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)
| |
2 | g.135817440C>A | CA429204523 | LCT | c.1608G>T (p.Leu536=)
| |
2 | g.135817440C>G | CA429204525 | LCT | c.1608G>C (p.Leu536=)
| |
2 | g.135817440C>T | CA429204524 | LCT | c.1608G>A (p.Leu536=)
| ClinVar gnomAD v4 |
2 | g.135817441A>C | CA348605791 | LCT | c.1607T>G (p.Leu536Arg)
| |
2 | g.135817441A>G | CA348605789 | LCT | c.1607T>C (p.Leu536Pro)
| |
2 | g.135817441A>T | CA348605790 | LCT | c.1607T>A (p.Leu536Gln)
| |
2 | g.135817442G>A | CA429204526 | LCT | c.1606C>T (p.Leu536=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817442G>C | CA348605792 | LCT | c.1606C>G (p.Leu536Val)
| |
2 | g.135817442G= | CA1290834788 | LCT | c.1606C= (p.Leu536=)
| |
2 | g.135817442G>T | CA348605793 | LCT | c.1606C>A (p.Leu536Met)
| dbSNP |
2 | g.135817443C>A | CA348605794 | LCT | c.1605G>T (p.Lys535Asn)
| |
2 | g.135817443C>G | CA348605795 | LCT | c.1605G>C (p.Lys535Asn)
| |
2 | g.135817443C>T | CA429204527 | LCT | c.1605G>A (p.Lys535=)
| |
2 | g.135817444T>A | CA348605796 | LCT | c.1604A>T (p.Lys535Met)
| |
2 | g.135817444T>C | CA348605797 | LCT | c.1604A>G (p.Lys535Arg)
| |
2 | g.135817444T>G | CA348605798 | LCT | c.1604A>C (p.Lys535Thr)
| |
2 | g.135817445T>A | CA348605799 | LCT | c.1603A>T (p.Lys535Ter)
| |
2 | g.135817445T>C | CA348605800 | LCT | c.1603A>G (p.Lys535Glu)
| |
2 | g.135817445T>G | CA348605801 | LCT | c.1603A>C (p.Lys535Gln)
| |
2 | g.135817446C>A | CA429204528 | LCT | c.1602G>T (p.Val534=)
| |
2 | g.135817446C>G | CA429204529 | LCT | c.1602G>C (p.Val534=)
| |
2 | g.135817446C>T | CA429204530 | LCT | c.1602G>A (p.Val534=)
| |
2 | g.135817447A>C | CA348605803 | LCT | c.1601T>G (p.Val534Gly)
| |
2 | g.135817447A>G | CA348605804 | LCT | c.1601T>C (p.Val534Ala)
| |
2 | g.135817447A>T | CA348605802 | LCT | c.1601T>A (p.Val534Glu)
| |
2 | g.135817448C>A | CA348605805 | LCT | c.1600G>T (p.Val534Leu)
| |
2 | g.135817448C>G | CA348605806 | LCT | c.1600G>C (p.Val534Leu)
| |
2 | g.135817448C>T | CA348605807 | LCT | c.1600G>A (p.Val534Met)
| gnomAD v4 |
2 | g.135817449A>C | CA429204532 | LCT | c.1599T>G (p.Arg533=)
| |
2 | g.135817449A>G | CA429204533 | LCT | c.1599T>C (p.Arg533=)
| |
2 | g.135817449A>T | CA429204531 | LCT | c.1599T>A (p.Arg533=)
| |
2 | g.135817450C>A | CA348605808 | LCT | c.1598G>T (p.Arg533Leu)
| COSMIC |
2 | g.135817450C= | CA1290834789 | LCT | c.1598G= (p.Arg533=)
| |
2 | g.135817450C>G | CA348605809 | LCT | c.1598G>C (p.Arg533Pro)
| |
2 | g.135817450C>T | CA348605810 | LCT | c.1598G>A (p.Arg533His)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817451G>A | CA348605811 | LCT | c.1597C>T (p.Arg533Cys)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817451G>C | CA348605813 | LCT | c.1597C>G (p.Arg533Gly)
| |
2 | g.135817451G= | CA1290834790 | LCT | c.1597C= (p.Arg533=)
| |
2 | g.135817451G>T | CA348605812 | LCT | c.1597C>A (p.Arg533Ser)
| |
2 | g.135817452G>A | CA429204534 | LCT | c.1596C>T (p.Asp532=)
| |
2 | g.135817452G>C | CA348605814 | LCT | c.1596C>G (p.Asp532Glu)
| |
2 | g.135817452G>T | CA348605815 | LCT | c.1596C>A (p.Asp532Glu)
| |
2 | g.135817453T>A | CA348605816 | LCT | c.1595A>T (p.Asp532Val)
| |
2 | g.135817453T>C | CA348605817 | LCT | c.1595A>G (p.Asp532Gly)
| |
2 | g.135817453T>G | CA348605818 | LCT | c.1595A>C (p.Asp532Ala)
| |
2 | g.135817454C>A | CA348605820 | LCT | c.1594G>T (p.Asp532Tyr)
| |
2 | g.135817454C>G | CA348605821 | LCT | c.1594G>C (p.Asp532His)
| |
2 | g.135817454C>T | CA348605819 | LCT | c.1594G>A (p.Asp532Asn)
| |
2 | g.135817455C>A | CA429204535 | LCT | c.1593G>T (p.Gly531=)
| |
2 | g.135817455C= | CA1290834791 | LCT | c.1593G= (p.Gly531=)
| |
2 | g.135817455C>G | CA429204536 | LCT | c.1593G>C (p.Gly531=)
| |
2 | g.135817455C>T | CA1888371 | LCT | c.1593G>A (p.Gly531=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817456C>A | CA348605824 | LCT | c.1592G>T (p.Gly531Val)
| |
2 | g.135817456C>G | CA348605822 | LCT | c.1592G>C (p.Gly531Ala)
| |
2 | g.135817456C>T | CA348605823 | LCT | c.1592G>A (p.Gly531Glu)
| gnomAD v4 |
2 | g.135817457C>A | CA348605825 | LCT | c.1591G>T (p.Gly531Trp)
| |
2 | g.135817457C>G | CA348605826 | LCT | c.1591G>C (p.Gly531Arg)
| |
2 | g.135817457C>T | CA348605827 | LCT | c.1591G>A (p.Gly531Arg)
| |
2 | g.135817458A>C | CA348605828 | LCT | c.1590T>G (p.Phe530Leu)
| |
2 | g.135817458A>G | CA429204537 | LCT | c.1590T>C (p.Phe530=)
| |
2 | g.135817458A>T | CA348605829 | LCT | c.1590T>A (p.Phe530Leu)
| |
2 | g.135817459A= | CA1290834792 | LCT | c.1589T= (p.Phe530=)
| |
2 | g.135817459A>C | CA348605830 | LCT | c.1589T>G (p.Phe530Cys)
| |
2 | g.135817459A>G | CA348605831 | LCT | c.1589T>C (p.Phe530Ser)
| dbSNP gnomAD v4 |
2 | g.135817459A>T | CA348605832 | LCT | c.1589T>A (p.Phe530Tyr)
| |
2 | g.135817460A= | CA1290834793 | LCT | c.1588T= (p.Phe530=)
| |
2 | g.135817460A>C | CA348605833 | LCT | c.1588T>G (p.Phe530Val)
| |
2 | g.135817460A>G | CA348605834 | LCT | c.1588T>C (p.Phe530Leu)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817460A>T | CA348605835 | LCT | c.1588T>A (p.Phe530Ile)
| |
2 | g.135817461T>A | CA429204538 | LCT | c.1587A>T (p.Thr529=)
| dbSNP |
2 | g.135817461T>C | CA429204539 | LCT | c.1587A>G (p.Thr529=)
| |
2 | g.135817461T>G | CA429204540 | LCT | c.1587A>C (p.Thr529=)
| dbSNP |
2 | g.135817461T= | CA1290834794 | LCT | c.1587A= (p.Thr529=)
| |
2 | g.135817462G>A | CA348605838 | LCT | c.1586C>T (p.Thr529Ile)
| gnomAD v4 |
2 | g.135817462G>C | CA348605836 | LCT | c.1586C>G (p.Thr529Arg)
| |
2 | g.135817462G>T | CA348605837 | LCT | c.1586C>A (p.Thr529Lys)
| |
2 | g.135817463T>A | CA348605839 | LCT | c.1585A>T (p.Thr529Ser)
| |
2 | g.135817463T>C | CA1888372 | LCT | c.1585A>G (p.Thr529Ala)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817463T>G | CA348605840 | LCT | c.1585A>C (p.Thr529Pro)
| |
2 | g.135817463T= | CA1290834795 | LCT | c.1585A= (p.Thr529=)
| |
2 | g.135817464G>A | CA429204541 | LCT | c.1584C>T (p.Ser528=)
| |
2 | g.135817464G>C | CA429204542 | LCT | c.1584C>G (p.Ser528=)
| |
2 | g.135817464G>T | CA429204543 | LCT | c.1584C>A (p.Ser528=)
| |
2 | g.135817465G>A | CA348605841 | LCT | c.1583C>T (p.Ser528Phe)
| |
2 | g.135817465G>C | CA348605842 | LCT | c.1583C>G (p.Ser528Cys)
| |
2 | g.135817465G>T | CA348605843 | LCT | c.1583C>A (p.Ser528Tyr)
| |
2 | g.135817466A>C | CA348605844 | LCT | c.1582T>G (p.Ser528Ala)
| |
2 | g.135817466A>G | CA348605845 | LCT | c.1582T>C (p.Ser528Pro)
| |
2 | g.135817466A>T | CA348605846 | LCT | c.1582T>A (p.Ser528Thr)
| |
2 | g.135817467G>A | CA429204544 | LCT | c.1581C>T (p.Phe527=)
| |
2 | g.135817467G>C | CA348605847 | LCT | c.1581C>G (p.Phe527Leu)
| |
2 | g.135817467G>T | CA348605848 | LCT | c.1581C>A (p.Phe527Leu)
| |
2 | g.135817468A>C | CA348605851 | LCT | c.1580T>G (p.Phe527Cys)
| |
2 | g.135817468A>G | CA348605850 | LCT | c.1580T>C (p.Phe527Ser)
| |
2 | g.135817468A>T | CA348605849 | LCT | c.1580T>A (p.Phe527Tyr)
| |
2 | g.135817469A>C | CA348605852 | LCT | c.1579T>G (p.Phe527Val)
| |
2 | g.135817469A>G | CA348605853 | LCT | c.1579T>C (p.Phe527Leu)
| |
2 | g.135817469A>T | CA348605854 | LCT | c.1579T>A (p.Phe527Ile)
| |
2 | g.135817470G>A | CA429204545 | LCT | c.1578C>T (p.Cys526=)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817470G>C | CA348605855 | LCT | c.1578C>G (p.Cys526Trp)
| |
2 | g.135817470G= | CA1290834796 | LCT | c.1578C= (p.Cys526=)
| |
2 | g.135817470G>T | CA348605856 | LCT | c.1578C>A (p.Cys526Ter)
| |
2 | g.135817471C>A | CA348605857 | LCT | c.1577G>T (p.Cys526Phe)
| |
2 | g.135817471C>G | CA348605858 | LCT | c.1577G>C (p.Cys526Ser)
| |
2 | g.135817471C>T | CA348605859 | LCT | c.1577G>A (p.Cys526Tyr)
| |
2 | g.135817472A>C | CA348605860 | LCT | c.1576T>G (p.Cys526Gly)
| |
2 | g.135817472A>G | CA348605861 | LCT | c.1576T>C (p.Cys526Arg)
| |
2 | g.135817472A>T | CA348605862 | LCT | c.1576T>A (p.Cys526Ser)
| |
2 | g.135817473G>A | CA429204546 | LCT | c.1575C>T (p.Phe525=)
| |
2 | g.135817473G>C | CA348605863 | LCT | c.1575C>G (p.Phe525Leu)
| |
2 | g.135817473G= | CA1290834797 | LCT | c.1575C= (p.Phe525=)
| |
2 | g.135817473G>T | CA56623416 | LCT | c.1575C>A (p.Phe525Leu)
| dbSNP gnomAD v4 |
2 | g.135817474A>C | CA348605866 | LCT | c.1574T>G (p.Phe525Cys)
| |
2 | g.135817474A>G | CA348605864 | LCT | c.1574T>C (p.Phe525Ser)
| |
2 | g.135817474A>T | CA348605865 | LCT | c.1574T>A (p.Phe525Tyr)
| |
2 | g.135817475A>C | CA348605867 | LCT | c.1573T>G (p.Phe525Val)
| |
2 | g.135817475A>G | CA348605868 | LCT | c.1573T>C (p.Phe525Leu)
| |
2 | g.135817475A>T | CA348605869 | LCT | c.1573T>A (p.Phe525Ile)
| |
2 | g.135817476G>A | CA429204547 | LCT | c.1572C>T (p.Ala524=)
| |
2 | g.135817476G>C | CA429204548 | LCT | c.1572C>G (p.Ala524=)
| |
2 | g.135817476G>T | CA429204549 | LCT | c.1572C>A (p.Ala524=)
| |
2 | g.135817477G>A | CA348605870 | LCT | c.1571C>T (p.Ala524Val)
| |
2 | g.135817477G>C | CA348605871 | LCT | c.1571C>G (p.Ala524Gly)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817477G= | CA1290834798 | LCT | c.1571C= (p.Ala524=)
| |
2 | g.135817477G>T | CA348605872 | LCT | c.1571C>A (p.Ala524Asp)
| dbSNP |
2 | g.135817478C>A | CA348605873 | LCT | c.1570G>T (p.Ala524Ser)
| |
2 | g.135817478C= | CA1290834799 | LCT | c.1570G= (p.Ala524=)
| |
2 | g.135817478C>G | CA348605874 | LCT | c.1570G>C (p.Ala524Pro)
| |
2 | g.135817478C>T | CA1888373 | LCT | c.1570G>A (p.Ala524Thr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817479C>A | CA1888375 | LCT | c.1569G>T (p.Ala523=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817479C= | CA1290834800 | LCT | c.1569G= (p.Ala523=)
| |
2 | g.135817479C>G | CA429204550 | LCT | c.1569G>C (p.Ala523=)
| gnomAD v4 |
2 | g.135817479C>T | CA1888374 | LCT | c.1569G>A (p.Ala523=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817480G>A | CA1888376 | LCT | c.1568C>T (p.Ala523Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
2 | g.135817480G>C | CA348605876 | LCT | c.1568C>G (p.Ala523Gly)
| gnomAD v4 |
2 | g.135817480G= | CA1290834801 | LCT | c.1568C= (p.Ala523=)
| |
2 | g.135817480G>T | CA348605875 | LCT | c.1568C>A (p.Ala523Glu)
| gnomAD v4 |
2 | g.135817481C>A | CA348605877 | LCT | c.1567G>T (p.Ala523Ser)
| |
2 | g.135817481C>G | CA348605879 | LCT | c.1567G>C (p.Ala523Pro)
| |
2 | g.135817481C>T | CA348605878 | LCT | c.1567G>A (p.Ala523Thr)
| |
2 | g.135817482A= | CA1290834802 | LCT | c.1566T= (p.Tyr522=)
| |
2 | g.135817482A>C | CA348605880 | LCT | c.1566T>G (p.Tyr522Ter)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817482A>G | CA429204551 | LCT | c.1566T>C (p.Tyr522=)
| |
2 | g.135817482A>T | CA348605881 | LCT | c.1566T>A (p.Tyr522Ter)
| |
2 | g.135817483T>A | CA348605882 | LCT | c.1565A>T (p.Tyr522Phe)
| |
2 | g.135817483T>C | CA348605884 | LCT | c.1565A>G (p.Tyr522Cys)
| COSMIC |
2 | g.135817483T>G | CA348605883 | LCT | c.1565A>C (p.Tyr522Ser)
| |