2 | g.135817303C>A | CA2661275742 | LCT | c.1707+38G>T (n.1707+38G>T)
| gnomAD v4 |
2 | g.135817303C>G | CA2661275740 | LCT | c.1707+38G>C (n.1707+38G>C)
| gnomAD v4 |
2 | g.135817303C>T | CA2661275741 | LCT | c.1707+38G>A (n.1707+38G>A)
| gnomAD v4 |
2 | g.135817305C>T | CA2661275743 | LCT | c.1707+36G>A (n.1707+36G>A)
| gnomAD v4 |
2 | g.135817306C= | CA1290834722 | LCT | c.1707+35G= (n.1707+35G=)
| |
2 | g.135817306C>T | CA1290834721 | LCT | c.1707+35G>A (n.1707+35G>A)
| dbSNP |
2 | g.135817307T>A | CA1888354 | LCT | c.1707+34A>T (n.1707+34A>T)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817307T= | CA1290834723 | LCT | c.1707+34A= (n.1707+34A=)
| |
2 | g.135817308C>A | CA2556649901 | LCT | c.1707+33G>T (n.1707+33G>T)
| |
2 | g.135817309C= | CA1290834724 | LCT | c.1707+32G= (n.1707+32G=)
| |
2 | g.135817309C>T | CA1290834725 | LCT | c.1707+32G>A (n.1707+32G>A)
| dbSNP gnomAD v4 |
2 | g.135817310A>C | CA2661275744 | LCT | c.1707+31T>G (n.1707+31T>G)
| gnomAD v4 |
2 | g.135817311A= | CA1290834726 | LCT | c.1707+30T= (n.1707+30T=)
| |
2 | g.135817311A>C | CA2661275745 | LCT | c.1707+30T>G (n.1707+30T>G)
| gnomAD v4 |
2 | g.135817311A>G | CA536547368 | LCT | c.1707+30T>C (n.1707+30T>C)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817312T>G | CA536547369 | LCT | c.1707+29A>C (n.1707+29A>C)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817312T= | CA1290834727 | LCT | c.1707+29A= (n.1707+29A=)
| |
2 | g.135817313T>C | CA536547370 | LCT | c.1707+28A>G (n.1707+28A>G)
| dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817313T= | CA1290834728 | LCT | c.1707+28A= (n.1707+28A=)
| |
2 | g.135817314A= | CA1290834729 | LCT | c.1707+27T= (n.1707+27T=)
| |
2 | g.135817314A>C | CA1888355 | LCT | c.1707+27T>G (n.1707+27T>G)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817314A>T | CA2661275746 | LCT | c.1707+27T>A (n.1707+27T>A)
| gnomAD v4 |
2 | g.135817315G>C | CA1888356 | LCT | c.1707+26C>G (n.1707+26C>G)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817315G= | CA1290834730 | LCT | c.1707+26C= (n.1707+26C=)
| |
2 | g.135817317A= | CA1290834731 | LCT | c.1707+24T= (n.1707+24T=)
| |
2 | g.135817317A>G | CA1290834732 | LCT | c.1707+24T>C (n.1707+24T>C)
| dbSNP |
2 | g.135817321G>C | CA757437355 | LCT | c.1707+20C>G (n.1707+20C>G)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817321G= | CA1290834733 | LCT | c.1707+20C= (n.1707+20C=)
| |
2 | g.135817322C>A | CA1888357 | LCT | c.1707+19G>T (n.1707+19G>T)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817322C= | CA1290834734 | LCT | c.1707+19G= (n.1707+19G=)
| |
2 | g.135817322C>T | CA1036798866 | LCT | c.1707+19G>A (n.1707+19G>A)
| ClinVar dbSNP gnomAD v4 |
2 | g.135817323T>G | CA2661275747 | LCT | c.1707+18A>C (n.1707+18A>C)
| gnomAD v4 |
2 | g.135817324G>C | CA2577108012 | LCT | c.1707+17C>G (n.1707+17C>G)
| |
2 | g.135817324G= | CA1290834735 | LCT | c.1707+17C= (n.1707+17C=)
| |
2 | g.135817324G>T | CA536547371 | LCT | c.1707+17C>A (n.1707+17C>A)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
2 | g.135817325C= | CA1290834736 | LCT | c.1707+16G= (n.1707+16G=)
| |
2 | g.135817325C>T | CA1036798869 | LCT | c.1707+16G>A (n.1707+16G>A)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817326A= | CA1290834737 | LCT | c.1707+15T= (n.1707+15T=)
| |
2 | g.135817326A>G | CA1290834738 | LCT | c.1707+15T>C (n.1707+15T>C)
| dbSNP |
2 | g.135817327G>A | CA2661275748 | LCT | c.1707+14C>T (n.1707+14C>T)
| gnomAD v4 |
2 | g.135817327G>C | CA1036798874 | LCT | c.1707+14C>G (n.1707+14C>G)
| dbSNP gnomAD v3 gnomAD v4 |
2 | g.135817327G= | CA1290834739 | LCT | c.1707+14C= (n.1707+14C=)
| |
2 | g.135817328G>A | CA56623329 | LCT | c.1707+13C>T (n.1707+13C>T)
| dbSNP gnomAD v4 |
2 | g.135817328G= | CA1290834740 | LCT | c.1707+13C= (n.1707+13C=)
| |
2 | g.135817328G>T | CA2661275749 | LCT | c.1707+13C>A (n.1707+13C>A)
| gnomAD v4 |
2 | g.135817329G>A | CA2661275750 | LCT | c.1707+12C>T (n.1707+12C>T)
| gnomAD v4 |
2 | g.135817329G>T | CA2661275751 | LCT | c.1707+12C>A (n.1707+12C>A)
| gnomAD v4 |
2 | g.135817330T>A | CA2700693035 | LCT | c.1707+11A>T (n.1707+11A>T)
| dbSNP |
2 | g.135817332G>A | CA1888358 | LCT | c.1707+9C>T (n.1707+9C>T)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.135817332G= | CA1290834741 | LCT | c.1707+9C= (n.1707+9C=)
| |
2 | g.135817334del | CA2577108013 | LCT | c.1707+9del (n.1707+9del)
| gnomAD v4 |
2 | g.135817334G>C | CA2577108014 | LCT | c.1707+7C>G (n.1707+7C>G)
| gnomAD v4 |
2 | g.135817337G>A | CA1888359 | LCT | c.1707+4C>T (n.1707+4C>T)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
2 | g.135817337G= | CA1290834742 | LCT | c.1707+4C= (n.1707+4C=)
| |
2 | g.135817337G>T | CA2550940002 | LCT | c.1707+4C>A (n.1707+4C>A)
| gnomAD v4 |
2 | g.135817338T>C | CA645531703 | LCT | c.1707+3A>G (n.1707+3A>G)
| gnomAD v4 COSMIC |
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 |