| 20 | g.49905763G>A | CA9904825 | SPATA2 | c.1419C>T (p.Thr473=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.49905763G>C | CA511018152 | SPATA2 | c.1419C>G (p.Thr473=)
| |
| 20 | g.49905763G= | CA2368281279 | SPATA2 | c.1419C= (p.Thr473=)
| |
| 20 | g.49905763G>T | CA511018153 | SPATA2 | c.1419C>A (p.Thr473=)
| dbSNP gnomAD v4 |
| 20 | g.49905764G>A | CA408945728 | SPATA2 | c.1418C>T (p.Thr473Ile)
| |
| 20 | g.49905764G>C | CA408945729 | SPATA2 | c.1418C>G (p.Thr473Ser)
| |
| 20 | g.49905764G>T | CA408945730 | SPATA2 | c.1418C>A (p.Thr473Asn)
| |
| 20 | g.49905765T>A | CA408945737 | SPATA2 | c.1417A>T (p.Thr473Ser)
| dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.49905765T>C | CA408945735 | SPATA2 | c.1417A>G (p.Thr473Ala)
| gnomAD v4 |
| 20 | g.49905765T>G | CA408945733 | SPATA2 | c.1417A>C (p.Thr473Pro)
| |
| 20 | g.49905765T= | CA2368281280 | SPATA2 | c.1417A= (p.Thr473=)
| |
| 20 | g.49905766G>A | CA511018154 | SPATA2 | c.1416C>T (p.Cys472=)
| |
| 20 | g.49905766G>C | CA408945740 | SPATA2 | c.1416C>G (p.Cys472Trp)
| |
| 20 | g.49905766G>T | CA408945742 | SPATA2 | c.1416C>A (p.Cys472Ter)
| |
| 20 | g.49905767C>A | CA408945745 | SPATA2 | c.1415G>T (p.Cys472Phe)
| |
| 20 | g.49905767C>G | CA408945749 | SPATA2 | c.1415G>C (p.Cys472Ser)
| dbSNP |
| 20 | g.49905767C>T | CA408945747 | SPATA2 | c.1415G>A (p.Cys472Tyr)
| gnomAD v3 gnomAD v4 |
| 20 | g.49905768A= | CA2368281281 | SPATA2 | c.1414T= (p.Cys472=)
| |
| 20 | g.49905768A>C | CA408945752 | SPATA2 | c.1414T>G (p.Cys472Gly)
| |
| 20 | g.49905768A>G | CA408945757 | SPATA2 | c.1414T>C (p.Cys472Arg)
| dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.49905768A>T | CA408945754 | SPATA2 | c.1414T>A (p.Cys472Ser)
| |
| 20 | g.49905769G>A | CA511018158 | SPATA2 | c.1413C>T (p.Thr471=)
| |
| 20 | g.49905769G>C | CA511018159 | SPATA2 | c.1413C>G (p.Thr471=)
| |
| 20 | g.49905769G>T | CA511018160 | SPATA2 | c.1413C>A (p.Thr471=)
| |
| 20 | g.49905770G>A | CA408945760 | SPATA2 | c.1412C>T (p.Thr471Ile)
| gnomAD v3 gnomAD v4 |
| 20 | g.49905770G>C | CA408945761 | SPATA2 | c.1412C>G (p.Thr471Ser)
| dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.49905770G= | CA2368281282 | SPATA2 | c.1412C= (p.Thr471=)
| |
| 20 | g.49905770G>T | CA408945765 | SPATA2 | c.1412C>A (p.Thr471Asn)
| |
| 20 | g.49905771T>A | CA408945767 | SPATA2 | c.1411A>T (p.Thr471Ser)
| |
| 20 | g.49905771T>C | CA408945768 | SPATA2 | c.1411A>G (p.Thr471Ala)
| gnomAD v4 |
| 20 | g.49905771T>G | CA408945769 | SPATA2 | c.1411A>C (p.Thr471Pro)
| |
| 20 | g.49905772G>A | CA511018164 | SPATA2 | c.1410C>T (p.Asn470=)
| |
| 20 | g.49905772G>C | CA408945770 | SPATA2 | c.1410C>G (p.Asn470Lys)
| gnomAD v3 gnomAD v4 |
| 20 | g.49905772G>T | CA408945773 | SPATA2 | c.1410C>A (p.Asn470Lys)
| |
| 20 | g.49905773T>A | CA408945776 | SPATA2 | c.1409A>T (p.Asn470Ile)
| |
| 20 | g.49905773T>C | CA408945777 | SPATA2 | c.1409A>G (p.Asn470Ser)
| gnomAD v4 |
| 20 | g.49905773T>G | CA408945779 | SPATA2 | c.1409A>C (p.Asn470Thr)
| |
| 20 | g.49905773_49905776delinsTTGG | CA2368281283 | SPATA2 | c.1406_1409delinsCCAA (p.Thr469=)
| |
| 20 | g.49905774T>A | CA408945795 | SPATA2 | c.1408A>T (p.Asn470Tyr)
| |
| 20 | g.49905774T>C | CA408945783 | SPATA2 | c.1408A>G (p.Asn470Asp)
| gnomAD v3 gnomAD v4 |
| 20 | g.49905774T>G | CA408945794 | SPATA2 | c.1408A>C (p.Asn470His)
| |
| 20 | g.49905777_49905779del | CA9904826 | SPATA2 | c.1406_1408del (p.Thr469del)
| dbSNP ExAC gnomAD v2 |
| 20 | g.49905775G>A | CA511018168 | SPATA2 | c.1407C>T (p.Thr469=)
| dbSNP |
| 20 | g.49905775G>C | CA511018169 | SPATA2 | c.1407C>G (p.Thr469=)
| |
| 20 | g.49905775G= | CA2368281284 | SPATA2 | c.1407C= (p.Thr469=)
| |
| 20 | g.49905775G>T | CA511018170 | SPATA2 | c.1407C>A (p.Thr469=)
| gnomAD v4 |
| 20 | g.49905776G>A | CA315121801 | SPATA2 | c.1406C>T (p.Thr469Ile)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905776G>C | CA408945798 | SPATA2 | c.1406C>G (p.Thr469Ser)
| |
| 20 | g.49905776G= | CA2368281285 | SPATA2 | c.1406C= (p.Thr469=)
| |
| 20 | g.49905776G>T | CA408945805 | SPATA2 | c.1406C>A (p.Thr469Asn)
| |
| 20 | g.49905777T>A | CA408945809 | SPATA2 | c.1405A>T (p.Thr469Ser)
| |
| 20 | g.49905777T>C | CA408945814 | SPATA2 | c.1405A>G (p.Thr469Ala)
| |
| 20 | g.49905777T>G | CA408945816 | SPATA2 | c.1405A>C (p.Thr469Pro)
| |
| 20 | g.49905778G>A | CA511018173 | SPATA2 | c.1404C>T (p.Ala468=)
| |
| 20 | g.49905778G>C | CA511018174 | SPATA2 | c.1404C>G (p.Ala468=)
| |
| 20 | g.49905778G>T | CA511018175 | SPATA2 | c.1404C>A (p.Ala468=)
| |
| 20 | g.49905779G>A | CA408945818 | SPATA2 | c.1403C>T (p.Ala468Val)
| |
| 20 | g.49905779G>C | CA408945822 | SPATA2 | c.1403C>G (p.Ala468Gly)
| |
| 20 | g.49905779G>T | CA408945823 | SPATA2 | c.1403C>A (p.Ala468Asp)
| |
| 20 | g.49905779_49905780insT | CA1018246835 | SPATA2 | c.1402_1403insA (p.Ala468AspfsTer14)
| gnomAD v3 gnomAD v4 |
| 20 | g.49905780C>A | CA408945832 | SPATA2 | c.1402G>T (p.Ala468Ser)
| |
| 20 | g.49905780C= | CA2368281286 | SPATA2 | c.1402G= (p.Ala468=)
| |
| 20 | g.49905780C>G | CA408945828 | SPATA2 | c.1402G>C (p.Ala468Pro)
| |
| 20 | g.49905780C>T | CA9904827 | SPATA2 | c.1402G>A (p.Ala468Thr)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905781G>A | CA9904828 | SPATA2 | c.1401C>T (p.Gly467=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905781G>C | CA511018179 | SPATA2 | c.1401C>G (p.Gly467=)
| |
| 20 | g.49905781G= | CA2368281287 | SPATA2 | c.1401C= (p.Gly467=)
| |
| 20 | g.49905781G>T | CA511018180 | SPATA2 | c.1401C>A (p.Gly467=)
| |
| 20 | g.49905782C>A | CA408945838 | SPATA2 | c.1400G>T (p.Gly467Val)
| |
| 20 | g.49905782C>G | CA408945840 | SPATA2 | c.1400G>C (p.Gly467Ala)
| |
| 20 | g.49905782C>T | CA408945844 | SPATA2 | c.1400G>A (p.Gly467Asp)
| |
| 20 | g.49905783C>A | CA408945847 | SPATA2 | c.1399G>T (p.Gly467Cys)
| dbSNP |
| 20 | g.49905783C= | CA2368281288 | SPATA2 | c.1399G= (p.Gly467=)
| |
| 20 | g.49905783C>G | CA408945851 | SPATA2 | c.1399G>C (p.Gly467Arg)
| |
| 20 | g.49905783C>T | CA408945853 | SPATA2 | c.1399G>A (p.Gly467Ser)
| |
| 20 | g.49905784T>A | CA511018182 | SPATA2 | c.1398A>T (p.Pro466=)
| |
| 20 | g.49905784T>C | CA511018183 | SPATA2 | c.1398A>G (p.Pro466=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905784T>G | CA511018184 | SPATA2 | c.1398A>C (p.Pro466=)
| |
| 20 | g.49905784T= | CA2368281289 | SPATA2 | c.1398A= (p.Pro466=)
| |
| 20 | g.49905784_49905789del | CA1018246841 | SPATA2 | c.1393_1398del (p.Arg465_Pro466del)
| gnomAD v3 gnomAD v4 |
| 20 | g.49905785G>A | CA408945854 | SPATA2 | c.1397C>T (p.Pro466Leu)
| gnomAD v4 |
| 20 | g.49905785G>C | CA408945857 | SPATA2 | c.1397C>G (p.Pro466Arg)
| gnomAD v4 |
| 20 | g.49905785G>T | CA408945861 | SPATA2 | c.1397C>A (p.Pro466Gln)
| |
| 20 | g.49905787del | CA2816621289 | SPATA2 | c.1397del (p.Pro466GlnfsTer?)
| |
| 20 | g.49905786G>A | CA408945864 | SPATA2 | c.1396C>T (p.Pro466Ser)
| gnomAD v4 |
| 20 | g.49905786G>C | CA408945868 | SPATA2 | c.1396C>G (p.Pro466Ala)
| |
| 20 | g.49905786G>T | CA408945869 | SPATA2 | c.1396C>A (p.Pro466Thr)
| |
| 20 | g.49905787G>A | CA511018188 | SPATA2 | c.1395C>T (p.Arg465=)
| dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.49905787G>C | CA511018187 | SPATA2 | c.1395C>G (p.Arg465=)
| dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.49905787G= | CA2368281290 | SPATA2 | c.1395C= (p.Arg465=)
| |
| 20 | g.49905787G>T | CA511018186 | SPATA2 | c.1395C>A (p.Arg465=)
| |
| 20 | g.49905788C>A | CA408945874 | SPATA2 | c.1394G>T (p.Arg465Leu)
| |
| 20 | g.49905788C= | CA2368281291 | SPATA2 | c.1394G= (p.Arg465=)
| |
| 20 | g.49905788C>G | CA408945875 | SPATA2 | c.1394G>C (p.Arg465Pro)
| dbSNP |
| 20 | g.49905788C>T | CA9904829 | SPATA2 | c.1394G>A (p.Arg465His)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905789G>A | CA315121833 | SPATA2 | c.1393C>T (p.Arg465Cys)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 20 | g.49905789G>C | CA315121835 | SPATA2 | c.1393C>G (p.Arg465Gly)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905789G= | CA2368281292 | SPATA2 | c.1393C= (p.Arg465=)
| |
| 20 | g.49905789G>T | CA408945877 | SPATA2 | c.1393C>A (p.Arg465Ser)
| |
| 20 | g.49905790del | CA2653279971 | SPATA2 | c.1393del (p.Arg465AlafsTer?)
| gnomAD v4 |
| 20 | g.49905790G>A | CA511018191 | SPATA2 | c.1392C>T (p.Asn464=)
| |
| 20 | g.49905790G>C | CA408945879 | SPATA2 | c.1392C>G (p.Asn464Lys)
| |
| 20 | g.49905790G>T | CA408945884 | SPATA2 | c.1392C>A (p.Asn464Lys)
| |
| 20 | g.49905791T>A | CA408945902 | SPATA2 | c.1391A>T (p.Asn464Ile)
| |
| 20 | g.49905791T>C | CA408945904 | SPATA2 | c.1391A>G (p.Asn464Ser)
| |
| 20 | g.49905791T>G | CA408945906 | SPATA2 | c.1391A>C (p.Asn464Thr)
| |
| 20 | g.49905791_49905792insATCAT | CA1018246852 | SPATA2 | c.1391_1392insTGATA (p.Arg465AspfsTer?)
| gnomAD v3 gnomAD v4 |
| 20 | g.49905792T>A | CA408945908 | SPATA2 | c.1390A>T (p.Asn464Tyr)
| |
| 20 | g.49905792T>C | CA408945911 | SPATA2 | c.1390A>G (p.Asn464Asp)
| |
| 20 | g.49905792T>G | CA408945913 | SPATA2 | c.1390A>C (p.Asn464His)
| |
| 20 | g.49905793G>A | CA9904830 | SPATA2 | c.1389C>T (p.Cys463=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905793G>C | CA408945924 | SPATA2 | c.1389C>G (p.Cys463Trp)
| dbSNP |
| 20 | g.49905793G= | CA2368281293 | SPATA2 | c.1389C= (p.Cys463=)
| |
| 20 | g.49905793G>T | CA408945914 | SPATA2 | c.1389C>A (p.Cys463Ter)
| |
| 20 | g.49905794C>A | CA408945931 | SPATA2 | c.1388G>T (p.Cys463Phe)
| gnomAD v3 gnomAD v4 |
| 20 | g.49905794C>G | CA408945927 | SPATA2 | c.1388G>C (p.Cys463Ser)
| |
| 20 | g.49905794C>T | CA408945929 | SPATA2 | c.1388G>A (p.Cys463Tyr)
| |
| 20 | g.49905795A>C | CA408945934 | SPATA2 | c.1387T>G (p.Cys463Gly)
| |
| 20 | g.49905795A>G | CA408945936 | SPATA2 | c.1387T>C (p.Cys463Arg)
| |
| 20 | g.49905795A>T | CA408945939 | SPATA2 | c.1387T>A (p.Cys463Ser)
| |
| 20 | g.49905796G>A | CA511018197 | SPATA2 | c.1386C>T (p.Phe462=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905796G>C | CA408945942 | SPATA2 | c.1386C>G (p.Phe462Leu)
| |
| 20 | g.49905796G= | CA2368281294 | SPATA2 | c.1386C= (p.Phe462=)
| |
| 20 | g.49905796G>T | CA408945947 | SPATA2 | c.1386C>A (p.Phe462Leu)
| |
| 20 | g.49905797A>C | CA408945951 | SPATA2 | c.1385T>G (p.Phe462Cys)
| |
| 20 | g.49905797A>G | CA408945953 | SPATA2 | c.1385T>C (p.Phe462Ser)
| |
| 20 | g.49905797A>T | CA408945955 | SPATA2 | c.1385T>A (p.Phe462Tyr)
| |
| 20 | g.49905798A>C | CA408945959 | SPATA2 | c.1384T>G (p.Phe462Val)
| |
| 20 | g.49905798A>G | CA408945962 | SPATA2 | c.1384T>C (p.Phe462Leu)
| |
| 20 | g.49905798A>T | CA408945964 | SPATA2 | c.1384T>A (p.Phe462Ile)
| |
| 20 | g.49905799G>A | CA511018199 | SPATA2 | c.1383C>T (p.Gly461=)
| |
| 20 | g.49905799G>C | CA511018200 | SPATA2 | c.1383C>G (p.Gly461=)
| |
| 20 | g.49905799G>T | CA511018201 | SPATA2 | c.1383C>A (p.Gly461=)
| |
| 20 | g.49905800C>A | CA408945968 | SPATA2 | c.1382G>T (p.Gly461Val)
| |
| 20 | g.49905800C= | CA2368281295 | SPATA2 | c.1382G= (p.Gly461=)
| |
| 20 | g.49905800C>G | CA408945974 | SPATA2 | c.1382G>C (p.Gly461Ala)
| |
| 20 | g.49905800C>T | CA408945971 | SPATA2 | c.1382G>A (p.Gly461Asp)
| dbSNP gnomAD v2 |
| 20 | g.49905801del | CA2653279972 | SPATA2 | c.1382del (p.Gly461AlafsTer?)
| gnomAD v4 |
| 20 | g.49905801C>A | CA408945977 | SPATA2 | c.1381G>T (p.Gly461Cys)
| |
| 20 | g.49905801C>G | CA408945979 | SPATA2 | c.1381G>C (p.Gly461Arg)
| |
| 20 | g.49905801C>T | CA408945981 | SPATA2 | c.1381G>A (p.Gly461Ser)
| |
| 20 | g.49905802A= | CA2368281296 | SPATA2 | c.1380T= (p.Cys460=)
| |
| 20 | g.49905802A>C | CA408945983 | SPATA2 | c.1380T>G (p.Cys460Trp)
| |
| 20 | g.49905802A>G | CA315121842 | SPATA2 | c.1380T>C (p.Cys460=)
| dbSNP gnomAD v3 gnomAD v4 COSMIC |
| 20 | g.49905802A>T | CA408945985 | SPATA2 | c.1380T>A (p.Cys460Ter)
| |
| 20 | g.49905803C>A | CA408945988 | SPATA2 | c.1379G>T (p.Cys460Phe)
| |
| 20 | g.49905803C>G | CA408945990 | SPATA2 | c.1379G>C (p.Cys460Ser)
| |
| 20 | g.49905803C>T | CA408945992 | SPATA2 | c.1379G>A (p.Cys460Tyr)
| |
| 20 | g.49905804A= | CA2368281297 | SPATA2 | c.1378T= (p.Cys460=)
| |
| 20 | g.49905804A>C | CA408945993 | SPATA2 | c.1378T>G (p.Cys460Gly)
| |
| 20 | g.49905804A>G | CA408945994 | SPATA2 | c.1378T>C (p.Cys460Arg)
| dbSNP gnomAD v2 gnomAD v4 |
| 20 | g.49905804A>T | CA408945996 | SPATA2 | c.1378T>A (p.Cys460Ser)
| |
| 20 | g.49905805G>A | CA511018206 | SPATA2 | c.1377C>T (p.Arg459=)
| |
| 20 | g.49905805G>C | CA511018207 | SPATA2 | c.1377C>G (p.Arg459=)
| |
| 20 | g.49905805G>T | CA511018208 | SPATA2 | c.1377C>A (p.Arg459=)
| |
| 20 | g.49905806C>A | CA315121845 | SPATA2 | c.1376G>T (p.Arg459Leu)
| dbSNP gnomAD v4 |
| 20 | g.49905806C= | CA2368281298 | SPATA2 | c.1376G= (p.Arg459=)
| |
| 20 | g.49905806C>G | CA408946002 | SPATA2 | c.1376G>C (p.Arg459Pro)
| |
| 20 | g.49905806C>T | CA9904831 | SPATA2 | c.1376G>A (p.Arg459His)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905807G>A | CA9904832 | SPATA2 | c.1375C>T (p.Arg459Cys)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905807G>C | CA408946003 | SPATA2 | c.1375C>G (p.Arg459Gly)
| |
| 20 | g.49905807G= | CA2368281299 | SPATA2 | c.1375C= (p.Arg459=)
| |
| 20 | g.49905807G>T | CA408946004 | SPATA2 | c.1375C>A (p.Arg459Ser)
| |
| 20 | g.49905808G>A | CA9904833 | SPATA2 | c.1374C>T (p.Ser458=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.49905808G>C | CA511018210 | SPATA2 | c.1374C>G (p.Ser458=)
| |
| 20 | g.49905808G= | CA2368281300 | SPATA2 | c.1374C= (p.Ser458=)
| |
| 20 | g.49905808G>T | CA511018209 | SPATA2 | c.1374C>A (p.Ser458=)
| |
| 20 | g.49905809G>A | CA408946008 | SPATA2 | c.1373C>T (p.Ser458Phe)
| dbSNP gnomAD v4 |
| 20 | g.49905809G>C | CA9904834 | SPATA2 | c.1373C>G (p.Ser458Cys)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905809G= | CA2368281301 | SPATA2 | c.1373C= (p.Ser458=)
| |
| 20 | g.49905809G>T | CA408946009 | SPATA2 | c.1373C>A (p.Ser458Tyr)
| |
| 20 | g.49905810A>C | CA408946011 | SPATA2 | c.1372T>G (p.Ser458Ala)
| |
| 20 | g.49905810A>G | CA408946013 | SPATA2 | c.1372T>C (p.Ser458Pro)
| |
| 20 | g.49905810A>T | CA408946018 | SPATA2 | c.1372T>A (p.Ser458Thr)
| |
| 20 | g.49905811A= | CA2368281302 | SPATA2 | c.1371T= (p.Thr457=)
| |
| 20 | g.49905811A>C | CA511018214 | SPATA2 | c.1371T>G (p.Thr457=)
| |
| 20 | g.49905811A>G | CA511018212 | SPATA2 | c.1371T>C (p.Thr457=)
| dbSNP gnomAD v4 |
| 20 | g.49905811A>T | CA511018213 | SPATA2 | c.1371T>A (p.Thr457=)
| |
| 20 | g.49905812G>A | CA408946022 | SPATA2 | c.1370C>T (p.Thr457Ile)
| gnomAD v4 |
| 20 | g.49905812G>C | CA408946024 | SPATA2 | c.1370C>G (p.Thr457Ser)
| dbSNP gnomAD v4 |
| 20 | g.49905812G>T | CA408946027 | SPATA2 | c.1370C>A (p.Thr457Asn)
| |
| 20 | g.49905813T>A | CA408946037 | SPATA2 | c.1369A>T (p.Thr457Ser)
| |
| 20 | g.49905813T>C | CA408946032 | SPATA2 | c.1369A>G (p.Thr457Ala)
| gnomAD v4 |
| 20 | g.49905813T>G | CA408946030 | SPATA2 | c.1369A>C (p.Thr457Pro)
| dbSNP |
| 20 | g.49905813T= | CA2368281303 | SPATA2 | c.1369A= (p.Thr457=)
| |
| 20 | g.49905814G>A | CA511018218 | SPATA2 | c.1368C>T (p.Pro456=)
| dbSNP gnomAD v4 |
| 20 | g.49905814G>C | CA511018220 | SPATA2 | c.1368C>G (p.Pro456=)
| |
| 20 | g.49905814G= | CA2368281304 | SPATA2 | c.1368C= (p.Pro456=)
| |
| 20 | g.49905814G>T | CA511018219 | SPATA2 | c.1368C>A (p.Pro456=)
| |
| 20 | g.49905815G>A | CA408946041 | SPATA2 | c.1367C>T (p.Pro456Leu)
| |
| 20 | g.49905815G>C | CA408946044 | SPATA2 | c.1367C>G (p.Pro456Arg)
| |
| 20 | g.49905815G>T | CA408946047 | SPATA2 | c.1367C>A (p.Pro456His)
| |
| 20 | g.49905816G>A | CA408946051 | SPATA2 | c.1366C>T (p.Pro456Ser)
| gnomAD v4 |
| 20 | g.49905816G>C | CA408946053 | SPATA2 | c.1366C>G (p.Pro456Ala)
| gnomAD v4 |
| 20 | g.49905816G>T | CA408946057 | SPATA2 | c.1366C>A (p.Pro456Thr)
| gnomAD v4 |
| 20 | g.49905817C>A | CA315121855 | SPATA2 | c.1365G>T (p.Thr455=)
| dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.49905817C= | CA2368281305 | SPATA2 | c.1365G= (p.Thr455=)
| |
| 20 | g.49905817C>G | CA511018224 | SPATA2 | c.1365G>C (p.Thr455=)
| |
| 20 | g.49905817C>T | CA9904835 | SPATA2 | c.1365G>A (p.Thr455=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905818G>A | CA9904836 | SPATA2 | c.1364C>T (p.Thr455Met)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905818G>C | CA315121859 | SPATA2 | c.1364C>G (p.Thr455Arg)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905818G= | CA2368281306 | SPATA2 | c.1364C= (p.Thr455=)
| |
| 20 | g.49905818G>T | CA408946070 | SPATA2 | c.1364C>A (p.Thr455Lys)
| |
| 20 | g.49905819T>A | CA408946073 | SPATA2 | c.1363A>T (p.Thr455Ser)
| |
| 20 | g.49905819T>C | CA9904837 | SPATA2 | c.1363A>G (p.Thr455Ala)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.49905819T>G | CA408946077 | SPATA2 | c.1363A>C (p.Thr455Pro)
| |
| 20 | g.49905819T= | CA2368281307 | SPATA2 | c.1363A= (p.Thr455=)
| |
| 20 | g.49905820G>A | CA511018226 | SPATA2 | c.1362C>T (p.Thr454=)
| |
| 20 | g.49905820G>C | CA511018227 | SPATA2 | c.1362C>G (p.Thr454=)
| |
| 20 | g.49905820G>T | CA511018228 | SPATA2 | c.1362C>A (p.Thr454=)
| |
| 20 | g.49905821G>A | CA9904838 | SPATA2 | c.1361C>T (p.Thr454Ile)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905821G>C | CA408946084 | SPATA2 | c.1361C>G (p.Thr454Ser)
| |
| 20 | g.49905821G= | CA2368281308 | SPATA2 | c.1361C= (p.Thr454=)
| |
| 20 | g.49905821G>T | CA408946080 | SPATA2 | c.1361C>A (p.Thr454Asn)
| |
| 20 | g.49905822T>A | CA408946090 | SPATA2 | c.1360A>T (p.Thr454Ser)
| |
| 20 | g.49905822T>C | CA408946099 | SPATA2 | c.1360A>G (p.Thr454Ala)
| dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.49905822T>G | CA408946096 | SPATA2 | c.1360A>C (p.Thr454Pro)
| |
| 20 | g.49905822T= | CA2368281309 | SPATA2 | c.1360A= (p.Thr454=)
| |
| 20 | g.49905823G>A | CA9904839 | SPATA2 | c.1359C>T (p.Ser453=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905823G>C | CA511018232 | SPATA2 | c.1359C>G (p.Ser453=)
| |
| 20 | g.49905823G= | CA2368281310 | SPATA2 | c.1359C= (p.Ser453=)
| |
| 20 | g.49905823G>T | CA511018233 | SPATA2 | c.1359C>A (p.Ser453=)
| |
| 20 | g.49905824G>A | CA9904840 | SPATA2 | c.1358C>T (p.Ser453Phe)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905824G>C | CA9904841 | SPATA2 | c.1358C>G (p.Ser453Cys)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.49905824G= | CA2368281311 | SPATA2 | c.1358C= (p.Ser453=)
| |
| 20 | g.49905824G>T | CA408946119 | SPATA2 | c.1358C>A (p.Ser453Tyr)
| |
| 20 | g.49905825A>C | CA408946123 | SPATA2 | c.1357T>G (p.Ser453Ala)
| |
| 20 | g.49905825A>G | CA408946126 | SPATA2 | c.1357T>C (p.Ser453Pro)
| |
| 20 | g.49905825A>T | CA408946129 | SPATA2 | c.1357T>A (p.Ser453Thr)
| |
| 20 | g.49905826G>A | CA511018235 | SPATA2 | c.1356C>T (p.Pro452=)
| |
| 20 | g.49905826G>C | CA511018236 | SPATA2 | c.1356C>G (p.Pro452=)
| gnomAD v4 |
| 20 | g.49905826G>T | CA511018237 | SPATA2 | c.1356C>A (p.Pro452=)
| |
| 20 | g.49905828del | CA2653279973 | SPATA2 | c.1356del (p.Ser453ProfsTer?)
| gnomAD v4 |
| 20 | g.49905827G>A | CA408946137 | SPATA2 | c.1355C>T (p.Pro452Leu)
| |
| 20 | g.49905827G>C | CA408946133 | SPATA2 | c.1355C>G (p.Pro452Arg)
| |
| 20 | g.49905827G>T | CA408946135 | SPATA2 | c.1355C>A (p.Pro452His)
| |
| 20 | g.49905828G>A | CA408946140 | SPATA2 | c.1354C>T (p.Pro452Ser)
| |
| 20 | g.49905828G>C | CA408946142 | SPATA2 | c.1354C>G (p.Pro452Ala)
| |
| 20 | g.49905828G>T | CA408946144 | SPATA2 | c.1354C>A (p.Pro452Thr)
| |
| 20 | g.49905829_49905832del | CA2816621298 | SPATA2 | c.1351_1354del (p.Lys451ProfsTer?)
| |
| 20 | g.49905829C>A | CA408946149 | SPATA2 | c.1353G>T (p.Lys451Asn)
| |
| 20 | g.49905829C>G | CA408946152 | SPATA2 | c.1353G>C (p.Lys451Asn)
| |
| 20 | g.49905829C>T | CA511018240 | SPATA2 | c.1353G>A (p.Lys451=)
| |
| 20 | g.49905830T>A | CA408946156 | SPATA2 | c.1352A>T (p.Lys451Met)
| |
| 20 | g.49905830T>C | CA408946161 | SPATA2 | c.1352A>G (p.Lys451Arg)
| |
| 20 | g.49905830T>G | CA408946158 | SPATA2 | c.1352A>C (p.Lys451Thr)
| |
| 20 | g.49905831T>A | CA408946162 | SPATA2 | c.1351A>T (p.Lys451Ter)
| |
| 20 | g.49905831T>C | CA408946164 | SPATA2 | c.1351A>G (p.Lys451Glu)
| |
| 20 | g.49905831T>G | CA408946167 | SPATA2 | c.1351A>C (p.Lys451Gln)
| |
| 20 | g.49905832G>A | CA511018244 | SPATA2 | c.1350C>T (p.Ser450=)
| |
| 20 | g.49905832G>C | CA511018245 | SPATA2 | c.1350C>G (p.Ser450=)
| |
| 20 | g.49905832G>T | CA511018246 | SPATA2 | c.1350C>A (p.Ser450=)
| |
| 20 | g.49905833G>A | CA408946171 | SPATA2 | c.1349C>T (p.Ser450Phe)
| |
| 20 | g.49905833G>C | CA408946173 | SPATA2 | c.1349C>G (p.Ser450Cys)
| |
| 20 | g.49905833G>T | CA408946176 | SPATA2 | c.1349C>A (p.Ser450Tyr)
| |
| 20 | g.49905834A>C | CA408946179 | SPATA2 | c.1348T>G (p.Ser450Ala)
| |
| 20 | g.49905834A>G | CA408946180 | SPATA2 | c.1348T>C (p.Ser450Pro)
| |
| 20 | g.49905834A>T | CA408946181 | SPATA2 | c.1348T>A (p.Ser450Thr)
| |
| 20 | g.49905835T>A | CA408946183 | SPATA2 | c.1347A>T (p.Lys449Asn)
| COSMIC |
| 20 | g.49905835T>C | CA511018251 | SPATA2 | c.1347A>G (p.Lys449=)
| |
| 20 | g.49905835T>G | CA408946185 | SPATA2 | c.1347A>C (p.Lys449Asn)
| |
| 20 | g.49905836T>A | CA408946188 | SPATA2 | c.1346A>T (p.Lys449Ile)
| |
| 20 | g.49905836T>C | CA408946193 | SPATA2 | c.1346A>G (p.Lys449Arg)
| |
| 20 | g.49905836T>G | CA408946190 | SPATA2 | c.1346A>C (p.Lys449Thr)
| |
| 20 | g.49905837T>A | CA408946197 | SPATA2 | c.1345A>T (p.Lys449Ter)
| |
| 20 | g.49905837T>C | CA408946201 | SPATA2 | c.1345A>G (p.Lys449Glu)
| |
| 20 | g.49905837T>G | CA408946204 | SPATA2 | c.1345A>C (p.Lys449Gln)
| |
| 20 | g.49905838G>A | CA511018255 | SPATA2 | c.1344C>T (p.Ser448=)
| |
| 20 | g.49905838G>C | CA511018256 | SPATA2 | c.1344C>G (p.Ser448=)
| dbSNP |
| 20 | g.49905838G= | CA2368281312 | SPATA2 | c.1344C= (p.Ser448=)
| |
| 20 | g.49905838G>T | CA511018257 | SPATA2 | c.1344C>A (p.Ser448=)
| |
| 20 | g.49905839G>A | CA408946209 | SPATA2 | c.1343C>T (p.Ser448Phe)
| |
| 20 | g.49905839G>C | CA408946211 | SPATA2 | c.1343C>G (p.Ser448Cys)
| |
| 20 | g.49905839G= | CA2368281313 | SPATA2 | c.1343C= (p.Ser448=)
| |
| 20 | g.49905839G>T | CA408946212 | SPATA2 | c.1343C>A (p.Ser448Tyr)
| dbSNP gnomAD v4 |
| 20 | g.49905840A>C | CA408946216 | SPATA2 | c.1342T>G (p.Ser448Ala)
| |
| 20 | g.49905840A>G | CA408946218 | SPATA2 | c.1342T>C (p.Ser448Pro)
| gnomAD v4 |
| 20 | g.49905840A>T | CA408946222 | SPATA2 | c.1342T>A (p.Ser448Thr)
| ClinVar |
| 20 | g.49905841G>A | CA9904842 | SPATA2 | c.1341C>T (p.His447=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905841G>C | CA408946228 | SPATA2 | c.1341C>G (p.His447Gln)
| |
| 20 | g.49905841G= | CA2368281314 | SPATA2 | c.1341C= (p.His447=)
| |
| 20 | g.49905841G>T | CA408946231 | SPATA2 | c.1341C>A (p.His447Gln)
| COSMIC |
| 20 | g.49905842T>A | CA408946240 | SPATA2 | c.1340A>T (p.His447Leu)
| |
| 20 | g.49905842T>C | CA9904843 | SPATA2 | c.1340A>G (p.His447Arg)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.49905842T>G | CA408946237 | SPATA2 | c.1340A>C (p.His447Pro)
| |
| 20 | g.49905842T= | CA2368281315 | SPATA2 | c.1340A= (p.His447=)
| |
| 20 | g.49905843G>A | CA408946244 | SPATA2 | c.1339C>T (p.His447Tyr)
| gnomAD v4 |
| 20 | g.49905843G>C | CA408946247 | SPATA2 | c.1339C>G (p.His447Asp)
| |
| 20 | g.49905843G>T | CA408946250 | SPATA2 | c.1339C>A (p.His447Asn)
| |
| 20 | g.49905844A>C | CA511018258 | SPATA2 | c.1338T>G (p.Leu446=)
| gnomAD v4 |
| 20 | g.49905844A>G | CA511018260 | SPATA2 | c.1338T>C (p.Leu446=)
| gnomAD v4 |
| 20 | g.49905844A>T | CA511018261 | SPATA2 | c.1338T>A (p.Leu446=)
| |
| 20 | g.49905845A>C | CA408946254 | SPATA2 | c.1337T>G (p.Leu446Arg)
| |
| 20 | g.49905845A>G | CA408946256 | SPATA2 | c.1337T>C (p.Leu446Pro)
| |
| 20 | g.49905845A>T | CA408946260 | SPATA2 | c.1337T>A (p.Leu446His)
| |
| 20 | g.49905846G>A | CA408946262 | SPATA2 | c.1336C>T (p.Leu446Phe)
| |
| 20 | g.49905846G>C | CA408946264 | SPATA2 | c.1336C>G (p.Leu446Val)
| |
| 20 | g.49905846G>T | CA408946267 | SPATA2 | c.1336C>A (p.Leu446Ile)
| gnomAD v4 |
| 20 | g.49905847G>A | CA511018264 | SPATA2 | c.1335C>T (p.His445=)
| dbSNP gnomAD v4 |
| 20 | g.49905847G>C | CA408946273 | SPATA2 | c.1335C>G (p.His445Gln)
| |
| 20 | g.49905847G= | CA2368281316 | SPATA2 | c.1335C= (p.His445=)
| |
| 20 | g.49905847G>T | CA408946277 | SPATA2 | c.1335C>A (p.His445Gln)
| gnomAD v4 |
| 20 | g.49905848T>A | CA408946289 | SPATA2 | c.1334A>T (p.His445Leu)
| |
| 20 | g.49905848T>C | CA408946286 | SPATA2 | c.1334A>G (p.His445Arg)
| |
| 20 | g.49905848T>G | CA408946282 | SPATA2 | c.1334A>C (p.His445Pro)
| |
| 20 | g.49905849G>A | CA315121874 | SPATA2 | c.1333C>T (p.His445Tyr)
| dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.49905849G>C | CA408946308 | SPATA2 | c.1333C>G (p.His445Asp)
| |
| 20 | g.49905849G= | CA2368281317 | SPATA2 | c.1333C= (p.His445=)
| |
| 20 | g.49905849G>T | CA9904844 | SPATA2 | c.1333C>A (p.His445Asn)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.49905850C>A | CA511018270 | SPATA2 | c.1332G>T (p.Pro444=)
| |
| 20 | g.49905850C= | CA2368281318 | SPATA2 | c.1332G= (p.Pro444=)
| |
| 20 | g.49905850C>G | CA511018271 | SPATA2 | c.1332G>C (p.Pro444=)
| |
| 20 | g.49905850C>T | CA9904845 | SPATA2 | c.1332G>A (p.Pro444=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 20 | g.49905851G>A | CA9904846 | SPATA2 | c.1331C>T (p.Pro444Leu)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905851G>C | CA408946312 | SPATA2 | c.1331C>G (p.Pro444Arg)
| |
| 20 | g.49905851G= | CA2368281319 | SPATA2 | c.1331C= (p.Pro444=)
| |
| 20 | g.49905851G>T | CA408946315 | SPATA2 | c.1331C>A (p.Pro444Gln)
| |
| 20 | g.49905852G>A | CA408946318 | SPATA2 | c.1330C>T (p.Pro444Ser)
| gnomAD v4 |
| 20 | g.49905852G>C | CA408946321 | SPATA2 | c.1330C>G (p.Pro444Ala)
| |
| 20 | g.49905852G>T | CA408946323 | SPATA2 | c.1330C>A (p.Pro444Thr)
| |
| 20 | g.49905853G>A | CA511018273 | SPATA2 | c.1329C>T (p.Leu443=)
| COSMIC |
| 20 | g.49905853G>C | CA511018275 | SPATA2 | c.1329C>G (p.Leu443=)
| |
| 20 | g.49905853G>T | CA511018274 | SPATA2 | c.1329C>A (p.Leu443=)
| |
| 20 | g.49905854A>C | CA408946327 | SPATA2 | c.1328T>G (p.Leu443Arg)
| |
| 20 | g.49905854A>G | CA408946329 | SPATA2 | c.1328T>C (p.Leu443Pro)
| |
| 20 | g.49905854A>T | CA408946333 | SPATA2 | c.1328T>A (p.Leu443His)
| |
| 20 | g.49905855G>A | CA9904847 | SPATA2 | c.1327C>T (p.Leu443Phe)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 20 | g.49905855G>C | CA408946337 | SPATA2 | c.1327C>G (p.Leu443Val)
| |
| 20 | g.49905855G= | CA2368281320 | SPATA2 | c.1327C= (p.Leu443=)
| |
| 20 | g.49905855G>T | CA408946340 | SPATA2 | c.1327C>A (p.Leu443Ile)
| |
| 20 | g.49905857_49905859del | CA2816621301 | SPATA2 | c.1325_1327del (p.Arg442del)
| |
| 20 | g.49905856G>A | CA511018279 | SPATA2 | c.1326C>T (p.Arg442=)
| |
| 20 | g.49905856G>C | CA511018280 | SPATA2 | c.1326C>G (p.Arg442=)
| |
| 20 | g.49905856G>T | CA511018281 | SPATA2 | c.1326C>A (p.Arg442=)
| |
| 20 | g.49905857C>A | CA9904848 | SPATA2 | c.1325G>T (p.Arg442Leu)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905857C= | CA2368281321 | SPATA2 | c.1325G= (p.Arg442=)
| |
| 20 | g.49905857C>G | CA408946348 | SPATA2 | c.1325G>C (p.Arg442Pro)
| |
| 20 | g.49905857C>T | CA9904849 | SPATA2 | c.1325G>A (p.Arg442His)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.49905858G>A | CA9904850 | SPATA2 | c.1324C>T (p.Arg442Cys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905858G>C | CA408946351 | SPATA2 | c.1324C>G (p.Arg442Gly)
| gnomAD v4 |
| 20 | g.49905858G= | CA2368281322 | SPATA2 | c.1324C= (p.Arg442=)
| |
| 20 | g.49905858G>T | CA408946352 | SPATA2 | c.1324C>A (p.Arg442Ser)
| |
| 20 | g.49905858_49905859insAA | CA2816621304 | SPATA2 | c.1323_1324insTT (p.Arg442PhefsTer?)
| |
| 20 | g.49905859G>A | CA511018285 | SPATA2 | c.1323C>T (p.Asp441=)
| |
| 20 | g.49905859G>C | CA315121886 | SPATA2 | c.1323C>G (p.Asp441Glu)
| dbSNP gnomAD v3 gnomAD v4 |
| 20 | g.49905859G= | CA2368281323 | SPATA2 | c.1323C= (p.Asp441=)
| |
| 20 | g.49905859G>T | CA408946355 | SPATA2 | c.1323C>A (p.Asp441Glu)
| |
| 20 | g.49905868_49905934del | CA2816621305 | SPATA2 | c.1257_1323del (p.His420AlafsTer?)
| |
| 20 | g.49905860T>A | CA408946359 | SPATA2 | c.1322A>T (p.Asp441Val)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905860T>C | CA408946365 | SPATA2 | c.1322A>G (p.Asp441Gly)
| |
| 20 | g.49905860T>G | CA408946366 | SPATA2 | c.1322A>C (p.Asp441Ala)
| |
| 20 | g.49905860T= | CA2368281324 | SPATA2 | c.1322A= (p.Asp441=)
| |
| 20 | g.49905860_49905861insAC | CA2816621306 | SPATA2 | c.1321_1322insGT (p.Asp441GlyfsTer?)
| |
| 20 | g.49905861C>A | CA408946370 | SPATA2 | c.1321G>T (p.Asp441Tyr)
| |
| 20 | g.49905861C= | CA2368281325 | SPATA2 | c.1321G= (p.Asp441=)
| |
| 20 | g.49905861C>G | CA408946373 | SPATA2 | c.1321G>C (p.Asp441His)
| |
| 20 | g.49905861C>T | CA9904851 | SPATA2 | c.1321G>A (p.Asp441Asn)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 20 | g.49905862G>A | CA9904852 | SPATA2 | c.1320C>T (p.Leu440=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
| 20 | g.49905862G>C | CA511018288 | SPATA2 | c.1320C>G (p.Leu440=)
| |
| 20 | g.49905862G= | CA2368281326 | SPATA2 | c.1320C= (p.Leu440=)
| |
| 20 | g.49905862G>T | CA511018289 | SPATA2 | c.1320C>A (p.Leu440=)
| |
| 20 | g.49905863A>C | CA408946393 | SPATA2 | c.1319T>G (p.Leu440Arg)
| |
| 20 | g.49905863A>G | CA408946388 | SPATA2 | c.1319T>C (p.Leu440Pro)
| |
| 20 | g.49905863A>T | CA408946391 | SPATA2 | c.1319T>A (p.Leu440His)
| |
