Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.7568464A>C | CA362676338 | DSP | c.1294A>C (p.Lys432Gln) n.1479A>C | |
6 | g.7568464A>G | CA362676339 | DSP | c.1294A>G (p.Lys432Glu) n.1479A>G | gnomAD v4 |
6 | g.7568464A>T | CA362676340 | DSP | c.1294A>T (p.Lys432Ter) n.1479A>T | |
6 | g.7568465A>C | CA362676341 | DSP | c.1295A>C (p.Lys432Thr) n.1480A>C | |
6 | g.7568465A>G | CA362676342 | DSP | c.1295A>G (p.Lys432Arg) n.1480A>G | |
6 | g.7568465A>T | CA362676343 | DSP | c.1295A>T (p.Lys432Met) n.1480A>T | |
6 | g.7568466G>A | CA448521769 | DSP | c.1296G>A (p.Lys432=) n.1481G>A | gnomAD v4 |
6 | g.7568466G>C | CA362676344 | DSP | c.1296G>C (p.Lys432Asn) n.1481G>C | |
6 | g.7568466G>T | CA362676345 | DSP | c.1296G>T (p.Lys432Asn) n.1481G>T | |
6 | g.7568467C>A | CA362676346 | DSP | c.1297C>A (p.Arg433Ser) n.1482C>A | |
6 | g.7568467C= | CA1608622917 | DSP | c.1297C= (p.Arg433=) n.1482C= | |
6 | g.7568467C>G | CA362676347 | DSP | c.1297C>G (p.Arg433Gly) n.1482C>G | |
6 | g.7568467C>T | CA027596 | DSP | c.1297C>T (p.Arg433Cys) n.1482C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7568468G>A | CA027614 | DSP | c.1298G>A (p.Arg433His) n.1483G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.7568468G>C | CA362676348 | DSP | c.1298G>C (p.Arg433Pro) n.1483G>C | |
6 | g.7568468G= | CA1608622920 | DSP | c.1298G= (p.Arg433=) n.1483G= | |
6 | g.7568468G>T | CA362676349 | DSP | c.1298G>T (p.Arg433Leu) n.1483G>T | dbSNP gnomAD v3 gnomAD v4 |
6 | g.7568469T>A | CA448521777 | DSP | c.1299T>A (p.Arg433=) n.1484T>A | |
6 | g.7568469T>C | CA448521778 | DSP | c.1299T>C (p.Arg433=) n.1484T>C | gnomAD v4 |
6 | g.7568469T>G | CA448521780 | DSP | c.1299T>G (p.Arg433=) n.1484T>G | |
6 | g.7568470C>A | CA362676350 | DSP | c.1300C>A (p.Gln434Lys) n.1485C>A | |
6 | g.7568470C>G | CA362676351 | DSP | c.1300C>G (p.Gln434Glu) n.1485C>G | |
6 | g.7568470C>T | CA362676352 | DSP | c.1300C>T (p.Gln434Ter) n.1485C>T | gnomAD v4 |
6 | g.7568471A>C | CA362676353 | DSP | c.1301A>C (p.Gln434Pro) n.1486A>C | gnomAD v4 |
6 | g.7568471A>G | CA362676354 | DSP | c.1301A>G (p.Gln434Arg) n.1486A>G | |
6 | g.7568471A>T | CA362676355 | DSP | c.1301A>T (p.Gln434Leu) n.1486A>T | |
6 | g.7568472G>A | CA448521787 | DSP | c.1302G>A (p.Gln434=) n.1487G>A | ClinVar dbSNP gnomAD v2 |
6 | g.7568472G>C | CA362676356 | DSP | c.1302G>C (p.Gln434His) n.1487G>C | dbSNP gnomAD v3 gnomAD v4 |
6 | g.7568472G= | CA1608622923 | DSP | c.1302G= (p.Gln434=) n.1487G= | |
6 | g.7568472G>T | CA362676357 | DSP | c.1302G>T (p.Gln434His) n.1487G>T | |
6 | g.7568473G>A | CA362676358 | DSP | c.1303G>A (p.Val435Met) n.1488G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7568473G>C | CA362676359 | DSP | c.1303G>C (p.Val435Leu) n.1488G>C | |
6 | g.7568473G= | CA1608622926 | DSP | c.1303G= (p.Val435=) n.1488G= | |
6 | g.7568473G>T | CA362676360 | DSP | c.1303G>T (p.Val435Leu) n.1488G>T | |
6 | g.7568474T>A | CA362676363 | DSP | c.1304T>A (p.Val435Glu) n.1489T>A | |
6 | g.7568474T>C | CA362676362 | DSP | c.1304T>C (p.Val435Ala) n.1489T>C | |
6 | g.7568474T>G | CA362676361 | DSP | c.1304T>G (p.Val435Gly) n.1489T>G | |
6 | g.7568475G>A | CA448521800 | DSP | c.1305G>A (p.Val435=) n.1490G>A | |
6 | g.7568475G>C | CA448521799 | DSP | c.1305G>C (p.Val435=) n.1490G>C | |
6 | g.7568475G>T | CA448521797 | DSP | c.1305G>T (p.Val435=) n.1490G>T | |
6 | g.7568476C>A | CA362676364 | DSP | c.1306C>A (p.Gln436Lys) n.1491C>A | |
6 | g.7568476C>G | CA362676365 | DSP | c.1306C>G (p.Gln436Glu) n.1491C>G | |
6 | g.7568476C>T | CA362676366 | DSP | c.1306C>T (p.Gln436Ter) n.1491C>T | |
6 | g.7568477A>C | CA362676367 | DSP | c.1307A>C (p.Gln436Pro) n.1492A>C | |
6 | g.7568477A>G | CA362676368 | DSP | c.1307A>G (p.Gln436Arg) n.1492A>G | dbSNP |
6 | g.7568477A>T | CA362676369 | DSP | c.1307A>T (p.Gln436Leu) n.1492A>T | |
6 | g.7568478G>A | CA16605129 | DSP | c.1308G>A (p.Gln436=) n.1493G>A | ClinVar dbSNP |
6 | g.7568478G>C | CA362676370 | DSP | c.1308G>C (p.Gln436His) n.1493G>C | ClinVar dbSNP gnomAD v4 |
6 | g.7568478G= | CA1608622932 | DSP | c.1308G= (p.Gln436=) n.1493G= | |
6 | g.7568478G>T | CA362676371 | DSP | c.1308G>T (p.Gln436His) n.1493G>T | |
6 | g.7568479A>C | CA362676372 | DSP | c.1309A>C (p.Asn437His) n.1494A>C | |
6 | g.7568479A>G | CA362676373 | DSP | c.1309A>G (p.Asn437Asp) n.1494A>G | |
6 | g.7568479A>T | CA362676374 | DSP | c.1309A>T (p.Asn437Tyr) n.1494A>T | |
6 | g.7568480A>C | CA362676375 | DSP | c.1310A>C (p.Asn437Thr) n.1495A>C | |
6 | g.7568480A>G | CA362676377 | DSP | c.1310A>G (p.Asn437Ser) n.1495A>G | ClinVar dbSNP COSMIC |
6 | g.7568480A>T | CA362676379 | DSP | c.1310A>T (p.Asn437Ile) n.1495A>T | |
6 | g.7568481C>A | CA362676381 | DSP | c.1311C>A (p.Asn437Lys) n.1496C>A | |
6 | g.7568481C>G | CA362676383 | DSP | c.1311C>G (p.Asn437Lys) n.1496C>G | |
6 | g.7568481C>T | CA448521818 | DSP | c.1311C>T (p.Asn437=) n.1496C>T | |
6 | g.7568482T>A | CA362676385 | DSP | c.1312T>A (p.Leu438Met) n.1497T>A | |
6 | g.7568482T>C | CA448521822 | DSP | c.1312T>C (p.Leu438=) n.1497T>C | |
6 | g.7568482T>G | CA362676386 | DSP | c.1312T>G (p.Leu438Val) n.1497T>G | |
6 | g.7568483T>A | CA362676388 | DSP | c.1313T>A (p.Leu438Ter) n.1498T>A | |
6 | g.7568483T>C | CA362676390 | DSP | c.1313T>C (p.Leu438Ser) n.1498T>C | |
6 | g.7568483T>G | CA362676389 | DSP | c.1313T>G (p.Leu438Trp) n.1498T>G | |
6 | g.7568484G>A | CA448521828 | DSP | c.1314G>A (p.Leu438=) n.1499G>A | |
6 | g.7568484G>C | CA362676394 | DSP | c.1314G>C (p.Leu438Phe) n.1499G>C | |
6 | g.7568484G>T | CA362676395 | DSP | c.1314G>T (p.Leu438Phe) n.1499G>T | |
6 | g.7568485G>A | CA004888 | DSP | c.1315G>A (p.Val439Ile) n.1500G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.7568485G>C | CA362676398 | DSP | c.1315G>C (p.Val439Leu) n.1500G>C | |
6 | g.7568485G= | CA1608622940 | DSP | c.1315G= (p.Val439=) n.1500G= | |
6 | g.7568485G>T | CA362676400 | DSP | c.1315G>T (p.Val439Leu) n.1500G>T | |
6 | g.7568486T>A | CA362676402 | DSP | c.1316T>A (p.Val439Glu) n.1501T>A | |
6 | g.7568486T>C | CA362676404 | DSP | c.1316T>C (p.Val439Ala) n.1501T>C | |
6 | g.7568486T>G | CA362676407 | DSP | c.1316T>G (p.Val439Gly) n.1501T>G | |
6 | g.7568487A>C | CA448521838 | DSP | c.1317A>C (p.Val439=) n.1502A>C | |
6 | g.7568487A>G | CA448521835 | DSP | c.1317A>G (p.Val439=) n.1502A>G | |
6 | g.7568487A>T | CA448521836 | DSP | c.1317A>T (p.Val439=) n.1502A>T | |
6 | g.7568488_7568501del | CA2573334497 | DSP | c.1318_1331del (p.Asn440AspfsTer8) | |
6 | g.7568488A>C | CA362676409 | DSP | c.1318A>C (p.Asn440His) n.1503A>C | |
6 | g.7568488A>G | CA362676412 | DSP | c.1318A>G (p.Asn440Asp) n.1503A>G | |
6 | g.7568488A>T | CA362676414 | DSP | c.1318A>T (p.Asn440Tyr) n.1503A>T | |
6 | g.7568489A>C | CA362676417 | DSP | c.1319A>C (p.Asn440Thr) n.1504A>C | |
6 | g.7568489A>G | CA362676419 | DSP | c.1319A>G (p.Asn440Ser) n.1504A>G | |
6 | g.7568489A>T | CA362676420 | DSP | c.1319A>T (p.Asn440Ile) n.1504A>T | |
6 | g.7568490C>A | CA362676421 | DSP | c.1320C>A (p.Asn440Lys) n.1505C>A | |
6 | g.7568490C= | CA1608622946 | DSP | c.1320C= (p.Asn440=) n.1505C= | |
6 | g.7568490C>G | CA362676423 | DSP | c.1320C>G (p.Asn440Lys) n.1505C>G | dbSNP |
6 | g.7568490C>T | CA448521847 | DSP | c.1320C>T (p.Asn440=) n.1505C>T | |
6 | g.7568491A>C | CA362676425 | DSP | c.1321A>C (p.Lys441Gln) n.1506A>C | |
6 | g.7568491A>G | CA362676426 | DSP | c.1321A>G (p.Lys441Glu) n.1506A>G | |
6 | g.7568491A>T | CA362676428 | DSP | c.1321A>T (p.Lys441Ter) n.1506A>T | |
6 | g.7568492A>C | CA362676430 | DSP | c.1322A>C (p.Lys441Thr) n.1507A>C | |
6 | g.7568492A>G | CA362676431 | DSP | c.1322A>G (p.Lys441Arg) n.1507A>G | |
6 | g.7568492A>T | CA362676433 | DSP | c.1322A>T (p.Lys441Met) n.1507A>T | |
6 | g.7568493G>A | CA448521858 | DSP | c.1323G>A (p.Lys441=) n.1508G>A | gnomAD v4 |
6 | g.7568493G>C | CA133956074 | DSP | c.1323G>C (p.Lys441Asn) n.1508G>C | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7568493G= | CA1608622951 | DSP | c.1323G= (p.Lys441=) n.1508G= | |
6 | g.7568493G>T | CA362676435 | DSP | c.1323G>T (p.Lys441Asn) n.1508G>T | |
6 | g.7568494T>A | CA362676436 | DSP | c.1324T>A (p.Ser442Thr) | |
6 | g.7568494T>C | CA362676437 | DSP | c.1324T>C (p.Ser442Pro) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7568494T>G | CA027687 | DSP | c.1324T>G (p.Ser442Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7568494T= | CA1608622967 | DSP | c.1324T= (p.Ser442=) | |
6 | g.7568495C>A | CA362676441 | DSP | c.1325C>A (p.Ser442Tyr) | |
6 | g.7568495C= | CA1608622976 | DSP | c.1325C= (p.Ser442=) | |
6 | g.7568495C>G | CA362676442 | DSP | c.1325C>G (p.Ser442Cys) | |
6 | g.7568495C>T | CA362676439 | DSP | c.1325C>T (p.Ser442Phe) | ClinVar dbSNP |
6 | g.7568496T>A | CA448521867 | DSP | c.1326T>A (p.Ser442=) | |
6 | g.7568496T>C | CA448521869 | DSP | c.1326T>C (p.Ser442=) | |
6 | g.7568496T>G | CA448521871 | DSP | c.1326T>G (p.Ser442=) | |
6 | g.7568497A>C | CA362676443 | DSP | c.1327A>C (p.Lys443Gln) | |
6 | g.7568497A>G | CA362676445 | DSP | c.1327A>G (p.Lys443Glu) | |
6 | g.7568497A>T | CA362676446 | DSP | c.1327A>T (p.Lys443Ter) | |
6 | g.7568498A= | CA1608622980 | DSP | c.1328A= (p.Lys443=) | |
6 | g.7568498A>C | CA362676447 | DSP | c.1328A>C (p.Lys443Thr) | |
6 | g.7568498A>G | CA362676449 | DSP | c.1328A>G (p.Lys443Arg) | gnomAD v4 |
6 | g.7568498A>T | CA362676450 | DSP | c.1328A>T (p.Lys443Met) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.7568499G>A | CA027703 | DSP | c.1329G>A (p.Lys443=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.7568499G>C | CA362676452 | DSP | c.1329G>C (p.Lys443Asn) | |
6 | g.7568499G= | CA1608622987 | DSP | c.1329G= (p.Lys443=) | |
6 | g.7568499G>T | CA362676454 | DSP | c.1329G>T (p.Lys443Asn) | |
6 | g.7568500A>C | CA362676456 | DSP | c.1330A>C (p.Lys444Gln) | |
6 | g.7568500A>G | CA362676458 | DSP | c.1330A>G (p.Lys444Glu) | |
6 | g.7568500A>T | CA362676459 | DSP | c.1330A>T (p.Lys444Ter) | |
6 | g.7568501A= | CA1608622989 | DSP | c.1331A= (p.Lys444=) | |
6 | g.7568501A>C | CA362676463 | DSP | c.1331A>C (p.Lys444Thr) | ClinVar dbSNP |
6 | g.7568501A>G | CA362676460 | DSP | c.1331A>G (p.Lys444Arg) | |
6 | g.7568501A>T | CA362676461 | DSP | c.1331A>T (p.Lys444Met) | |
6 | g.7568502G>A | CA448521888 | DSP | c.1332G>A (p.Lys444=) | |
6 | g.7568502G>C | CA362676465 | DSP | c.1332G>C (p.Lys444Asn) | |
6 | g.7568502G>T | CA362676466 | DSP | c.1332G>T (p.Lys444Asn) | |
6 | g.7568503A= | CA1608622996 | DSP | c.1333A= (p.Ile445=) | |
6 | g.7568503A>C | CA362676467 | DSP | c.1333A>C (p.Ile445Leu) | |
6 | g.7568503A>G | CA133956077 | DSP | c.1333A>G (p.Ile445Val) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.7568503A>T | CA362676468 | DSP | c.1333A>T (p.Ile445Phe) | |
6 | g.7568504T>A | CA362676470 | DSP | c.1334T>A (p.Ile445Asn) | |
6 | g.7568504T>C | CA362676471 | DSP | c.1334T>C (p.Ile445Thr) | gnomAD v4 |
6 | g.7568504T>G | CA362676473 | DSP | c.1334T>G (p.Ile445Ser) | |
6 | g.7568505T>A | CA448521901 | DSP | c.1335T>A (p.Ile445=) | dbSNP |
6 | g.7568505T>C | CA448521903 | DSP | c.1335T>C (p.Ile445=) | |
6 | g.7568505T>G | CA133956079 | DSP | c.1335T>G (p.Ile445Met) | ClinVar dbSNP |
6 | g.7568505T= | CA1608623027 | DSP | c.1335T= (p.Ile445=) | |
6 | g.7568506G>A | CA362676475 | DSP | c.1336G>A (p.Val446Ile) | gnomAD v4 |
6 | g.7568506G>C | CA362676476 | DSP | c.1336G>C (p.Val446Leu) | |
6 | g.7568506G>T | CA362676478 | DSP | c.1336G>T (p.Val446Leu) | |
6 | g.7568507T>A | CA362676481 | DSP | c.1337T>A (p.Val446Glu) | |
6 | g.7568507T>C | CA362676480 | DSP | c.1337T>C (p.Val446Ala) | |
6 | g.7568507T>G | CA362676479 | DSP | c.1337T>G (p.Val446Gly) | |
6 | g.7568508A>C | CA448521912 | DSP | c.1338A>C (p.Val446=) | |
6 | g.7568508A>G | CA448521914 | DSP | c.1338A>G (p.Val446=) | gnomAD v4 |
6 | g.7568508A>T | CA448521916 | DSP | c.1338A>T (p.Val446=) | |
6 | g.7568509C>A | CA362676482 | DSP | c.1339C>A (p.Gln447Lys) | |
6 | g.7568509C>G | CA362676486 | DSP | c.1339C>G (p.Gln447Glu) | |
6 | g.7568509C>T | CA362676483 | DSP | c.1339C>T (p.Gln447Ter) | ClinVar dbSNP |
6 | g.7568510A>C | CA362676490 | DSP | c.1340A>C (p.Gln447Pro) | |
6 | g.7568510A>G | CA362676495 | DSP | c.1340A>G (p.Gln447Arg) | |
6 | g.7568510A>T | CA362676497 | DSP | c.1340A>T (p.Gln447Leu) | |
6 | g.7568511G>A | CA448521923 | DSP | c.1341G>A (p.Gln447=) | |
6 | g.7568511G>C | CA362676499 | DSP | c.1341G>C (p.Gln447His) | |
6 | g.7568511G>T | CA362676501 | DSP | c.1341G>T (p.Gln447His) | |
6 | g.7568512C>A | CA362676503 | DSP | c.1342C>A (p.Leu448Met) | |
6 | g.7568512C>G | CA362676504 | DSP | c.1342C>G (p.Leu448Val) | gnomAD v4 |
6 | g.7568512C>T | CA448521929 | DSP | c.1342C>T (p.Leu448=) | |
6 | g.7568513T>A | CA362676511 | DSP | c.1343T>A (p.Leu448Gln) | |
6 | g.7568513T>C | CA362676513 | DSP | c.1343T>C (p.Leu448Pro) | |
6 | g.7568513T>G | CA362676514 | DSP | c.1343T>G (p.Leu448Arg) | |
6 | g.7568514G>A | CA004898 | DSP | c.1344G>A (p.Leu448=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7568514G>C | CA448521937 | DSP | c.1344G>C (p.Leu448=) | |
6 | g.7568514G= | CA1608623034 | DSP | c.1344G= (p.Leu448=) | |
6 | g.7568514G>T | CA448521935 | DSP | c.1344G>T (p.Leu448=) | |
6 | g.7568515A>C | CA362676518 | DSP | c.1345A>C (p.Lys449Gln) | |
6 | g.7568515A>G | CA362676517 | DSP | c.1345A>G (p.Lys449Glu) | |
6 | g.7568515A>T | CA362676516 | DSP | c.1345A>T (p.Lys449Ter) | |
6 | g.7568516A= | CA1608623040 | DSP | c.1346A= (p.Lys449=) | |
6 | g.7568516A>C | CA362676519 | DSP | c.1346A>C (p.Lys449Thr) | dbSNP gnomAD v4 |
6 | g.7568516A>G | CA133956085 | DSP | c.1346A>G (p.Lys449Arg) | dbSNP gnomAD v4 |
6 | g.7568516A>T | CA362676520 | DSP | c.1346A>T (p.Lys449Met) | |
6 | g.7568517G>A | CA448521947 | DSP | c.1347G>A (p.Lys449=) | gnomAD v4 |
6 | g.7568517G>C | CA362676522 | DSP | c.1347G>C (p.Lys449Asn) | |
6 | g.7568517G>T | CA362676523 | DSP | c.1347G>T (p.Lys449Asn) | |
6 | g.7568518C>A | CA362676525 | DSP | c.1348C>A (p.Pro450Thr) | |
6 | g.7568518C= | CA1608623047 | DSP | c.1348C= (p.Pro450=) | |
6 | g.7568518C>G | CA351976 | DSP | c.1348C>G (p.Pro450Ala) | ClinVar dbSNP |
6 | g.7568518C>T | CA362676528 | DSP | c.1348C>T (p.Pro450Ser) | |
6 | g.7568519C>A | CA362676530 | DSP | c.1349C>A (p.Pro450His) | |
6 | g.7568519C= | CA1608623054 | DSP | c.1349C= (p.Pro450=) | |
6 | g.7568519C>G | CA362676531 | DSP | c.1349C>G (p.Pro450Arg) | |
6 | g.7568519C>T | CA027738 | DSP | c.1349C>T (p.Pro450Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7568520T>A | CA448521958 | DSP | c.1350T>A (p.Pro450=) | |
6 | g.7568520T>C | CA448521960 | DSP | c.1350T>C (p.Pro450=) | |
6 | g.7568520T>G | CA448521961 | DSP | c.1350T>G (p.Pro450=) | |
6 | g.7568520T= | CA1608623060 | DSP | c.1350T= (p.Pro450=) | |
6 | g.7568520_7568521insTTA | CA915944141 | DSP | c.1350_1351insTTA (p.Pro450_Arg451insLeu) | ClinVar dbSNP |
6 | g.7568521C>A | CA362676534 | DSP | c.1351C>A (p.Arg451Ser) | ClinVar |
6 | g.7568521C= | CA1608623065 | DSP | c.1351C= (p.Arg451=) | |
6 | g.7568521C>G | CA362676532 | DSP | c.1351C>G (p.Arg451Gly) | ClinVar dbSNP gnomAD v4 |
6 | g.7568521C>T | CA16042676 | DSP | c.1351C>T (p.Arg451Cys) | ClinVar dbSNP COSMIC |
6 | g.7568522G>A | CA004905 | DSP | c.1352G>A (p.Arg451His) | ClinVar dbSNP gnomAD v4 COSMIC |
6 | g.7568522G>C | CA362676535 | DSP | c.1352G>C (p.Arg451Pro) | ClinVar |
6 | g.7568522G= | CA1608623075 | DSP | c.1352G= (p.Arg451=) | |
6 | g.7568522G>T | CA362676536 | DSP | c.1352G>T (p.Arg451Leu) | ClinVar dbSNP |
6 | g.7568523T>A | CA448521969 | DSP | c.1353T>A (p.Arg451=) | |
6 | g.7568523T>C | CA448521972 | DSP | c.1353T>C (p.Arg451=) | |
6 | g.7568523T>G | CA448521974 | DSP | c.1353T>G (p.Arg451=) | |
6 | g.7568524A>C | CA362676538 | DSP | c.1354A>C (p.Asn452His) | |
6 | g.7568524A>G | CA362676539 | DSP | c.1354A>G (p.Asn452Asp) | |
6 | g.7568524A>T | CA362676540 | DSP | c.1354A>T (p.Asn452Tyr) | |
6 | g.7568525A>C | CA362676545 | DSP | c.1355A>C (p.Asn452Thr) | |
6 | g.7568525A>G | CA362676542 | DSP | c.1355A>G (p.Asn452Ser) | |
6 | g.7568525A>T | CA362676544 | DSP | c.1355A>T (p.Asn452Ile) | |
6 | g.7568526C>A | CA362676547 | DSP | c.1356C>A (p.Asn452Lys) | |
6 | g.7568526C= | CA1608623080 | DSP | c.1356C= (p.Asn452=) | |
6 | g.7568526C>G | CA362676548 | DSP | c.1356C>G (p.Asn452Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7568526C>T | CA448521981 | DSP | c.1356C>T (p.Asn452=) | ClinVar dbSNP |
6 | g.7568527C>A | CA362676550 | DSP | c.1357C>A (p.Pro453Thr) | ClinVar |
6 | g.7568527C= | CA1608623087 | DSP | c.1357C= (p.Pro453=) | |
6 | g.7568527C>G | CA362676551 | DSP | c.1357C>G (p.Pro453Ala) | |
6 | g.7568527C>T | CA362676552 | DSP | c.1357C>T (p.Pro453Ser) | ClinVar dbSNP gnomAD v4 |
6 | g.7568528C>A | CA362676553 | DSP | c.1358C>A (p.Pro453Gln) | |
6 | g.7568528C>G | CA362676555 | DSP | c.1358C>G (p.Pro453Arg) | |
6 | g.7568528C>T | CA362676554 | DSP | c.1358C>T (p.Pro453Leu) | |
6 | g.7568529A= | CA1608623089 | DSP | c.1359A= (p.Pro453=) | |
6 | g.7568529A>C | CA448521988 | DSP | c.1359A>C (p.Pro453=) | |
6 | g.7568529A>G | CA448521989 | DSP | c.1359A>G (p.Pro453=) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.7568529A>T | CA448521990 | DSP | c.1359A>T (p.Pro453=) | |
6 | g.7568530G>A | CA362676557 | DSP | c.1360G>A (p.Asp454Asn) | |
6 | g.7568530G>C | CA362676559 | DSP | c.1360G>C (p.Asp454His) | |
6 | g.7568530G>T | CA362676560 | DSP | c.1360G>T (p.Asp454Tyr) | COSMIC |
6 | g.7568531A= | CA1608623091 | DSP | c.1361A= (p.Asp454=) | |
6 | g.7568531A>C | CA362676561 | DSP | c.1361A>C (p.Asp454Ala) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.7568531A>G | CA362676562 | DSP | c.1361A>G (p.Asp454Gly) | |
6 | g.7568531A>T | CA362676563 | DSP | c.1361A>T (p.Asp454Val) | |
6 | g.7568532C>A | CA027756 | DSP | c.1362C>A (p.Asp454Glu) | dbSNP ExAC gnomAD v2 |
6 | g.7568532C= | CA1608623096 | DSP | c.1362C= (p.Asp454=) | |
6 | g.7568532C>G | CA362676566 | DSP | c.1362C>G (p.Asp454Glu) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.7568532C>T | CA448521996 | DSP | c.1362C>T (p.Asp454=) | ClinVar dbSNP |
6 | g.7568533T>A | CA362676567 | DSP | c.1363T>A (p.Tyr455Asn) | |
6 | g.7568533T>C | CA362676569 | DSP | c.1363T>C (p.Tyr455His) | |
6 | g.7568533T>G | CA362676571 | DSP | c.1363T>G (p.Tyr455Asp) | |
6 | g.7568534A= | CA1608623100 | DSP | c.1364A= (p.Tyr455=) | |
6 | g.7568534A>C | CA362676576 | DSP | c.1364A>C (p.Tyr455Ser) | |
6 | g.7568534A>G | CA362676577 | DSP | c.1364A>G (p.Tyr455Cys) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.7568534A>T | CA362676573 | DSP | c.1364A>T (p.Tyr455Phe) | |
6 | g.7568535C>A | CA362676580 | DSP | c.1365C>A (p.Tyr455Ter) | |
6 | g.7568535C>G | CA362676579 | DSP | c.1365C>G (p.Tyr455Ter) | |
6 | g.7568535C>T | CA448522014 | DSP | c.1365C>T (p.Tyr455=) | |
6 | g.7568536A= | CA1608623116 | DSP | c.1366A= (p.Arg456=) | |
6 | g.7568536A>C | CA448522016 | DSP | c.1366A>C (p.Arg456=) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.7568536A>G | CA362676581 | DSP | c.1366A>G (p.Arg456Gly) | |
6 | g.7568536A>T | CA362676582 | DSP | c.1366A>T (p.Arg456Ter) | |
6 | g.7568537G>A | CA362676583 | DSP | c.1367G>A (p.Arg456Lys) | |
6 | g.7568537G>C | CA362676584 | DSP | c.1367G>C (p.Arg456Thr) | |
6 | g.7568537G>T | CA362676586 | DSP | c.1367G>T (p.Arg456Ile) | |
6 | g.7568538A>C | CA362676587 | DSP | c.1368A>C (p.Arg456Ser) | |
6 | g.7568538A>G | CA448522021 | DSP | c.1368A>G (p.Arg456=) | |
6 | g.7568538A>T | CA362676588 | DSP | c.1368A>T (p.Arg456Ser) | |
6 | g.7568539A>C | CA362676589 | DSP | c.1369A>C (p.Ser457Arg) | |
6 | g.7568539A>G | CA362676590 | DSP | c.1369A>G (p.Ser457Gly) | |
6 | g.7568539A>T | CA362676591 | DSP | c.1369A>T (p.Ser457Cys) | |
6 | g.7568540G>A | CA362676592 | DSP | c.1370G>A (p.Ser457Asn) | |
6 | g.7568540G>C | CA362676593 | DSP | c.1370G>C (p.Ser457Thr) | |
6 | g.7568540G>T | CA362676594 | DSP | c.1370G>T (p.Ser457Ile) | |
6 | g.7568541C>A | CA362676597 | DSP | c.1371C>A (p.Ser457Arg) | gnomAD v4 |
6 | g.7568541C>G | CA362676595 | DSP | c.1371C>G (p.Ser457Arg) | |
6 | g.7568541C>T | CA448522042 | DSP | c.1371C>T (p.Ser457=) | |
6 | g.7568542A= | CA1608623121 | DSP | c.1372A= (p.Asn458=) | |
6 | g.7568542A>C | CA362676599 | DSP | c.1372A>C (p.Asn458His) | dbSNP |
6 | g.7568542A>G | CA362676601 | DSP | c.1372A>G (p.Asn458Asp) | |
6 | g.7568542A>T | CA362676602 | DSP | c.1372A>T (p.Asn458Tyr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.7568543A>C | CA362676603 | DSP | c.1373A>C (p.Asn458Thr) | |
6 | g.7568543A>G | CA362676604 | DSP | c.1373A>G (p.Asn458Ser) | gnomAD v4 |
6 | g.7568543A>T | CA362676605 | DSP | c.1373A>T (p.Asn458Ile) | |
6 | g.7568544T>A | CA362676608 | DSP | c.1374T>A (p.Asn458Lys) | |
6 | g.7568544T>C | CA448522054 | DSP | c.1374T>C (p.Asn458=) | |
6 | g.7568544T>G | CA362676609 | DSP | c.1374T>G (p.Asn458Lys) | gnomAD v4 |
6 | g.7568545A>C | CA362676613 | DSP | c.1375A>C (p.Lys459Gln) | |
6 | g.7568545A>G | CA362676614 | DSP | c.1375A>G (p.Lys459Glu) | |
6 | g.7568545A>T | CA362676615 | DSP | c.1375A>T (p.Lys459Ter) | |
6 | g.7568546A>C | CA362676620 | DSP | c.1376A>C (p.Lys459Thr) | |
6 | g.7568546A>G | CA362676621 | DSP | c.1376A>G (p.Lys459Arg) | |
6 | g.7568546A>T | CA362676622 | DSP | c.1376A>T (p.Lys459Ile) | |
6 | g.7568547A>C | CA362676623 | DSP | c.1377A>C (p.Lys459Asn) | |
6 | g.7568547A>G | CA448522070 | DSP | c.1377A>G (p.Lys459=) | |
6 | g.7568547A>T | CA362676624 | DSP | c.1377A>T (p.Lys459Asn) | |
6 | g.7568548C>A | CA362676625 | DSP | c.1378C>A (p.Pro460Thr) | |
6 | g.7568548C= | CA1608623123 | DSP | c.1378C= (p.Pro460=) | |
6 | g.7568548C>G | CA027784 | DSP | c.1378C>G (p.Pro460Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.7568548C>T | CA362676626 | DSP | c.1378C>T (p.Pro460Ser) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.7568549C>A | CA362676635 | DSP | c.1379C>A (p.Pro460His) | |
6 | g.7568549C= | CA1608623133 | DSP | c.1379C= (p.Pro460=) | |
6 | g.7568549C>G | CA362676637 | DSP | c.1379C>G (p.Pro460Arg) | |
6 | g.7568549C>T | CA027800 | DSP | c.1379C>T (p.Pro460Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.7568550C>A | CA448522081 | DSP | c.1380C>A (p.Pro460=) | |
6 | g.7568550C= | CA1608623139 | DSP | c.1380C= (p.Pro460=) | |
6 | g.7568550C>G | CA448522082 | DSP | c.1380C>G (p.Pro460=) | gnomAD v4 |
6 | g.7568550C>T | CA448522083 | DSP | c.1380C>T (p.Pro460=) | ClinVar dbSNP gnomAD v4 |
6 | g.7568550_7568553delinsCATT | CA1608623137 | DSP | c.1380_1383delinsCATT (p.Pro460=) | |
6 | g.7568551A>C | CA362676638 | DSP | c.1381A>C (p.Ile461Leu) | |
6 | g.7568551A>G | CA362676639 | DSP | c.1381A>G (p.Ile461Val) | gnomAD v4 |
6 | g.7568551A>T | CA362676641 | DSP | c.1381A>T (p.Ile461Phe) | |
6 | g.7568554_7568556del | CA004913 | DSP | c.1384_1386del (p.Ile462del) | ClinVar dbSNP |
6 | g.7568552T>A | CA362676644 | DSP | c.1382T>A (p.Ile461Asn) | |
6 | g.7568552T>C | CA362676645 | DSP | c.1382T>C (p.Ile461Thr) | ClinVar dbSNP gnomAD v4 |
6 | g.7568552T>G | CA362676649 | DSP | c.1382T>G (p.Ile461Ser) | |
6 | g.7568552T= | CA1608623145 | DSP | c.1382T= (p.Ile461=) | |
6 | g.7568553T>A | CA448522090 | DSP | c.1383T>A (p.Ile461=) | |
6 | g.7568553T>C | CA448522093 | DSP | c.1383T>C (p.Ile461=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.7568553T>G | CA362676652 | DSP | c.1383T>G (p.Ile461Met) | |
6 | g.7568553T= | CA1608623149 | DSP | c.1383T= (p.Ile461=) | |
6 | g.7568554A>C | CA362676656 | DSP | c.1384A>C (p.Ile462Leu) | |
6 | g.7568554A>G | CA362676655 | DSP | c.1384A>G (p.Ile462Val) | |
6 | g.7568554A>T | CA362676654 | DSP | c.1384A>T (p.Ile462Phe) | |
6 | g.7568554_7568555delinsAT | CA1608623151 | DSP | c.1384_1385delinsAT (p.Ile462=) | |
6 | g.7568555T>A | CA362676657 | DSP | c.1385T>A (p.Ile462Asn) | |
6 | g.7568555T>C | CA362676658 | DSP | c.1385T>C (p.Ile462Thr) | |
6 | g.7568555T>G | CA362676660 | DSP | c.1385T>G (p.Ile462Ser) | gnomAD v4 |
6 | g.7568556del | CA913187583 | DSP | c.1386del (p.Leu463SerfsTer22) | ClinVar dbSNP |
6 | g.7568556T>A | CA448522098 | DSP | c.1386T>A (p.Ile462=) | |
6 | g.7568556T>C | CA448522104 | DSP | c.1386T>C (p.Ile462=) | dbSNP gnomAD v4 |
6 | g.7568556T>G | CA362676661 | DSP | c.1386T>G (p.Ile462Met) | |
6 | g.7568556T= | CA1608623159 | DSP | c.1386T= (p.Ile462=) | |
6 | g.7568556_7568559del | CA2677222923 | DSP | c.1386_1389del (p.Leu463GlufsTer21) | ClinVar gnomAD v4 |
6 | g.7568557C>A | CA362676673 | DSP | c.1387C>A (p.Leu463Ile) | |
6 | g.7568557C>G | CA362676674 | DSP | c.1387C>G (p.Leu463Val) | |
6 | g.7568557C>T | CA362676675 | DSP | c.1387C>T (p.Leu463Phe) | |
6 | g.7568558T>A | CA362676678 | DSP | c.1388T>A (p.Leu463His) | |
6 | g.7568558T>C | CA362676681 | DSP | c.1388T>C (p.Leu463Pro) | ClinVar dbSNP |
6 | g.7568558T>G | CA362676685 | DSP | c.1388T>G (p.Leu463Arg) | |
6 | g.7568558T= | CA1608623163 | DSP | c.1388T= (p.Leu463=) | |
6 | g.7568559C>A | CA448522116 | DSP | c.1389C>A (p.Leu463=) | |
6 | g.7568559C>G | CA448522118 | DSP | c.1389C>G (p.Leu463=) | |
6 | g.7568559C>T | CA448522120 | DSP | c.1389C>T (p.Leu463=) | |
6 | g.7568560A>C | CA448522122 | DSP | c.1390A>C (p.Arg464=) | |
6 | g.7568560A>G | CA362676692 | DSP | c.1390A>G (p.Arg464Gly) | |
6 | g.7568560A>T | CA362676694 | DSP | c.1390A>T (p.Arg464Ter) | |
6 | g.7568561G>A | CA362676697 | DSP | c.1391G>A (p.Arg464Lys) | |
6 | g.7568561G>C | CA362676707 | DSP | c.1391G>C (p.Arg464Thr) | |
6 | g.7568561G>T | CA362676700 | DSP | c.1391G>T (p.Arg464Ile) | |
6 | g.7568562A= | CA1608623173 | DSP | c.1392A= (p.Arg464=) | |
6 | g.7568562A>C | CA362676709 | DSP | c.1392A>C (p.Arg464Ser) | ClinVar dbSNP |
6 | g.7568562A>G | CA448522137 | DSP | c.1392A>G (p.Arg464=) | |
6 | g.7568562A>T | CA362676712 | DSP | c.1392A>T (p.Arg464Ser) | |
6 | g.7568563G>A | CA362676715 | DSP | c.1393G>A (p.Ala465Thr) | |
6 | g.7568563G>C | CA362676717 | DSP | c.1393G>C (p.Ala465Pro) | |
6 | g.7568563G>T | CA362676719 | DSP | c.1393G>T (p.Ala465Ser) | |
6 | g.7568564C>A | CA362676721 | DSP | c.1394C>A (p.Ala465Asp) | |
6 | g.7568564C>G | CA362676723 | DSP | c.1394C>G (p.Ala465Gly) | |
6 | g.7568564C>T | CA362676724 | DSP | c.1394C>T (p.Ala465Val) | |
6 | g.7568568_7568569del | CA2677222928 | DSP | c.1398_1399del (p.Cys467Ter) | gnomAD v4 |