Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.47607912T>A | CA3844371 | CD2AP | c.1531-15T>A (n.1531-15T>A) n.41T>A c.1519-15T>A (n.1519-15T>A) c.1384-15T>A (n.1384-15T>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.47607912T>C | CA3844372 | CD2AP | c.1531-15T>C (n.1531-15T>C) n.41T>C c.1519-15T>C (n.1519-15T>C) c.1384-15T>C (n.1384-15T>C) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.47607912T= | CA1626460724 | CD2AP | c.1531-15T= (n.1531-15T=) n.41T= c.1519-15T= (n.1519-15T=) c.1384-15T= (n.1384-15T=) | |
6 | g.47607912_47607913delinsTA | CA1626460728 | CD2AP | c.1531-15_1531-14delinsTA (n.1531-15_1531-14delinsTA) n.41_42delinsTA c.1519-15_1519-14delinsTA (n.1519-15_1519-14delinsTA) c.1384-15_1384-14delinsTA (n.1384-15_1384-14delinsTA) | |
6 | g.47607918dup | CA3844373 | CD2AP | c.1531-9dup (n.1531-9dup) n.47dup c.1519-9dup (n.1519-9dup) c.1384-9dup (n.1384-9dup) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.47607918del | CA566924913 | CD2AP | c.1531-9del (n.1531-9del) n.47del c.1519-9del (n.1519-9del) c.1384-9del (n.1384-9del) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.47607917_47607918del | CA2679027818 | CD2AP | c.1531-10_1531-9del (n.1531-10_1531-9del) n.46_47del c.1519-10_1519-9del (n.1519-10_1519-9del) c.1384-10_1384-9del (n.1384-10_1384-9del) | gnomAD v4 |
6 | g.47607916A= | CA1626460734 | CD2AP | c.1531-11A= (n.1531-11A=) n.45A= c.1519-11A= (n.1519-11A=) c.1384-11A= (n.1384-11A=) | |
6 | g.47607916A>T | CA566924915 | CD2AP | c.1531-11A>T (n.1531-11A>T) n.45A>T c.1519-11A>T (n.1519-11A>T) c.1384-11A>T (n.1384-11A>T) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.47607918A>C | CA2573140867 | CD2AP | c.1531-9A>C (n.1531-9A>C) n.47A>C c.1519-9A>C (n.1519-9A>C) c.1384-9A>C (n.1384-9A>C) | ClinVar dbSNP |
6 | g.47607919T>C | CA137927434 | CD2AP | c.1531-8T>C (n.1531-8T>C) n.48T>C c.1519-8T>C (n.1519-8T>C) c.1384-8T>C (n.1384-8T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.47607919T= | CA1626460738 | CD2AP | c.1531-8T= (n.1531-8T=) n.48T= c.1519-8T= (n.1519-8T=) c.1384-8T= (n.1384-8T=) | |
6 | g.47607920C>A | CA3844374 | CD2AP | c.1531-7C>A (n.1531-7C>A) n.49C>A c.1519-7C>A (n.1519-7C>A) c.1384-7C>A (n.1384-7C>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.47607920C= | CA1626460741 | CD2AP | c.1531-7C= (n.1531-7C=) n.49C= c.1519-7C= (n.1519-7C=) c.1384-7C= (n.1384-7C=) | |
6 | g.47607923T>A | CA2679027819 | CD2AP | c.1531-4T>A (n.1531-4T>A) n.52T>A c.1519-4T>A (n.1519-4T>A) c.1384-4T>A (n.1384-4T>A) | gnomAD v4 |
6 | g.47607924T>C | CA2578708012 | CD2AP | c.1531-3T>C (n.1531-3T>C) n.53T>C c.1519-3T>C (n.1519-3T>C) c.1384-3T>C (n.1384-3T>C) | |
6 | g.47607925A>C | CA363941355 | CD2AP | c.1531-2A>C (n.1531-2A>C) n.54A>C c.1519-2A>C (n.1519-2A>C) c.1384-2A>C (n.1384-2A>C) | |
6 | g.47607925A>G | CA363941357 | CD2AP | c.1531-2A>G (n.1531-2A>G) n.54A>G c.1519-2A>G (n.1519-2A>G) c.1384-2A>G (n.1384-2A>G) | |
6 | g.47607925A>T | CA363941358 | CD2AP | c.1531-2A>T (n.1531-2A>T) n.54A>T c.1519-2A>T (n.1519-2A>T) c.1384-2A>T (n.1384-2A>T) | |
6 | g.47607926G>A | CA363941360 | CD2AP | c.1531-1G>A (n.1531-1G>A) n.55G>A c.1519-1G>A (n.1519-1G>A) c.1384-1G>A (n.1384-1G>A) | |
6 | g.47607926G>C | CA363941361 | CD2AP | c.1531-1G>C (n.1531-1G>C) n.55G>C c.1519-1G>C (n.1519-1G>C) c.1384-1G>C (n.1384-1G>C) | |
6 | g.47607926G>T | CA363941363 | CD2AP | c.1531-1G>T (n.1531-1G>T) n.55G>T c.1519-1G>T (n.1519-1G>T) c.1384-1G>T (n.1384-1G>T) | |
6 | g.47607927C>A | CA363941366 | CD2AP | c.1531C>A (p.Pro511Thr) n.56C>A c.1519C>A (p.Pro507Thr) c.1384C>A (p.Pro462Thr) | gnomAD v4 |
6 | g.47607927C>G | CA363941368 | CD2AP | c.1531C>G (p.Pro511Ala) n.56C>G c.1519C>G (p.Pro507Ala) c.1384C>G (p.Pro462Ala) | |
6 | g.47607927C>T | CA363941371 | CD2AP | c.1531C>T (p.Pro511Ser) n.56C>T c.1519C>T (p.Pro507Ser) c.1384C>T (p.Pro462Ser) | gnomAD v4 |
6 | g.47607928C>A | CA363941374 | CD2AP | c.1532C>A (p.Pro511Gln) n.57C>A c.1520C>A (p.Pro507Gln) c.1385C>A (p.Pro462Gln) | gnomAD v4 |
6 | g.47607928C>G | CA363941376 | CD2AP | c.1532C>G (p.Pro511Arg) n.57C>G c.1520C>G (p.Pro507Arg) c.1385C>G (p.Pro462Arg) | |
6 | g.47607928C>T | CA363941378 | CD2AP | c.1532C>T (p.Pro511Leu) n.57C>T c.1520C>T (p.Pro507Leu) c.1385C>T (p.Pro462Leu) | gnomAD v4 |
6 | g.47607929A>C | CA450395713 | CD2AP | c.1533A>C (p.Pro511=) n.58A>C c.1521A>C (p.Pro507=) c.1386A>C (p.Pro462=) | |
6 | g.47607929A>G | CA450395717 | CD2AP | c.1533A>G (p.Pro511=) n.58A>G c.1521A>G (p.Pro507=) c.1386A>G (p.Pro462=) | |
6 | g.47607929A>T | CA450395716 | CD2AP | c.1533A>T (p.Pro511=) n.58A>T c.1521A>T (p.Pro507=) c.1386A>T (p.Pro462=) | |
6 | g.47607930A= | CA1626460745 | CD2AP | c.1534A= (p.Thr512=) n.59A= c.1522A= (p.Thr508=) c.1387A= (p.Thr463=) | |
6 | g.47607930A>C | CA363941385 | CD2AP | c.1534A>C (p.Thr512Pro) n.59A>C c.1522A>C (p.Thr508Pro) c.1387A>C (p.Thr463Pro) | |
6 | g.47607930A>G | CA363941383 | CD2AP | c.1534A>G (p.Thr512Ala) n.59A>G c.1522A>G (p.Thr508Ala) c.1387A>G (p.Thr463Ala) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.47607930A>T | CA363941380 | CD2AP | c.1534A>T (p.Thr512Ser) n.59A>T c.1522A>T (p.Thr508Ser) c.1387A>T (p.Thr463Ser) | |
6 | g.47607931C>A | CA363941389 | CD2AP | c.1535C>A (p.Thr512Asn) n.60C>A c.1523C>A (p.Thr508Asn) c.1388C>A (p.Thr463Asn) | |
6 | g.47607931C>G | CA363941388 | CD2AP | c.1535C>G (p.Thr512Ser) n.60C>G c.1523C>G (p.Thr508Ser) c.1388C>G (p.Thr463Ser) | |
6 | g.47607931C>T | CA363941390 | CD2AP | c.1535C>T (p.Thr512Ile) n.60C>T c.1523C>T (p.Thr508Ile) c.1388C>T (p.Thr463Ile) | gnomAD v4 |
6 | g.47607932T>A | CA450395731 | CD2AP | c.1536T>A (p.Thr512=) n.61T>A c.1524T>A (p.Thr508=) c.1389T>A (p.Thr463=) | |
6 | g.47607932T>C | CA450395728 | CD2AP | c.1536T>C (p.Thr512=) n.61T>C c.1524T>C (p.Thr508=) c.1389T>C (p.Thr463=) | gnomAD v4 |
6 | g.47607932T>G | CA450395726 | CD2AP | c.1536T>G (p.Thr512=) n.61T>G c.1524T>G (p.Thr508=) c.1389T>G (p.Thr463=) | |
6 | g.47607933C>A | CA363941392 | CD2AP | c.1537C>A (p.His513Asn) n.62C>A c.1525C>A (p.His509Asn) c.1390C>A (p.His464Asn) | |
6 | g.47607933C= | CA1626460751 | CD2AP | c.1537C= (p.His513=) n.62C= c.1525C= (p.His509=) c.1390C= (p.His464=) | |
6 | g.47607933C>G | CA363941394 | CD2AP | c.1537C>G (p.His513Asp) n.62C>G c.1525C>G (p.His509Asp) c.1390C>G (p.His464Asp) | gnomAD v4 |
6 | g.47607933C>T | CA363941396 | CD2AP | c.1537C>T (p.His513Tyr) n.62C>T c.1525C>T (p.His509Tyr) c.1390C>T (p.His464Tyr) | |
6 | g.47607935_47607936del | CA2679027820 | CD2AP | c.1539_1540del (p.His513GlnfsTer21) n.64_65del c.1527_1528del (p.His509GlnfsTer21) c.1392_1393del (p.His464GlnfsTer21) | gnomAD v4 |
6 | g.47607934A>C | CA363941400 | CD2AP | c.1538A>C (p.His513Pro) n.63A>C c.1526A>C (p.His509Pro) c.1391A>C (p.His464Pro) | |
6 | g.47607934A>G | CA363941402 | CD2AP | c.1538A>G (p.His513Arg) n.63A>G c.1526A>G (p.His509Arg) c.1391A>G (p.His464Arg) | |
6 | g.47607934A>T | CA363941405 | CD2AP | c.1538A>T (p.His513Leu) n.63A>T c.1526A>T (p.His509Leu) c.1391A>T (p.His464Leu) | |
6 | g.47607934dup | CA3844375 | CD2AP | c.1538dup (p.His513GlnfsTer22) n.63dup c.1526dup (p.His509GlnfsTer22) c.1391dup (p.His464GlnfsTer22) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.47607935C>A | CA363941408 | CD2AP | c.1539C>A (p.His513Gln) n.64C>A c.1527C>A (p.His509Gln) c.1392C>A (p.His464Gln) | gnomAD v4 |
6 | g.47607935C>G | CA363941409 | CD2AP | c.1539C>G (p.His513Gln) n.64C>G c.1527C>G (p.His509Gln) c.1392C>G (p.His464Gln) | |
6 | g.47607935C>T | CA450395749 | CD2AP | c.1539C>T (p.His513=) n.64C>T c.1527C>T (p.His509=) c.1392C>T (p.His464=) | gnomAD v4 |
6 | g.47607936A= | CA1626460758 | CD2AP | c.1540A= (p.Ser514=) n.65A= c.1528A= (p.Ser510=) c.1393A= (p.Ser465=) | |
6 | g.47607936A>C | CA363941412 | CD2AP | c.1540A>C (p.Ser514Arg) n.65A>C c.1528A>C (p.Ser510Arg) c.1393A>C (p.Ser465Arg) | |
6 | g.47607936A>G | CA363941414 | CD2AP | c.1540A>G (p.Ser514Gly) n.65A>G c.1528A>G (p.Ser510Gly) c.1393A>G (p.Ser465Gly) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.47607936A>T | CA363941417 | CD2AP | c.1540A>T (p.Ser514Cys) n.65A>T c.1528A>T (p.Ser510Cys) c.1393A>T (p.Ser465Cys) | |
6 | g.47607937G>A | CA363941425 | CD2AP | c.1541G>A (p.Ser514Asn) n.66G>A c.1529G>A (p.Ser510Asn) c.1394G>A (p.Ser465Asn) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.47607937G>C | CA363941422 | CD2AP | c.1541G>C (p.Ser514Thr) n.66G>C c.1529G>C (p.Ser510Thr) c.1394G>C (p.Ser465Thr) | |
6 | g.47607937G= | CA1626460762 | CD2AP | c.1541G= (p.Ser514=) n.66G= c.1529G= (p.Ser510=) c.1394G= (p.Ser465=) | |
6 | g.47607937G>T | CA363941420 | CD2AP | c.1541G>T (p.Ser514Ile) n.66G>T c.1529G>T (p.Ser510Ile) c.1394G>T (p.Ser465Ile) | |
6 | g.47607938C>A | CA363941428 | CD2AP | c.1542C>A (p.Ser514Arg) n.67C>A c.1530C>A (p.Ser510Arg) c.1395C>A (p.Ser465Arg) | |
6 | g.47607938C>G | CA363941430 | CD2AP | c.1542C>G (p.Ser514Arg) n.67C>G c.1530C>G (p.Ser510Arg) c.1395C>G (p.Ser465Arg) | |
6 | g.47607938C>T | CA450395762 | CD2AP | c.1542C>T (p.Ser514=) n.67C>T c.1530C>T (p.Ser510=) c.1395C>T (p.Ser465=) | gnomAD v4 |
6 | g.47607939C>A | CA363941432 | CD2AP | c.1543C>A (p.Pro515Thr) n.68C>A c.1531C>A (p.Pro511Thr) c.1396C>A (p.Pro466Thr) | dbSNP |
6 | g.47607939C= | CA1626460767 | CD2AP | c.1543C= (p.Pro515=) n.68C= c.1531C= (p.Pro511=) c.1396C= (p.Pro466=) | |
6 | g.47607939C>G | CA363941434 | CD2AP | c.1543C>G (p.Pro515Ala) n.68C>G c.1531C>G (p.Pro511Ala) c.1396C>G (p.Pro466Ala) | |
6 | g.47607939C>T | CA363941437 | CD2AP | c.1543C>T (p.Pro515Ser) n.68C>T c.1531C>T (p.Pro511Ser) c.1396C>T (p.Pro466Ser) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.47607940C>A | CA363941439 | CD2AP | c.1544C>A (p.Pro515His) n.69C>A c.1532C>A (p.Pro511His) c.1397C>A (p.Pro466His) | |
6 | g.47607940C= | CA1626460770 | CD2AP | c.1544C= (p.Pro515=) n.69C= c.1532C= (p.Pro511=) c.1397C= (p.Pro466=) | |
6 | g.47607940C>G | CA363941441 | CD2AP | c.1544C>G (p.Pro515Arg) n.69C>G c.1532C>G (p.Pro511Arg) c.1397C>G (p.Pro466Arg) | |
6 | g.47607940C>T | CA363941443 | CD2AP | c.1544C>T (p.Pro515Leu) n.69C>T c.1532C>T (p.Pro511Leu) c.1397C>T (p.Pro466Leu) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.47607941C>A | CA450395776 | CD2AP | c.1545C>A (p.Pro515=) n.70C>A c.1533C>A (p.Pro511=) c.1398C>A (p.Pro466=) | |
6 | g.47607941C= | CA1626460774 | CD2AP | c.1545C= (p.Pro515=) n.70C= c.1533C= (p.Pro511=) c.1398C= (p.Pro466=) | |
6 | g.47607941C>G | CA450395778 | CD2AP | c.1545C>G (p.Pro515=) n.70C>G c.1533C>G (p.Pro511=) c.1398C>G (p.Pro466=) | |
6 | g.47607941C>T | CA3844376 | CD2AP | c.1545C>T (p.Pro515=) n.70C>T c.1533C>T (p.Pro511=) c.1398C>T (p.Pro466=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.47607942G>A | CA3844378 | CD2AP | c.1546G>A (p.Glu516Lys) n.71G>A c.1534G>A (p.Glu512Lys) c.1399G>A (p.Glu467Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.47607942G>C | CA363941449 | CD2AP | c.1546G>C (p.Glu516Gln) n.71G>C c.1534G>C (p.Glu512Gln) c.1399G>C (p.Glu467Gln) | |
6 | g.47607942G= | CA1626460781 | CD2AP | c.1546G= (p.Glu516=) n.71G= c.1534G= (p.Glu512=) c.1399G= (p.Glu467=) | |
6 | g.47607942G>T | CA363941451 | CD2AP | c.1546G>T (p.Glu516Ter) n.71G>T c.1534G>T (p.Glu512Ter) c.1399G>T (p.Glu467Ter) | |
6 | g.47607943A>C | CA363941457 | CD2AP | c.1547A>C (p.Glu516Ala) n.72A>C c.1535A>C (p.Glu512Ala) c.1400A>C (p.Glu467Ala) | |
6 | g.47607943A>G | CA363941461 | CD2AP | c.1547A>G (p.Glu516Gly) n.72A>G c.1535A>G (p.Glu512Gly) c.1400A>G (p.Glu467Gly) | |
6 | g.47607943A>T | CA363941455 | CD2AP | c.1547A>T (p.Glu516Val) n.72A>T c.1535A>T (p.Glu512Val) c.1400A>T (p.Glu467Val) | |
6 | g.47607948dup | CA3844377 | CD2AP | c.1552dup (p.Ile518AsnfsTer17) n.77dup c.1540dup (p.Ile514AsnfsTer17) c.1405dup (p.Ile469AsnfsTer17) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.47607948del | CA2679027821 | CD2AP | c.1552del (p.Ile518SerfsTer2) n.77del c.1540del (p.Ile514SerfsTer2) c.1405del (p.Ile469SerfsTer2) | gnomAD v4 |
6 | g.47607944A= | CA1626460790 | CD2AP | c.1548A= (p.Glu516=) n.73A= c.1536A= (p.Glu512=) c.1401A= (p.Glu467=) | |
6 | g.47607944A>C | CA363941464 | CD2AP | c.1548A>C (p.Glu516Asp) n.73A>C c.1536A>C (p.Glu512Asp) c.1401A>C (p.Glu467Asp) | |
6 | g.47607944A>G | CA450395791 | CD2AP | c.1548A>G (p.Glu516=) n.73A>G c.1536A>G (p.Glu512=) c.1401A>G (p.Glu467=) | dbSNP gnomAD v4 |
6 | g.47607944A>T | CA363941466 | CD2AP | c.1548A>T (p.Glu516Asp) n.73A>T c.1536A>T (p.Glu512Asp) c.1401A>T (p.Glu467Asp) | |
6 | g.47607945A= | CA1626460793 | CD2AP | c.1549A= (p.Lys517=) n.74A= c.1537A= (p.Lys513=) c.1402A= (p.Lys468=) | |
6 | g.47607945A>C | CA363941469 | CD2AP | c.1549A>C (p.Lys517Gln) n.74A>C c.1537A>C (p.Lys513Gln) c.1402A>C (p.Lys468Gln) | |
6 | g.47607945A>G | CA363941470 | CD2AP | c.1549A>G (p.Lys517Glu) n.74A>G c.1537A>G (p.Lys513Glu) c.1402A>G (p.Lys468Glu) | gnomAD v4 |
6 | g.47607945A>T | CA363941473 | CD2AP | c.1549A>T (p.Lys517Ter) n.74A>T c.1537A>T (p.Lys513Ter) c.1402A>T (p.Lys468Ter) | dbSNP gnomAD v4 |
6 | g.47607946A>C | CA363941480 | CD2AP | c.1550A>C (p.Lys517Thr) n.75A>C c.1538A>C (p.Lys513Thr) c.1403A>C (p.Lys468Thr) | |
6 | g.47607946A>G | CA363941476 | CD2AP | c.1550A>G (p.Lys517Arg) n.75A>G c.1538A>G (p.Lys513Arg) c.1403A>G (p.Lys468Arg) | |
6 | g.47607946A>T | CA363941477 | CD2AP | c.1550A>T (p.Lys517Ile) n.75A>T c.1538A>T (p.Lys513Ile) c.1403A>T (p.Lys468Ile) | |
6 | g.47607947A>C | CA363941482 | CD2AP | c.1551A>C (p.Lys517Asn) n.76A>C c.1539A>C (p.Lys513Asn) c.1404A>C (p.Lys468Asn) | |
6 | g.47607947A>G | CA450395800 | CD2AP | c.1551A>G (p.Lys517=) n.76A>G c.1539A>G (p.Lys513=) c.1404A>G (p.Lys468=) | |
6 | g.47607947A>T | CA363941485 | CD2AP | c.1551A>T (p.Lys517Asn) n.76A>T c.1539A>T (p.Lys513Asn) c.1404A>T (p.Lys468Asn) | |
6 | g.47607948A>C | CA363941488 | CD2AP | c.1552A>C (p.Ile518Leu) n.77A>C c.1540A>C (p.Ile514Leu) c.1405A>C (p.Ile469Leu) | |
6 | g.47607948A>G | CA363941490 | CD2AP | c.1552A>G (p.Ile518Val) n.77A>G c.1540A>G (p.Ile514Val) c.1405A>G (p.Ile469Val) | |
6 | g.47607948A>T | CA363941492 | CD2AP | c.1552A>T (p.Ile518Phe) n.77A>T c.1540A>T (p.Ile514Phe) c.1405A>T (p.Ile469Phe) | |
6 | g.47607949T>A | CA137927471 | CD2AP | c.1553T>A (p.Ile518Asn) n.78T>A c.1541T>A (p.Ile514Asn) c.1406T>A (p.Ile469Asn) | dbSNP gnomAD v4 |
6 | g.47607949T>C | CA363941499 | CD2AP | c.1553T>C (p.Ile518Thr) n.78T>C c.1541T>C (p.Ile514Thr) c.1406T>C (p.Ile469Thr) | |
6 | g.47607949T>G | CA363941496 | CD2AP | c.1553T>G (p.Ile518Ser) n.78T>G c.1541T>G (p.Ile514Ser) c.1406T>G (p.Ile469Ser) | |
6 | g.47607949T= | CA1626460798 | CD2AP | c.1553T= (p.Ile518=) n.78T= c.1541T= (p.Ile514=) c.1406T= (p.Ile469=) | |
6 | g.47607950C>A | CA450395809 | CD2AP | c.1554C>A (p.Ile518=) n.79C>A c.1542C>A (p.Ile514=) c.1407C>A (p.Ile469=) | |
6 | g.47607950C>G | CA363941501 | CD2AP | c.1554C>G (p.Ile518Met) n.79C>G c.1542C>G (p.Ile514Met) c.1407C>G (p.Ile469Met) | gnomAD v4 |
6 | g.47607950C>T | CA450395812 | CD2AP | c.1554C>T (p.Ile518=) n.79C>T c.1542C>T (p.Ile514=) c.1407C>T (p.Ile469=) | COSMIC |
6 | g.47607951T>A | CA363941503 | CD2AP | c.1555T>A (p.Leu519Met) n.80T>A c.1543T>A (p.Leu515Met) c.1408T>A (p.Leu470Met) | |
6 | g.47607951T>C | CA450395820 | CD2AP | c.1555T>C (p.Leu519=) n.80T>C c.1543T>C (p.Leu515=) c.1408T>C (p.Leu470=) | |
6 | g.47607951T>G | CA363941506 | CD2AP | c.1555T>G (p.Leu519Val) n.80T>G c.1543T>G (p.Leu515Val) c.1408T>G (p.Leu470Val) | gnomAD v4 |
6 | g.47607952T>A | CA363941509 | CD2AP | c.1556T>A (p.Leu519Ter) n.81T>A c.1544T>A (p.Leu515Ter) c.1409T>A (p.Leu470Ter) | |
6 | g.47607952T>C | CA363941512 | CD2AP | c.1556T>C (p.Leu519Ser) n.81T>C c.1544T>C (p.Leu515Ser) c.1409T>C (p.Leu470Ser) | |
6 | g.47607952T>G | CA363941514 | CD2AP | c.1556T>G (p.Leu519Trp) n.81T>G c.1544T>G (p.Leu515Trp) c.1409T>G (p.Leu470Trp) | |
6 | g.47607953G>A | CA450395825 | CD2AP | c.1557G>A (p.Leu519=) n.82G>A c.1545G>A (p.Leu515=) c.1410G>A (p.Leu470=) | |
6 | g.47607953G>C | CA137927476 | CD2AP | c.1557G>C (p.Leu519Phe) n.82G>C c.1545G>C (p.Leu515Phe) c.1410G>C (p.Leu470Phe) | dbSNP gnomAD v4 |
6 | g.47607953G= | CA1626460800 | CD2AP | c.1557G= (p.Leu519=) n.82G= c.1545G= (p.Leu515=) c.1410G= (p.Leu470=) | |
6 | g.47607953G>T | CA363941518 | CD2AP | c.1557G>T (p.Leu519Phe) n.82G>T c.1545G>T (p.Leu515Phe) c.1410G>T (p.Leu470Phe) | |
6 | g.47607954A>C | CA363941521 | CD2AP | c.1558A>C (p.Lys520Gln) n.83A>C c.1546A>C (p.Lys516Gln) c.1411A>C (p.Lys471Gln) | |
6 | g.47607954A>G | CA363941523 | CD2AP | c.1558A>G (p.Lys520Glu) n.83A>G c.1546A>G (p.Lys516Glu) c.1411A>G (p.Lys471Glu) | |
6 | g.47607954A>T | CA363941525 | CD2AP | c.1558A>T (p.Lys520Ter) n.83A>T c.1546A>T (p.Lys516Ter) c.1411A>T (p.Lys471Ter) | |
6 | g.47607955A= | CA1626460805 | CD2AP | c.1559A= (p.Lys520=) n.84A= c.1547A= (p.Lys516=) c.1412A= (p.Lys471=) | |
6 | g.47607955A>C | CA3844379 | CD2AP | c.1559A>C (p.Lys520Thr) n.84A>C c.1547A>C (p.Lys516Thr) c.1412A>C (p.Lys471Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.47607955A>G | CA363941530 | CD2AP | c.1559A>G (p.Lys520Arg) n.84A>G c.1547A>G (p.Lys516Arg) c.1412A>G (p.Lys471Arg) | dbSNP gnomAD v4 |
6 | g.47607955A>T | CA363941528 | CD2AP | c.1559A>T (p.Lys520Met) n.84A>T c.1547A>T (p.Lys516Met) c.1412A>T (p.Lys471Met) | |
6 | g.47607956G>A | CA450395844 | CD2AP | c.1560G>A (p.Lys520=) n.85G>A c.1548G>A (p.Lys516=) c.1413G>A (p.Lys471=) | gnomAD v4 |
6 | g.47607956G>C | CA363941533 | CD2AP | c.1560G>C (p.Lys520Asn) n.85G>C c.1548G>C (p.Lys516Asn) c.1413G>C (p.Lys471Asn) | |
6 | g.47607956G>T | CA363941535 | CD2AP | c.1560G>T (p.Lys520Asn) n.85G>T c.1548G>T (p.Lys516Asn) c.1413G>T (p.Lys471Asn) | |
6 | g.47607957T>A | CA363941538 | CD2AP | c.1561T>A (p.Leu521Ile) n.86T>A c.1549T>A (p.Leu517Ile) c.1414T>A (p.Leu472Ile) | |
6 | g.47607957T>C | CA450395847 | CD2AP | c.1561T>C (p.Leu521=) n.86T>C c.1549T>C (p.Leu517=) c.1414T>C (p.Leu472=) | |
6 | g.47607957T>G | CA363941540 | CD2AP | c.1561T>G (p.Leu521Val) n.86T>G c.1549T>G (p.Leu517Val) c.1414T>G (p.Leu472Val) | |
6 | g.47607958T>A | CA363941543 | CD2AP | c.1562T>A (p.Leu521Ter) n.87T>A c.1550T>A (p.Leu517Ter) c.1415T>A (p.Leu472Ter) | |
6 | g.47607958T>C | CA363941545 | CD2AP | c.1562T>C (p.Leu521Ser) n.87T>C c.1550T>C (p.Leu517Ser) c.1415T>C (p.Leu472Ser) | |
6 | g.47607958T>G | CA137927481 | CD2AP | c.1562T>G (p.Leu521Ter) n.87T>G c.1550T>G (p.Leu517Ter) c.1415T>G (p.Leu472Ter) | dbSNP |
6 | g.47607958T= | CA1626460810 | CD2AP | c.1562T= (p.Leu521=) n.87T= c.1550T= (p.Leu517=) c.1415T= (p.Leu472=) | |
6 | g.47607959A= | CA1626460813 | CD2AP | c.1563A= (p.Leu521=) n.88A= c.1551A= (p.Leu517=) c.1416A= (p.Leu472=) | |
6 | g.47607959A>C | CA363941549 | CD2AP | c.1563A>C (p.Leu521Phe) n.88A>C c.1551A>C (p.Leu517Phe) c.1416A>C (p.Leu472Phe) | |
6 | g.47607959A>G | CA450395854 | CD2AP | c.1563A>G (p.Leu521=) n.88A>G c.1551A>G (p.Leu517=) c.1416A>G (p.Leu472=) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.47607959A>T | CA363941551 | CD2AP | c.1563A>T (p.Leu521Phe) n.88A>T c.1551A>T (p.Leu517Phe) c.1416A>T (p.Leu472Phe) | |
6 | g.47607960C>A | CA363941555 | CD2AP | c.1564C>A (p.Pro522Thr) n.89C>A c.1552C>A (p.Pro518Thr) c.1417C>A (p.Pro473Thr) | |
6 | g.47607960C>G | CA363941558 | CD2AP | c.1564C>G (p.Pro522Ala) n.89C>G c.1552C>G (p.Pro518Ala) c.1417C>G (p.Pro473Ala) | |
6 | g.47607960C>T | CA363941559 | CD2AP | c.1564C>T (p.Pro522Ser) n.89C>T c.1552C>T (p.Pro518Ser) c.1417C>T (p.Pro473Ser) | |
6 | g.47607961C>A | CA363941563 | CD2AP | c.1565C>A (p.Pro522Gln) n.90C>A c.1553C>A (p.Pro518Gln) c.1418C>A (p.Pro473Gln) | |
6 | g.47607961C>G | CA363941564 | CD2AP | c.1565C>G (p.Pro522Arg) n.90C>G c.1553C>G (p.Pro518Arg) c.1418C>G (p.Pro473Arg) | |
6 | g.47607961C>T | CA363941566 | CD2AP | c.1565C>T (p.Pro522Leu) n.90C>T c.1553C>T (p.Pro518Leu) c.1418C>T (p.Pro473Leu) | |
6 | g.47607962A= | CA1626460816 | CD2AP | c.1566A= (p.Pro522=) n.91A= c.1554A= (p.Pro518=) c.1419A= (p.Pro473=) | |
6 | g.47607962A>C | CA3844380 | CD2AP | c.1566A>C (p.Pro522=) n.91A>C c.1554A>C (p.Pro518=) c.1419A>C (p.Pro473=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.47607962A>G | CA450395866 | CD2AP | c.1566A>G (p.Pro522=) n.91A>G c.1554A>G (p.Pro518=) c.1419A>G (p.Pro473=) | |
6 | g.47607962A>T | CA450395869 | CD2AP | c.1566A>T (p.Pro522=) n.91A>T c.1554A>T (p.Pro518=) c.1419A>T (p.Pro473=) | |
6 | g.47607963A= | CA1626460819 | CD2AP | c.1567A= (p.Lys523=) n.92A= c.1555A= (p.Lys519=) c.1420A= (p.Lys474=) | |
6 | g.47607963A>C | CA363941577 | CD2AP | c.1567A>C (p.Lys523Gln) n.92A>C c.1555A>C (p.Lys519Gln) c.1420A>C (p.Lys474Gln) | |
6 | g.47607963A>G | CA363941572 | CD2AP | c.1567A>G (p.Lys523Glu) n.92A>G c.1555A>G (p.Lys519Glu) c.1420A>G (p.Lys474Glu) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.47607963A>T | CA363941575 | CD2AP | c.1567A>T (p.Lys523Ter) n.92A>T c.1555A>T (p.Lys519Ter) c.1420A>T (p.Lys474Ter) | |
6 | g.47607963_47607966delinsAAAG | CA1626460821 | CD2AP | c.1567_1570delinsAAAG (p.Lys523=) n.92_95delinsAAAG c.1555_1558delinsAAAG (p.Lys519=) c.1420_1423delinsAAAG (p.Lys474=) | |
6 | g.47607964A>C | CA363941586 | CD2AP | c.1568A>C (p.Lys523Thr) n.93A>C c.1556A>C (p.Lys519Thr) c.1421A>C (p.Lys474Thr) | |
6 | g.47607964A>G | CA363941588 | CD2AP | c.1568A>G (p.Lys523Arg) n.93A>G c.1556A>G (p.Lys519Arg) c.1421A>G (p.Lys474Arg) | gnomAD v4 |
6 | g.47607964A>T | CA363941590 | CD2AP | c.1568A>T (p.Lys523Ile) n.93A>T c.1556A>T (p.Lys519Ile) c.1421A>T (p.Lys474Ile) | |
6 | g.47607971_47607973del | CA3844381 | CD2AP | c.1575_1577del (p.Glu525del) n.100_102del c.1563_1565del (p.Glu521del) c.1428_1430del (p.Glu476del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.47607965A= | CA1626460828 | CD2AP | c.1569A= (p.Lys523=) n.94A= c.1557A= (p.Lys519=) c.1422A= (p.Lys474=) | |
6 | g.47607965A>C | CA363941598 | CD2AP | c.1569A>C (p.Lys523Asn) n.94A>C c.1557A>C (p.Lys519Asn) c.1422A>C (p.Lys474Asn) | |
6 | g.47607965A>G | CA450395888 | CD2AP | c.1569A>G (p.Lys523=) n.94A>G c.1557A>G (p.Lys519=) c.1422A>G (p.Lys474=) | gnomAD v4 |
6 | g.47607965A>T | CA363941600 | CD2AP | c.1569A>T (p.Lys523Asn) n.94A>T c.1557A>T (p.Lys519Asn) c.1422A>T (p.Lys474Asn) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.47607966G>A | CA363941603 | CD2AP | c.1570G>A (p.Glu524Lys) n.95G>A c.1558G>A (p.Glu520Lys) c.1423G>A (p.Glu475Lys) | |
6 | g.47607966G>C | CA363941605 | CD2AP | c.1570G>C (p.Glu524Gln) n.95G>C c.1558G>C (p.Glu520Gln) c.1423G>C (p.Glu475Gln) | |
6 | g.47607966G>T | CA363941607 | CD2AP | c.1570G>T (p.Glu524Ter) n.95G>T c.1558G>T (p.Glu520Ter) c.1423G>T (p.Glu475Ter) | |
6 | g.47607967A= | CA1626460831 | CD2AP | c.1571A= (p.Glu524=) n.96A= c.1559A= (p.Glu520=) c.1424A= (p.Glu475=) | |
6 | g.47607967A>C | CA363941612 | CD2AP | c.1571A>C (p.Glu524Ala) n.96A>C c.1559A>C (p.Glu520Ala) c.1424A>C (p.Glu475Ala) | |
6 | g.47607967A>G | CA363941609 | CD2AP | c.1571A>G (p.Glu524Gly) n.96A>G c.1559A>G (p.Glu520Gly) c.1424A>G (p.Glu475Gly) | dbSNP |
6 | g.47607967A>T | CA363941614 | CD2AP | c.1571A>T (p.Glu524Val) n.96A>T c.1559A>T (p.Glu520Val) c.1424A>T (p.Glu475Val) | |
6 | g.47607968A>C | CA363941617 | CD2AP | c.1572A>C (p.Glu524Asp) n.97A>C c.1560A>C (p.Glu520Asp) c.1425A>C (p.Glu475Asp) | |
6 | g.47607968A>G | CA450395909 | CD2AP | c.1572A>G (p.Glu524=) n.97A>G c.1560A>G (p.Glu520=) c.1425A>G (p.Glu475=) | gnomAD v4 |
6 | g.47607968A>T | CA363941619 | CD2AP | c.1572A>T (p.Glu524Asp) n.97A>T c.1560A>T (p.Glu520Asp) c.1425A>T (p.Glu475Asp) | |
6 | g.47607969G>A | CA363941624 | CD2AP | c.1573G>A (p.Glu525Lys) n.98G>A c.1561G>A (p.Glu521Lys) c.1426G>A (p.Glu476Lys) | |
6 | g.47607969G>C | CA363941626 | CD2AP | c.1573G>C (p.Glu525Gln) n.98G>C c.1561G>C (p.Glu521Gln) c.1426G>C (p.Glu476Gln) | |
6 | g.47607969G>T | CA363941629 | CD2AP | c.1573G>T (p.Glu525Ter) n.98G>T c.1561G>T (p.Glu521Ter) c.1426G>T (p.Glu476Ter) | |
6 | g.47607970A= | CA1626460836 | CD2AP | c.1574A= (p.Glu525=) n.99A= c.1562A= (p.Glu521=) c.1427A= (p.Glu476=) | |
6 | g.47607970A>C | CA363941631 | CD2AP | c.1574A>C (p.Glu525Ala) n.99A>C c.1562A>C (p.Glu521Ala) c.1427A>C (p.Glu476Ala) | |
6 | g.47607970A>G | CA363941632 | CD2AP | c.1574A>G (p.Glu525Gly) n.99A>G c.1562A>G (p.Glu521Gly) c.1427A>G (p.Glu476Gly) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.47607970A>T | CA363941634 | CD2AP | c.1574A>T (p.Glu525Val) n.99A>T c.1562A>T (p.Glu521Val) c.1427A>T (p.Glu476Val) | |
6 | g.47607971A= | CA1626460837 | CD2AP | c.1575A= (p.Glu525=) n.100A= c.1563A= (p.Glu521=) c.1428A= (p.Glu476=) | |
6 | g.47607971A>C | CA137927518 | CD2AP | c.1575A>C (p.Glu525Asp) n.100A>C c.1563A>C (p.Glu521Asp) c.1428A>C (p.Glu476Asp) | dbSNP gnomAD v4 |
6 | g.47607971A>G | CA450395933 | CD2AP | c.1575A>G (p.Glu525=) n.100A>G c.1563A>G (p.Glu521=) c.1428A>G (p.Glu476=) | |
6 | g.47607971A>T | CA363941637 | CD2AP | c.1575A>T (p.Glu525Asp) n.100A>T c.1563A>T (p.Glu521Asp) c.1428A>T (p.Glu476Asp) | |
6 | g.47607972G>A | CA363941645 | CD2AP | c.1576G>A (p.Asp526Asn) n.101G>A c.1564G>A (p.Asp522Asn) c.1429G>A (p.Asp477Asn) | COSMIC |
6 | g.47607972G>C | CA363941643 | CD2AP | c.1576G>C (p.Asp526His) n.101G>C c.1564G>C (p.Asp522His) c.1429G>C (p.Asp477His) | |
6 | g.47607972G>T | CA363941640 | CD2AP | c.1576G>T (p.Asp526Tyr) n.101G>T c.1564G>T (p.Asp522Tyr) c.1429G>T (p.Asp477Tyr) | |
6 | g.47607973A>C | CA363941647 | CD2AP | c.1577A>C (p.Asp526Ala) n.102A>C c.1565A>C (p.Asp522Ala) c.1430A>C (p.Asp477Ala) | |
6 | g.47607973A>G | CA363941648 | CD2AP | c.1577A>G (p.Asp526Gly) n.102A>G c.1565A>G (p.Asp522Gly) c.1430A>G (p.Asp477Gly) | |
6 | g.47607973A>T | CA363941650 | CD2AP | c.1577A>T (p.Asp526Val) n.102A>T c.1565A>T (p.Asp522Val) c.1430A>T (p.Asp477Val) | |
6 | g.47607974C>A | CA363941657 | CD2AP | c.1578C>A (p.Asp526Glu) n.103C>A c.1566C>A (p.Asp522Glu) c.1431C>A (p.Asp477Glu) | |
6 | g.47607974C>G | CA363941658 | CD2AP | c.1578C>G (p.Asp526Glu) n.103C>G c.1566C>G (p.Asp522Glu) c.1431C>G (p.Asp477Glu) | |
6 | g.47607974C>T | CA450395952 | CD2AP | c.1578C>T (p.Asp526=) n.103C>T c.1566C>T (p.Asp522=) c.1431C>T (p.Asp477=) | |
6 | g.47607975A>C | CA363941661 | CD2AP | c.1579A>C (p.Ser527Arg) n.104A>C c.1567A>C (p.Ser523Arg) c.1432A>C (p.Ser478Arg) | |
6 | g.47607975A>G | CA363941663 | CD2AP | c.1579A>G (p.Ser527Gly) n.104A>G c.1567A>G (p.Ser523Gly) c.1432A>G (p.Ser478Gly) | |
6 | g.47607975A>T | CA363941665 | CD2AP | c.1579A>T (p.Ser527Cys) n.104A>T c.1567A>T (p.Ser523Cys) c.1432A>T (p.Ser478Cys) | |
6 | g.47607976G>A | CA3844382 | CD2AP | c.1580G>A (p.Ser527Asn) n.105G>A c.1568G>A (p.Ser523Asn) c.1433G>A (p.Ser478Asn) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.47607976G>C | CA363941670 | CD2AP | c.1580G>C (p.Ser527Thr) n.105G>C c.1568G>C (p.Ser523Thr) c.1433G>C (p.Ser478Thr) | |
6 | g.47607976G= | CA1626460839 | CD2AP | c.1580G= (p.Ser527=) n.105G= c.1568G= (p.Ser523=) c.1433G= (p.Ser478=) | |
6 | g.47607976G>T | CA363941672 | CD2AP | c.1580G>T (p.Ser527Ile) n.105G>T c.1568G>T (p.Ser523Ile) c.1433G>T (p.Ser478Ile) | |
6 | g.47607977T>A | CA363941678 | CD2AP | c.1581T>A (p.Ser527Arg) n.106T>A c.1569T>A (p.Ser523Arg) c.1434T>A (p.Ser478Arg) | |
6 | g.47607977T>C | CA450395965 | CD2AP | c.1581T>C (p.Ser527=) n.106T>C c.1569T>C (p.Ser523=) c.1434T>C (p.Ser478=) | |
6 | g.47607977T>G | CA363941679 | CD2AP | c.1581T>G (p.Ser527Arg) n.106T>G c.1569T>G (p.Ser523Arg) c.1434T>G (p.Ser478Arg) | |
6 | g.47607978G>A | CA363941684 | CD2AP | c.1582G>A (p.Ala528Thr) n.107G>A c.1570G>A (p.Ala524Thr) c.1435G>A (p.Ala479Thr) | gnomAD v4 |
6 | g.47607978G>C | CA363941686 | CD2AP | c.1582G>C (p.Ala528Pro) n.107G>C c.1570G>C (p.Ala524Pro) c.1435G>C (p.Ala479Pro) | |
6 | g.47607978G>T | CA363941682 | CD2AP | c.1582G>T (p.Ala528Ser) n.107G>T c.1570G>T (p.Ala524Ser) c.1435G>T (p.Ala479Ser) | |
6 | g.47607979C>A | CA363941695 | CD2AP | c.1583C>A (p.Ala528Asp) n.108C>A c.1571C>A (p.Ala524Asp) c.1436C>A (p.Ala479Asp) | |
6 | g.47607979C>G | CA363941689 | CD2AP | c.1583C>G (p.Ala528Gly) n.108C>G c.1571C>G (p.Ala524Gly) c.1436C>G (p.Ala479Gly) | |
6 | g.47607979C>T | CA363941692 | CD2AP | c.1583C>T (p.Ala528Val) n.108C>T c.1571C>T (p.Ala524Val) c.1436C>T (p.Ala479Val) | ClinVar |
6 | g.47607980C>A | CA450395980 | CD2AP | c.1584C>A (p.Ala528=) n.109C>A c.1572C>A (p.Ala524=) c.1437C>A (p.Ala479=) | |
6 | g.47607980C= | CA1626460842 | CD2AP | c.1584C= (p.Ala528=) n.109C= c.1572C= (p.Ala524=) c.1437C= (p.Ala479=) | |
6 | g.47607980C>G | CA450395985 | CD2AP | c.1584C>G (p.Ala528=) n.109C>G c.1572C>G (p.Ala524=) c.1437C>G (p.Ala479=) | |
6 | g.47607980C>T | CA137927547 | CD2AP | c.1584C>T (p.Ala528=) n.109C>T c.1572C>T (p.Ala524=) c.1437C>T (p.Ala479=) | dbSNP gnomAD v4 |
6 | g.47607981A>C | CA363941700 | CD2AP | c.1585A>C (p.Asn529His) n.110A>C c.1573A>C (p.Asn525His) c.1438A>C (p.Asn480His) | |
6 | g.47607981A>G | CA363941703 | CD2AP | c.1585A>G (p.Asn529Asp) n.110A>G c.1573A>G (p.Asn525Asp) c.1438A>G (p.Asn480Asp) | |
6 | g.47607981A>T | CA363941706 | CD2AP | c.1585A>T (p.Asn529Tyr) n.110A>T c.1573A>T (p.Asn525Tyr) c.1438A>T (p.Asn480Tyr) | |
6 | g.47607982A>C | CA363941711 | CD2AP | c.1586A>C (p.Asn529Thr) n.111A>C c.1574A>C (p.Asn525Thr) c.1439A>C (p.Asn480Thr) | |
6 | g.47607982A>G | CA363941714 | CD2AP | c.1586A>G (p.Asn529Ser) n.111A>G c.1574A>G (p.Asn525Ser) c.1439A>G (p.Asn480Ser) | |
6 | g.47607982A>T | CA363941717 | CD2AP | c.1586A>T (p.Asn529Ile) n.111A>T c.1574A>T (p.Asn525Ile) c.1439A>T (p.Asn480Ile) | |
6 | g.47607983C>A | CA363941720 | CD2AP | c.1587C>A (p.Asn529Lys) n.112C>A c.1575C>A (p.Asn525Lys) c.1440C>A (p.Asn480Lys) | |
6 | g.47607983C= | CA1626460844 | CD2AP | c.1587C= (p.Asn529=) n.112C= c.1575C= (p.Asn525=) c.1440C= (p.Asn480=) | |
6 | g.47607983C>G | CA363941723 | CD2AP | c.1587C>G (p.Asn529Lys) n.112C>G c.1575C>G (p.Asn525Lys) c.1440C>G (p.Asn480Lys) | |
6 | g.47607983C>T | CA450396020 | CD2AP | c.1587C>T (p.Asn529=) n.112C>T c.1575C>T (p.Asn525=) c.1440C>T (p.Asn480=) | dbSNP |
6 | g.47607984C>A | CA363941727 | CD2AP | c.1588C>A (p.Leu530Met) n.113C>A c.1576C>A (p.Leu526Met) c.1441C>A (p.Leu481Met) | |
6 | g.47607984C= | CA1626460846 | CD2AP | c.1588C= (p.Leu530=) n.113C= c.1576C= (p.Leu526=) c.1441C= (p.Leu481=) | |
6 | g.47607984C>G | CA3844383 | CD2AP | c.1588C>G (p.Leu530Val) n.113C>G c.1576C>G (p.Leu526Val) c.1441C>G (p.Leu481Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.47607984C>T | CA450396022 | CD2AP | c.1588C>T (p.Leu530=) n.113C>T c.1576C>T (p.Leu526=) c.1441C>T (p.Leu481=) | |
6 | g.47607985T>A | CA363941738 | CD2AP | c.1589T>A (p.Leu530Gln) n.114T>A c.1577T>A (p.Leu526Gln) c.1442T>A (p.Leu481Gln) | |
6 | g.47607985T>C | CA363941742 | CD2AP | c.1589T>C (p.Leu530Pro) n.114T>C c.1577T>C (p.Leu526Pro) c.1442T>C (p.Leu481Pro) | |
6 | g.47607985T>G | CA363941735 | CD2AP | c.1589T>G (p.Leu530Arg) n.114T>G c.1577T>G (p.Leu526Arg) c.1442T>G (p.Leu481Arg) | |
6 | g.47607986G>A | CA450396027 | CD2AP | c.1590G>A (p.Leu530=) n.115G>A c.1578G>A (p.Leu526=) c.1443G>A (p.Leu481=) | dbSNP |
6 | g.47607986G>C | CA450396029 | CD2AP | c.1590G>C (p.Leu530=) n.115G>C c.1578G>C (p.Leu526=) c.1443G>C (p.Leu481=) | |
6 | g.47607986G= | CA1626460849 | CD2AP | c.1590G= (p.Leu530=) n.115G= c.1578G= (p.Leu526=) c.1443G= (p.Leu481=) | |
6 | g.47607986G>T | CA450396033 | CD2AP | c.1590G>T (p.Leu530=) n.115G>T c.1578G>T (p.Leu526=) c.1443G>T (p.Leu481=) | |
6 | g.47607987A>C | CA363941747 | CD2AP | c.1591A>C (p.Lys531Gln) n.116A>C c.1579A>C (p.Lys527Gln) c.1444A>C (p.Lys482Gln) | |
6 | g.47607987A>G | CA363941752 | CD2AP | c.1591A>G (p.Lys531Glu) n.116A>G c.1579A>G (p.Lys527Glu) c.1444A>G (p.Lys482Glu) | |
6 | g.47607987A>T | CA363941754 | CD2AP | c.1591A>T (p.Lys531Ter) n.116A>T c.1579A>T (p.Lys527Ter) c.1444A>T (p.Lys482Ter) | |
6 | g.47607988A>C | CA363941761 | CD2AP | c.1592A>C (p.Lys531Thr) n.117A>C c.1580A>C (p.Lys527Thr) c.1445A>C (p.Lys482Thr) | |
6 | g.47607988A>G | CA363941762 | CD2AP | c.1592A>G (p.Lys531Arg) n.117A>G c.1580A>G (p.Lys527Arg) c.1445A>G (p.Lys482Arg) | |
6 | g.47607988A>T | CA363941777 | CD2AP | c.1592A>T (p.Lys531Met) n.117A>T c.1580A>T (p.Lys527Met) c.1445A>T (p.Lys482Met) | |
6 | g.47607989G>A | CA450396040 | CD2AP | c.1593G>A (p.Lys531=) n.118G>A c.1581G>A (p.Lys527=) c.1446G>A (p.Lys482=) | |
6 | g.47607989G>C | CA363941782 | CD2AP | c.1593G>C (p.Lys531Asn) n.118G>C c.1581G>C (p.Lys527Asn) c.1446G>C (p.Lys482Asn) | gnomAD v4 |
6 | g.47607989G>T | CA363941784 | CD2AP | c.1593G>T (p.Lys531Asn) n.118G>T c.1581G>T (p.Lys527Asn) c.1446G>T (p.Lys482Asn) | |
6 | g.47607990C>A | CA363941788 | CD2AP | c.1594C>A (p.Pro532Thr) n.119C>A c.1582C>A (p.Pro528Thr) c.1447C>A (p.Pro483Thr) | |
6 | g.47607990C= | CA1626460853 | CD2AP | c.1594C= (p.Pro532=) n.119C= c.1582C= (p.Pro528=) c.1447C= (p.Pro483=) | |
6 | g.47607990C>G | CA363941791 | CD2AP | c.1594C>G (p.Pro532Ala) n.119C>G c.1582C>G (p.Pro528Ala) c.1447C>G (p.Pro483Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.47607990C>T | CA363941794 | CD2AP | c.1594C>T (p.Pro532Ser) n.119C>T c.1582C>T (p.Pro528Ser) c.1447C>T (p.Pro483Ser) | ClinVar dbSNP gnomAD v4 |
6 | g.47607991C>A | CA363941800 | CD2AP | c.1595C>A (p.Pro532Gln) n.120C>A c.1583C>A (p.Pro528Gln) c.1448C>A (p.Pro483Gln) | |
6 | g.47607991C>G | CA363941801 | CD2AP | c.1595C>G (p.Pro532Arg) n.120C>G c.1583C>G (p.Pro528Arg) c.1448C>G (p.Pro483Arg) | |
6 | g.47607991C>T | CA363941804 | CD2AP | c.1595C>T (p.Pro532Leu) n.120C>T c.1583C>T (p.Pro528Leu) c.1448C>T (p.Pro483Leu) | |
6 | g.47607992A= | CA1626460856 | CD2AP | c.1596A= (p.Pro532=) n.121A= c.1584A= (p.Pro528=) c.1449A= (p.Pro483=) | |
6 | g.47607992A>C | CA450396054 | CD2AP | c.1596A>C (p.Pro532=) n.121A>C c.1584A>C (p.Pro528=) c.1449A>C (p.Pro483=) | |
6 | g.47607992A>G | CA3844384 | CD2AP | c.1596A>G (p.Pro532=) n.121A>G c.1584A>G (p.Pro528=) c.1449A>G (p.Pro483=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.47607992A>T | CA450396058 | CD2AP | c.1596A>T (p.Pro532=) n.121A>T c.1584A>T (p.Pro528=) c.1449A>T (p.Pro483=) | |
6 | g.47607993T>A | CA363941829 | CD2AP | c.1597T>A (p.Ser533Thr) n.122T>A c.1585T>A (p.Ser529Thr) c.1450T>A (p.Ser484Thr) | |
6 | g.47607993T>C | CA363941815 | CD2AP | c.1597T>C (p.Ser533Pro) n.122T>C c.1585T>C (p.Ser529Pro) c.1450T>C (p.Ser484Pro) | |
6 | g.47607993T>G | CA363941824 | CD2AP | c.1597T>G (p.Ser533Ala) n.122T>G c.1585T>G (p.Ser529Ala) c.1450T>G (p.Ser484Ala) | |
6 | g.47607994C>A | CA137927554 | CD2AP | c.1598C>A (p.Ser533Tyr) n.123C>A c.1586C>A (p.Ser529Tyr) c.1451C>A (p.Ser484Tyr) | dbSNP gnomAD v3 gnomAD v4 |
6 | g.47607994C= | CA1626460860 | CD2AP | c.1598C= (p.Ser533=) n.123C= c.1586C= (p.Ser529=) c.1451C= (p.Ser484=) | |
6 | g.47607994C>G | CA363941836 | CD2AP | c.1598C>G (p.Ser533Cys) n.123C>G c.1586C>G (p.Ser529Cys) c.1451C>G (p.Ser484Cys) | |
6 | g.47607994C>T | CA363941838 | CD2AP | c.1598C>T (p.Ser533Phe) n.123C>T c.1586C>T (p.Ser529Phe) c.1451C>T (p.Ser484Phe) | gnomAD v4 |
6 | g.47607995T>A | CA450396083 | CD2AP | c.1599T>A (p.Ser533=) n.124T>A c.1587T>A (p.Ser529=) c.1452T>A (p.Ser484=) | |
6 | g.47607995T>C | CA450396087 | CD2AP | c.1599T>C (p.Ser533=) n.124T>C c.1587T>C (p.Ser529=) c.1452T>C (p.Ser484=) | |
6 | g.47607995T>G | CA450396085 | CD2AP | c.1599T>G (p.Ser533=) n.124T>G c.1587T>G (p.Ser529=) c.1452T>G (p.Ser484=) | |
6 | g.47607996G>A | CA137927561 | CD2AP | c.1600G>A (p.Glu534Lys) n.125G>A c.1588G>A (p.Glu530Lys) c.1453G>A (p.Glu485Lys) | dbSNP gnomAD v2 gnomAD v4 |
6 | g.47607996G>C | CA363941839 | CD2AP | c.1600G>C (p.Glu534Gln) n.125G>C c.1588G>C (p.Glu530Gln) c.1453G>C (p.Glu485Gln) | |
6 | g.47607996G= | CA1626460864 | CD2AP | c.1600G= (p.Glu534=) n.125G= c.1588G= (p.Glu530=) c.1453G= (p.Glu485=) | |
6 | g.47607996G>T | CA363941840 | CD2AP | c.1600G>T (p.Glu534Ter) n.125G>T c.1588G>T (p.Glu530Ter) c.1453G>T (p.Glu485Ter) | |
6 | g.47607997A>C | CA363941842 | CD2AP | c.1601A>C (p.Glu534Ala) n.126A>C c.1589A>C (p.Glu530Ala) c.1454A>C (p.Glu485Ala) | |
6 | g.47607997A>G | CA363941843 | CD2AP | c.1601A>G (p.Glu534Gly) n.126A>G c.1589A>G (p.Glu530Gly) c.1454A>G (p.Glu485Gly) | |
6 | g.47607997A>T | CA363941845 | CD2AP | c.1601A>T (p.Glu534Val) n.126A>T c.1589A>T (p.Glu530Val) c.1454A>T (p.Glu485Val) | dbSNP gnomAD v4 |
6 | g.47607998A= | CA1626460870 | CD2AP | c.1602A= (p.Glu534=) n.127A= c.1590A= (p.Glu530=) c.1455A= (p.Glu485=) | |
6 | g.47607998A>C | CA363941852 | CD2AP | c.1602A>C (p.Glu534Asp) n.127A>C c.1590A>C (p.Glu530Asp) c.1455A>C (p.Glu485Asp) | |
6 | g.47607998A>G | CA3844385 | CD2AP | c.1602A>G (p.Glu534=) n.127A>G c.1590A>G (p.Glu530=) c.1455A>G (p.Glu485=) | dbSNP ExAC gnomAD v2 |
6 | g.47607998A>T | CA363941861 | CD2AP | c.1602A>T (p.Glu534Asp) n.127A>T c.1590A>T (p.Glu530Asp) c.1455A>T (p.Glu485Asp) | |
6 | g.47607999T>A | CA363941865 | CD2AP | c.1603T>A (p.Leu535Ile) n.128T>A c.1591T>A (p.Leu531Ile) c.1456T>A (p.Leu486Ile) | |
6 | g.47607999T>C | CA450396106 | CD2AP | c.1603T>C (p.Leu535=) n.128T>C c.1591T>C (p.Leu531=) c.1456T>C (p.Leu486=) | dbSNP |
6 | g.47607999T>G | CA363941868 | CD2AP | c.1603T>G (p.Leu535Val) n.128T>G c.1591T>G (p.Leu531Val) c.1456T>G (p.Leu486Val) | |
6 | g.47607999T= | CA1626460874 | CD2AP | c.1603T= (p.Leu535=) n.128T= c.1591T= (p.Leu531=) c.1456T= (p.Leu486=) | |
6 | g.47608000T>A | CA363941872 | CD2AP | c.1604T>A (p.Leu535Ter) n.129T>A c.1592T>A (p.Leu531Ter) c.1457T>A (p.Leu486Ter) | |
6 | g.47608000T>C | CA363941876 | CD2AP | c.1604T>C (p.Leu535Ser) n.129T>C c.1592T>C (p.Leu531Ser) c.1457T>C (p.Leu486Ser) | |
6 | g.47608000T>G | CA363941880 | CD2AP | c.1604T>G (p.Leu535Ter) n.129T>G c.1592T>G (p.Leu531Ter) c.1457T>G (p.Leu486Ter) | |
6 | g.47608000_47608003delinsTAAA | CA1626460877 | CD2AP | c.1604_1607delinsTAAA (p.Leu535=) n.129_132delinsTAAA c.1592_1595delinsTAAA (p.Leu531=) c.1457_1460delinsTAAA (p.Leu486=) | |
6 | g.47608001A= | CA1626460881 | CD2AP | c.1605A= (p.Leu535=) n.130A= c.1593A= (p.Leu531=) c.1458A= (p.Leu486=) | |
6 | g.47608001A>C | CA363941883 | CD2AP | c.1605A>C (p.Leu535Phe) n.130A>C c.1593A>C (p.Leu531Phe) c.1458A>C (p.Leu486Phe) | |
6 | g.47608001A>G | CA450396140 | CD2AP | c.1605A>G (p.Leu535=) n.130A>G c.1593A>G (p.Leu531=) c.1458A>G (p.Leu486=) | |
6 | g.47608001A>T | CA3844387 | CD2AP | c.1605A>T (p.Leu535Phe) n.130A>T c.1593A>T (p.Leu531Phe) c.1458A>T (p.Leu486Phe) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.47608007dup | CA3844386 | CD2AP | c.1611dup (p.Asp538ArgfsTer20) n.136dup c.1599dup (p.Asp534ArgfsTer20) c.1464dup (p.Asp489ArgfsTer20) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.47608007del | CA645549884 | CD2AP | c.1611del (p.Asp538IlefsTer27) n.136del c.1599del (p.Asp534IlefsTer27) c.1464del (p.Asp489IlefsTer27) | gnomAD v4 COSMIC |
6 | g.47608006_47608007del | CA2679027822 | CD2AP | c.1610_1611del (p.Lys537ArgfsTer20) n.135_136del c.1598_1599del (p.Lys533ArgfsTer20) c.1463_1464del (p.Lys488ArgfsTer20) | gnomAD v4 |
6 | g.47608005_47608007del | CA137927574 | CD2AP | c.1609_1611del (p.Lys537del) n.134_136del c.1597_1599del (p.Lys533del) c.1462_1464del (p.Lys488del) | dbSNP |
6 | g.47608002A>C | CA363941884 | CD2AP | c.1606A>C (p.Lys536Gln) n.131A>C c.1594A>C (p.Lys532Gln) c.1459A>C (p.Lys487Gln) | |
6 | g.47608002A>G | CA363941886 | CD2AP | c.1606A>G (p.Lys536Glu) n.131A>G c.1594A>G (p.Lys532Glu) c.1459A>G (p.Lys487Glu) | |
6 | g.47608002A>T | CA363941888 | CD2AP | c.1606A>T (p.Lys536Ter) n.131A>T c.1594A>T (p.Lys532Ter) c.1459A>T (p.Lys487Ter) | gnomAD v4 |
6 | g.47608003A>C | CA363941892 | CD2AP | c.1607A>C (p.Lys536Thr) n.132A>C c.1595A>C (p.Lys532Thr) c.1460A>C (p.Lys487Thr) | |
6 | g.47608003A>G | CA363941895 | CD2AP | c.1607A>G (p.Lys536Arg) n.132A>G c.1595A>G (p.Lys532Arg) c.1460A>G (p.Lys487Arg) | gnomAD v4 |
6 | g.47608003A>T | CA363941897 | CD2AP | c.1607A>T (p.Lys536Ile) n.132A>T c.1595A>T (p.Lys532Ile) c.1460A>T (p.Lys487Ile) | |
6 | g.47608004A= | CA1626460885 | CD2AP | c.1608A= (p.Lys536=) n.133A= c.1596A= (p.Lys532=) c.1461A= (p.Lys487=) | |
6 | g.47608004A>C | CA363941909 | CD2AP | c.1608A>C (p.Lys536Asn) n.133A>C c.1596A>C (p.Lys532Asn) c.1461A>C (p.Lys487Asn) | |
6 | g.47608004A>G | CA3844388 | CD2AP | c.1608A>G (p.Lys536=) n.133A>G c.1596A>G (p.Lys532=) c.1461A>G (p.Lys487=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.47608004A>T | CA363941903 | CD2AP | c.1608A>T (p.Lys536Asn) n.133A>T c.1596A>T (p.Lys532Asn) c.1461A>T (p.Lys487Asn) | |
6 | g.47608005A>C | CA363941915 | CD2AP | c.1609A>C (p.Lys537Gln) n.134A>C c.1597A>C (p.Lys533Gln) c.1462A>C (p.Lys488Gln) | |
6 | g.47608005A>G | CA363941921 | CD2AP | c.1609A>G (p.Lys537Glu) n.134A>G c.1597A>G (p.Lys533Glu) c.1462A>G (p.Lys488Glu) | |
6 | g.47608005A>T | CA363941918 | CD2AP | c.1609A>T (p.Lys537Ter) n.134A>T c.1597A>T (p.Lys533Ter) c.1462A>T (p.Lys488Ter) | |
6 | g.47608006A>C | CA363941922 | CD2AP | c.1610A>C (p.Lys537Thr) n.135A>C c.1598A>C (p.Lys533Thr) c.1463A>C (p.Lys488Thr) | |
6 | g.47608006A>G | CA363941925 | CD2AP | c.1610A>G (p.Lys537Arg) n.135A>G c.1598A>G (p.Lys533Arg) c.1463A>G (p.Lys488Arg) | |
6 | g.47608006A>T | CA363941923 | CD2AP | c.1610A>T (p.Lys537Ile) n.135A>T c.1598A>T (p.Lys533Ile) c.1463A>T (p.Lys488Ile) | |
6 | g.47608007A>C | CA363941928 | CD2AP | c.1611A>C (p.Lys537Asn) n.136A>C c.1599A>C (p.Lys533Asn) c.1464A>C (p.Lys488Asn) | |
6 | g.47608007A>G | CA450396172 | CD2AP | c.1611A>G (p.Lys537=) n.136A>G c.1599A>G (p.Lys533=) c.1464A>G (p.Lys488=) | |
6 | g.47608007A>T | CA363941932 | CD2AP | c.1611A>T (p.Lys537Asn) n.136A>T c.1599A>T (p.Lys533Asn) c.1464A>T (p.Lys488Asn) | |
6 | g.47608008G>A | CA3844390 | CD2AP | c.1612G>A (p.Asp538Asn) n.137G>A c.1600G>A (p.Asp534Asn) c.1465G>A (p.Asp489Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.47608008G>C | CA363941938 | CD2AP | c.1612G>C (p.Asp538His) n.137G>C c.1600G>C (p.Asp534His) c.1465G>C (p.Asp489His) | |
6 | g.47608008G= | CA1626460888 | CD2AP | c.1612G= (p.Asp538=) n.137G= c.1600G= (p.Asp534=) c.1465G= (p.Asp489=) | |
6 | g.47608008G>T | CA3844389 | CD2AP | c.1612G>T (p.Asp538Tyr) n.137G>T c.1600G>T (p.Asp534Tyr) c.1465G>T (p.Asp489Tyr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.47608009A>C | CA363941953 | CD2AP | c.1613A>C (p.Asp538Ala) n.138A>C c.1601A>C (p.Asp534Ala) c.1466A>C (p.Asp489Ala) | |
6 | g.47608009A>G | CA363941957 | CD2AP | c.1613A>G (p.Asp538Gly) n.138A>G c.1601A>G (p.Asp534Gly) c.1466A>G (p.Asp489Gly) | |
6 | g.47608009A>T | CA363941959 | CD2AP | c.1613A>T (p.Asp538Val) n.138A>T c.1601A>T (p.Asp534Val) c.1466A>T (p.Asp489Val) | |
6 | g.47608010T>A | CA363941963 | CD2AP | c.1614T>A (p.Asp538Glu) n.139T>A c.1602T>A (p.Asp534Glu) c.1467T>A (p.Asp489Glu) | |
6 | g.47608010T>C | CA450396185 | CD2AP | c.1614T>C (p.Asp538=) n.139T>C c.1602T>C (p.Asp534=) c.1467T>C (p.Asp489=) | gnomAD v4 |
6 | g.47608010T>G | CA363941967 | CD2AP | c.1614T>G (p.Asp538Glu) n.139T>G c.1602T>G (p.Asp534Glu) c.1467T>G (p.Asp489Glu) | |
6 | g.47608011A= | CA1626460890 | CD2AP | c.1615A= (p.Thr539=) n.140A= c.1603A= (p.Thr535=) c.1468A= (p.Thr490=) | |
6 | g.47608011A>C | CA363941972 | CD2AP | c.1615A>C (p.Thr539Pro) n.140A>C c.1603A>C (p.Thr535Pro) c.1468A>C (p.Thr490Pro) | |
6 | g.47608011A>G | CA363941976 | CD2AP | c.1615A>G (p.Thr539Ala) n.140A>G c.1603A>G (p.Thr535Ala) c.1468A>G (p.Thr490Ala) | dbSNP gnomAD v4 |
6 | g.47608011A>T | CA363941978 | CD2AP | c.1615A>T (p.Thr539Ser) n.140A>T c.1603A>T (p.Thr535Ser) c.1468A>T (p.Thr490Ser) | |
6 | g.47608012C>A | CA363941995 | CD2AP | c.1616C>A (p.Thr539Lys) n.141C>A c.1604C>A (p.Thr535Lys) c.1469C>A (p.Thr490Lys) | |
6 | g.47608012C>G | CA363941990 | CD2AP | c.1616C>G (p.Thr539Arg) n.141C>G c.1604C>G (p.Thr535Arg) c.1469C>G (p.Thr490Arg) | |
6 | g.47608012C>T | CA363941983 | CD2AP | c.1616C>T (p.Thr539Ile) n.141C>T c.1604C>T (p.Thr535Ile) c.1469C>T (p.Thr490Ile) | ClinVar |