UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.153770141_153770148del | CA2695051102 | PLXNB3 | c.1679_1686del (p.Phe560CysfsTer6) c.1748_1755del (p.Phe583CysfsTer6) | gnomAD v4 |
| X | g.153770143C>A | CA415101403 | PLXNB3 | c.1681C>A (p.His561Asn) c.1750C>A (p.His584Asn) | |
| X | g.153770143C>G | CA415101405 | PLXNB3 | c.1681C>G (p.His561Asp) c.1750C>G (p.His584Asp) | |
| X | g.153770143C>T | CA415101407 | PLXNB3 | c.1681C>T (p.His561Tyr) c.1750C>T (p.His584Tyr) | |
| X | g.153770144A>C | CA415101409 | PLXNB3 | c.1682A>C (p.His561Pro) c.1751A>C (p.His584Pro) | |
| X | g.153770144A>G | CA415101416 | PLXNB3 | c.1682A>G (p.His561Arg) c.1751A>G (p.His584Arg) | |
| X | g.153770144A>T | CA415101415 | PLXNB3 | c.1682A>T (p.His561Leu) c.1751A>T (p.His584Leu) | |
| X | g.153770145T>A | CA415101418 | PLXNB3 | c.1683T>A (p.His561Gln) c.1752T>A (p.His584Gln) | |
| X | g.153770145T>C | CA10550909 | PLXNB3 | c.1683T>C (p.His561=) c.1752T>C (p.His584=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.153770145T>G | CA415101420 | PLXNB3 | c.1683T>G (p.His561Gln) c.1752T>G (p.His584Gln) | |
| X | g.153770145T= | CA2466468338 | PLXNB3 | c.1683T= (p.His561=) c.1752T= (p.His584=) | |
| X | g.153770146T>A | CA415101422 | PLXNB3 | c.1684T>A (p.Cys562Ser) c.1753T>A (p.Cys585Ser) | |
| X | g.153770146T>C | CA415101424 | PLXNB3 | c.1684T>C (p.Cys562Arg) c.1753T>C (p.Cys585Arg) | |
| X | g.153770146T>G | CA415101426 | PLXNB3 | c.1684T>G (p.Cys562Gly) c.1753T>G (p.Cys585Gly) | ClinVar |
| X | g.153770147G>A | CA415101429 | PLXNB3 | c.1685G>A (p.Cys562Tyr) c.1754G>A (p.Cys585Tyr) | |
| X | g.153770147G>C | CA415101430 | PLXNB3 | c.1685G>C (p.Cys562Ser) c.1754G>C (p.Cys585Ser) | |
| X | g.153770147G>T | CA415101432 | PLXNB3 | c.1685G>T (p.Cys562Phe) c.1754G>T (p.Cys585Phe) | |
| X | g.153770148T>A | CA415101434 | PLXNB3 | c.1686T>A (p.Cys562Ter) c.1755T>A (p.Cys585Ter) | gnomAD v4 |
| X | g.153770148T>C | CA519346922 | PLXNB3 | c.1686T>C (p.Cys562=) c.1755T>C (p.Cys585=) | |
| X | g.153770148T>G | CA415101436 | PLXNB3 | c.1686T>G (p.Cys562Trp) c.1755T>G (p.Cys585Trp) | |
| X | g.153770149G>A | CA415101441 | PLXNB3 | c.1687G>A (p.Ala563Thr) c.1756G>A (p.Ala586Thr) | gnomAD v4 |
| X | g.153770149G>C | CA415101438 | PLXNB3 | c.1687G>C (p.Ala563Pro) c.1756G>C (p.Ala586Pro) | |
| X | g.153770149G>T | CA415101439 | PLXNB3 | c.1687G>T (p.Ala563Ser) c.1756G>T (p.Ala586Ser) | |
| X | g.153770150C>A | CA415101444 | PLXNB3 | c.1688C>A (p.Ala563Glu) c.1757C>A (p.Ala586Glu) | |
| X | g.153770150C= | CA2466468339 | PLXNB3 | c.1688C= (p.Ala563=) c.1757C= (p.Ala586=) | |
| X | g.153770150C>G | CA415101445 | PLXNB3 | c.1688C>G (p.Ala563Gly) c.1757C>G (p.Ala586Gly) | |
| X | g.153770150C>T | CA10550910 | PLXNB3 | c.1688C>T (p.Ala563Val) c.1757C>T (p.Ala586Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.153770151G>A | CA10550911 | PLXNB3 | c.1689G>A (p.Ala563=) c.1758G>A (p.Ala586=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.153770151G>C | CA519346927 | PLXNB3 | c.1689G>C (p.Ala563=) c.1758G>C (p.Ala586=) | |
| X | g.153770151G= | CA2466468340 | PLXNB3 | c.1689G= (p.Ala563=) c.1758G= (p.Ala586=) | |
| X | g.153770151G>T | CA519346926 | PLXNB3 | c.1689G>T (p.Ala563=) c.1758G>T (p.Ala586=) | |
| X | g.153770151_153770153del | CA2695051105 | PLXNB3 | c.1689_1691del (p.Phe564del) c.1758_1760del (p.Phe587del) | gnomAD v4 |
| X | g.153770152T>A | CA415101449 | PLXNB3 | c.1690T>A (p.Phe564Ile) c.1759T>A (p.Phe587Ile) | |
| X | g.153770152T>C | CA415101451 | PLXNB3 | c.1690T>C (p.Phe564Leu) c.1759T>C (p.Phe587Leu) | |
| X | g.153770152T>G | CA415101452 | PLXNB3 | c.1690T>G (p.Phe564Val) c.1759T>G (p.Phe587Val) | |
| X | g.153770153T>A | CA415101454 | PLXNB3 | c.1691T>A (p.Phe564Tyr) c.1760T>A (p.Phe587Tyr) | |
| X | g.153770153T>C | CA415101455 | PLXNB3 | c.1691T>C (p.Phe564Ser) c.1760T>C (p.Phe587Ser) | |
| X | g.153770153T>G | CA415101457 | PLXNB3 | c.1691T>G (p.Phe564Cys) c.1760T>G (p.Phe587Cys) | |
| X | g.153770154C>A | CA415101462 | PLXNB3 | c.1692C>A (p.Phe564Leu) c.1761C>A (p.Phe587Leu) | gnomAD v4 |
| X | g.153770154C= | CA2466468341 | PLXNB3 | c.1692C= (p.Phe564=) c.1761C= (p.Phe587=) | |
| X | g.153770154C>G | CA415101460 | PLXNB3 | c.1692C>G (p.Phe564Leu) c.1761C>G (p.Phe587Leu) | |
| X | g.153770154C>T | CA10550912 | PLXNB3 | c.1692C>T (p.Phe564=) c.1761C>T (p.Phe587=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.153770155G>A | CA10550913 | PLXNB3 | c.1693G>A (p.Gly565Arg) c.1762G>A (p.Gly588Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.153770155G>C | CA415101464 | PLXNB3 | c.1693G>C (p.Gly565Arg) c.1762G>C (p.Gly588Arg) | dbSNP |
| X | g.153770155G= | CA2466468342 | PLXNB3 | c.1693G= (p.Gly565=) c.1762G= (p.Gly588=) | |
| X | g.153770155G>T | CA415101466 | PLXNB3 | c.1693G>T (p.Gly565Trp) c.1762G>T (p.Gly588Trp) | |
| X | g.153770156G>A | CA415101469 | PLXNB3 | c.1694G>A (p.Gly565Glu) c.1763G>A (p.Gly588Glu) | gnomAD v4 |
| X | g.153770156G>C | CA415101470 | PLXNB3 | c.1694G>C (p.Gly565Ala) c.1763G>C (p.Gly588Ala) | |
| X | g.153770156G>T | CA415101472 | PLXNB3 | c.1694G>T (p.Gly565Val) c.1763G>T (p.Gly588Val) | gnomAD v4 |
| X | g.153770157G>A | CA519346935 | PLXNB3 | c.1695G>A (p.Gly565=) c.1764G>A (p.Gly588=) | |
| X | g.153770157G>C | CA519346936 | PLXNB3 | c.1695G>C (p.Gly565=) c.1764G>C (p.Gly588=) | |
| X | g.153770157G>T | CA519346938 | PLXNB3 | c.1695G>T (p.Gly565=) c.1764G>T (p.Gly588=) | |
| X | g.153770158G>A | CA10550914 | PLXNB3 | c.1696G>A (p.Asp566Asn) c.1765G>A (p.Asp589Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.153770158G>C | CA415101475 | PLXNB3 | c.1696G>C (p.Asp566His) c.1765G>C (p.Asp589His) | gnomAD v4 |
| X | g.153770158G= | CA2466468343 | PLXNB3 | c.1696G= (p.Asp566=) c.1765G= (p.Asp589=) | |
| X | g.153770158G>T | CA415101476 | PLXNB3 | c.1696G>T (p.Asp566Tyr) c.1765G>T (p.Asp589Tyr) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.153770159A>C | CA415101480 | PLXNB3 | c.1697A>C (p.Asp566Ala) c.1766A>C (p.Asp589Ala) | |
| X | g.153770159A>G | CA415101482 | PLXNB3 | c.1697A>G (p.Asp566Gly) c.1766A>G (p.Asp589Gly) | gnomAD v4 |
| X | g.153770159A>T | CA415101483 | PLXNB3 | c.1697A>T (p.Asp566Val) c.1766A>T (p.Asp589Val) | |
| X | g.153770160C>A | CA415101487 | PLXNB3 | c.1698C>A (p.Asp566Glu) c.1767C>A (p.Asp589Glu) | |
| X | g.153770160C>G | CA415101490 | PLXNB3 | c.1698C>G (p.Asp566Glu) c.1767C>G (p.Asp589Glu) | |
| X | g.153770160C>T | CA519346944 | PLXNB3 | c.1698C>T (p.Asp566=) c.1767C>T (p.Asp589=) | |
| X | g.153770161T>A | CA415101495 | PLXNB3 | c.1699T>A (p.Tyr567Asn) c.1768T>A (p.Tyr590Asn) | |
| X | g.153770161T>C | CA415101492 | PLXNB3 | c.1699T>C (p.Tyr567His) c.1768T>C (p.Tyr590His) | gnomAD v4 |
| X | g.153770161T>G | CA415101494 | PLXNB3 | c.1699T>G (p.Tyr567Asp) c.1768T>G (p.Tyr590Asp) | |
| X | g.153770162A>C | CA415101497 | PLXNB3 | c.1700A>C (p.Tyr567Ser) c.1769A>C (p.Tyr590Ser) | |
| X | g.153770162A>G | CA415101499 | PLXNB3 | c.1700A>G (p.Tyr567Cys) c.1769A>G (p.Tyr590Cys) | gnomAD v4 |
| X | g.153770162A>T | CA415101500 | PLXNB3 | c.1700A>T (p.Tyr567Phe) c.1769A>T (p.Tyr590Phe) | |
| X | g.153770163T>A | CA415101501 | PLXNB3 | c.1701T>A (p.Tyr567Ter) c.1770T>A (p.Tyr590Ter) | |
| X | g.153770163T>C | CA519346948 | PLXNB3 | c.1701T>C (p.Tyr567=) c.1770T>C (p.Tyr590=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.153770163T>G | CA415101502 | PLXNB3 | c.1701T>G (p.Tyr567Ter) c.1770T>G (p.Tyr590Ter) | |
| X | g.153770163T= | CA2466468344 | PLXNB3 | c.1701T= (p.Tyr567=) c.1770T= (p.Tyr590=) | |
| X | g.153770164G>A | CA415101504 | PLXNB3 | c.1702G>A (p.Asp568Asn) c.1771G>A (p.Asp591Asn) | dbSNP |
| X | g.153770164G>C | CA415101505 | PLXNB3 | c.1702G>C (p.Asp568His) c.1771G>C (p.Asp591His) | |
| X | g.153770164G= | CA2466468345 | PLXNB3 | c.1702G= (p.Asp568=) c.1771G= (p.Asp591=) | |
| X | g.153770164G>T | CA415101506 | PLXNB3 | c.1702G>T (p.Asp568Tyr) c.1771G>T (p.Asp591Tyr) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.153770165A>C | CA415101509 | PLXNB3 | c.1703A>C (p.Asp568Ala) c.1772A>C (p.Asp591Ala) | |
| X | g.153770165A>G | CA415101510 | PLXNB3 | c.1703A>G (p.Asp568Gly) c.1772A>G (p.Asp591Gly) | |
| X | g.153770165A>T | CA415101511 | PLXNB3 | c.1703A>T (p.Asp568Val) c.1772A>T (p.Asp591Val) | |
| X | g.153770166C>A | CA415101514 | PLXNB3 | c.1704C>A (p.Asp568Glu) c.1773C>A (p.Asp591Glu) | |
| X | g.153770166C>G | CA415101515 | PLXNB3 | c.1704C>G (p.Asp568Glu) c.1773C>G (p.Asp591Glu) | |
| X | g.153770166C>T | CA519346960 | PLXNB3 | c.1704C>T (p.Asp568=) c.1773C>T (p.Asp591=) | |
| X | g.153770167A>C | CA415101518 | PLXNB3 | c.1705A>C (p.Ser569Arg) c.1774A>C (p.Ser592Arg) | |
| X | g.153770167A>G | CA415101520 | PLXNB3 | c.1705A>G (p.Ser569Gly) c.1774A>G (p.Ser592Gly) | |
| X | g.153770167A>T | CA415101519 | PLXNB3 | c.1705A>T (p.Ser569Cys) c.1774A>T (p.Ser592Cys) | |
| X | g.153770168G>A | CA415101521 | PLXNB3 | c.1706G>A (p.Ser569Asn) c.1775G>A (p.Ser592Asn) | |
| X | g.153770168G>C | CA415101522 | PLXNB3 | c.1706G>C (p.Ser569Thr) c.1775G>C (p.Ser592Thr) | dbSNP |
| X | g.153770168G= | CA2466468346 | PLXNB3 | c.1706G= (p.Ser569=) c.1775G= (p.Ser592=) | |
| X | g.153770168G>T | CA415101523 | PLXNB3 | c.1706G>T (p.Ser569Ile) c.1775G>T (p.Ser592Ile) | |
| X | g.153770169C>A | CA415101524 | PLXNB3 | c.1707C>A (p.Ser569Arg) c.1776C>A (p.Ser592Arg) | |
| X | g.153770169C>G | CA415101525 | PLXNB3 | c.1707C>G (p.Ser569Arg) c.1776C>G (p.Ser592Arg) | |
| X | g.153770169C>T | CA519346964 | PLXNB3 | c.1707C>T (p.Ser569=) c.1776C>T (p.Ser592=) | gnomAD v4 |
| X | g.153770170T>A | CA415101526 | PLXNB3 | c.1708T>A (p.Leu570Met) c.1777T>A (p.Leu593Met) | |
| X | g.153770170T>C | CA519346965 | PLXNB3 | c.1708T>C (p.Leu570=) c.1777T>C (p.Leu593=) | |
| X | g.153770170T>G | CA415101527 | PLXNB3 | c.1708T>G (p.Leu570Val) c.1777T>G (p.Leu593Val) | |
| X | g.153770171T>A | CA415101528 | PLXNB3 | c.1709T>A (p.Leu570Ter) c.1778T>A (p.Leu593Ter) | |
| X | g.153770171T>C | CA415101529 | PLXNB3 | c.1709T>C (p.Leu570Ser) c.1778T>C (p.Leu593Ser) | |
| X | g.153770171T>G | CA415101530 | PLXNB3 | c.1709T>G (p.Leu570Trp) c.1778T>G (p.Leu593Trp) | |
| X | g.153770172G>A | CA519346966 | PLXNB3 | c.1710G>A (p.Leu570=) c.1779G>A (p.Leu593=) | |
| X | g.153770172G>C | CA415101532 | PLXNB3 | c.1710G>C (p.Leu570Phe) c.1779G>C (p.Leu593Phe) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.153770172G= | CA2466468347 | PLXNB3 | c.1710G= (p.Leu570=) c.1779G= (p.Leu593=) | |
| X | g.153770172G>T | CA415101534 | PLXNB3 | c.1710G>T (p.Leu570Phe) c.1779G>T (p.Leu593Phe) | |
| X | g.153770173G>A | CA415101539 | PLXNB3 | c.1711G>A (p.Ala571Thr) c.1780G>A (p.Ala594Thr) | |
| X | g.153770173G>C | CA415101536 | PLXNB3 | c.1711G>C (p.Ala571Pro) c.1780G>C (p.Ala594Pro) | |
| X | g.153770173G>T | CA415101537 | PLXNB3 | c.1711G>T (p.Ala571Ser) c.1780G>T (p.Ala594Ser) | |
| X | g.153770174C>A | CA415101541 | PLXNB3 | c.1712C>A (p.Ala571Asp) c.1781C>A (p.Ala594Asp) | |
| X | g.153770174C>G | CA415101543 | PLXNB3 | c.1712C>G (p.Ala571Gly) c.1781C>G (p.Ala594Gly) | gnomAD v4 |
| X | g.153770174C>T | CA415101545 | PLXNB3 | c.1712C>T (p.Ala571Val) c.1781C>T (p.Ala594Val) | gnomAD v4 |
| X | g.153770175T>A | CA519346970 | PLXNB3 | c.1713T>A (p.Ala571=) c.1782T>A (p.Ala594=) | |
| X | g.153770175T>C | CA519346971 | PLXNB3 | c.1713T>C (p.Ala571=) c.1782T>C (p.Ala594=) | |
| X | g.153770175T>G | CA519346973 | PLXNB3 | c.1713T>G (p.Ala571=) c.1782T>G (p.Ala594=) | |
| X | g.153770176C>A | CA415101547 | PLXNB3 | c.1714C>A (p.His572Asn) c.1783C>A (p.His595Asn) | COSMIC COSMIC |
| X | g.153770176C>G | CA415101549 | PLXNB3 | c.1714C>G (p.His572Asp) c.1783C>G (p.His595Asp) | |
| X | g.153770176C>T | CA415101551 | PLXNB3 | c.1714C>T (p.His572Tyr) c.1783C>T (p.His595Tyr) | |
| X | g.153770177A>C | CA415101552 | PLXNB3 | c.1715A>C (p.His572Pro) c.1784A>C (p.His595Pro) | gnomAD v4 |
| X | g.153770177A>G | CA415101554 | PLXNB3 | c.1715A>G (p.His572Arg) c.1784A>G (p.His595Arg) | |
| X | g.153770177A>T | CA415101556 | PLXNB3 | c.1715A>T (p.His572Leu) c.1784A>T (p.His595Leu) | |
| X | g.153770178T>A | CA337228297 | PLXNB3 | c.1716T>A (p.His572Gln) c.1785T>A (p.His595Gln) | dbSNP |
| X | g.153770178T>C | CA519346977 | PLXNB3 | c.1716T>C (p.His572=) c.1785T>C (p.His595=) | |
| X | g.153770178T>G | CA415101559 | PLXNB3 | c.1716T>G (p.His572Gln) c.1785T>G (p.His595Gln) | |
| X | g.153770178T= | CA2466468348 | PLXNB3 | c.1716T= (p.His572=) c.1785T= (p.His595=) | |
| X | g.153770179G>A | CA10550915 | PLXNB3 | c.1717G>A (p.Val573Met) c.1786G>A (p.Val596Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.153770179G>C | CA415101568 | PLXNB3 | c.1717G>C (p.Val573Leu) c.1786G>C (p.Val596Leu) | |
| X | g.153770179G= | CA2466468349 | PLXNB3 | c.1717G= (p.Val573=) c.1786G= (p.Val596=) | |
| X | g.153770179G>T | CA415101567 | PLXNB3 | c.1717G>T (p.Val573Leu) c.1786G>T (p.Val596Leu) | |
| X | g.153770180T>A | CA415101570 | PLXNB3 | c.1718T>A (p.Val573Glu) c.1787T>A (p.Val596Glu) | |
| X | g.153770180T>C | CA415101574 | PLXNB3 | c.1718T>C (p.Val573Ala) c.1787T>C (p.Val596Ala) | |
| X | g.153770180T>G | CA415101572 | PLXNB3 | c.1718T>G (p.Val573Gly) c.1787T>G (p.Val596Gly) | |
| X | g.153770181G>A | CA519346980 | PLXNB3 | c.1719G>A (p.Val573=) c.1788G>A (p.Val596=) | |
| X | g.153770181G>C | CA519346982 | PLXNB3 | c.1719G>C (p.Val573=) c.1788G>C (p.Val596=) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.153770181G= | CA2466468350 | PLXNB3 | c.1719G= (p.Val573=) c.1788G= (p.Val596=) | |
| X | g.153770181G>T | CA519346983 | PLXNB3 | c.1719G>T (p.Val573=) c.1788G>T (p.Val596=) | |
| X | g.153770182G>A | CA415101576 | PLXNB3 | c.1720G>A (p.Glu574Lys) c.1789G>A (p.Glu597Lys) | |
| X | g.153770182G>C | CA415101578 | PLXNB3 | c.1720G>C (p.Glu574Gln) c.1789G>C (p.Glu597Gln) | |
| X | g.153770182G>T | CA415101580 | PLXNB3 | c.1720G>T (p.Glu574Ter) c.1789G>T (p.Glu597Ter) | |
| X | g.153770183A>C | CA415101581 | PLXNB3 | c.1721A>C (p.Glu574Ala) c.1790A>C (p.Glu597Ala) | |
| X | g.153770183A>G | CA415101582 | PLXNB3 | c.1721A>G (p.Glu574Gly) c.1790A>G (p.Glu597Gly) | |
| X | g.153770183A>T | CA415101583 | PLXNB3 | c.1721A>T (p.Glu574Val) c.1790A>T (p.Glu597Val) | |
| X | g.153770184A>C | CA415101584 | PLXNB3 | c.1722A>C (p.Glu574Asp) c.1791A>C (p.Glu597Asp) | |
| X | g.153770184A>G | CA519346988 | PLXNB3 | c.1722A>G (p.Glu574=) c.1791A>G (p.Glu597=) | |
| X | g.153770184A>T | CA415101585 | PLXNB3 | c.1722A>T (p.Glu574Asp) c.1791A>T (p.Glu597Asp) | |
| X | g.153770185G>A | CA415101586 | PLXNB3 | c.1723G>A (p.Gly575Arg) c.1792G>A (p.Gly598Arg) | dbSNP gnomAD v4 |
| X | g.153770185G>C | CA415101587 | PLXNB3 | c.1723G>C (p.Gly575Arg) c.1792G>C (p.Gly598Arg) | |
| X | g.153770185G= | CA2466468351 | PLXNB3 | c.1723G= (p.Gly575=) c.1792G= (p.Gly598=) | |
| X | g.153770185G>T | CA415101589 | PLXNB3 | c.1723G>T (p.Gly575Trp) c.1792G>T (p.Gly598Trp) | dbSNP |
| X | g.153770186G>A | CA415101591 | PLXNB3 | c.1724G>A (p.Gly575Glu) c.1793G>A (p.Gly598Glu) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.153770186G>C | CA415101597 | PLXNB3 | c.1724G>C (p.Gly575Ala) c.1793G>C (p.Gly598Ala) | |
| X | g.153770186G= | CA2466468352 | PLXNB3 | c.1724G= (p.Gly575=) c.1793G= (p.Gly598=) | |
| X | g.153770186G>T | CA415101595 | PLXNB3 | c.1724G>T (p.Gly575Val) c.1793G>T (p.Gly598Val) | |
| X | g.153770187G>A | CA519346999 | PLXNB3 | c.1725G>A (p.Gly575=) c.1794G>A (p.Gly598=) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.153770187G>C | CA519346997 | PLXNB3 | c.1725G>C (p.Gly575=) c.1794G>C (p.Gly598=) | |
| X | g.153770187G= | CA2466468353 | PLXNB3 | c.1725G= (p.Gly575=) c.1794G= (p.Gly598=) | |
| X | g.153770187G>T | CA519346996 | PLXNB3 | c.1725G>T (p.Gly575=) c.1794G>T (p.Gly598=) | |
| X | g.153770188C>A | CA415101599 | PLXNB3 | c.1726C>A (p.Pro576Thr) c.1795C>A (p.Pro599Thr) | |
| X | g.153770188C>G | CA415101600 | PLXNB3 | c.1726C>G (p.Pro576Ala) c.1795C>G (p.Pro599Ala) | |
| X | g.153770188C>T | CA415101601 | PLXNB3 | c.1726C>T (p.Pro576Ser) c.1795C>T (p.Pro599Ser) | gnomAD v4 |
| X | g.153770189C>A | CA415101602 | PLXNB3 | c.1727C>A (p.Pro576His) c.1796C>A (p.Pro599His) | gnomAD v4 |
| X | g.153770189C>G | CA415101603 | PLXNB3 | c.1727C>G (p.Pro576Arg) c.1796C>G (p.Pro599Arg) | |
| X | g.153770189C>T | CA415101606 | PLXNB3 | c.1727C>T (p.Pro576Leu) c.1796C>T (p.Pro599Leu) | |
| X | g.153770190C>A | CA519347012 | PLXNB3 | c.1728C>A (p.Pro576=) c.1797C>A (p.Pro599=) | |
| X | g.153770190C>G | CA519347011 | PLXNB3 | c.1728C>G (p.Pro576=) c.1797C>G (p.Pro599=) | |
| X | g.153770190C>T | CA519347010 | PLXNB3 | c.1728C>T (p.Pro576=) c.1797C>T (p.Pro599=) | |
| X | g.153770191C>A | CA415101609 | PLXNB3 | c.1729C>A (p.His577Asn) c.1798C>A (p.His600Asn) | gnomAD v4 |
| X | g.153770191C= | CA2466468354 | PLXNB3 | c.1729C= (p.His577=) c.1798C= (p.His600=) | |
| X | g.153770191C>G | CA415101610 | PLXNB3 | c.1729C>G (p.His577Asp) c.1798C>G (p.His600Asp) | |
| X | g.153770191C>T | CA337228314 | PLXNB3 | c.1729C>T (p.His577Tyr) c.1798C>T (p.His600Tyr) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.153770192A>C | CA415101616 | PLXNB3 | c.1730A>C (p.His577Pro) c.1799A>C (p.His600Pro) | |
| X | g.153770192A>G | CA415101619 | PLXNB3 | c.1730A>G (p.His577Arg) c.1799A>G (p.His600Arg) | |
| X | g.153770192A>T | CA415101615 | PLXNB3 | c.1730A>T (p.His577Leu) c.1799A>T (p.His600Leu) | |
| X | g.153770193C>A | CA415101621 | PLXNB3 | c.1731C>A (p.His577Gln) c.1800C>A (p.His600Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.153770193C= | CA2466468355 | PLXNB3 | c.1731C= (p.His577=) c.1800C= (p.His600=) | |
| X | g.153770193C>G | CA415101623 | PLXNB3 | c.1731C>G (p.His577Gln) c.1800C>G (p.His600Gln) | |
| X | g.153770193C>T | CA10550916 | PLXNB3 | c.1731C>T (p.His577=) c.1800C>T (p.His600=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
| X | g.153770194G>A | CA10550917 | PLXNB3 | c.1732G>A (p.Val578Met) c.1801G>A (p.Val601Met) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| X | g.153770194G>C | CA415101627 | PLXNB3 | c.1732G>C (p.Val578Leu) c.1801G>C (p.Val601Leu) | |
| X | g.153770194G= | CA2466468356 | PLXNB3 | c.1732G= (p.Val578=) c.1801G= (p.Val601=) | |
| X | g.153770194G>T | CA415101629 | PLXNB3 | c.1732G>T (p.Val578Leu) c.1801G>T (p.Val601Leu) | |
| X | g.153770195T>A | CA415101631 | PLXNB3 | c.1733T>A (p.Val578Glu) c.1802T>A (p.Val601Glu) | |
| X | g.153770195T>C | CA415101633 | PLXNB3 | c.1733T>C (p.Val578Ala) c.1802T>C (p.Val601Ala) | |
| X | g.153770195T>G | CA415101635 | PLXNB3 | c.1733T>G (p.Val578Gly) c.1802T>G (p.Val601Gly) | |
| X | g.153770196G>A | CA519347074 | PLXNB3 | c.1734G>A (p.Val578=) c.1803G>A (p.Val601=) | |
| X | g.153770196G>C | CA519347075 | PLXNB3 | c.1734G>C (p.Val578=) c.1803G>C (p.Val601=) | |
| X | g.153770196G= | CA2466468357 | PLXNB3 | c.1734G= (p.Val578=) c.1803G= (p.Val601=) | |
| X | g.153770196G>T | CA519347076 | PLXNB3 | c.1734G>T (p.Val578=) c.1803G>T (p.Val601=) | dbSNP gnomAD v2 |
| X | g.153770197G>A | CA415101638 | PLXNB3 | c.1735G>A (p.Ala579Thr) c.1804G>A (p.Ala602Thr) | COSMIC COSMIC COSMIC |
| X | g.153770197G>C | CA415101641 | PLXNB3 | c.1735G>C (p.Ala579Pro) c.1804G>C (p.Ala602Pro) | |
| X | g.153770197G= | CA2466468358 | PLXNB3 | c.1735G= (p.Ala579=) c.1804G= (p.Ala602=) | |
| X | g.153770197G>T | CA415101643 | PLXNB3 | c.1735G>T (p.Ala579Ser) c.1804G>T (p.Ala602Ser) | dbSNP gnomAD v2 |
| X | g.153770198C>A | CA415101649 | PLXNB3 | c.1736C>A (p.Ala579Asp) c.1805C>A (p.Ala602Asp) | |
| X | g.153770198C>G | CA415101646 | PLXNB3 | c.1736C>G (p.Ala579Gly) c.1805C>G (p.Ala602Gly) | |
| X | g.153770198C>T | CA415101647 | PLXNB3 | c.1736C>T (p.Ala579Val) c.1805C>T (p.Ala602Val) | |
| X | g.153770199C>A | CA519347091 | PLXNB3 | c.1737C>A (p.Ala579=) c.1806C>A (p.Ala602=) | |
| X | g.153770199C>G | CA519347092 | PLXNB3 | c.1737C>G (p.Ala579=) c.1806C>G (p.Ala602=) | |
| X | g.153770199C>T | CA519347094 | PLXNB3 | c.1737C>T (p.Ala579=) c.1806C>T (p.Ala602=) | |
| X | g.153770200T>A | CA415101652 | PLXNB3 | c.1738T>A (p.Cys580Ser) c.1807T>A (p.Cys603Ser) | |
| X | g.153770200T>C | CA415101653 | PLXNB3 | c.1738T>C (p.Cys580Arg) c.1807T>C (p.Cys603Arg) | |
| X | g.153770200T>G | CA415101655 | PLXNB3 | c.1738T>G (p.Cys580Gly) c.1807T>G (p.Cys603Gly) | |
| X | g.153770201G>A | CA415101658 | PLXNB3 | c.1739G>A (p.Cys580Tyr) c.1808G>A (p.Cys603Tyr) | |
| X | g.153770201G>C | CA10550918 | PLXNB3 | c.1739G>C (p.Cys580Ser) c.1808G>C (p.Cys603Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.153770201G= | CA2466468359 | PLXNB3 | c.1739G= (p.Cys580=) c.1808G= (p.Cys603=) | |
| X | g.153770201G>T | CA415101661 | PLXNB3 | c.1739G>T (p.Cys580Phe) c.1808G>T (p.Cys603Phe) | |
| X | g.153770202T>A | CA415101663 | PLXNB3 | c.1740T>A (p.Cys580Ter) c.1809T>A (p.Cys603Ter) | |
| X | g.153770202T>C | CA519347105 | PLXNB3 | c.1740T>C (p.Cys580=) c.1809T>C (p.Cys603=) | gnomAD v4 |
| X | g.153770202T>G | CA415101665 | PLXNB3 | c.1740T>G (p.Cys580Trp) c.1809T>G (p.Cys603Trp) | |
| X | g.153770203G>A | CA415101669 | PLXNB3 | c.1741G>A (p.Val581Ile) c.1810G>A (p.Val604Ile) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.153770203G>C | CA415101673 | PLXNB3 | c.1741G>C (p.Val581Leu) c.1810G>C (p.Val604Leu) | |
| X | g.153770203G= | CA2466468360 | PLXNB3 | c.1741G= (p.Val581=) c.1810G= (p.Val604=) | |
| X | g.153770203G>T | CA415101674 | PLXNB3 | c.1741G>T (p.Val581Phe) c.1810G>T (p.Val604Phe) | |
| X | g.153770204T>A | CA415101679 | PLXNB3 | c.1742T>A (p.Val581Asp) c.1811T>A (p.Val604Asp) | |
| X | g.153770204T>C | CA415101685 | PLXNB3 | c.1742T>C (p.Val581Ala) c.1811T>C (p.Val604Ala) | gnomAD v4 |
| X | g.153770204T>G | CA415101682 | PLXNB3 | c.1742T>G (p.Val581Gly) c.1811T>G (p.Val604Gly) | |
| X | g.153770205C>A | CA519347115 | PLXNB3 | c.1743C>A (p.Val581=) c.1812C>A (p.Val604=) | |
| X | g.153770205C= | CA2466468361 | PLXNB3 | c.1743C= (p.Val581=) c.1812C= (p.Val604=) | |
| X | g.153770205C>G | CA10550919 | PLXNB3 | c.1743C>G (p.Val581=) c.1812C>G (p.Val604=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.153770205C>T | CA519347117 | PLXNB3 | c.1743C>T (p.Val581=) c.1812C>T (p.Val604=) | |
| X | g.153770206A>C | CA415101695 | PLXNB3 | c.1744A>C (p.Thr582Pro) c.1813A>C (p.Thr605Pro) | |
| X | g.153770206A>G | CA415101692 | PLXNB3 | c.1744A>G (p.Thr582Ala) c.1813A>G (p.Thr605Ala) | |
| X | g.153770206A>T | CA415101697 | PLXNB3 | c.1744A>T (p.Thr582Ser) c.1813A>T (p.Thr605Ser) | |
| X | g.153770207C>A | CA415101701 | PLXNB3 | c.1745C>A (p.Thr582Asn) c.1814C>A (p.Thr605Asn) | |
| X | g.153770207C>G | CA415101703 | PLXNB3 | c.1745C>G (p.Thr582Ser) c.1814C>G (p.Thr605Ser) | |
| X | g.153770207C>T | CA415101704 | PLXNB3 | c.1745C>T (p.Thr582Ile) c.1814C>T (p.Thr605Ile) | |
| X | g.153770208C>A | CA519347121 | PLXNB3 | c.1746C>A (p.Thr582=) c.1815C>A (p.Thr605=) | |
| X | g.153770208C>G | CA519347122 | PLXNB3 | c.1746C>G (p.Thr582=) c.1815C>G (p.Thr605=) | |
| X | g.153770208C>T | CA519347120 | PLXNB3 | c.1746C>T (p.Thr582=) c.1815C>T (p.Thr605=) | |
| X | g.153770209C>A | CA415101708 | PLXNB3 | c.1747C>A (p.Pro583Thr) c.1816C>A (p.Pro606Thr) | |
| X | g.153770209C= | CA2466468362 | PLXNB3 | c.1747C= (p.Pro583=) c.1816C= (p.Pro606=) | |
| X | g.153770209C>G | CA415101710 | PLXNB3 | c.1747C>G (p.Pro583Ala) c.1816C>G (p.Pro606Ala) | |
| X | g.153770209C>T | CA415101712 | PLXNB3 | c.1747C>T (p.Pro583Ser) c.1816C>T (p.Pro606Ser) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.153770210C>A | CA415101716 | PLXNB3 | c.1748C>A (p.Pro583His) c.1817C>A (p.Pro606His) | |
| X | g.153770210C>G | CA415101717 | PLXNB3 | c.1748C>G (p.Pro583Arg) c.1817C>G (p.Pro606Arg) | |
| X | g.153770210C>T | CA415101719 | PLXNB3 | c.1748C>T (p.Pro583Leu) c.1817C>T (p.Pro606Leu) | |
| X | g.153770211del | CA2579730231 | PLXNB3 | c.1749del (p.Gln585LysfsTer20) c.1818del (p.Gln608LysfsTer20) | |
| X | g.153770211T>A | CA519347130 | PLXNB3 | c.1749T>A (p.Pro583=) c.1818T>A (p.Pro606=) | |
| X | g.153770211T>C | CA519347129 | PLXNB3 | c.1749T>C (p.Pro583=) c.1818T>C (p.Pro606=) | |
| X | g.153770211T>G | CA519347127 | PLXNB3 | c.1749T>G (p.Pro583=) c.1818T>G (p.Pro606=) | |
| X | g.153770212C>A | CA415101721 | PLXNB3 | c.1750C>A (p.Pro584Thr) c.1819C>A (p.Pro607Thr) | |
| X | g.153770212C= | CA2466468363 | PLXNB3 | c.1750C= (p.Pro584=) c.1819C= (p.Pro607=) | |
| X | g.153770212C>G | CA415101722 | PLXNB3 | c.1750C>G (p.Pro584Ala) c.1819C>G (p.Pro607Ala) | |
| X | g.153770212C>T | CA415101725 | PLXNB3 | c.1750C>T (p.Pro584Ser) c.1819C>T (p.Pro607Ser) | dbSNP gnomAD v2 |
| X | g.153770213C>A | CA415101728 | PLXNB3 | c.1751C>A (p.Pro584His) c.1820C>A (p.Pro607His) | |
| X | g.153770213C>G | CA415101733 | PLXNB3 | c.1751C>G (p.Pro584Arg) c.1820C>G (p.Pro607Arg) | |
| X | g.153770213C>T | CA415101730 | PLXNB3 | c.1751C>T (p.Pro584Leu) c.1820C>T (p.Pro607Leu) | gnomAD v4 |
| X | g.153770214C>A | CA519347135 | PLXNB3 | c.1752C>A (p.Pro584=) c.1821C>A (p.Pro607=) | gnomAD v4 |
| X | g.153770214C>G | CA519347138 | PLXNB3 | c.1752C>G (p.Pro584=) c.1821C>G (p.Pro607=) | |
| X | g.153770214C>T | CA519347137 | PLXNB3 | c.1752C>T (p.Pro584=) c.1821C>T (p.Pro607=) | gnomAD v4 |
| X | g.153770215C>A | CA415101735 | PLXNB3 | c.1753C>A (p.Gln585Lys) c.1822C>A (p.Gln608Lys) | |
| X | g.153770215C>G | CA415101737 | PLXNB3 | c.1753C>G (p.Gln585Glu) c.1822C>G (p.Gln608Glu) | |
| X | g.153770215C>T | CA415101740 | PLXNB3 | c.1753C>T (p.Gln585Ter) c.1822C>T (p.Gln608Ter) | |
| X | g.153770216A= | CA2466468364 | PLXNB3 | c.1754A= (p.Gln585=) c.1823A= (p.Gln608=) | |
| X | g.153770216A>C | CA10550920 | PLXNB3 | c.1754A>C (p.Gln585Pro) c.1823A>C (p.Gln608Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.153770216A>G | CA415101745 | PLXNB3 | c.1754A>G (p.Gln585Arg) c.1823A>G (p.Gln608Arg) | |
| X | g.153770216A>T | CA415101747 | PLXNB3 | c.1754A>T (p.Gln585Leu) c.1823A>T (p.Gln608Leu) | |
| X | g.153770217A>C | CA415101750 | PLXNB3 | c.1755A>C (p.Gln585His) c.1824A>C (p.Gln608His) | |
| X | g.153770217A>G | CA519347144 | PLXNB3 | c.1755A>G (p.Gln585=) c.1824A>G (p.Gln608=) | gnomAD v4 |
| X | g.153770217A>T | CA415101757 | PLXNB3 | c.1755A>T (p.Gln585His) c.1824A>T (p.Gln608His) | |
| X | g.153770218G>A | CA415101765 | PLXNB3 | c.1756G>A (p.Asp586Asn) c.1825G>A (p.Asp609Asn) | gnomAD v4 |
| X | g.153770218G>C | CA10550921 | PLXNB3 | c.1756G>C (p.Asp586His) c.1825G>C (p.Asp609His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.153770218G= | CA2466468365 | PLXNB3 | c.1756G= (p.Asp586=) c.1825G= (p.Asp609=) | |
| X | g.153770218G>T | CA415101761 | PLXNB3 | c.1756G>T (p.Asp586Tyr) c.1825G>T (p.Asp609Tyr) | |
| X | g.153770219A>C | CA415101768 | PLXNB3 | c.1757A>C (p.Asp586Ala) c.1826A>C (p.Asp609Ala) | |
| X | g.153770219A>G | CA415101770 | PLXNB3 | c.1757A>G (p.Asp586Gly) c.1826A>G (p.Asp609Gly) | |
| X | g.153770219A>T | CA415101772 | PLXNB3 | c.1757A>T (p.Asp586Val) c.1826A>T (p.Asp609Val) | |
| X | g.153770220C>A | CA415101775 | PLXNB3 | c.1758C>A (p.Asp586Glu) c.1827C>A (p.Asp609Glu) | |
| X | g.153770220C>G | CA415101777 | PLXNB3 | c.1758C>G (p.Asp586Glu) c.1827C>G (p.Asp609Glu) | |
| X | g.153770220C>T | CA519347150 | PLXNB3 | c.1758C>T (p.Asp586=) c.1827C>T (p.Asp609=) | gnomAD v4 |
| X | g.153770221C>A | CA415101780 | PLXNB3 | c.1759C>A (p.Gln587Lys) c.1828C>A (p.Gln610Lys) | |
| X | g.153770221C>G | CA415101783 | PLXNB3 | c.1759C>G (p.Gln587Glu) c.1828C>G (p.Gln610Glu) | |
| X | g.153770221C>T | CA415101785 | PLXNB3 | c.1759C>T (p.Gln587Ter) c.1828C>T (p.Gln610Ter) | |
| X | g.153770222A>C | CA415101789 | PLXNB3 | c.1760A>C (p.Gln587Pro) c.1829A>C (p.Gln610Pro) | |
| X | g.153770222A>G | CA415101791 | PLXNB3 | c.1760A>G (p.Gln587Arg) c.1829A>G (p.Gln610Arg) | |
| X | g.153770222A>T | CA415101794 | PLXNB3 | c.1760A>T (p.Gln587Leu) c.1829A>T (p.Gln610Leu) | |
| X | g.153770223G>A | CA519347155 | PLXNB3 | c.1761G>A (p.Gln587=) c.1830G>A (p.Gln610=) | gnomAD v4 |
| X | g.153770223G>C | CA415101799 | PLXNB3 | c.1761G>C (p.Gln587His) c.1830G>C (p.Gln610His) | dbSNP gnomAD v4 |
| X | g.153770223G= | CA2466468366 | PLXNB3 | c.1761G= (p.Gln587=) c.1830G= (p.Gln610=) | |
| X | g.153770223G>T | CA415101797 | PLXNB3 | c.1761G>T (p.Gln587His) c.1830G>T (p.Gln610His) | |
| X | g.153770224G>A | CA415101803 | PLXNB3 | c.1762G>A (p.Val588Met) c.1831G>A (p.Val611Met) | gnomAD v4 |
| X | g.153770224G>C | CA415101805 | PLXNB3 | c.1762G>C (p.Val588Leu) c.1831G>C (p.Val611Leu) | gnomAD v4 |
| X | g.153770224G>T | CA415101807 | PLXNB3 | c.1762G>T (p.Val588Leu) c.1831G>T (p.Val611Leu) | |
| X | g.153770225T>A | CA415101810 | PLXNB3 | c.1763T>A (p.Val588Glu) c.1832T>A (p.Val611Glu) | |
| X | g.153770225T>C | CA415101812 | PLXNB3 | c.1763T>C (p.Val588Ala) c.1832T>C (p.Val611Ala) | dbSNP |
| X | g.153770225T>G | CA415101814 | PLXNB3 | c.1763T>G (p.Val588Gly) c.1832T>G (p.Val611Gly) | |
| X | g.153770225T= | CA2466468367 | PLXNB3 | c.1763T= (p.Val588=) c.1832T= (p.Val611=) | |
| X | g.153770226G>A | CA337228384 | PLXNB3 | c.1764G>A (p.Val588=) c.1833G>A (p.Val611=) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.153770226G>C | CA519347162 | PLXNB3 | c.1764G>C (p.Val588=) c.1833G>C (p.Val611=) | |
| X | g.153770226G= | CA2466468368 | PLXNB3 | c.1764G= (p.Val588=) c.1833G= (p.Val611=) | |
| X | g.153770226G>T | CA519347163 | PLXNB3 | c.1764G>T (p.Val588=) c.1833G>T (p.Val611=) | dbSNP |
| X | g.153770227C>A | CA415101817 | PLXNB3 | c.1765C>A (p.Pro589Thr) c.1834C>A (p.Pro612Thr) | |
| X | g.153770227C>G | CA415101819 | PLXNB3 | c.1765C>G (p.Pro589Ala) c.1834C>G (p.Pro612Ala) | |
| X | g.153770227C>T | CA415101822 | PLXNB3 | c.1765C>T (p.Pro589Ser) c.1834C>T (p.Pro612Ser) | gnomAD v4 |
| X | g.153770228C>A | CA415101825 | PLXNB3 | c.1766C>A (p.Pro589Gln) c.1835C>A (p.Pro612Gln) | |
| X | g.153770228C>G | CA415101827 | PLXNB3 | c.1766C>G (p.Pro589Arg) c.1835C>G (p.Pro612Arg) | |
| X | g.153770228C>T | CA415101829 | PLXNB3 | c.1766C>T (p.Pro589Leu) c.1835C>T (p.Pro612Leu) | |
| X | g.153770229A>C | CA519347168 | PLXNB3 | c.1767A>C (p.Pro589=) c.1836A>C (p.Pro612=) | |
| X | g.153770229A>G | CA519347170 | PLXNB3 | c.1767A>G (p.Pro589=) c.1836A>G (p.Pro612=) | |
| X | g.153770229A>T | CA519347169 | PLXNB3 | c.1767A>T (p.Pro589=) c.1836A>T (p.Pro612=) | |
| X | g.153770230C>A | CA415101833 | PLXNB3 | c.1768C>A (p.Leu590Ile) c.1837C>A (p.Leu613Ile) | |
| X | g.153770230C>G | CA415101834 | PLXNB3 | c.1768C>G (p.Leu590Val) c.1837C>G (p.Leu613Val) | |
| X | g.153770230C>T | CA415101832 | PLXNB3 | c.1768C>T (p.Leu590Phe) c.1837C>T (p.Leu613Phe) | |
| X | g.153770231T>A | CA415101835 | PLXNB3 | c.1769T>A (p.Leu590His) c.1838T>A (p.Leu613His) | |
| X | g.153770231T>C | CA415101836 | PLXNB3 | c.1769T>C (p.Leu590Pro) c.1838T>C (p.Leu613Pro) | |
| X | g.153770231T>G | CA415101837 | PLXNB3 | c.1769T>G (p.Leu590Arg) c.1838T>G (p.Leu613Arg) | |
| X | g.153770232T>A | CA519347173 | PLXNB3 | c.1770T>A (p.Leu590=) c.1839T>A (p.Leu613=) | |
| X | g.153770232T>C | CA519347174 | PLXNB3 | c.1770T>C (p.Leu590=) c.1839T>C (p.Leu613=) | dbSNP gnomAD v4 |
| X | g.153770232T>G | CA519347175 | PLXNB3 | c.1770T>G (p.Leu590=) c.1839T>G (p.Leu613=) | |
| X | g.153770232T= | CA2466468369 | PLXNB3 | c.1770T= (p.Leu590=) c.1839T= (p.Leu613=) | |
| X | g.153770233A= | CA2466468370 | PLXNB3 | c.1771A= (p.Asn591=) c.1840A= (p.Asn614=) | |
| X | g.153770233A>C | CA415101838 | PLXNB3 | c.1771A>C (p.Asn591His) c.1840A>C (p.Asn614His) | |
| X | g.153770233A>G | CA10550922 | PLXNB3 | c.1771A>G (p.Asn591Asp) c.1840A>G (p.Asn614Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.153770233A>T | CA415101839 | PLXNB3 | c.1771A>T (p.Asn591Tyr) c.1840A>T (p.Asn614Tyr) | |
| X | g.153770234A= | CA2466468371 | PLXNB3 | c.1772A= (p.Asn591=) c.1841A= (p.Asn614=) | |
| X | g.153770234A>C | CA415101840 | PLXNB3 | c.1772A>C (p.Asn591Thr) c.1841A>C (p.Asn614Thr) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.153770234A>G | CA415101841 | PLXNB3 | c.1772A>G (p.Asn591Ser) c.1841A>G (p.Asn614Ser) | |
| X | g.153770234A>T | CA415101842 | PLXNB3 | c.1772A>T (p.Asn591Ile) c.1841A>T (p.Asn614Ile) | |
| X | g.153770235C>A | CA415101843 | PLXNB3 | c.1773C>A (p.Asn591Lys) c.1842C>A (p.Asn614Lys) | |
| X | g.153770235C>G | CA415101845 | PLXNB3 | c.1773C>G (p.Asn591Lys) c.1842C>G (p.Asn614Lys) | |
| X | g.153770235C>T | CA519347179 | PLXNB3 | c.1773C>T (p.Asn591=) c.1842C>T (p.Asn614=) | gnomAD v4 |
| X | g.153770236C>A | CA415101853 | PLXNB3 | c.1774C>A (p.Pro592Thr) c.1843C>A (p.Pro615Thr) | |
| X | g.153770236C= | CA2466468372 | PLXNB3 | c.1774C= (p.Pro592=) c.1843C= (p.Pro615=) | |
| X | g.153770236C>G | CA415101851 | PLXNB3 | c.1774C>G (p.Pro592Ala) c.1843C>G (p.Pro615Ala) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.153770236C>T | CA415101848 | PLXNB3 | c.1774C>T (p.Pro592Ser) c.1843C>T (p.Pro615Ser) | dbSNP gnomAD v2 gnomAD v4 |
| X | g.153770237C>A | CA415101856 | PLXNB3 | c.1775C>A (p.Pro592His) c.1844C>A (p.Pro615His) | |
| X | g.153770237C>G | CA415101858 | PLXNB3 | c.1775C>G (p.Pro592Arg) c.1844C>G (p.Pro615Arg) | |
| X | g.153770237C>T | CA415101860 | PLXNB3 | c.1775C>T (p.Pro592Leu) c.1844C>T (p.Pro615Leu) | |
| X | g.153770238T>A | CA519347181 | PLXNB3 | c.1776T>A (p.Pro592=) c.1845T>A (p.Pro615=) | |
| X | g.153770238T>C | CA10550923 | PLXNB3 | c.1776T>C (p.Pro592=) c.1845T>C (p.Pro615=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.153770238T>G | CA519347182 | PLXNB3 | c.1776T>G (p.Pro592=) c.1845T>G (p.Pro615=) | |
| X | g.153770238T= | CA2466468373 | PLXNB3 | c.1776T= (p.Pro592=) c.1845T= (p.Pro615=) | |
| X | g.153770239C>A | CA415101865 | PLXNB3 | c.1777C>A (p.Pro593Thr) c.1846C>A (p.Pro616Thr) | |
| X | g.153770239C= | CA2466468374 | PLXNB3 | c.1777C= (p.Pro593=) c.1846C= (p.Pro616=) | |
| X | g.153770239C>G | CA10550924 | PLXNB3 | c.1777C>G (p.Pro593Ala) c.1846C>G (p.Pro616Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.153770239C>T | CA415101869 | PLXNB3 | c.1777C>T (p.Pro593Ser) c.1846C>T (p.Pro616Ser) | COSMIC COSMIC COSMIC |
| X | g.153770240C>A | CA415101872 | PLXNB3 | c.1778C>A (p.Pro593Gln) c.1847C>A (p.Pro616Gln) | dbSNP gnomAD v3 gnomAD v4 |
| X | g.153770240C= | CA2466468375 | PLXNB3 | c.1778C= (p.Pro593=) c.1847C= (p.Pro616=) | |
| X | g.153770240C>G | CA415101874 | PLXNB3 | c.1778C>G (p.Pro593Arg) c.1847C>G (p.Pro616Arg) | |
| X | g.153770240C>T | CA415101876 | PLXNB3 | c.1778C>T (p.Pro593Leu) c.1847C>T (p.Pro616Leu) | gnomAD v4 |
| X | g.153770241A>C | CA519347186 | PLXNB3 | c.1779A>C (p.Pro593=) c.1848A>C (p.Pro616=) | |
| X | g.153770241A>G | CA519347187 | PLXNB3 | c.1779A>G (p.Pro593=) c.1848A>G (p.Pro616=) | |
| X | g.153770241A>T | CA519347188 | PLXNB3 | c.1779A>T (p.Pro593=) c.1848A>T (p.Pro616=) | |
| X | g.153770241_153770242delinsAG | CA2466468376 | PLXNB3 | c.1779_1780delinsAG (p.Pro593=) c.1848_1849delinsAG (p.Pro616=) | |
| X | g.153770242G>A | CA10550925 | PLXNB3 | c.1780G>A (p.Gly594Ser) c.1849G>A (p.Gly617Ser) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| X | g.153770242G>C | CA415101879 | PLXNB3 | c.1780G>C (p.Gly594Arg) c.1849G>C (p.Gly617Arg) | |
| X | g.153770242G= | CA2466468378 | PLXNB3 | c.1780G= (p.Gly594=) c.1849G= (p.Gly617=) | |
| X | g.153770242G>T | CA415101883 | PLXNB3 | c.1780G>T (p.Gly594Cys) c.1849G>T (p.Gly617Cys) | |
| X | g.153770243del | CA2466468377 | PLXNB3 | c.1781del (p.Gly594AlafsTer11) c.1850del (p.Gly617AlafsTer11) | dbSNP |
| X | g.153770243G>A | CA415101887 | PLXNB3 | c.1781G>A (p.Gly594Asp) c.1850G>A (p.Gly617Asp) | gnomAD v4 |
| X | g.153770243G>C | CA415101890 | PLXNB3 | c.1781G>C (p.Gly594Ala) c.1850G>C (p.Gly617Ala) | |
| X | g.153770243G>T | CA415101885 | PLXNB3 | c.1781G>T (p.Gly594Val) c.1850G>T (p.Gly617Val) |