6 | g.49457937A= | CA1627395349 | MMUT | c.507T= (p.Asp169=)
| |
6 | g.49457937A>C | CA364404582 | MMUT | c.507T>G (p.Asp169Glu)
| |
6 | g.49457937A>G | CA450608626 | MMUT | c.507T>C (p.Asp169=)
| ClinVar dbSNP |
6 | g.49457937A>T | CA364404583 | MMUT | c.507T>A (p.Asp169Glu)
| |
6 | g.49457938T>A | CA364404584 | MMUT | c.506A>T (p.Asp169Val)
| |
6 | g.49457938T>C | CA364404585 | MMUT | c.506A>G (p.Asp169Gly)
| |
6 | g.49457938T>G | CA364404586 | MMUT | c.506A>C (p.Asp169Ala)
| |
6 | g.49457939C>A | CA364404587 | MMUT | c.505G>T (p.Asp169Tyr)
| |
6 | g.49457939C>G | CA364404588 | MMUT | c.505G>C (p.Asp169His)
| |
6 | g.49457939C>T | CA364404589 | MMUT | c.505G>A (p.Asp169Asn)
| |
6 | g.49457940T>A | CA364404590 | MMUT | c.504A>T (p.Glu168Asp)
| |
6 | g.49457940T>C | CA450608627 | MMUT | c.504A>G (p.Glu168=)
| |
6 | g.49457940T>G | CA364404591 | MMUT | c.504A>C (p.Glu168Asp)
| |
6 | g.49457941del | CA2695206688 | MMUT | c.504del (p.Asp169IlefsTer11)
| |
6 | g.49457940_49457941insATTAGACTTG | CA2841020023 | MMUT | c.503_504insCAAGTCTAAT (p.Glu168AspfsTer11)
| |
6 | g.49457941T>A | CA364404592 | MMUT | c.503A>T (p.Glu168Val)
| |
6 | g.49457941T>C | CA364404593 | MMUT | c.503A>G (p.Glu168Gly)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.49457941T>G | CA364404594 | MMUT | c.503A>C (p.Glu168Ala)
| |
6 | g.49457941T= | CA1627395352 | MMUT | c.503A= (p.Glu168=)
| |
6 | g.49457942C>A | CA364404595 | MMUT | c.502G>T (p.Glu168Ter)
| |
6 | g.49457942C>G | CA364404596 | MMUT | c.502G>C (p.Glu168Gln)
| |
6 | g.49457942C>T | CA364404597 | MMUT | c.502G>A (p.Glu168Lys)
| |
6 | g.49457943C>A | CA450608628 | MMUT | c.501G>T (p.Val167=)
| |
6 | g.49457943C>G | CA450608629 | MMUT | c.501G>C (p.Val167=)
| |
6 | g.49457943C>T | CA450608630 | MMUT | c.501G>A (p.Val167=)
| |
6 | g.49457944A= | CA1627395356 | MMUT | c.500T= (p.Val167=)
| |
6 | g.49457944A>C | CA364404598 | MMUT | c.500T>G (p.Val167Gly)
| |
6 | g.49457944A>G | CA364404599 | MMUT | c.500T>C (p.Val167Ala)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.49457944A>T | CA364404600 | MMUT | c.500T>A (p.Val167Glu)
| |
6 | g.49457945C>A | CA364404601 | MMUT | c.499G>T (p.Val167Leu)
| |
6 | g.49457945C= | CA1627395361 | MMUT | c.499G= (p.Val167=)
| |
6 | g.49457945C>G | CA364404602 | MMUT | c.499G>C (p.Val167Leu)
| |
6 | g.49457945C>T | CA3847100 | MMUT | c.499G>A (p.Val167Met)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49457946A>C | CA450608633 | MMUT | c.498T>G (p.Thr166=)
| |
6 | g.49457946A>G | CA450608632 | MMUT | c.498T>C (p.Thr166=)
| ClinVar gnomAD v4 |
6 | g.49457946A>T | CA450608631 | MMUT | c.498T>A (p.Thr166=)
| |
6 | g.49457947_49457953del | CA2841020024 | MMUT | c.492_498del (p.Ile164MetfsTer14)
| |
6 | g.49457947G>A | CA364404605 | MMUT | c.497C>T (p.Thr166Ile)
| |
6 | g.49457947G>C | CA364404604 | MMUT | c.497C>G (p.Thr166Ser)
| |
6 | g.49457947G>T | CA364404603 | MMUT | c.497C>A (p.Thr166Asn)
| |
6 | g.49457948T>A | CA364404606 | MMUT | c.496A>T (p.Thr166Ser)
| |
6 | g.49457948T>C | CA364404607 | MMUT | c.496A>G (p.Thr166Ala)
| dbSNP gnomAD v3 gnomAD v4 |
6 | g.49457948T>G | CA364404608 | MMUT | c.496A>C (p.Thr166Pro)
| |
6 | g.49457948T= | CA1627395367 | MMUT | c.496A= (p.Thr166=)
| |
6 | g.49457949G>A | CA450608634 | MMUT | c.495C>T (p.Asp165=)
| |
6 | g.49457949G>C | CA364404609 | MMUT | c.495C>G (p.Asp165Glu)
| |
6 | g.49457949G>T | CA364404610 | MMUT | c.495C>A (p.Asp165Glu)
| |
6 | g.49457950T>A | CA364404611 | MMUT | c.494A>T (p.Asp165Val)
| |
6 | g.49457950T>C | CA138799926 | MMUT | c.494A>G (p.Asp165Gly)
| ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
6 | g.49457950T>G | CA364404612 | MMUT | c.494A>C (p.Asp165Ala)
| |
6 | g.49457950T= | CA1627395373 | MMUT | c.494A= (p.Asp165=)
| |
6 | g.49457951C>A | CA364404613 | MMUT | c.493G>T (p.Asp165Tyr)
| |
6 | g.49457951C>G | CA364404614 | MMUT | c.493G>C (p.Asp165His)
| |
6 | g.49457951C>T | CA364404615 | MMUT | c.493G>A (p.Asp165Asn)
| |
6 | g.49457952A>C | CA364404616 | MMUT | c.492T>G (p.Ile164Met)
| |
6 | g.49457952A>G | CA450608636 | MMUT | c.492T>C (p.Ile164=)
| |
6 | g.49457952A>T | CA450608635 | MMUT | c.492T>A (p.Ile164=)
| |
6 | g.49457953A= | CA1627395377 | MMUT | c.491T= (p.Ile164=)
| |
6 | g.49457953A>C | CA364404618 | MMUT | c.491T>G (p.Ile164Ser)
| |
6 | g.49457953A>G | CA364404617 | MMUT | c.491T>C (p.Ile164Thr)
| |
6 | g.49457953A>T | CA3847101 | MMUT | c.491T>A (p.Ile164Asn)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49457954T>A | CA364404619 | MMUT | c.490A>T (p.Ile164Phe)
| |
6 | g.49457954T>C | CA364404621 | MMUT | c.490A>G (p.Ile164Val)
| dbSNP gnomAD v4 |
6 | g.49457954T>G | CA364404620 | MMUT | c.490A>C (p.Ile164Leu)
| |
6 | g.49457954T= | CA1627395381 | MMUT | c.490A= (p.Ile164=)
| |
6 | g.49457955A>C | CA450608637 | MMUT | c.489T>G (p.Ala163=)
| |
6 | g.49457955A>G | CA450608638 | MMUT | c.489T>C (p.Ala163=)
| ClinVar |
6 | g.49457955A>T | CA450608639 | MMUT | c.489T>A (p.Ala163=)
| |
6 | g.49457956G>A | CA364404622 | MMUT | c.488C>T (p.Ala163Val)
| dbSNP gnomAD v3 gnomAD v4 |
6 | g.49457956G>C | CA364404623 | MMUT | c.488C>G (p.Ala163Gly)
| gnomAD v4 |
6 | g.49457956G= | CA1627395383 | MMUT | c.488C= (p.Ala163=)
| |
6 | g.49457956G>T | CA364404624 | MMUT | c.488C>A (p.Ala163Asp)
| |
6 | g.49457957C>A | CA364404625 | MMUT | c.487G>T (p.Ala163Ser)
| |
6 | g.49457957C>G | CA364404626 | MMUT | c.487G>C (p.Ala163Pro)
| |
6 | g.49457957C>T | CA364404627 | MMUT | c.487G>A (p.Ala163Thr)
| |
6 | g.49457958A>C | CA450608640 | MMUT | c.486T>G (p.Val162=)
| |
6 | g.49457958A>G | CA450608642 | MMUT | c.486T>C (p.Val162=)
| |
6 | g.49457958A>T | CA450608641 | MMUT | c.486T>A (p.Val162=)
| |
6 | g.49457959A= | CA1627395386 | MMUT | c.485T= (p.Val162=)
| |
6 | g.49457959A>C | CA364404628 | MMUT | c.485T>G (p.Val162Gly)
| dbSNP gnomAD v4 |
6 | g.49457959A>G | CA364404629 | MMUT | c.485T>C (p.Val162Ala)
| COSMIC |
6 | g.49457959A>T | CA364404630 | MMUT | c.485T>A (p.Val162Asp)
| |
6 | g.49457960C>A | CA364404631 | MMUT | c.484G>T (p.Val162Phe)
| |
6 | g.49457960C>G | CA364404632 | MMUT | c.484G>C (p.Val162Leu)
| |
6 | g.49457960C>T | CA364404633 | MMUT | c.484G>A (p.Val162Ile)
| |
6 | g.49457961T>A | CA450608643 | MMUT | c.483A>T (p.Gly161=)
| |
6 | g.49457961T>C | CA3847102 | MMUT | c.483A>G (p.Gly161=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49457961T>G | CA450608644 | MMUT | c.483A>C (p.Gly161=)
| ClinVar gnomAD v4 |
6 | g.49457961T= | CA1627395388 | MMUT | c.483A= (p.Gly161=)
| |
6 | g.49457962C>A | CA364404636 | MMUT | c.482G>T (p.Gly161Val)
| |
6 | g.49457962C>G | CA364404634 | MMUT | c.482G>C (p.Gly161Ala)
| |
6 | g.49457962C>T | CA364404635 | MMUT | c.482G>A (p.Gly161Glu)
| |
6 | g.49457963C>A | CA364404637 | MMUT | c.481G>T (p.Gly161Ter)
| |
6 | g.49457963C>G | CA364404638 | MMUT | c.481G>C (p.Gly161Arg)
| |
6 | g.49457963C>T | CA364404639 | MMUT | c.481G>A (p.Gly161Arg)
| ClinVar dbSNP gnomAD v4 |
6 | g.49457964A>C | CA450608645 | MMUT | c.480T>G (p.Ala160=)
| |
6 | g.49457964A>G | CA450608646 | MMUT | c.480T>C (p.Ala160=)
| |
6 | g.49457964A>T | CA450608647 | MMUT | c.480T>A (p.Ala160=)
| |
6 | g.49457965G>A | CA364404640 | MMUT | c.479C>T (p.Ala160Val)
| gnomAD v4 |
6 | g.49457965G>C | CA364404641 | MMUT | c.479C>G (p.Ala160Gly)
| |
6 | g.49457965G>T | CA364404642 | MMUT | c.479C>A (p.Ala160Asp)
| |
6 | g.49457966C>A | CA364404643 | MMUT | c.478G>T (p.Ala160Ser)
| dbSNP |
6 | g.49457966C>G | CA364404644 | MMUT | c.478G>C (p.Ala160Pro)
| |
6 | g.49457966C>T | CA364404645 | MMUT | c.478G>A (p.Ala160Thr)
| |
6 | g.49457967dup | CA2841020025 | MMUT | c.478dup (p.Ala160GlyfsTer6)
| |
6 | g.49457967C>A | CA364404646 | MMUT | c.477G>T (p.Met159Ile)
| |
6 | g.49457967C>G | CA364404647 | MMUT | c.477G>C (p.Met159Ile)
| |
6 | g.49457967C>T | CA364404648 | MMUT | c.477G>A (p.Met159Ile)
| |
6 | g.49457968A>C | CA364404649 | MMUT | c.476T>G (p.Met159Arg)
| |
6 | g.49457968A>G | CA364404651 | MMUT | c.476T>C (p.Met159Thr)
| |
6 | g.49457968A>T | CA364404650 | MMUT | c.476T>A (p.Met159Lys)
| |
6 | g.49457969T>A | CA364404652 | MMUT | c.475A>T (p.Met159Leu)
| |
6 | g.49457969T>C | CA364404653 | MMUT | c.475A>G (p.Met159Val)
| |
6 | g.49457969T>G | CA364404654 | MMUT | c.475A>C (p.Met159Leu)
| |
6 | g.49457970T>A | CA450608648 | MMUT | c.474A>T (p.Gly158=)
| |
6 | g.49457970T>C | CA450608649 | MMUT | c.474A>G (p.Gly158=)
| |
6 | g.49457970T>G | CA450608650 | MMUT | c.474A>C (p.Gly158=)
| |
6 | g.49457971C>A | CA364404655 | MMUT | c.473G>T (p.Gly158Val)
| |
6 | g.49457971C>G | CA364404656 | MMUT | c.473G>C (p.Gly158Ala)
| |
6 | g.49457971C>T | CA364404657 | MMUT | c.473G>A (p.Gly158Glu)
| |
6 | g.49457972C>A | CA364404658 | MMUT | c.472G>T (p.Gly158Ter)
| |
6 | g.49457972C>G | CA364404659 | MMUT | c.472G>C (p.Gly158Arg)
| gnomAD v4 |
6 | g.49457972C>T | CA364404660 | MMUT | c.472G>A (p.Gly158Arg)
| gnomAD v4 |
6 | g.49457973A>C | CA450608651 | MMUT | c.471T>G (p.Val157=)
| |
6 | g.49457973A>G | CA450608652 | MMUT | c.471T>C (p.Val157=)
| |
6 | g.49457973A>T | CA450608653 | MMUT | c.471T>A (p.Val157=)
| |
6 | g.49457974A>C | CA364404661 | MMUT | c.470T>G (p.Val157Gly)
| |
6 | g.49457974A>G | CA364404662 | MMUT | c.470T>C (p.Val157Ala)
| |
6 | g.49457974A>T | CA364404663 | MMUT | c.470T>A (p.Val157Asp)
| |
6 | g.49457975C>A | CA364404666 | MMUT | c.469G>T (p.Val157Phe)
| |
6 | g.49457975C>G | CA364404664 | MMUT | c.469G>C (p.Val157Leu)
| |
6 | g.49457975C>T | CA364404665 | MMUT | c.469G>A (p.Val157Ile)
| |
6 | g.49457976A= | CA1627395391 | MMUT | c.468T= (p.Asp156=)
| |
6 | g.49457976A>C | CA364404667 | MMUT | c.468T>G (p.Asp156Glu)
| |
6 | g.49457976A>G | CA450608655 | MMUT | c.468T>C (p.Asp156=)
| gnomAD v4 |
6 | g.49457976A>T | CA364404668 | MMUT | c.468T>A (p.Asp156Glu)
| dbSNP |
6 | g.49457977T>A | CA3847103 | MMUT | c.467A>T (p.Asp156Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49457977T>C | CA364404669 | MMUT | c.467A>G (p.Asp156Gly)
| dbSNP gnomAD v3 gnomAD v4 |
6 | g.49457977T>G | CA364404670 | MMUT | c.467A>C (p.Asp156Ala)
| |
6 | g.49457977T= | CA1627395396 | MMUT | c.467A= (p.Asp156=)
| |
6 | g.49457978C>A | CA364404671 | MMUT | c.466G>T (p.Asp156Tyr)
| |
6 | g.49457978C>G | CA364404672 | MMUT | c.466G>C (p.Asp156His)
| |
6 | g.49457978C>T | CA364404673 | MMUT | c.466G>A (p.Asp156Asn)
| ClinVar gnomAD v4 |
6 | g.49457981_49457983del | CA2695206689 | MMUT | c.464_466del (p.Gly155del)
| |
6 | g.49457979A>C | CA450608658 | MMUT | c.465T>G (p.Gly155=)
| |
6 | g.49457979A>G | CA450608659 | MMUT | c.465T>C (p.Gly155=)
| |
6 | g.49457979A>T | CA450608660 | MMUT | c.465T>A (p.Gly155=)
| |
6 | g.49457980C>A | CA364404674 | MMUT | c.464G>T (p.Gly155Val)
| gnomAD v4 |
6 | g.49457980C= | CA1627395403 | MMUT | c.464G= (p.Gly155=)
| |
6 | g.49457980C>G | CA364404675 | MMUT | c.464G>C (p.Gly155Ala)
| |
6 | g.49457980C>T | CA3847104 | MMUT | c.464G>A (p.Gly155Asp)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49457981C>A | CA364404677 | MMUT | c.463G>T (p.Gly155Cys)
| gnomAD v4 |
6 | g.49457981C>G | CA364404678 | MMUT | c.463G>C (p.Gly155Arg)
| |
6 | g.49457981C>T | CA364404676 | MMUT | c.463G>A (p.Gly155Ser)
| |
6 | g.49457982A>C | CA450608661 | MMUT | c.462T>G (p.Arg154=)
| |
6 | g.49457982A>G | CA450608662 | MMUT | c.462T>C (p.Arg154=)
| |
6 | g.49457982A>T | CA450608663 | MMUT | c.462T>A (p.Arg154=)
| gnomAD v4 |
6 | g.49457983C>A | CA364404680 | MMUT | c.461G>T (p.Arg154Leu)
| gnomAD v4 |
6 | g.49457983C= | CA1627395411 | MMUT | c.461G= (p.Arg154=)
| |
6 | g.49457983C>G | CA364404679 | MMUT | c.461G>C (p.Arg154Pro)
| |
6 | g.49457983C>T | CA3847105 | MMUT | c.461G>A (p.Arg154His)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49457984G>A | CA364404681 | MMUT | c.460C>T (p.Arg154Cys)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49457984G>C | CA364404682 | MMUT | c.460C>G (p.Arg154Gly)
| |
6 | g.49457984G= | CA1627395419 | MMUT | c.460C= (p.Arg154=)
| |
6 | g.49457984G>T | CA364404683 | MMUT | c.460C>A (p.Arg154Ser)
| gnomAD v4 |
6 | g.49457985A>C | CA450608665 | MMUT | c.459T>G (p.Val153=)
| |
6 | g.49457985A>G | CA450608666 | MMUT | c.459T>C (p.Val153=)
| |
6 | g.49457985A>T | CA450608667 | MMUT | c.459T>A (p.Val153=)
| |
6 | g.49457986del | CA2695206690 | MMUT | c.459del (p.Arg154ValfsTer26)
| |
6 | g.49457986A>C | CA364404684 | MMUT | c.458T>G (p.Val153Gly)
| |
6 | g.49457986A>G | CA364404685 | MMUT | c.458T>C (p.Val153Ala)
| |
6 | g.49457986A>T | CA364404686 | MMUT | c.458T>A (p.Val153Asp)
| |
6 | g.49457987C>A | CA364404687 | MMUT | c.457G>T (p.Val153Phe)
| |
6 | g.49457987C= | CA1627395424 | MMUT | c.457G= (p.Val153=)
| |
6 | g.49457987C>G | CA364404688 | MMUT | c.457G>C (p.Val153Leu)
| |
6 | g.49457987C>T | CA364404689 | MMUT | c.457G>A (p.Val153Ile)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.49457988T>A | CA450608670 | MMUT | c.456A>T (p.Arg152=)
| |
6 | g.49457988T>C | CA450608669 | MMUT | c.456A>G (p.Arg152=)
| |
6 | g.49457988T>G | CA450608668 | MMUT | c.456A>C (p.Arg152=)
| |
6 | g.49457989C>A | CA364404691 | MMUT | c.455G>T (p.Arg152Leu)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49457989C= | CA1627395431 | MMUT | c.455G= (p.Arg152=)
| |
6 | g.49457989C>G | CA364404690 | MMUT | c.455G>C (p.Arg152Pro)
| |
6 | g.49457989C>T | CA3847106 | MMUT | c.455G>A (p.Arg152Gln)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
6 | g.49457990G>A | CA3847107 | MMUT | c.454C>T (p.Arg152Ter)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49457990G>C | CA364404692 | MMUT | c.454C>G (p.Arg152Gly)
| |
6 | g.49457990G= | CA1627395439 | MMUT | c.454C= (p.Arg152=)
| |
6 | g.49457990G>T | CA450608671 | MMUT | c.454C>A (p.Arg152=)
| |
6 | g.49457991A>C | CA450608672 | MMUT | c.453T>G (p.Pro151=)
| |
6 | g.49457991A>G | CA450608673 | MMUT | c.453T>C (p.Pro151=)
| |
6 | g.49457991A>T | CA450608674 | MMUT | c.453T>A (p.Pro151=)
| |
6 | g.49457992G>A | CA364404693 | MMUT | c.452C>T (p.Pro151Leu)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.49457992G>C | CA364404694 | MMUT | c.452C>G (p.Pro151Arg)
| gnomAD v4 |
6 | g.49457992G= | CA1627395441 | MMUT | c.452C= (p.Pro151=)
| |
6 | g.49457992G>T | CA364404695 | MMUT | c.452C>A (p.Pro151His)
| |
6 | g.49457993G>A | CA364404696 | MMUT | c.451C>T (p.Pro151Ser)
| gnomAD v4 COSMIC |
6 | g.49457993G>C | CA364404697 | MMUT | c.451C>G (p.Pro151Ala)
| |
6 | g.49457993G>T | CA364404698 | MMUT | c.451C>A (p.Pro151Thr)
| |
6 | g.49457994G>A | CA450608675 | MMUT | c.450C>T (p.Asn150=)
| ClinVar dbSNP gnomAD v4 |
6 | g.49457994G>C | CA364404699 | MMUT | c.450C>G (p.Asn150Lys)
| |
6 | g.49457994G= | CA1627395443 | MMUT | c.450C= (p.Asn150=)
| |
6 | g.49457994G>T | CA364404700 | MMUT | c.450C>A (p.Asn150Lys)
| |
6 | g.49457995T>A | CA364404701 | MMUT | c.449A>T (p.Asn150Ile)
| |
6 | g.49457995T>C | CA138799965 | MMUT | c.449A>G (p.Asn150Ser)
| dbSNP gnomAD v3 gnomAD v4 |
6 | g.49457995T>G | CA364404702 | MMUT | c.449A>C (p.Asn150Thr)
| |
6 | g.49457995T= | CA1627395447 | MMUT | c.449A= (p.Asn150=)
| |
6 | g.49457996T>A | CA364404704 | MMUT | c.448A>T (p.Asn150Tyr)
| |
6 | g.49457996T>C | CA364404705 | MMUT | c.448A>G (p.Asn150Asp)
| |
6 | g.49457996T>G | CA364404703 | MMUT | c.448A>C (p.Asn150His)
| |
6 | g.49457997G>A | CA450608676 | MMUT | c.447C>T (p.Asp149=)
| gnomAD v4 |
6 | g.49457997G>C | CA364404706 | MMUT | c.447C>G (p.Asp149Glu)
| |
6 | g.49457997G= | CA1627395449 | MMUT | c.447C= (p.Asp149=)
| |
6 | g.49457997G>T | CA364404707 | MMUT | c.447C>A (p.Asp149Glu)
| ClinVar |
6 | g.49457998T>A | CA364404708 | MMUT | c.446A>T (p.Asp149Val)
| ClinVar dbSNP |
6 | g.49457998T>C | CA364404709 | MMUT | c.446A>G (p.Asp149Gly)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
6 | g.49457998T>G | CA364404710 | MMUT | c.446A>C (p.Asp149Ala)
| |
6 | g.49457998T= | CA1627395460 | MMUT | c.446A= (p.Asp149=)
| |
6 | g.49457998dup | CA1139659603 | MMUT | c.446dup (p.Asp149GlufsTer8)
| ClinVar dbSNP |
6 | g.49457999C>A | CA364404711 | MMUT | c.445G>T (p.Asp149Tyr)
| |
6 | g.49457999C>G | CA364404712 | MMUT | c.445G>C (p.Asp149His)
| |
6 | g.49457999C>T | CA364404713 | MMUT | c.445G>A (p.Asp149Asn)
| |
6 | g.49458000T>A | CA450608677 | MMUT | c.444A>T (p.Ser148=)
| |
6 | g.49458000T>C | CA450608678 | MMUT | c.444A>G (p.Ser148=)
| |
6 | g.49458000T>G | CA450608679 | MMUT | c.444A>C (p.Ser148=)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.49458000T= | CA1627395465 | MMUT | c.444A= (p.Ser148=)
| |
6 | g.49458001G>A | CA364404714 | MMUT | c.443C>T (p.Ser148Leu)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
6 | g.49458001G>C | CA364404715 | MMUT | c.443C>G (p.Ser148Ter)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.49458001G= | CA1627395469 | MMUT | c.443C= (p.Ser148=)
| |
6 | g.49458001G>T | CA364404716 | MMUT | c.443C>A (p.Ser148Ter)
| |
6 | g.49458002A>C | CA364404717 | MMUT | c.442T>G (p.Ser148Ala)
| |
6 | g.49458002A>G | CA364404718 | MMUT | c.442T>C (p.Ser148Pro)
| |
6 | g.49458002A>T | CA364404719 | MMUT | c.442T>A (p.Ser148Thr)
| |
6 | g.49458003A>C | CA364404721 | MMUT | c.441T>G (p.Asp147Glu)
| |
6 | g.49458003A>G | CA450608680 | MMUT | c.441T>C (p.Asp147=)
| gnomAD v4 |
6 | g.49458003A>T | CA364404720 | MMUT | c.441T>A (p.Asp147Glu)
| |
6 | g.49458004T>A | CA364404722 | MMUT | c.440A>T (p.Asp147Val)
| |
6 | g.49458004T>C | CA364404723 | MMUT | c.440A>G (p.Asp147Gly)
| |
6 | g.49458004T>G | CA364404724 | MMUT | c.440A>C (p.Asp147Ala)
| |
6 | g.49458005C>A | CA364404725 | MMUT | c.439G>T (p.Asp147Tyr)
| gnomAD v4 |
6 | g.49458005C>G | CA364404726 | MMUT | c.439G>C (p.Asp147His)
| |
6 | g.49458005C>T | CA364404727 | MMUT | c.439G>A (p.Asp147Asn)
| |
6 | g.49458006del | CA2582341703 | MMUT | c.438del (p.Tyr146Ter)
| ClinVar |
6 | g.49458006A= | CA1627395472 | MMUT | c.438T= (p.Tyr146=)
| |
6 | g.49458006A>C | CA364404729 | MMUT | c.438T>G (p.Tyr146Ter)
| |
6 | g.49458006A>G | CA3847108 | MMUT | c.438T>C (p.Tyr146=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49458006A>T | CA364404728 | MMUT | c.438T>A (p.Tyr146Ter)
| ClinVar dbSNP |
6 | g.49458007T>A | CA364404730 | MMUT | c.437A>T (p.Tyr146Phe)
| |
6 | g.49458007T>C | CA3847109 | MMUT | c.437A>G (p.Tyr146Cys)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49458007T>G | CA364404731 | MMUT | c.437A>C (p.Tyr146Ser)
| |
6 | g.49458007T= | CA1627395476 | MMUT | c.437A= (p.Tyr146=)
| |
6 | g.49458008A>C | CA364404732 | MMUT | c.436T>G (p.Tyr146Asp)
| |
6 | g.49458008A>G | CA364404733 | MMUT | c.436T>C (p.Tyr146His)
| |
6 | g.49458008A>T | CA364404734 | MMUT | c.436T>A (p.Tyr146Asn)
| |
6 | g.49458008dup | CA2695206691 | MMUT | c.436dup (p.Tyr146LeufsTer2)
| |
6 | g.49458009G>A | CA450608681 | MMUT | c.435C>T (p.Gly145=)
| ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC |
6 | g.49458009G>C | CA450608682 | MMUT | c.435C>G (p.Gly145=)
| |
6 | g.49458009G= | CA1627395481 | MMUT | c.435C= (p.Gly145=)
| |
6 | g.49458009G>T | CA450608683 | MMUT | c.435C>A (p.Gly145=)
| |
6 | g.49458010C>A | CA364404736 | MMUT | c.434G>T (p.Gly145Val)
| dbSNP gnomAD v2 gnomAD v4 |
6 | g.49458010C= | CA1627395482 | MMUT | c.434G= (p.Gly145=)
| |
6 | g.49458010C>G | CA364404737 | MMUT | c.434G>C (p.Gly145Ala)
| |
6 | g.49458010C>T | CA364404735 | MMUT | c.434G>A (p.Gly145Asp)
| gnomAD v4 COSMIC |
6 | g.49458011C>A | CA364404738 | MMUT | c.433G>T (p.Gly145Cys)
| dbSNP gnomAD v2 |
6 | g.49458011C= | CA1627395484 | MMUT | c.433G= (p.Gly145=)
| |
6 | g.49458011C>G | CA364404740 | MMUT | c.433G>C (p.Gly145Arg)
| |
6 | g.49458011C>T | CA364404739 | MMUT | c.433G>A (p.Gly145Ser)
| dbSNP gnomAD v4 |
6 | g.49458012A>C | CA450608684 | MMUT | c.432T>G (p.Arg144=)
| |
6 | g.49458012A>G | CA450608685 | MMUT | c.432T>C (p.Arg144=)
| |
6 | g.49458012A>T | CA450608686 | MMUT | c.432T>A (p.Arg144=)
| |
6 | g.49458013C>A | CA364404741 | MMUT | c.431G>T (p.Arg144Leu)
| |
6 | g.49458013C= | CA1627395489 | MMUT | c.431G= (p.Arg144=)
| |
6 | g.49458013C>G | CA364404742 | MMUT | c.431G>C (p.Arg144Pro)
| |
6 | g.49458013C>T | CA3847110 | MMUT | c.431G>A (p.Arg144His)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49458014G>A | CA364404743 | MMUT | c.430C>T (p.Arg144Cys)
| ClinVar gnomAD v4 |
6 | g.49458014G>C | CA364404745 | MMUT | c.430C>G (p.Arg144Gly)
| gnomAD v4 |
6 | g.49458014G>T | CA364404744 | MMUT | c.430C>A (p.Arg144Ser)
| |
6 | g.49458015A>C | CA364404746 | MMUT | c.429T>G (p.His143Gln)
| |
6 | g.49458015A>G | CA450608687 | MMUT | c.429T>C (p.His143=)
| |
6 | g.49458015A>T | CA364404747 | MMUT | c.429T>A (p.His143Gln)
| |
6 | g.49458016T>A | CA364404748 | MMUT | c.428A>T (p.His143Leu)
| |
6 | g.49458016T>C | CA364404749 | MMUT | c.428A>G (p.His143Arg)
| gnomAD v4 |
6 | g.49458016T>G | CA364404750 | MMUT | c.428A>C (p.His143Pro)
| |
6 | g.49458017_49458020del | CA2578675210 | MMUT | c.425_428del (p.Thr142IlefsTer?)
| |
6 | g.49458017G>A | CA364404751 | MMUT | c.427C>T (p.His143Tyr)
| gnomAD v4 |
6 | g.49458017G>C | CA364404752 | MMUT | c.427C>G (p.His143Asp)
| |
6 | g.49458017G>T | CA364404753 | MMUT | c.427C>A (p.His143Asn)
| |
6 | g.49458018del | CA2573140887 | MMUT | c.426del (p.His143IlefsTer?)
| ClinVar dbSNP gnomAD v4 |
6 | g.49458018T>A | CA450608688 | MMUT | c.426A>T (p.Thr142=)
| |
6 | g.49458018T>C | CA450608689 | MMUT | c.426A>G (p.Thr142=)
| gnomAD v4 |
6 | g.49458018T>G | CA450608690 | MMUT | c.426A>C (p.Thr142=)
| |
6 | g.49458019G>A | CA364404754 | MMUT | c.425C>T (p.Thr142Ile)
| |
6 | g.49458019G>C | CA364404755 | MMUT | c.425C>G (p.Thr142Arg)
| |
6 | g.49458019G>T | CA364404756 | MMUT | c.425C>A (p.Thr142Lys)
| gnomAD v4 |
6 | g.49458020T>A | CA364404759 | MMUT | c.424A>T (p.Thr142Ser)
| |
6 | g.49458020T>C | CA364404758 | MMUT | c.424A>G (p.Thr142Ala)
| ClinVar |
6 | g.49458020T>G | CA364404757 | MMUT | c.424A>C (p.Thr142Pro)
| |
6 | g.49458021C>A | CA450608691 | MMUT | c.423G>T (p.Ala141=)
| ClinVar dbSNP |
6 | g.49458021C= | CA1627395492 | MMUT | c.423G= (p.Ala141=)
| |
6 | g.49458021C>G | CA450608692 | MMUT | c.423G>C (p.Ala141=)
| |
6 | g.49458021C>T | CA3847111 | MMUT | c.423G>A (p.Ala141=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49458021_49458022insAAA | CA2578675211 | MMUT | c.422_423insTTT (p.Ala141_Thr142insLeu)
| |
6 | g.49458022G>A | CA3847112 | MMUT | c.422C>T (p.Ala141Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.49458022G>C | CA364404760 | MMUT | c.422C>G (p.Ala141Gly)
| |
6 | g.49458022G= | CA1627395501 | MMUT | c.422C= (p.Ala141=)
| |
6 | g.49458022G>T | CA3847113 | MMUT | c.422C>A (p.Ala141Glu)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49458022_49458023delinsGC | CA1627395509 | MMUT | c.421_422delinsGC (p.Ala141=)
| |
6 | g.49458023C>A | CA364404761 | MMUT | c.421G>T (p.Ala141Ser)
| |
6 | g.49458023C= | CA1627395521 | MMUT | c.421G= (p.Ala141=)
| |
6 | g.49458023C>G | CA364404762 | MMUT | c.421G>C (p.Ala141Pro)
| |
6 | g.49458023C>T | CA364404763 | MMUT | c.421G>A (p.Ala141Thr)
| ClinVar dbSNP |
6 | g.49458024dup | CA2841020026 | MMUT | c.421dup (p.Ala141GlyfsTer7)
| |
6 | g.49458024del | CA1139659605 | MMUT | c.421del (p.Ala141ArgfsTer?)
| ClinVar dbSNP |
6 | g.49458024C>A | CA450608693 | MMUT | c.420G>T (p.Leu140=)
| |
6 | g.49458024C= | CA1627395532 | MMUT | c.420G= (p.Leu140=)
| |
6 | g.49458024C>G | CA450608694 | MMUT | c.420G>C (p.Leu140=)
| |
6 | g.49458024C>T | CA3847114 | MMUT | c.420G>A (p.Leu140=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.49458025A>C | CA364404764 | MMUT | c.419T>G (p.Leu140Arg)
| |
6 | g.49458025A>G | CA364404765 | MMUT | c.419T>C (p.Leu140Pro)
| |
6 | g.49458025A>T | CA364404766 | MMUT | c.419T>A (p.Leu140Gln)
| |
6 | g.49458026G>A | CA450608695 | MMUT | c.418C>T (p.Leu140=)
| gnomAD v4 |
6 | g.49458026G>C | CA364404767 | MMUT | c.418C>G (p.Leu140Val)
| |
6 | g.49458026G>T | CA364404768 | MMUT | c.418C>A (p.Leu140Met)
| gnomAD v4 |
6 | g.49458027A>C | CA364404770 | MMUT | c.417T>G (p.Asp139Glu)
| |
6 | g.49458027A>G | CA450608696 | MMUT | c.417T>C (p.Asp139=)
| gnomAD v4 |
6 | g.49458027A>T | CA364404769 | MMUT | c.417T>A (p.Asp139Glu)
| |
6 | g.49458028T>A | CA364404771 | MMUT | c.416A>T (p.Asp139Val)
| |
6 | g.49458028T>C | CA364404772 | MMUT | c.416A>G (p.Asp139Gly)
| |
6 | g.49458028T>G | CA364404773 | MMUT | c.416A>C (p.Asp139Ala)
| |
6 | g.49458029C>A | CA364404774 | MMUT | c.415G>T (p.Asp139Tyr)
| |
6 | g.49458029C= | CA1627395536 | MMUT | c.415G= (p.Asp139=)
| |
6 | g.49458029C>G | CA364404775 | MMUT | c.415G>C (p.Asp139His)
| |
6 | g.49458029C>T | CA10575882 | MMUT | c.415G>A (p.Asp139Asn)
| ClinVar dbSNP |
6 | g.49458030A>C | CA364404777 | MMUT | c.414T>G (p.Phe138Leu)
| |
6 | g.49458030A>G | CA450608697 | MMUT | c.414T>C (p.Phe138=)
| ClinVar dbSNP gnomAD v4 |
6 | g.49458030A>T | CA364404776 | MMUT | c.414T>A (p.Phe138Leu)
| |
6 | g.49458030_49458048delinsGTGGCTTTATATATT | CA2580075487 | MMUT | c.396_414delinsAATATATAAAGCCAC (p.Gly133IlefsTer?)
| ClinVar |
6 | g.49458031A>C | CA364404778 | MMUT | c.413T>G (p.Phe138Cys)
| |
6 | g.49458031A>G | CA364404779 | MMUT | c.413T>C (p.Phe138Ser)
| |
6 | g.49458031A>T | CA364404780 | MMUT | c.413T>A (p.Phe138Tyr)
| gnomAD v4 |
6 | g.49458032A>C | CA364404781 | MMUT | c.412T>G (p.Phe138Val)
| |
6 | g.49458032A>G | CA364404782 | MMUT | c.412T>C (p.Phe138Leu)
| |
6 | g.49458032A>T | CA364404783 | MMUT | c.412T>A (p.Phe138Ile)
| |
6 | g.49458033G>A | CA450608698 | MMUT | c.411C>T (p.Ala137=)
| |
6 | g.49458033G>C | CA450608699 | MMUT | c.411C>G (p.Ala137=)
| |
6 | g.49458033G>T | CA450608700 | MMUT | c.411C>A (p.Ala137=)
| |
6 | g.49458034G>A | CA364404785 | MMUT | c.410C>T (p.Ala137Val)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
6 | g.49458034G>C | CA138800018 | MMUT | c.410C>G (p.Ala137Gly)
| ClinVar dbSNP |
6 | g.49458034G= | CA1627395545 | MMUT | c.410C= (p.Ala137=)
| |
6 | g.49458034G>T | CA364404784 | MMUT | c.410C>A (p.Ala137Asp)
| |
6 | g.49458035C>A | CA364404786 | MMUT | c.409G>T (p.Ala137Ser)
| |
6 | g.49458035C>G | CA364404787 | MMUT | c.409G>C (p.Ala137Pro)
| |
6 | g.49458035C>T | CA364404788 | MMUT | c.409G>A (p.Ala137Thr)
| |
6 | g.49458036A= | CA1627395549 | MMUT | c.408T= (p.Val136=)
| |
6 | g.49458036A>C | CA450608702 | MMUT | c.408T>G (p.Val136=)
| dbSNP gnomAD v2 |
6 | g.49458036A>G | CA450608703 | MMUT | c.408T>C (p.Val136=)
| |
6 | g.49458036A>T | CA450608701 | MMUT | c.408T>A (p.Val136=)
| |
6 | g.49458037A>C | CA364404789 | MMUT | c.407T>G (p.Val136Gly)
| COSMIC |
6 | g.49458037A>G | CA364404790 | MMUT | c.407T>C (p.Val136Ala)
| |
6 | g.49458037A>T | CA364404791 | MMUT | c.407T>A (p.Val136Asp)
| gnomAD v4 |