| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 13 | g.52397636C>A | CA388037560 | THSD1 | c.617G>T (p.Cys206Phe) | |
| 13 | g.52397636C= | CA2091759549 | THSD1 | c.617G= (p.Cys206=) | |
| 13 | g.52397636C>G | CA388037557 | THSD1 | c.617G>C (p.Cys206Ser) | |
| 13 | g.52397636C>T | CA199702 | THSD1 | c.617G>A (p.Cys206Tyr) | ClinVar dbSNP gnomAD v4 |
| 13 | g.52397637A>C | CA388037564 | THSD1 | c.616T>G (p.Cys206Gly) | |
| 13 | g.52397637A>G | CA388037567 | THSD1 | c.616T>C (p.Cys206Arg) | |
| 13 | g.52397637A>T | CA388037570 | THSD1 | c.616T>A (p.Cys206Ser) | |
| 13 | g.52397638G>A | CA484028307 | THSD1 | c.615C>T (p.Gly205=) | dbSNP |
| 13 | g.52397638G>C | CA484028308 | THSD1 | c.615C>G (p.Gly205=) | |
| 13 | g.52397638G= | CA2091759553 | THSD1 | c.615C= (p.Gly205=) | |
| 13 | g.52397638G>T | CA484028309 | THSD1 | c.615C>A (p.Gly205=) | |
| 13 | g.52397639C>A | CA388037574 | THSD1 | c.614G>T (p.Gly205Val) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.52397639C= | CA2091759557 | THSD1 | c.614G= (p.Gly205=) | |
| 13 | g.52397639C>G | CA388037577 | THSD1 | c.614G>C (p.Gly205Ala) | |
| 13 | g.52397639C>T | CA250097282 | THSD1 | c.614G>A (p.Gly205Asp) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397640C>A | CA388037588 | THSD1 | c.613G>T (p.Gly205Cys) | |
| 13 | g.52397640C>G | CA388037594 | THSD1 | c.613G>C (p.Gly205Arg) | |
| 13 | g.52397640C>T | CA388037591 | THSD1 | c.613G>A (p.Gly205Ser) | |
| 13 | g.52397641A= | CA2091759562 | THSD1 | c.612T= (p.Phe204=) | |
| 13 | g.52397641A>C | CA388037599 | THSD1 | c.612T>G (p.Phe204Leu) | |
| 13 | g.52397641A>G | CA6992170 | THSD1 | c.612T>C (p.Phe204=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397641A>T | CA388037607 | THSD1 | c.612T>A (p.Phe204Leu) | |
| 13 | g.52397642A>C | CA388037610 | THSD1 | c.611T>G (p.Phe204Cys) | |
| 13 | g.52397642A>G | CA388037612 | THSD1 | c.611T>C (p.Phe204Ser) | |
| 13 | g.52397642A>T | CA388037615 | THSD1 | c.611T>A (p.Phe204Tyr) | |
| 13 | g.52397643A>C | CA388037620 | THSD1 | c.610T>G (p.Phe204Val) | gnomAD v4 |
| 13 | g.52397643A>G | CA388037622 | THSD1 | c.610T>C (p.Phe204Leu) | |
| 13 | g.52397643A>T | CA388037625 | THSD1 | c.610T>A (p.Phe204Ile) | |
| 13 | g.52397644C>A | CA388037629 | THSD1 | c.609G>T (p.Glu203Asp) | |
| 13 | g.52397644C>G | CA388037630 | THSD1 | c.609G>C (p.Glu203Asp) | |
| 13 | g.52397644C>T | CA484028327 | THSD1 | c.609G>A (p.Glu203=) | gnomAD v4 |
| 13 | g.52397645T>A | CA388037645 | THSD1 | c.608A>T (p.Glu203Val) | |
| 13 | g.52397645T>C | CA388037642 | THSD1 | c.608A>G (p.Glu203Gly) | |
| 13 | g.52397645T>G | CA388037635 | THSD1 | c.608A>C (p.Glu203Ala) | |
| 13 | g.52397646C>A | CA388037649 | THSD1 | c.607G>T (p.Glu203Ter) | |
| 13 | g.52397646C>G | CA388037654 | THSD1 | c.607G>C (p.Glu203Gln) | |
| 13 | g.52397646C>T | CA388037651 | THSD1 | c.607G>A (p.Glu203Lys) | |
| 13 | g.52397647A>C | CA484028334 | THSD1 | c.606T>G (p.Val202=) | |
| 13 | g.52397647A>G | CA484028335 | THSD1 | c.606T>C (p.Val202=) | |
| 13 | g.52397647A>T | CA484028338 | THSD1 | c.606T>A (p.Val202=) | |
| 13 | g.52397648A>C | CA388037658 | THSD1 | c.605T>G (p.Val202Gly) | |
| 13 | g.52397648A>G | CA388037664 | THSD1 | c.605T>C (p.Val202Ala) | |
| 13 | g.52397648A>T | CA388037660 | THSD1 | c.605T>A (p.Val202Asp) | |
| 13 | g.52397649C>A | CA388037665 | THSD1 | c.604G>T (p.Val202Phe) | |
| 13 | g.52397649C>G | CA388037670 | THSD1 | c.604G>C (p.Val202Leu) | |
| 13 | g.52397649C>T | CA388037667 | THSD1 | c.604G>A (p.Val202Ile) | |
| 13 | g.52397650C>A | CA388037673 | THSD1 | c.603G>T (p.Trp201Cys) | |
| 13 | g.52397650C>G | CA388037676 | THSD1 | c.603G>C (p.Trp201Cys) | |
| 13 | g.52397650C>T | CA388037679 | THSD1 | c.603G>A (p.Trp201Ter) | |
| 13 | g.52397651C>A | CA388037684 | THSD1 | c.602G>T (p.Trp201Leu) | gnomAD v4 |
| 13 | g.52397651C= | CA2091759564 | THSD1 | c.602G= (p.Trp201=) | |
| 13 | g.52397651C>G | CA388037686 | THSD1 | c.602G>C (p.Trp201Ser) | |
| 13 | g.52397651C>T | CA388037688 | THSD1 | c.602G>A (p.Trp201Ter) | dbSNP |
| 13 | g.52397652A>C | CA388037695 | THSD1 | c.601T>G (p.Trp201Gly) | |
| 13 | g.52397652A>G | CA388037691 | THSD1 | c.601T>C (p.Trp201Arg) | |
| 13 | g.52397652A>T | CA388037694 | THSD1 | c.601T>A (p.Trp201Arg) | |
| 13 | g.52397653C>A | CA388037698 | THSD1 | c.600G>T (p.Gln200His) | |
| 13 | g.52397653C>G | CA388037699 | THSD1 | c.600G>C (p.Gln200His) | |
| 13 | g.52397653C>T | CA484028353 | THSD1 | c.600G>A (p.Gln200=) | |
| 13 | g.52397654T>A | CA388037701 | THSD1 | c.599A>T (p.Gln200Leu) | |
| 13 | g.52397654T>C | CA388037703 | THSD1 | c.599A>G (p.Gln200Arg) | |
| 13 | g.52397654T>G | CA388037705 | THSD1 | c.599A>C (p.Gln200Pro) | |
| 13 | g.52397655G>A | CA388037707 | THSD1 | c.598C>T (p.Gln200Ter) | dbSNP gnomAD v4 |
| 13 | g.52397655G>C | CA388037710 | THSD1 | c.598C>G (p.Gln200Glu) | |
| 13 | g.52397655G= | CA2091759567 | THSD1 | c.598C= (p.Gln200=) | |
| 13 | g.52397655G>T | CA388037708 | THSD1 | c.598C>A (p.Gln200Lys) | |
| 13 | g.52397656A>C | CA484028361 | THSD1 | c.597T>G (p.Gly199=) | |
| 13 | g.52397656A>G | CA484028359 | THSD1 | c.597T>C (p.Gly199=) | gnomAD v4 |
| 13 | g.52397656A>T | CA484028360 | THSD1 | c.597T>A (p.Gly199=) | COSMIC |
| 13 | g.52397657C>A | CA388037713 | THSD1 | c.596G>T (p.Gly199Val) | |
| 13 | g.52397657C>G | CA388037715 | THSD1 | c.596G>C (p.Gly199Ala) | gnomAD v4 |
| 13 | g.52397657C>T | CA388037717 | THSD1 | c.596G>A (p.Gly199Asp) | COSMIC |
| 13 | g.52397658C>A | CA388037719 | THSD1 | c.595G>T (p.Gly199Cys) | |
| 13 | g.52397658C= | CA2091759572 | THSD1 | c.595G= (p.Gly199=) | |
| 13 | g.52397658C>G | CA388037720 | THSD1 | c.595G>C (p.Gly199Arg) | |
| 13 | g.52397658C>T | CA6992171 | THSD1 | c.595G>A (p.Gly199Ser) | dbSNP ExAC gnomAD v2 |
| 13 | g.52397659T>A | CA388037723 | THSD1 | c.594A>T (p.Gln198His) | |
| 13 | g.52397659T>C | CA484028364 | THSD1 | c.594A>G (p.Gln198=) | |
| 13 | g.52397659T>G | CA388037725 | THSD1 | c.594A>C (p.Gln198His) | |
| 13 | g.52397660T>A | CA388037727 | THSD1 | c.593A>T (p.Gln198Leu) | |
| 13 | g.52397660T>C | CA6992172 | THSD1 | c.593A>G (p.Gln198Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397660T>G | CA388037729 | THSD1 | c.593A>C (p.Gln198Pro) | |
| 13 | g.52397660T= | CA2091759575 | THSD1 | c.593A= (p.Gln198=) | |
| 13 | g.52397661G>A | CA388037731 | THSD1 | c.592C>T (p.Gln198Ter) | gnomAD v4 |
| 13 | g.52397661G>C | CA6992173 | THSD1 | c.592C>G (p.Gln198Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397661G= | CA2091759577 | THSD1 | c.592C= (p.Gln198=) | |
| 13 | g.52397661G>T | CA388037736 | THSD1 | c.592C>A (p.Gln198Lys) | |
| 13 | g.52397661_52397662insCG | CA2558563652 | THSD1 | c.592_593insGC (p.Gln198ArgfsTer23) | |
| 13 | g.52397662A>C | CA484028372 | THSD1 | c.591T>G (p.Ala197=) | |
| 13 | g.52397662A>G | CA484028371 | THSD1 | c.591T>C (p.Ala197=) | |
| 13 | g.52397662A>T | CA484028373 | THSD1 | c.591T>A (p.Ala197=) | |
| 13 | g.52397663G>A | CA388037739 | THSD1 | c.590C>T (p.Ala197Val) | |
| 13 | g.52397663G>C | CA388037741 | THSD1 | c.590C>G (p.Ala197Gly) | |
| 13 | g.52397663G>T | CA388037742 | THSD1 | c.590C>A (p.Ala197Asp) | |
| 13 | g.52397664C>A | CA388037746 | THSD1 | c.589G>T (p.Ala197Ser) | COSMIC |
| 13 | g.52397664C>G | CA388037748 | THSD1 | c.589G>C (p.Ala197Pro) | |
| 13 | g.52397664C>T | CA388037749 | THSD1 | c.589G>A (p.Ala197Thr) | |
| 13 | g.52397664_52397665del | CA2506648129 | THSD1 | c.588_589del (p.Ala197SerfsTer6) | |
| 13 | g.52397665A>C | CA484028376 | THSD1 | c.588T>G (p.Leu196=) | |
| 13 | g.52397665A>G | CA484028377 | THSD1 | c.588T>C (p.Leu196=) | |
| 13 | g.52397665A>T | CA484028378 | THSD1 | c.588T>A (p.Leu196=) | |
| 13 | g.52397666A>C | CA388037752 | THSD1 | c.587T>G (p.Leu196Arg) | |
| 13 | g.52397666A>G | CA388037754 | THSD1 | c.587T>C (p.Leu196Pro) | |
| 13 | g.52397666A>T | CA388037755 | THSD1 | c.587T>A (p.Leu196His) | |
| 13 | g.52397667G>A | CA388037757 | THSD1 | c.586C>T (p.Leu196Phe) | |
| 13 | g.52397667G>C | CA388037759 | THSD1 | c.586C>G (p.Leu196Val) | |
| 13 | g.52397667G>T | CA388037760 | THSD1 | c.586C>A (p.Leu196Ile) | |
| 13 | g.52397668T>A | CA388037764 | THSD1 | c.585A>T (p.Glu195Asp) | |
| 13 | g.52397668T>C | CA484028385 | THSD1 | c.585A>G (p.Glu195=) | |
| 13 | g.52397668T>G | CA388037763 | THSD1 | c.585A>C (p.Glu195Asp) | |
| 13 | g.52397669T>A | CA388037766 | THSD1 | c.584A>T (p.Glu195Val) | |
| 13 | g.52397669T>C | CA388037768 | THSD1 | c.584A>G (p.Glu195Gly) | |
| 13 | g.52397669T>G | CA388037770 | THSD1 | c.584A>C (p.Glu195Ala) | |
| 13 | g.52397670C>A | CA388037772 | THSD1 | c.583G>T (p.Glu195Ter) | |
| 13 | g.52397670C>G | CA388037774 | THSD1 | c.583G>C (p.Glu195Gln) | |
| 13 | g.52397670C>T | CA388037777 | THSD1 | c.583G>A (p.Glu195Lys) | gnomAD v4 |
| 13 | g.52397671T>A | CA484028391 | THSD1 | c.582A>T (p.Thr194=) | |
| 13 | g.52397671T>C | CA484028392 | THSD1 | c.582A>G (p.Thr194=) | gnomAD v4 |
| 13 | g.52397671T>G | CA484028395 | THSD1 | c.582A>C (p.Thr194=) | |
| 13 | g.52397672G>A | CA388037779 | THSD1 | c.581C>T (p.Thr194Ile) | |
| 13 | g.52397672G>C | CA388037781 | THSD1 | c.581C>G (p.Thr194Arg) | gnomAD v4 |
| 13 | g.52397672G>T | CA388037783 | THSD1 | c.581C>A (p.Thr194Lys) | |
| 13 | g.52397673T>A | CA388037785 | THSD1 | c.580A>T (p.Thr194Ser) | dbSNP gnomAD v4 |
| 13 | g.52397673T>C | CA388037787 | THSD1 | c.580A>G (p.Thr194Ala) | dbSNP gnomAD v4 |
| 13 | g.52397673T>G | CA388037789 | THSD1 | c.580A>C (p.Thr194Pro) | |
| 13 | g.52397673T= | CA2091759581 | THSD1 | c.580A= (p.Thr194=) | |
| 13 | g.52397674C>A | CA388037793 | THSD1 | c.579G>T (p.Arg193Ser) | |
| 13 | g.52397674C>G | CA388037792 | THSD1 | c.579G>C (p.Arg193Ser) | |
| 13 | g.52397674C>T | CA484028398 | THSD1 | c.579G>A (p.Arg193=) | |
| 13 | g.52397675C>A | CA388037795 | THSD1 | c.578G>T (p.Arg193Met) | |
| 13 | g.52397675C>G | CA388037797 | THSD1 | c.578G>C (p.Arg193Thr) | |
| 13 | g.52397675C>T | CA388037800 | THSD1 | c.578G>A (p.Arg193Lys) | |
| 13 | g.52397676T>A | CA388037802 | THSD1 | c.577A>T (p.Arg193Trp) | |
| 13 | g.52397676T>C | CA388037804 | THSD1 | c.577A>G (p.Arg193Gly) | |
| 13 | g.52397676T>G | CA484028402 | THSD1 | c.577A>C (p.Arg193=) | |
| 13 | g.52397677T>A | CA388037806 | THSD1 | c.576A>T (p.Lys192Asn) | |
| 13 | g.52397677T>C | CA484028406 | THSD1 | c.576A>G (p.Lys192=) | |
| 13 | g.52397677T>G | CA388037808 | THSD1 | c.576A>C (p.Lys192Asn) | |
| 13 | g.52397678T>A | CA388037815 | THSD1 | c.575A>T (p.Lys192Ile) | |
| 13 | g.52397678T>C | CA388037810 | THSD1 | c.575A>G (p.Lys192Arg) | |
| 13 | g.52397678T>G | CA388037813 | THSD1 | c.575A>C (p.Lys192Thr) | |
| 13 | g.52397679T>A | CA388037817 | THSD1 | c.574A>T (p.Lys192Ter) | |
| 13 | g.52397679T>C | CA388037818 | THSD1 | c.574A>G (p.Lys192Glu) | |
| 13 | g.52397679T>G | CA388037819 | THSD1 | c.574A>C (p.Lys192Gln) | |
| 13 | g.52397680G>A | CA484028411 | THSD1 | c.573C>T (p.Ser191=) | gnomAD v4 |
| 13 | g.52397680G>C | CA388037820 | THSD1 | c.573C>G (p.Ser191Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.52397680G= | CA2091759586 | THSD1 | c.573C= (p.Ser191=) | |
| 13 | g.52397680G>T | CA388037821 | THSD1 | c.573C>A (p.Ser191Arg) | |
| 13 | g.52397681C>A | CA388037822 | THSD1 | c.572G>T (p.Ser191Ile) | |
| 13 | g.52397681C>G | CA388037825 | THSD1 | c.572G>C (p.Ser191Thr) | |
| 13 | g.52397681C>T | CA388037823 | THSD1 | c.572G>A (p.Ser191Asn) | |
| 13 | g.52397682T>A | CA388037828 | THSD1 | c.571A>T (p.Ser191Cys) | |
| 13 | g.52397682T>C | CA388037829 | THSD1 | c.571A>G (p.Ser191Gly) | |
| 13 | g.52397682T>G | CA388037830 | THSD1 | c.571A>C (p.Ser191Arg) | |
| 13 | g.52397683G>A | CA6992174 | THSD1 | c.570C>T (p.Thr190=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397683G>C | CA484028420 | THSD1 | c.570C>G (p.Thr190=) | |
| 13 | g.52397683G= | CA2091759591 | THSD1 | c.570C= (p.Thr190=) | |
| 13 | g.52397683G>T | CA484028418 | THSD1 | c.570C>A (p.Thr190=) | |
| 13 | g.52397684G>A | CA388037833 | THSD1 | c.569C>T (p.Thr190Ile) | |
| 13 | g.52397684G>C | CA388037834 | THSD1 | c.569C>G (p.Thr190Ser) | |
| 13 | g.52397684G>T | CA388037835 | THSD1 | c.569C>A (p.Thr190Asn) | |
| 13 | g.52397685T>A | CA388037837 | THSD1 | c.568A>T (p.Thr190Ser) | |
| 13 | g.52397685T>C | CA388037839 | THSD1 | c.568A>G (p.Thr190Ala) | |
| 13 | g.52397685T>G | CA388037840 | THSD1 | c.568A>C (p.Thr190Pro) | |
| 13 | g.52397686T>A | CA388037841 | THSD1 | c.567A>T (p.Arg189Ser) | |
| 13 | g.52397686T>C | CA484028426 | THSD1 | c.567A>G (p.Arg189=) | |
| 13 | g.52397686T>G | CA388037842 | THSD1 | c.567A>C (p.Arg189Ser) | |
| 13 | g.52397687C>A | CA388037845 | THSD1 | c.566G>T (p.Arg189Ile) | |
| 13 | g.52397687C= | CA2091759595 | THSD1 | c.566G= (p.Arg189=) | |
| 13 | g.52397687C>G | CA388037853 | THSD1 | c.566G>C (p.Arg189Thr) | |
| 13 | g.52397687C>T | CA6992175 | THSD1 | c.566G>A (p.Arg189Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397688T>A | CA388037856 | THSD1 | c.565A>T (p.Arg189Ter) | |
| 13 | g.52397688T>C | CA388037857 | THSD1 | c.565A>G (p.Arg189Gly) | gnomAD v4 |
| 13 | g.52397688T>G | CA484028427 | THSD1 | c.565A>C (p.Arg189=) | |
| 13 | g.52397689T>A | CA484028429 | THSD1 | c.564A>T (p.Ile188=) | |
| 13 | g.52397689T>C | CA388037860 | THSD1 | c.564A>G (p.Ile188Met) | gnomAD v4 |
| 13 | g.52397689T>G | CA484028431 | THSD1 | c.564A>C (p.Ile188=) | |
| 13 | g.52397690A>C | CA388037863 | THSD1 | c.563T>G (p.Ile188Arg) | |
| 13 | g.52397690A>G | CA388037865 | THSD1 | c.563T>C (p.Ile188Thr) | |
| 13 | g.52397690A>T | CA388037867 | THSD1 | c.563T>A (p.Ile188Lys) | |
| 13 | g.52397691T>A | CA388037869 | THSD1 | c.562A>T (p.Ile188Leu) | |
| 13 | g.52397691T>C | CA388037870 | THSD1 | c.562A>G (p.Ile188Val) | |
| 13 | g.52397691T>G | CA388037871 | THSD1 | c.562A>C (p.Ile188Leu) | |
| 13 | g.52397692T>A | CA388037872 | THSD1 | c.561A>T (p.Glu187Asp) | |
| 13 | g.52397692T>C | CA484028436 | THSD1 | c.561A>G (p.Glu187=) | |
| 13 | g.52397692T>G | CA388037873 | THSD1 | c.561A>C (p.Glu187Asp) | |
| 13 | g.52397693T>A | CA388037880 | THSD1 | c.560A>T (p.Glu187Val) | |
| 13 | g.52397693T>C | CA388037878 | THSD1 | c.560A>G (p.Glu187Gly) | gnomAD v4 |
| 13 | g.52397693T>G | CA388037876 | THSD1 | c.560A>C (p.Glu187Ala) | |
| 13 | g.52397694C>A | CA388037881 | THSD1 | c.559G>T (p.Glu187Ter) | |
| 13 | g.52397694C>G | CA388037882 | THSD1 | c.559G>C (p.Glu187Gln) | |
| 13 | g.52397694C>T | CA388037884 | THSD1 | c.559G>A (p.Glu187Lys) | |
| 13 | g.52397695C>A | CA484028442 | THSD1 | c.558G>T (p.Leu186=) | gnomAD v4 |
| 13 | g.52397695C>G | CA484028443 | THSD1 | c.558G>C (p.Leu186=) | |
| 13 | g.52397695C>T | CA484028444 | THSD1 | c.558G>A (p.Leu186=) | |
| 13 | g.52397696A= | CA2091759598 | THSD1 | c.557T= (p.Leu186=) | |
| 13 | g.52397696A>C | CA388037886 | THSD1 | c.557T>G (p.Leu186Arg) | |
| 13 | g.52397696A>G | CA388037888 | THSD1 | c.557T>C (p.Leu186Pro) | |
| 13 | g.52397696A>T | CA388037891 | THSD1 | c.557T>A (p.Leu186Gln) | dbSNP gnomAD v4 |
| 13 | g.52397697G>A | CA484028446 | THSD1 | c.556C>T (p.Leu186=) | |
| 13 | g.52397697G>C | CA388037895 | THSD1 | c.556C>G (p.Leu186Val) | |
| 13 | g.52397697G>T | CA388037897 | THSD1 | c.556C>A (p.Leu186Met) | |
| 13 | g.52397698C>A | CA484028450 | THSD1 | c.555G>T (p.Pro185=) | |
| 13 | g.52397698C= | CA2091759600 | THSD1 | c.555G= (p.Pro185=) | |
| 13 | g.52397698C>G | CA484028451 | THSD1 | c.555G>C (p.Pro185=) | |
| 13 | g.52397698C>T | CA6992176 | THSD1 | c.555G>A (p.Pro185=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397699G>A | CA388037903 | THSD1 | c.554C>T (p.Pro185Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397699G>C | CA388037904 | THSD1 | c.554C>G (p.Pro185Arg) | |
| 13 | g.52397699G= | CA2091759605 | THSD1 | c.554C= (p.Pro185=) | |
| 13 | g.52397699G>T | CA388037907 | THSD1 | c.554C>A (p.Pro185Gln) | gnomAD v4 |
| 13 | g.52397700G>A | CA388037923 | THSD1 | c.553C>T (p.Pro185Ser) | |
| 13 | g.52397700G>C | CA388037920 | THSD1 | c.553C>G (p.Pro185Ala) | |
| 13 | g.52397700G= | CA2091759607 | THSD1 | c.553C= (p.Pro185=) | |
| 13 | g.52397700G>T | CA388037911 | THSD1 | c.553C>A (p.Pro185Thr) | dbSNP gnomAD v2 gnomAD v4 |
| 13 | g.52397701C>A | CA388037932 | THSD1 | c.552G>T (p.Gln184His) | |
| 13 | g.52397701C>G | CA388037934 | THSD1 | c.552G>C (p.Gln184His) | |
| 13 | g.52397701C>T | CA484028459 | THSD1 | c.552G>A (p.Gln184=) | gnomAD v4 |
| 13 | g.52397701_52397702insA | CA2557528149 | THSD1 | c.551_552insT (p.Gln184HisfsTer20) | |
| 13 | g.52397702T>A | CA388037938 | THSD1 | c.551A>T (p.Gln184Leu) | |
| 13 | g.52397702T>C | CA6992177 | THSD1 | c.551A>G (p.Gln184Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397702T>G | CA388037942 | THSD1 | c.551A>C (p.Gln184Pro) | |
| 13 | g.52397702T= | CA2091759610 | THSD1 | c.551A= (p.Gln184=) | |
| 13 | g.52397703G>A | CA6992178 | THSD1 | c.550C>T (p.Gln184Ter) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 13 | g.52397703G>C | CA250097302 | THSD1 | c.550C>G (p.Gln184Glu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397703G= | CA2091759614 | THSD1 | c.550C= (p.Gln184=) | |
| 13 | g.52397703G>T | CA388037946 | THSD1 | c.550C>A (p.Gln184Lys) | |
| 13 | g.52397704T>A | CA388037951 | THSD1 | c.549A>T (p.Arg183Ser) | |
| 13 | g.52397704T>C | CA484028467 | THSD1 | c.549A>G (p.Arg183=) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.52397704T>G | CA250097310 | THSD1 | c.549A>C (p.Arg183Ser) | dbSNP gnomAD v4 |
| 13 | g.52397704T= | CA2091759617 | THSD1 | c.549A= (p.Arg183=) | |
| 13 | g.52397705C>A | CA388037961 | THSD1 | c.548G>T (p.Arg183Ile) | |
| 13 | g.52397705C>G | CA388037962 | THSD1 | c.548G>C (p.Arg183Thr) | |
| 13 | g.52397705C>T | CA388037966 | THSD1 | c.548G>A (p.Arg183Lys) | |
| 13 | g.52397706T>A | CA388037971 | THSD1 | c.547A>T (p.Arg183Ter) | |
| 13 | g.52397706T>C | CA388037973 | THSD1 | c.547A>G (p.Arg183Gly) | dbSNP gnomAD v4 |
| 13 | g.52397706T>G | CA484028469 | THSD1 | c.547A>C (p.Arg183=) | |
| 13 | g.52397706T= | CA2091759620 | THSD1 | c.547A= (p.Arg183=) | |
| 13 | g.52397707T>A | CA484028470 | THSD1 | c.546A>T (p.Ser182=) | |
| 13 | g.52397707T>C | CA484028471 | THSD1 | c.546A>G (p.Ser182=) | dbSNP gnomAD v3 gnomAD v4 |
| 13 | g.52397707T>G | CA484028472 | THSD1 | c.546A>C (p.Ser182=) | |
| 13 | g.52397707T= | CA2091759623 | THSD1 | c.546A= (p.Ser182=) | |
| 13 | g.52397708G>A | CA388037982 | THSD1 | c.545C>T (p.Ser182Leu) | |
| 13 | g.52397708G>C | CA388037979 | THSD1 | c.545C>G (p.Ser182Ter) | |
| 13 | g.52397708G>T | CA388037977 | THSD1 | c.545C>A (p.Ser182Ter) | |
| 13 | g.52397709A>C | CA388037983 | THSD1 | c.544T>G (p.Ser182Ala) | |
| 13 | g.52397709A>G | CA388037986 | THSD1 | c.544T>C (p.Ser182Pro) | |
| 13 | g.52397709A>T | CA388037989 | THSD1 | c.544T>A (p.Ser182Thr) | |
| 13 | g.52397710A>C | CA388037992 | THSD1 | c.543T>G (p.Asn181Lys) | |
| 13 | g.52397710A>G | CA484028476 | THSD1 | c.543T>C (p.Asn181=) | |
| 13 | g.52397710A>T | CA388037994 | THSD1 | c.543T>A (p.Asn181Lys) | |
| 13 | g.52397710_52397716del | CA2569554637 | THSD1 | c.537_543del (p.Arg179SerfsTer8) | |
| 13 | g.52397711T>A | CA388037999 | THSD1 | c.542A>T (p.Asn181Ile) | |
| 13 | g.52397711T>C | CA388038000 | THSD1 | c.542A>G (p.Asn181Ser) | |
| 13 | g.52397711T>G | CA388038002 | THSD1 | c.542A>C (p.Asn181Thr) | |
| 13 | g.52397712T>A | CA388038006 | THSD1 | c.541A>T (p.Asn181Tyr) | |
| 13 | g.52397712T>C | CA388038009 | THSD1 | c.541A>G (p.Asn181Asp) | |
| 13 | g.52397712T>G | CA388038012 | THSD1 | c.541A>C (p.Asn181His) | |
| 13 | g.52397713T>A | CA388038016 | THSD1 | c.540A>T (p.Arg180Ser) | |
| 13 | g.52397713T>C | CA484028478 | THSD1 | c.540A>G (p.Arg180=) | |
| 13 | g.52397713T>G | CA388038017 | THSD1 | c.540A>C (p.Arg180Ser) | |
| 13 | g.52397714C>A | CA388038023 | THSD1 | c.539G>T (p.Arg180Ile) | |
| 13 | g.52397714C>G | CA388038026 | THSD1 | c.539G>C (p.Arg180Thr) | |
| 13 | g.52397714C>T | CA388038020 | THSD1 | c.539G>A (p.Arg180Lys) | |
| 13 | g.52397715T>A | CA388038029 | THSD1 | c.538A>T (p.Arg180Ter) | |
| 13 | g.52397715T>C | CA388038032 | THSD1 | c.538A>G (p.Arg180Gly) | |
| 13 | g.52397715T>G | CA484028481 | THSD1 | c.538A>C (p.Arg180=) | |
| 13 | g.52397716T>A | CA388038035 | THSD1 | c.537A>T (p.Arg179Ser) | |
| 13 | g.52397716T>C | CA484028482 | THSD1 | c.537A>G (p.Arg179=) | |
| 13 | g.52397716T>G | CA388038038 | THSD1 | c.537A>C (p.Arg179Ser) | |
| 13 | g.52397717C>A | CA388038042 | THSD1 | c.536G>T (p.Arg179Ile) | |
| 13 | g.52397717C>G | CA388038044 | THSD1 | c.536G>C (p.Arg179Thr) | |
| 13 | g.52397717C>T | CA388038047 | THSD1 | c.536G>A (p.Arg179Lys) | gnomAD v4 |
| 13 | g.52397717_52397718insCCGCCC | CA2565195912 | THSD1 | c.536_537insGGCGGG (p.Arg179_Arg180insAlaGly) | |
| 13 | g.52397718T>A | CA388038049 | THSD1 | c.535A>T (p.Arg179Ter) | |
| 13 | g.52397718T>C | CA388038052 | THSD1 | c.535A>G (p.Arg179Gly) | |
| 13 | g.52397718T>G | CA484028484 | THSD1 | c.535A>C (p.Arg179=) | |
| 13 | g.52397719T>A | CA484028487 | THSD1 | c.534A>T (p.Ala178=) | |
| 13 | g.52397719T>C | CA484028488 | THSD1 | c.534A>G (p.Ala178=) | |
| 13 | g.52397719T>G | CA484028490 | THSD1 | c.534A>C (p.Ala178=) | |
| 13 | g.52397720G>A | CA388038056 | THSD1 | c.533C>T (p.Ala178Val) | |
| 13 | g.52397720G>C | CA388038059 | THSD1 | c.533C>G (p.Ala178Gly) | |
| 13 | g.52397720G>T | CA388038064 | THSD1 | c.533C>A (p.Ala178Glu) | |
| 13 | g.52397721C>A | CA388038077 | THSD1 | c.532G>T (p.Ala178Ser) | |
| 13 | g.52397721C>G | CA388038067 | THSD1 | c.532G>C (p.Ala178Pro) | |
| 13 | g.52397721C>T | CA388038075 | THSD1 | c.532G>A (p.Ala178Thr) | |
| 13 | g.52397722C>A | CA388038080 | THSD1 | c.531G>T (p.Glu177Asp) | |
| 13 | g.52397722C>G | CA388038082 | THSD1 | c.531G>C (p.Glu177Asp) | |
| 13 | g.52397722C>T | CA484028491 | THSD1 | c.531G>A (p.Glu177=) | gnomAD v4 |
| 13 | g.52397723T>A | CA388038083 | THSD1 | c.530A>T (p.Glu177Val) | |
| 13 | g.52397723T>C | CA388038084 | THSD1 | c.530A>G (p.Glu177Gly) | COSMIC |
| 13 | g.52397723T>G | CA388038086 | THSD1 | c.530A>C (p.Glu177Ala) | |
| 13 | g.52397724C>A | CA388038088 | THSD1 | c.529G>T (p.Glu177Ter) | |
| 13 | g.52397724C= | CA2091759625 | THSD1 | c.529G= (p.Glu177=) | |
| 13 | g.52397724C>G | CA388038091 | THSD1 | c.529G>C (p.Glu177Gln) | |
| 13 | g.52397724C>T | CA6992179 | THSD1 | c.529G>A (p.Glu177Lys) | dbSNP ExAC gnomAD v2 COSMIC |
| 13 | g.52397725A= | CA2091759629 | THSD1 | c.528T= (p.Pro176=) | |
| 13 | g.52397725A>C | CA484028494 | THSD1 | c.528T>G (p.Pro176=) | dbSNP gnomAD v4 |
| 13 | g.52397725A>G | CA484028495 | THSD1 | c.528T>C (p.Pro176=) | |
| 13 | g.52397725A>T | CA484028496 | THSD1 | c.528T>A (p.Pro176=) | |
| 13 | g.52397726G>A | CA6992180 | THSD1 | c.527C>T (p.Pro176Leu) | dbSNP ExAC |
| 13 | g.52397726G>C | CA388038095 | THSD1 | c.527C>G (p.Pro176Arg) | dbSNP |
| 13 | g.52397726G= | CA2091759633 | THSD1 | c.527C= (p.Pro176=) | |
| 13 | g.52397726G>T | CA388038100 | THSD1 | c.527C>A (p.Pro176His) | |
| 13 | g.52397727G>A | CA388038109 | THSD1 | c.526C>T (p.Pro176Ser) | |
| 13 | g.52397727G>C | CA388038108 | THSD1 | c.526C>G (p.Pro176Ala) | |
| 13 | g.52397727G= | CA2091759638 | THSD1 | c.526C= (p.Pro176=) | |
| 13 | g.52397727G>T | CA6992181 | THSD1 | c.526C>A (p.Pro176Thr) | dbSNP ExAC |
| 13 | g.52397728A= | CA2091759641 | THSD1 | c.525T= (p.Leu175=) | |
| 13 | g.52397728A>C | CA484028501 | THSD1 | c.525T>G (p.Leu175=) | |
| 13 | g.52397728A>G | CA484028502 | THSD1 | c.525T>C (p.Leu175=) | dbSNP |
| 13 | g.52397728A>T | CA484028503 | THSD1 | c.525T>A (p.Leu175=) | |
| 13 | g.52397729A= | CA2091759645 | THSD1 | c.524T= (p.Leu175=) | |
| 13 | g.52397729A>C | CA388038111 | THSD1 | c.524T>G (p.Leu175Arg) | ClinVar dbSNP gnomAD v4 |
| 13 | g.52397729A>G | CA388038117 | THSD1 | c.524T>C (p.Leu175Pro) | |
| 13 | g.52397729A>T | CA388038114 | THSD1 | c.524T>A (p.Leu175His) | |
| 13 | g.52397730G>A | CA388038121 | THSD1 | c.523C>T (p.Leu175Phe) | |
| 13 | g.52397730G>C | CA388038123 | THSD1 | c.523C>G (p.Leu175Val) | |
| 13 | g.52397730G>T | CA388038125 | THSD1 | c.523C>A (p.Leu175Ile) | |
| 13 | g.52397731A>C | CA388038128 | THSD1 | c.522T>G (p.Ser174Arg) | |
| 13 | g.52397731A>G | CA484028509 | THSD1 | c.522T>C (p.Ser174=) | gnomAD v4 |
| 13 | g.52397731A>T | CA388038131 | THSD1 | c.522T>A (p.Ser174Arg) | |
| 13 | g.52397732C>A | CA388038135 | THSD1 | c.521G>T (p.Ser174Ile) | |
| 13 | g.52397732C>G | CA388038140 | THSD1 | c.521G>C (p.Ser174Thr) | |
| 13 | g.52397732C>T | CA388038142 | THSD1 | c.521G>A (p.Ser174Asn) | gnomAD v4 |
| 13 | g.52397733T>A | CA388038143 | THSD1 | c.520A>T (p.Ser174Cys) | |
| 13 | g.52397733T>C | CA388038148 | THSD1 | c.520A>G (p.Ser174Gly) | |
| 13 | g.52397733T>G | CA388038150 | THSD1 | c.520A>C (p.Ser174Arg) | |
| 13 | g.52397734G>A | CA6992182 | THSD1 | c.519C>T (p.Asn173=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 13 | g.52397734G>C | CA388038158 | THSD1 | c.519C>G (p.Asn173Lys) | |
| 13 | g.52397734G= | CA2091759647 | THSD1 | c.519C= (p.Asn173=) | |
| 13 | g.52397734G>T | CA388038155 | THSD1 | c.519C>A (p.Asn173Lys) | gnomAD v4 |
| 13 | g.52397735T>A | CA388038165 | THSD1 | c.518A>T (p.Asn173Ile) | |
| 13 | g.52397735T>C | CA388038167 | THSD1 | c.518A>G (p.Asn173Ser) | |
| 13 | g.52397735T>G | CA388038171 | THSD1 | c.518A>C (p.Asn173Thr) | |
| 13 | g.52397735_52397738delinsTTGG | CA2091759651 | THSD1 | c.515_518delinsCCAA (p.Thr172=) | |
| 13 | g.52397736T>A | CA388038175 | THSD1 | c.517A>T (p.Asn173Tyr) | |
| 13 | g.52397736T>C | CA388038177 | THSD1 | c.517A>G (p.Asn173Asp) | |
| 13 | g.52397736T>G | CA388038178 | THSD1 | c.517A>C (p.Asn173His) | |
| 13 | g.52397738_52397740del | CA2091759654 | THSD1 | c.515_517del (p.Thr172del) | dbSNP |