,KCNQ1-AS1 | c.1551C>G (p.Ala517=) c.1908C>G (p.Ala636=) c.1527C>G (p.Ala509=) c.312C>G (p.Ala104=) n.415C>G n.778-7438G>C | ClinVar dbSNP gnomAD v4 |
11 | g.2847880C>T | CA033688 | KCNQ1,KCNQ1-AS1 | c.1551C>T (p.Ala517=) c.1908C>T (p.Ala636=) c.1527C>T (p.Ala509=) c.312C>T (p.Ala104=) n.415C>T n.778-7438G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.2847881C>A | CA379140405 | KCNQ1,KCNQ1-AS1 | c.1552C>A (p.His518Asn) c.1909C>A (p.His637Asn) c.1528C>A (p.His510Asn) c.313C>A (p.His105Asn) n.416C>A n.778-7439G>T | gnomAD v4 |
11 | g.2847881C= | CA1948349659 | KCNQ1,KCNQ1-AS1 | c.1552C= (p.His518=) c.1909C= (p.His637=) c.1528C= (p.His510=) c.313C= (p.His105=) n.416C= n.778-7439G= | |
11 | g.2847881C>G | CA379140406 | KCNQ1,KCNQ1-AS1 | c.1552C>G (p.His518Asp) c.1909C>G (p.His637Asp) c.1528C>G (p.His510Asp) c.313C>G (p.His105Asp) n.416C>G n.778-7439G>C | |
11 | g.2847881C>T | CA379140407 | KCNQ1,KCNQ1-AS1 | c.1552C>T (p.His518Tyr) c.1909C>T (p.His637Tyr) c.1528C>T (p.His510Tyr) c.313C>T (p.His105Tyr) n.416C>T n.778-7439G>A | dbSNP gnomAD v2 gnomAD v4 |
11 | g.2847882A>C | CA379140408 | KCNQ1,KCNQ1-AS1 | c.1553A>C (p.His518Pro) c.1910A>C (p.His637Pro) c.1529A>C (p.His510Pro) c.314A>C (p.His105Pro) n.417A>C n.778-7440T>G | |
11 | g.2847882A>G | CA379140410 | KCNQ1,KCNQ1-AS1 | c.1553A>G (p.His518Arg) c.1910A>G (p.His637Arg) c.1529A>G (p.His510Arg) c.314A>G (p.His105Arg) n.417A>G n.778-7440T>C | gnomAD v4 |
11 | g.2847882A>T | CA379140409 | KCNQ1,KCNQ1-AS1 | c.1553A>T (p.His518Leu) c.1910A>T (p.His637Leu) c.1529A>T (p.His510Leu) c.314A>T (p.His105Leu) n.417A>T n.778-7440T>A | |
11 | g.2847883C>A | CA379140411 | KCNQ1,KCNQ1-AS1 | c.1554C>A (p.His518Gln) c.1911C>A (p.His637Gln) c.1530C>A (p.His510Gln) c.315C>A (p.His105Gln) n.418C>A n.778-7441G>T | gnomAD v4 |
11 | g.2847883C>G | CA379140412 | KCNQ1,KCNQ1-AS1 | c.1554C>G (p.His518Gln) c.1911C>G (p.His637Gln) c.1530C>G (p.His510Gln) c.315C>G (p.His105Gln) n.418C>G n.778-7441G>C | |
11 | g.2847883C>T | CA472466682 | KCNQ1,KCNQ1-AS1 | c.1554C>T (p.His518=) c.1911C>T (p.His637=) c.1530C>T (p.His510=) c.315C>T (p.His105=) n.418C>T n.778-7441G>A | ClinVar dbSNP gnomAD v4 |
11 | g.2847884A= | CA1948349660 | KCNQ1,KCNQ1-AS1 | c.1555A= (p.Ile519=) c.1912A= (p.Ile638=) c.1531A= (p.Ile511=) c.316A= (p.Ile106=) n.419A= n.778-7442T= | |
11 | g.2847884A>C | CA379140413 | KCNQ1,KCNQ1-AS1 | c.1555A>C (p.Ile519Leu) c.1912A>C (p.Ile638Leu) c.1531A>C (p.Ile511Leu) c.316A>C (p.Ile106Leu) n.419A>C n.778-7442T>G | |
11 | g.2847884A>G | CA379140414 | KCNQ1,KCNQ1-AS1 | c.1555A>G (p.Ile519Val) c.1912A>G (p.Ile638Val) c.1531A>G (p.Ile511Val) c.316A>G (p.Ile106Val) n.419A>G n.778-7442T>C | dbSNP gnomAD v4 |
11 | g.2847884A>T | CA379140415 | KCNQ1,KCNQ1-AS1 | c.1555A>T (p.Ile519Phe) c.1912A>T (p.Ile638Phe) c.1531A>T (p.Ile511Phe) c.316A>T (p.Ile106Phe) n.419A>T n.778-7442T>A | gnomAD v4 |
11 | g.2847885T>A | CA379140416 | KCNQ1,KCNQ1-AS1 | c.1556T>A (p.Ile519Asn) c.1913T>A (p.Ile638Asn) c.1532T>A (p.Ile511Asn) c.317T>A (p.Ile106Asn) n.420T>A n.778-7443A>T | gnomAD v4 |
11 | g.2847885T>C | CA379140417 | KCNQ1,KCNQ1-AS1 | c.1556T>C (p.Ile519Thr) c.1913T>C (p.Ile638Thr) c.1532T>C (p.Ile511Thr) c.317T>C (p.Ile106Thr) n.420T>C n.778-7443A>G | gnomAD v4 |
11 | g.2847885T>G | CA379140418 | KCNQ1,KCNQ1-AS1 | c.1556T>G (p.Ile519Ser) c.1913T>G (p.Ile638Ser) c.1532T>G (p.Ile511Ser) c.317T>G (p.Ile106Ser) n.420T>G n.778-7443A>C | |
11 | g.2847886C>A | CA472466701 | KCNQ1,KCNQ1-AS1 | c.1557C>A (p.Ile519=) c.1914C>A (p.Ile638=) c.1533C>A (p.Ile511=) c.318C>A (p.Ile106=) n.421C>A n.778-7444G>T | gnomAD v4 |
11 | g.2847886C>G | CA379140419 | KCNQ1,KCNQ1-AS1 | c.1557C>G (p.Ile519Met) c.1914C>G (p.Ile638Met) c.1533C>G (p.Ile511Met) c.318C>G (p.Ile106Met) n.421C>G n.778-7444G>C | |
11 | g.2847886C>T | CA472466705 | KCNQ1,KCNQ1-AS1 | c.1557C>T (p.Ile519=) c.1914C>T (p.Ile638=) c.1533C>T (p.Ile511=) c.318C>T (p.Ile106=) n.421C>T n.778-7444G>A | gnomAD v4 |
11 | g.2847887A= | CA1948349661 | KCNQ1,KCNQ1-AS1 | c.1558A= (p.Thr520=) c.1915A= (p.Thr639=) c.1534A= (p.Thr512=) c.319A= (p.Thr107=) n.422A= n.778-7445T= | |
11 | g.2847887A>C | CA379140422 | KCNQ1,KCNQ1-AS1 | c.1558A>C (p.Thr520Pro) c.1915A>C (p.Thr639Pro) c.1534A>C (p.Thr512Pro) c.319A>C (p.Thr107Pro) n.422A>C n.778-7445T>G | dbSNP gnomAD v4 |
11 | g.2847887A>G | CA379140421 | KCNQ1,KCNQ1-AS1 | c.1558A>G (p.Thr520Ala) c.1915A>G (p.Thr639Ala) c.1534A>G (p.Thr512Ala) c.319A>G (p.Thr107Ala) n.422A>G n.778-7445T>C | |
11 | g.2847887A>T | CA379140420 | KCNQ1,KCNQ1-AS1 | c.1558A>T (p.Thr520Ser) c.1915A>T (p.Thr639Ser) c.1534A>T (p.Thr512Ser) c.319A>T (p.Thr107Ser) n.422A>T n.778-7445T>A |