2 | g.135817339A>C | CA348605560 | LCT | c.1707+2T>G (n.1707+2T>G)
| |
2 | g.135817339A>G | CA348605561 | LCT | c.1707+2T>C (n.1707+2T>C)
| |
2 | g.135817339A>T | CA348605562 | LCT | c.1707+2T>A (n.1707+2T>A)
| |
2 | g.135817340C>A | CA348605563 | LCT | c.1707+1G>T (n.1707+1G>T)
| |
2 | g.135817340C= | CA1290834743 | LCT | c.1707+1G= (n.1707+1G=)
| |
2 | g.135817340C>G | CA348605565 | LCT | c.1707+1G>C (n.1707+1G>C)
| |
2 | g.135817340C>T | CA348605564 | LCT | c.1707+1G>A (n.1707+1G>A)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817341C>A | CA348605566 | LCT | c.1707G>T (p.Lys569Asn)
| |
2 | g.135817341C>G | CA348605567 | LCT | c.1707G>C (p.Lys569Asn)
| |
2 | g.135817341C>T | CA429204351 | LCT | c.1707G>A (p.Lys569=)
| |
2 | g.135817342T>A | CA348605568 | LCT | c.1706A>T (p.Lys569Met)
| |
2 | g.135817342T>C | CA348605569 | LCT | c.1706A>G (p.Lys569Arg)
| |
2 | g.135817342T>G | CA348605570 | LCT | c.1706A>C (p.Lys569Thr)
| |
2 | g.135817343T>A | CA348605571 | LCT | c.1705A>T (p.Lys569Ter)
| |
2 | g.135817343T>C | CA348605572 | LCT | c.1705A>G (p.Lys569Glu)
| |
2 | g.135817343T>G | CA348605573 | LCT | c.1705A>C (p.Lys569Gln)
| |
2 | g.135817344A>C | CA348605574 | LCT | c.1704T>G (p.Phe568Leu)
| |
2 | g.135817344A>G | CA429204356 | LCT | c.1704T>C (p.Phe568=)
| |
2 | g.135817344A>T | CA348605575 | LCT | c.1704T>A (p.Phe568Leu)
| |
2 | g.135817345A>C | CA348605578 | LCT | c.1703T>G (p.Phe568Cys)
| |
2 | g.135817345A>G | CA348605577 | LCT | c.1703T>C (p.Phe568Ser)
| |
2 | g.135817345A>T | CA348605576 | LCT | c.1703T>A (p.Phe568Tyr)
| |
2 | g.135817346A>C | CA348605579 | LCT | c.1702T>G (p.Phe568Val)
| |
2 | g.135817346A>G | CA348605580 | LCT | c.1702T>C (p.Phe568Leu)
| |
2 | g.135817346A>T | CA348605581 | LCT | c.1702T>A (p.Phe568Ile)
| |
2 | g.135817347A>C | CA429204467 | LCT | c.1701T>G (p.Ser567=)
| |
2 | g.135817347A>G | CA429204468 | LCT | c.1701T>C (p.Ser567=)
| |
2 | g.135817347A>T | CA429204469 | LCT | c.1701T>A (p.Ser567=)
| |
2 | g.135817348G>A | CA348605582 | LCT | c.1700C>T (p.Ser567Phe)
| |
2 | g.135817348G>C | CA348605583 | LCT | c.1700C>G (p.Ser567Cys)
| |
2 | g.135817348G>T | CA348605584 | LCT | c.1700C>A (p.Ser567Tyr)
| |
2 | g.135817349A>C | CA348605585 | LCT | c.1699T>G (p.Ser567Ala)
| |
2 | g.135817349A>G | CA348605586 | LCT | c.1699T>C (p.Ser567Pro)
| |
2 | g.135817349A>T | CA348605587 | LCT | c.1699T>A (p.Ser567Thr)
| |
2 | g.135817349_135817357del | CA645531704 | LCT | c.1691_1699del (p.Gly564_Ser567delinsAla)
| COSMIC |
2 | g.135817350G>A | CA1888360 | LCT | c.1698C>T (p.Ala566=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817350G>C | CA429204470 | LCT | c.1698C>G (p.Ala566=)
| |
2 | g.135817350G= | CA1290834744 | LCT | c.1698C= (p.Ala566=)
| |
2 | g.135817350G>T | CA429204471 | LCT | c.1698C>A (p.Ala566=)
| |
2 | g.135817351G>A | CA348605588 | LCT | c.1697C>T (p.Ala566Val)
| |
2 | g.135817351G>C | CA348605589 | LCT | c.1697C>G (p.Ala566Gly)
| |
2 | g.135817351G>T | CA348605590 | LCT | c.1697C>A (p.Ala566Asp)
| |
2 | g.135817351_135817356delinsGCCACT | CA1290834745 | LCT | c.1692_1697delinsAGTGGC (p.Gly564=)
| |
2 | g.135817352C>A | CA348605593 | LCT | c.1696G>T (p.Ala566Ser)
| |
2 | g.135817352C= | CA1290834746 | LCT | c.1696G= (p.Ala566=)
| |
2 | g.135817352C>G | CA348605592 | LCT | c.1696G>C (p.Ala566Pro)
| |
2 | g.135817352C>T | CA348605591 | LCT | c.1696G>A (p.Ala566Thr)
| dbSNP |
2 | g.135817354_135817358del | CA144312 | LCT | c.1692_1696del (p.Val565LeufsTer3)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817353C>A | CA429204472 | LCT | c.1695G>T (p.Val565=)
| |
2 | g.135817353C>G | CA429204474 | LCT | c.1695G>C (p.Val565=)
| |
2 | g.135817353C>T | CA429204473 | LCT | c.1695G>A (p.Val565=)
| |
2 | g.135817354A>C | CA348605594 | LCT | c.1694T>G (p.Val565Gly)
| |
2 | g.135817354A>G | CA348605595 | LCT | c.1694T>C (p.Val565Ala)
| gnomAD v4 |
2 | g.135817354A>T | CA348605596 | LCT | c.1694T>A (p.Val565Glu)
| COSMIC |
2 | g.135817355C>A | CA348605597 | LCT | c.1693G>T (p.Val565Leu)
| |
2 | g.135817355C>G | CA348605598 | LCT | c.1693G>C (p.Val565Leu)
| |
2 | g.135817355C>T | CA348605599 | LCT | c.1693G>A (p.Val565Met)
| gnomAD v4 |
2 | g.135817356T>A | CA429204475 | LCT | c.1692A>T (p.Gly564=)
| |
2 | g.135817356T>C | CA1888361 | LCT | c.1692A>G (p.Gly564=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817356T>G | CA429204476 | LCT | c.1692A>C (p.Gly564=)
| |
2 | g.135817356T= | CA1290834747 | LCT | c.1692A= (p.Gly564=)
| |
2 | g.135817357C>A | CA348605600 | LCT | c.1691G>T (p.Gly564Val)
| |
2 | g.135817357C>G | CA348605601 | LCT | c.1691G>C (p.Gly564Ala)
| |
2 | g.135817357C>T | CA348605602 | LCT | c.1691G>A (p.Gly564Glu)
| |
2 | g.135817358C>A | CA348605603 | LCT | c.1690G>T (p.Gly564Ter)
| |
2 | g.135817358C>G | CA348605604 | LCT | c.1690G>C (p.Gly564Arg)
| gnomAD v4 |
2 | g.135817358C>T | CA348605605 | LCT | c.1690G>A (p.Gly564Arg)
| |
2 | g.135817359T>A | CA429204477 | LCT | c.1689A>T (p.Pro563=)
| |
2 | g.135817359T>C | CA429204478 | LCT | c.1689A>G (p.Pro563=)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817359T>G | CA429204479 | LCT | c.1689A>C (p.Pro563=)
| |
2 | g.135817359T= | CA1290834748 | LCT | c.1689A= (p.Pro563=)
| |
2 | g.135817360G>A | CA348605606 | LCT | c.1688C>T (p.Pro563Leu)
| |
2 | g.135817360G>C | CA348605608 | LCT | c.1688C>G (p.Pro563Arg)
| |
2 | g.135817360G>T | CA348605607 | LCT | c.1688C>A (p.Pro563Gln)
| |
2 | g.135817361G>A | CA348605609 | LCT | c.1687C>T (p.Pro563Ser)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817361G>C | CA348605610 | LCT | c.1687C>G (p.Pro563Ala)
| |
2 | g.135817361G= | CA1290834749 | LCT | c.1687C= (p.Pro563=)
| |
2 | g.135817361G>T | CA348605611 | LCT | c.1687C>A (p.Pro563Thr)
| |
2 | g.135817362G>A | CA429204480 | LCT | c.1686C>T (p.Asp562=)
| |
2 | g.135817362G>C | CA348605612 | LCT | c.1686C>G (p.Asp562Glu)
| |
2 | g.135817362G>T | CA348605613 | LCT | c.1686C>A (p.Asp562Glu)
| |
2 | g.135817363T>A | CA348605616 | LCT | c.1685A>T (p.Asp562Val)
| |
2 | g.135817363T>C | CA348605615 | LCT | c.1685A>G (p.Asp562Gly)
| |
2 | g.135817363T>G | CA348605614 | LCT | c.1685A>C (p.Asp562Ala)
| |
2 | g.135817364C>A | CA348605617 | LCT | c.1684G>T (p.Asp562Tyr)
| |
2 | g.135817364C>G | CA348605618 | LCT | c.1684G>C (p.Asp562His)
| |
2 | g.135817364C>T | CA348605619 | LCT | c.1684G>A (p.Asp562Asn)
| |
2 | g.135817365A= | CA1290834750 | LCT | c.1683T= (p.Ser561=)
| |
2 | g.135817365A>C | CA429204481 | LCT | c.1683T>G (p.Ser561=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817365A>G | CA429204482 | LCT | c.1683T>C (p.Ser561=)
| |
2 | g.135817365A>T | CA429204483 | LCT | c.1683T>A (p.Ser561=)
| |
2 | g.135817366G>A | CA348605620 | LCT | c.1682C>T (p.Ser561Phe)
| |
2 | g.135817366G>C | CA348605621 | LCT | c.1682C>G (p.Ser561Cys)
| dbSNP gnomAD v4 COSMIC |
2 | g.135817366G= | CA1290834751 | LCT | c.1682C= (p.Ser561=)
| |
2 | g.135817366G>T | CA348605622 | LCT | c.1682C>A (p.Ser561Tyr)
| |
2 | g.135817367A>C | CA348605623 | LCT | c.1681T>G (p.Ser561Ala)
| |
2 | g.135817367A>G | CA348605625 | LCT | c.1681T>C (p.Ser561Pro)
| |
2 | g.135817367A>T | CA348605624 | LCT | c.1681T>A (p.Ser561Thr)
| |
2 | g.135817368G>A | CA429204484 | LCT | c.1680C>T (p.Ile560=)
| |
2 | g.135817368G>C | CA56623340 | LCT | c.1680C>G (p.Ile560Met)
| dbSNP gnomAD v4 |
2 | g.135817368G= | CA1290834752 | LCT | c.1680C= (p.Ile560=)
| |
2 | g.135817368G>T | CA429204485 | LCT | c.1680C>A (p.Ile560=)
| |
2 | g.135817369A>C | CA348605626 | LCT | c.1679T>G (p.Ile560Ser)
| |
2 | g.135817369A>G | CA348605627 | LCT | c.1679T>C (p.Ile560Thr)
| |
2 | g.135817369A>T | CA348605628 | LCT | c.1679T>A (p.Ile560Asn)
| |
2 | g.135817370T>A | CA348605629 | LCT | c.1678A>T (p.Ile560Phe)
| |
2 | g.135817370T>C | CA348605630 | LCT | c.1678A>G (p.Ile560Val)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817370T>G | CA348605631 | LCT | c.1678A>C (p.Ile560Leu)
| |
2 | g.135817370T= | CA1290834753 | LCT | c.1678A= (p.Ile560=)
| |
2 | g.135817371G>A | CA429204486 | LCT | c.1677C>T (p.Gly559=)
| |
2 | g.135817371G>C | CA429204487 | LCT | c.1677C>G (p.Gly559=)
| gnomAD v4 |
2 | g.135817371G>T | CA429204488 | LCT | c.1677C>A (p.Gly559=)
| |
2 | g.135817372C>A | CA348605632 | LCT | c.1676G>T (p.Gly559Val)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817372C= | CA1290834754 | LCT | c.1676G= (p.Gly559=)
| |
2 | g.135817372C>G | CA348605633 | LCT | c.1676G>C (p.Gly559Ala)
| |
2 | g.135817372C>T | CA348605634 | LCT | c.1676G>A (p.Gly559Asp)
| gnomAD v4 |
2 | g.135817373C>A | CA348605636 | LCT | c.1675G>T (p.Gly559Cys)
| |
2 | g.135817373C= | CA1290834755 | LCT | c.1675G= (p.Gly559=)
| |
2 | g.135817373C>G | CA348605635 | LCT | c.1675G>C (p.Gly559Arg)
| COSMIC |
2 | g.135817373C>T | CA1888362 | LCT | c.1675G>A (p.Gly559Ser)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817374G>A | CA1888363 | LCT | c.1674C>T (p.Pro558=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817374G>C | CA429204489 | LCT | c.1674C>G (p.Pro558=)
| |
2 | g.135817374G= | CA1290834756 | LCT | c.1674C= (p.Pro558=)
| |
2 | g.135817374G>T | CA429204490 | LCT | c.1674C>A (p.Pro558=)
| dbSNP |
2 | g.135817375G>A | CA348605637 | LCT | c.1673C>T (p.Pro558Leu)
| |
2 | g.135817375G>C | CA348605638 | LCT | c.1673C>G (p.Pro558Arg)
| |
2 | g.135817375G>T | CA348605639 | LCT | c.1673C>A (p.Pro558His)
| gnomAD v4 |
2 | g.135817376G>A | CA348605640 | LCT | c.1672C>T (p.Pro558Ser)
| dbSNP |
2 | g.135817376G>C | CA348605641 | LCT | c.1672C>G (p.Pro558Ala)
| |
2 | g.135817376G= | CA1290834757 | LCT | c.1672C= (p.Pro558=)
| |
2 | g.135817376G>T | CA348605642 | LCT | c.1672C>A (p.Pro558Thr)
| |
2 | g.135817377A>C | CA429204493 | LCT | c.1671T>G (p.Pro557=)
| |
2 | g.135817377A>G | CA429204492 | LCT | c.1671T>C (p.Pro557=)
| |
2 | g.135817377A>T | CA429204491 | LCT | c.1671T>A (p.Pro557=)
| |
2 | g.135817378G>A | CA348605645 | LCT | c.1670C>T (p.Pro557Leu)
| |
2 | g.135817378G>C | CA348605643 | LCT | c.1670C>G (p.Pro557Arg)
| dbSNP |
2 | g.135817378G= | CA1290834758 | LCT | c.1670C= (p.Pro557=)
| |
2 | g.135817378G>T | CA348605644 | LCT | c.1670C>A (p.Pro557His)
| |
2 | g.135817379G>A | CA348605646 | LCT | c.1669C>T (p.Pro557Ser)
| dbSNP gnomAD v3 gnomAD v4 COSMIC |
2 | g.135817379G>C | CA348605647 | LCT | c.1669C>G (p.Pro557Ala)
| |
2 | g.135817379G= | CA1290834759 | LCT | c.1669C= (p.Pro557=)
| |
2 | g.135817379G>T | CA348605648 | LCT | c.1669C>A (p.Pro557Thr)
| |
2 | g.135817380G>A | CA429204494 | LCT | c.1668C>T (p.His556=)
| |
2 | g.135817380G>C | CA348605649 | LCT | c.1668C>G (p.His556Gln)
| |
2 | g.135817380G>T | CA348605650 | LCT | c.1668C>A (p.His556Gln)
| |
2 | g.135817381T>A | CA348605653 | LCT | c.1667A>T (p.His556Leu)
| |
2 | g.135817381T>C | CA348605651 | LCT | c.1667A>G (p.His556Arg)
| |
2 | g.135817381T>G | CA348605652 | LCT | c.1667A>C (p.His556Pro)
| dbSNP |
2 | g.135817381T= | CA1290834760 | LCT | c.1667A= (p.His556=)
| |
2 | g.135817382G>A | CA348605654 | LCT | c.1666C>T (p.His556Tyr)
| |
2 | g.135817382G>C | CA348605655 | LCT | c.1666C>G (p.His556Asp)
| |
2 | g.135817382G>T | CA348605656 | LCT | c.1666C>A (p.His556Asn)
| |
2 | g.135817383C>A | CA348605657 | LCT | c.1665G>T (p.Gln555His)
| |
2 | g.135817383C>G | CA348605658 | LCT | c.1665G>C (p.Gln555His)
| |
2 | g.135817383C>T | CA429204495 | LCT | c.1665G>A (p.Gln555=)
| |
2 | g.135817384T>A | CA348605661 | LCT | c.1664A>T (p.Gln555Leu)
| |
2 | g.135817384T>C | CA348605660 | LCT | c.1664A>G (p.Gln555Arg)
| |
2 | g.135817384T>G | CA348605659 | LCT | c.1664A>C (p.Gln555Pro)
| |
2 | g.135817385G>A | CA348605662 | LCT | c.1663C>T (p.Gln555Ter)
| |
2 | g.135817385G>C | CA348605663 | LCT | c.1663C>G (p.Gln555Glu)
| ClinVar dbSNP |
2 | g.135817385G>T | CA348605664 | LCT | c.1663C>A (p.Gln555Lys)
| |
2 | g.135817386G>A | CA429204496 | LCT | c.1662C>T (p.Gly554=)
| dbSNP gnomAD v4 |
2 | g.135817386G>C | CA429204497 | LCT | c.1662C>G (p.Gly554=)
| |
2 | g.135817386G= | CA1290834761 | LCT | c.1662C= (p.Gly554=)
| |
2 | g.135817386G>T | CA429204498 | LCT | c.1662C>A (p.Gly554=)
| |
2 | g.135817387C>A | CA348605665 | LCT | c.1661G>T (p.Gly554Val)
| |
2 | g.135817387C>G | CA348605666 | LCT | c.1661G>C (p.Gly554Ala)
| |
2 | g.135817387C>T | CA348605667 | LCT | c.1661G>A (p.Gly554Asp)
| gnomAD v4 |
2 | g.135817388C>A | CA348605668 | LCT | c.1660G>T (p.Gly554Cys)
| |
2 | g.135817388C= | CA1290834762 | LCT | c.1660G= (p.Gly554=)
| |
2 | g.135817388C>G | CA348605669 | LCT | c.1660G>C (p.Gly554Arg)
| dbSNP |
2 | g.135817388C>T | CA56623342 | LCT | c.1660G>A (p.Gly554Ser)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817389G>A | CA1888364 | LCT | c.1659C>T (p.Thr553=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135817389G>C | CA429204499 | LCT | c.1659C>G (p.Thr553=)
| |
2 | g.135817389G= | CA1290834763 | LCT | c.1659C= (p.Thr553=)
| |
2 | g.135817389G>T | CA429204500 | LCT | c.1659C>A (p.Thr553=)
| |
2 | g.135817390G>A | CA348605670 | LCT | c.1658C>T (p.Thr553Ile)
| |
2 | g.135817390G>C | CA348605671 | LCT | c.1658C>G (p.Thr553Ser)
| |
2 | g.135817390G= | CA1290834764 | LCT | c.1658C= (p.Thr553=)
| |
2 | g.135817390G>T | CA56623353 | LCT | c.1658C>A (p.Thr553Asn)
| dbSNP |
2 | g.135817391T>A | CA348605672 | LCT | c.1657A>T (p.Thr553Ser)
| |
2 | g.135817391T>C | CA348605673 | LCT | c.1657A>G (p.Thr553Ala)
| |
2 | g.135817391T>G | CA348605674 | LCT | c.1657A>C (p.Thr553Pro)
| |
2 | g.135817392G>A | CA429204501 | LCT | c.1656C>T (p.Gly552=)
| |
2 | g.135817392G>C | CA429204502 | LCT | c.1656C>G (p.Gly552=)
| |
2 | g.135817392G>T | CA429204503 | LCT | c.1656C>A (p.Gly552=)
| |
2 | g.135817393C>A | CA348605675 | LCT | c.1655G>T (p.Gly552Val)
| |
2 | g.135817393C>G | CA348605676 | LCT | c.1655G>C (p.Gly552Ala)
| |
2 | g.135817393C>T | CA348605677 | LCT | c.1655G>A (p.Gly552Asp)
| gnomAD v4 |
2 | g.135817394C>A | CA348605678 | LCT | c.1654G>T (p.Gly552Cys)
| |
2 | g.135817394C>G | CA348605679 | LCT | c.1654G>C (p.Gly552Arg)
| |
2 | g.135817394C>T | CA348605680 | LCT | c.1654G>A (p.Gly552Ser)
| |
2 | g.135817395A= | CA1290834765 | LCT | c.1653T= (p.Tyr551=)
| |
2 | g.135817395A>C | CA348605682 | LCT | c.1653T>G (p.Tyr551Ter)
| |
2 | g.135817395A>G | CA429204504 | LCT | c.1653T>C (p.Tyr551=)
| dbSNP gnomAD v4 |
2 | g.135817395A>T | CA348605681 | LCT | c.1653T>A (p.Tyr551Ter)
| |
2 | g.135817396T>A | CA348605683 | LCT | c.1652A>T (p.Tyr551Phe)
| |
2 | g.135817396T>C | CA348605684 | LCT | c.1652A>G (p.Tyr551Cys)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817396T>G | CA348605685 | LCT | c.1652A>C (p.Tyr551Ser)
| |
2 | g.135817396T= | CA1290834766 | LCT | c.1652A= (p.Tyr551=)
| |
2 | g.135817397A>C | CA348605686 | LCT | c.1651T>G (p.Tyr551Asp)
| |
2 | g.135817397A>G | CA348605687 | LCT | c.1651T>C (p.Tyr551His)
| |
2 | g.135817397A>T | CA348605688 | LCT | c.1651T>A (p.Tyr551Asn)
| |
2 | g.135817398G>A | CA429204505 | LCT | c.1650C>T (p.Gly550=)
| |
2 | g.135817398G>C | CA1888365 | LCT | c.1650C>G (p.Gly550=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817398G= | CA1290834767 | LCT | c.1650C= (p.Gly550=)
| |
2 | g.135817398G>T | CA429204506 | LCT | c.1650C>A (p.Gly550=)
| |
2 | g.135817399C>A | CA348605689 | LCT | c.1649G>T (p.Gly550Val)
| |
2 | g.135817399C>G | CA348605690 | LCT | c.1649G>C (p.Gly550Ala)
| |
2 | g.135817399C>T | CA348605691 | LCT | c.1649G>A (p.Gly550Asp)
| gnomAD v4 |
2 | g.135817400C>A | CA348605692 | LCT | c.1648G>T (p.Gly550Cys)
| |
2 | g.135817400C= | CA1290834768 | LCT | c.1648G= (p.Gly550=)
| |
2 | g.135817400C>G | CA348605693 | LCT | c.1648G>C (p.Gly550Arg)
| |
2 | g.135817400C>T | CA56623378 | LCT | c.1648G>A (p.Gly550Ser)
| dbSNP |
2 | g.135817401T>A | CA429204507 | LCT | c.1647A>T (p.Ala549=)
| |
2 | g.135817401T>C | CA429204508 | LCT | c.1647A>G (p.Ala549=)
| dbSNP |
2 | g.135817401T>G | CA429204509 | LCT | c.1647A>C (p.Ala549=)
| |
2 | g.135817401T= | CA1290834769 | LCT | c.1647A= (p.Ala549=)
| |
2 | g.135817402G>A | CA348605696 | LCT | c.1646C>T (p.Ala549Val)
| gnomAD v4 |
2 | g.135817402G>C | CA348605694 | LCT | c.1646C>G (p.Ala549Gly)
| |
2 | g.135817402G>T | CA348605695 | LCT | c.1646C>A (p.Ala549Glu)
| |
2 | g.135817403C>A | CA348605697 | LCT | c.1645G>T (p.Ala549Ser)
| |
2 | g.135817403C= | CA1290834770 | LCT | c.1645G= (p.Ala549=)
| |
2 | g.135817403C>G | CA348605699 | LCT | c.1645G>C (p.Ala549Pro)
| |
2 | g.135817403C>T | CA348605698 | LCT | c.1645G>A (p.Ala549Thr)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817404G>A | CA1888366 | LCT | c.1644C>T (p.Tyr548=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817404G>C | CA348605700 | LCT | c.1644C>G (p.Tyr548Ter)
| gnomAD v4 |
2 | g.135817404G= | CA1290834771 | LCT | c.1644C= (p.Tyr548=)
| |
2 | g.135817404G>T | CA348605701 | LCT | c.1644C>A (p.Tyr548Ter)
| |
2 | g.135817405T>A | CA348605702 | LCT | c.1643A>T (p.Tyr548Phe)
| gnomAD v4 |
2 | g.135817405T>C | CA348605703 | LCT | c.1643A>G (p.Tyr548Cys)
| |
2 | g.135817405T>G | CA348605704 | LCT | c.1643A>C (p.Tyr548Ser)
| |
2 | g.135817406A= | CA1290834772 | LCT | c.1642T= (p.Tyr548=)
| |
2 | g.135817406A>C | CA348605705 | LCT | c.1642T>G (p.Tyr548Asp)
| |
2 | g.135817406A>G | CA348605706 | LCT | c.1642T>C (p.Tyr548His)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817406A>T | CA348605707 | LCT | c.1642T>A (p.Tyr548Asn)
| |
2 | g.135817407G>A | CA429204510 | LCT | c.1641C>T (p.Ser547=)
| |
2 | g.135817407G>C | CA348605708 | LCT | c.1641C>G (p.Ser547Arg)
| |
2 | g.135817407G>T | CA348605709 | LCT | c.1641C>A (p.Ser547Arg)
| |
2 | g.135817408C>A | CA348605712 | LCT | c.1640G>T (p.Ser547Ile)
| |
2 | g.135817408C>G | CA348605711 | LCT | c.1640G>C (p.Ser547Thr)
| |
2 | g.135817408C>T | CA348605710 | LCT | c.1640G>A (p.Ser547Asn)
| |
2 | g.135817409T>A | CA348605713 | LCT | c.1639A>T (p.Ser547Cys)
| |
2 | g.135817409T>C | CA348605714 | LCT | c.1639A>G (p.Ser547Gly)
| |
2 | g.135817409T>G | CA348605715 | LCT | c.1639A>C (p.Ser547Arg)
| |
2 | g.135817410C>A | CA348605716 | LCT | c.1638G>T (p.Met546Ile)
| dbSNP |
2 | g.135817410C= | CA1290834773 | LCT | c.1638G= (p.Met546=)
| |
2 | g.135817410C>G | CA348605717 | LCT | c.1638G>C (p.Met546Ile)
| |
2 | g.135817410C>T | CA348605718 | LCT | c.1638G>A (p.Met546Ile)
| |
2 | g.135817411A>C | CA348605719 | LCT | c.1637T>G (p.Met546Arg)
| |
2 | g.135817411A>G | CA348605720 | LCT | c.1637T>C (p.Met546Thr)
| |
2 | g.135817411A>T | CA348605721 | LCT | c.1637T>A (p.Met546Lys)
| |
2 | g.135817412T>A | CA348605722 | LCT | c.1636A>T (p.Met546Leu)
| |
2 | g.135817412T>C | CA348605723 | LCT | c.1636A>G (p.Met546Val)
| |
2 | g.135817412T>G | CA348605724 | LCT | c.1636A>C (p.Met546Leu)
| |
2 | g.135817413C>A | CA429204513 | LCT | c.1635G>T (p.Val545=)
| dbSNP |
2 | g.135817413C= | CA1290834774 | LCT | c.1635G= (p.Val545=)
| |
2 | g.135817413C>G | CA429204511 | LCT | c.1635G>C (p.Val545=)
| |
2 | g.135817413C>T | CA429204512 | LCT | c.1635G>A (p.Val545=)
| |
2 | g.135817414A>C | CA348605727 | LCT | c.1634T>G (p.Val545Gly)
| |
2 | g.135817414A>G | CA348605726 | LCT | c.1634T>C (p.Val545Ala)
| |
2 | g.135817414A>T | CA348605725 | LCT | c.1634T>A (p.Val545Glu)
| |
2 | g.135817415C>A | CA348605730 | LCT | c.1633G>T (p.Val545Leu)
| |
2 | g.135817415C>G | CA348605728 | LCT | c.1633G>C (p.Val545Leu)
| |
2 | g.135817415C>T | CA348605729 | LCT | c.1633G>A (p.Val545Met)
| |
2 | g.135817416C>A | CA348605731 | LCT | c.1632G>T (p.Trp544Cys)
| |
2 | g.135817416C>G | CA348605732 | LCT | c.1632G>C (p.Trp544Cys)
| |
2 | g.135817416C>T | CA348605733 | LCT | c.1632G>A (p.Trp544Ter)
| |
2 | g.135817417C>A | CA348605734 | LCT | c.1631G>T (p.Trp544Leu)
| |
2 | g.135817417C>G | CA348605735 | LCT | c.1631G>C (p.Trp544Ser)
| |
2 | g.135817417C>T | CA348605736 | LCT | c.1631G>A (p.Trp544Ter)
| COSMIC |
2 | g.135817418A>C | CA348605737 | LCT | c.1630T>G (p.Trp544Gly)
| |
2 | g.135817418A>G | CA348605738 | LCT | c.1630T>C (p.Trp544Arg)
| |
2 | g.135817418A>T | CA348605739 | LCT | c.1630T>A (p.Trp544Arg)
| |
2 | g.135817419C>A | CA429204514 | LCT | c.1629G>T (p.Pro543=)
| |
2 | g.135817419C= | CA1290834775 | LCT | c.1629G= (p.Pro543=)
| |
2 | g.135817419C>G | CA429204515 | LCT | c.1629G>C (p.Pro543=)
| |
2 | g.135817419C>T | CA1888367 | LCT | c.1629G>A (p.Pro543=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817420G>A | CA348605741 | LCT | c.1628C>T (p.Pro543Leu)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817420G>C | CA348605742 | LCT | c.1628C>G (p.Pro543Arg)
| |
2 | g.135817420G= | CA1290834776 | LCT | c.1628C= (p.Pro543=)
| |
2 | g.135817420G>T | CA348605740 | LCT | c.1628C>A (p.Pro543Gln)
| |
2 | g.135817421G>A | CA348605743 | LCT | c.1627C>T (p.Pro543Ser)
| |
2 | g.135817421G>C | CA348605744 | LCT | c.1627C>G (p.Pro543Ala)
| |
2 | g.135817421G= | CA1290834777 | LCT | c.1627C= (p.Pro543=)
| |
2 | g.135817421G>T | CA348605745 | LCT | c.1627C>A (p.Pro543Thr)
| dbSNP gnomAD v4 COSMIC |
2 | g.135817422C>A | CA348605746 | LCT | c.1626G>T (p.Glu542Asp)
| |
2 | g.135817422C= | CA1290834778 | LCT | c.1626G= (p.Glu542=)
| |
2 | g.135817422C>G | CA348605747 | LCT | c.1626G>C (p.Glu542Asp)
| |
2 | g.135817422C>T | CA429204516 | LCT | c.1626G>A (p.Glu542=)
| dbSNP |
2 | g.135817423T>A | CA348605750 | LCT | c.1625A>T (p.Glu542Val)
| |
2 | g.135817423T>C | CA348605748 | LCT | c.1625A>G (p.Glu542Gly)
| |
2 | g.135817423T>G | CA348605749 | LCT | c.1625A>C (p.Glu542Ala)
| |
2 | g.135817424C>A | CA348605751 | LCT | c.1624G>T (p.Glu542Ter)
| |
2 | g.135817424C= | CA1290834779 | LCT | c.1624G= (p.Glu542=)
| |
2 | g.135817424C>G | CA348605752 | LCT | c.1624G>C (p.Glu542Gln)
| |
2 | g.135817424C>T | CA348605753 | LCT | c.1624G>A (p.Glu542Lys)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817425A= | CA1290834780 | LCT | c.1623T= (p.His541=)
| |
2 | g.135817425A>C | CA348605754 | LCT | c.1623T>G (p.His541Gln)
| |
2 | g.135817425A>G | CA1888368 | LCT | c.1623T>C (p.His541=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817425A>T | CA348605755 | LCT | c.1623T>A (p.His541Gln)
| |
2 | g.135817426T>A | CA348605757 | LCT | c.1622A>T (p.His541Leu)
| |
2 | g.135817426T>C | CA1888369 | LCT | c.1622A>G (p.His541Arg)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817426T>G | CA348605756 | LCT | c.1622A>C (p.His541Pro)
| COSMIC |
2 | g.135817426T= | CA1290834781 | LCT | c.1622A= (p.His541=)
| |
2 | g.135817427G>A | CA348605758 | LCT | c.1621C>T (p.His541Tyr)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817427G>C | CA348605760 | LCT | c.1621C>G (p.His541Asp)
| |
2 | g.135817427G= | CA1290834782 | LCT | c.1621C= (p.His541=)
| |
2 | g.135817427G>T | CA348605759 | LCT | c.1621C>A (p.His541Asn)
| |
2 | g.135817428del | CA2661275752 | LCT | c.1621del (p.His541MetfsTer5)
| gnomAD v4 |
2 | g.135817428G>A | CA429204517 | LCT | c.1620C>T (p.Phe540=)
| |
2 | g.135817428G>C | CA348605761 | LCT | c.1620C>G (p.Phe540Leu)
| |
2 | g.135817428G>T | CA348605762 | LCT | c.1620C>A (p.Phe540Leu)
| |
2 | g.135817429A= | CA1290834783 | LCT | c.1619T= (p.Phe540=)
| |
2 | g.135817429A>C | CA348605763 | LCT | c.1619T>G (p.Phe540Cys)
| dbSNP |
2 | g.135817429A>G | CA348605764 | LCT | c.1619T>C (p.Phe540Ser)
| |
2 | g.135817429A>T | CA348605765 | LCT | c.1619T>A (p.Phe540Tyr)
| |
2 | g.135817430A>C | CA348605766 | LCT | c.1618T>G (p.Phe540Val)
| |
2 | g.135817430A>G | CA348605767 | LCT | c.1618T>C (p.Phe540Leu)
| |
2 | g.135817430A>T | CA348605768 | LCT | c.1618T>A (p.Phe540Ile)
| |
2 | g.135817431G>A | CA1888370 | LCT | c.1617C>T (p.Thr539=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817431G>C | CA429204518 | LCT | c.1617C>G (p.Thr539=)
| |
2 | g.135817431G= | CA1290834784 | LCT | c.1617C= (p.Thr539=)
| |
2 | g.135817431G>T | CA429204519 | LCT | c.1617C>A (p.Thr539=)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817432G>A | CA348605769 | LCT | c.1616C>T (p.Thr539Ile)
| |
2 | g.135817432G>C | CA348605770 | LCT | c.1616C>G (p.Thr539Ser)
| |
2 | g.135817432G>T | CA348605771 | LCT | c.1616C>A (p.Thr539Asn)
| |
2 | g.135817433T>A | CA348605774 | LCT | c.1615A>T (p.Thr539Ser)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817433T>C | CA348605772 | LCT | c.1615A>G (p.Thr539Ala)
| |
2 | g.135817433T>G | CA348605773 | LCT | c.1615A>C (p.Thr539Pro)
| |
2 | g.135817433T= | CA1290834785 | LCT | c.1615A= (p.Thr539=)
| |
2 | g.135817434C>A | CA429204522 | LCT | c.1614G>T (p.Val538=)
| |
2 | g.135817434C>G | CA429204521 | LCT | c.1614G>C (p.Val538=)
| ClinVar |
2 | g.135817434C>T | CA429204520 | LCT | c.1614G>A (p.Val538=)
| |
2 | g.135817435A= | CA1290834786 | LCT | c.1613T= (p.Val538=)
| |
2 | g.135817435A>C | CA348605775 | LCT | c.1613T>G (p.Val538Gly)
| |
2 | g.135817435A>G | CA348605776 | LCT | c.1613T>C (p.Val538Ala)
| |
2 | g.135817435A>T | CA348605777 | LCT | c.1613T>A (p.Val538Glu)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817436C>A | CA348605778 | LCT | c.1612G>T (p.Val538Leu)
| |
2 | g.135817436C= | CA1290834787 | LCT | c.1612G= (p.Val538=)
| |
2 | g.135817436C>G | CA348605779 | LCT | c.1612G>C (p.Val538Leu)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817436C>T | CA56623402 | LCT | c.1612G>A (p.Val538Met)
| dbSNP |
2 | g.135817437C>A | CA348605780 | LCT | c.1611G>T (p.Trp537Cys)
| gnomAD v4 |
2 | g.135817437C>G | CA348605781 | LCT | c.1611G>C (p.Trp537Cys)
| |
2 | g.135817437C>T | CA348605782 | LCT | c.1611G>A (p.Trp537Ter)
| |
2 | g.135817438C>A | CA348605783 | LCT | c.1610G>T (p.Trp537Leu)
| |
2 | g.135817438C>G | CA348605784 | LCT | c.1610G>C (p.Trp537Ser)
| |
2 | g.135817438C>T | CA348605785 | LCT | c.1610G>A (p.Trp537Ter)
| |
2 | g.135817439A>C | CA348605788 | LCT | c.1609T>G (p.Trp537Gly)
| |
2 | g.135817439A>G | CA348605787 | LCT | c.1609T>C (p.Trp537Arg)
| |
2 | g.135817439A>T | CA348605786 | LCT | c.1609T>A (p.Trp537Arg)
| |