Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.176093445G>ACA430224562HOXD13c.555G>A (p.Ala185=)
c.725-1035G>A (n.725-1035G>A)
 dbSNP
2g.176093445G>CCA430224561HOXD13c.555G>C (p.Ala185=)
c.725-1035G>C (n.725-1035G>C)
 dbSNP
2g.176093445G=CA1309431425HOXD13c.555G= (p.Ala185=)
c.725-1035G= (n.725-1035G=)
2g.176093445G>TCA430224560HOXD13c.555G>T (p.Ala185=)
c.725-1035G>T (n.725-1035G>T)
2g.176093446C>ACA430224563HOXD13c.556C>A (p.Arg186=)
c.725-1034C>A (n.725-1034C>A)
 dbSNP
2g.176093446C=CA1309431426HOXD13c.556C= (p.Arg186=)
c.725-1034C= (n.725-1034C=)
2g.176093446C>GCA60846418HOXD13c.556C>G (p.Arg186Gly)
c.725-1034C>G (n.725-1034C>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093446C>TCA349352989HOXD13c.556C>T (p.Arg186Ter)
c.725-1034C>T (n.725-1034C>T)
 dbSNP
2g.176093447G>ACA1976623HOXD13c.557G>A (p.Arg186Gln)
c.725-1033G>A (n.725-1033G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093447G>CCA349352990HOXD13c.557G>C (p.Arg186Pro)
c.725-1033G>C (n.725-1033G>C)
 dbSNP
2g.176093447G=CA1309431427HOXD13c.557G= (p.Arg186=)
c.725-1033G= (n.725-1033G=)
2g.176093447G>TCA1976624HOXD13c.557G>T (p.Arg186Leu)
c.725-1033G>T (n.725-1033G>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093448A>CCA430224564HOXD13c.558A>C (p.Arg186=)
c.725-1032A>C (n.725-1032A>C)
2g.176093448A>GCA430224565HOXD13c.558A>G (p.Arg186=)
c.725-1032A>G (n.725-1032A>G)
 dbSNP
2g.176093448A>TCA430224566HOXD13c.558A>T (p.Arg186=)
c.725-1032A>T (n.725-1032A>T)
 dbSNP
2g.176093449G>ACA1976625HOXD13c.559G>A (p.Ala187Thr)
c.725-1031G>A (n.725-1031G>A)
 dbSNP ExAC gnomAD v2
2g.176093449G>CCA349352991HOXD13c.559G>C (p.Ala187Pro)
c.725-1031G>C (n.725-1031G>C)
2g.176093449G=CA1309431428HOXD13c.559G= (p.Ala187=)
c.725-1031G= (n.725-1031G=)
2g.176093449G>TCA349352992HOXD13c.559G>T (p.Ala187Ser)
c.725-1031G>T (n.725-1031G>T)
2g.176093450C>ACA349352993HOXD13c.560C>A (p.Ala187Asp)
c.725-1030C>A (n.725-1030C>A)
 dbSNP
2g.176093450C=CA1309431429HOXD13c.560C= (p.Ala187=)
c.725-1030C= (n.725-1030C=)
2g.176093450C>GCA349352994HOXD13c.560C>G (p.Ala187Gly)
c.725-1030C>G (n.725-1030C>G)
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.176093450C>TCA349352995HOXD13c.560C>T (p.Ala187Val)
c.725-1030C>T (n.725-1030C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093451C>ACA430224567HOXD13c.561C>A (p.Ala187=)
c.725-1029C>A (n.725-1029C>A)
 dbSNP
2g.176093451C=CA1309431430HOXD13c.561C= (p.Ala187=)
c.725-1029C= (n.725-1029C=)
2g.176093451C>GCA430224568HOXD13c.561C>G (p.Ala187=)
c.725-1029C>G (n.725-1029C>G)
 dbSNP
2g.176093451C>TCA430224569HOXD13c.561C>T (p.Ala187=)
c.725-1029C>T (n.725-1029C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093452A=CA1309431431HOXD13c.562A= (p.Lys188=)
c.725-1028A= (n.725-1028A=)
2g.176093452A>CCA349352996HOXD13c.562A>C (p.Lys188Gln)
c.725-1028A>C (n.725-1028A>C)
 dbSNP
2g.176093452A>GCA1976626HOXD13c.562A>G (p.Lys188Glu)
c.725-1028A>G (n.725-1028A>G)
 dbSNP ExAC gnomAD v3 gnomAD v4
2g.176093452A>TCA349352997HOXD13c.562A>T (p.Lys188Ter)
c.725-1028A>T (n.725-1028A>T)
 dbSNP gnomAD v4
2g.176093453A=CA1309431432HOXD13c.563A= (p.Lys188=)
c.725-1027A= (n.725-1027A=)
2g.176093453A>CCA349352999HOXD13c.563A>C (p.Lys188Thr)
c.725-1027A>C (n.725-1027A>C)
2g.176093453A>GCA1976627HOXD13c.563A>G (p.Lys188Arg)
c.725-1027A>G (n.725-1027A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093453A>TCA349352998HOXD13c.563A>T (p.Lys188Met)
c.725-1027A>T (n.725-1027A>T)
 dbSNP
2g.176093454G>ACA430224570HOXD13c.564G>A (p.Lys188=)
c.725-1026G>A (n.725-1026G>A)
 dbSNP gnomAD v3 gnomAD v4
2g.176093454G>CCA349353000HOXD13c.564G>C (p.Lys188Asn)
c.725-1026G>C (n.725-1026G>C)
 dbSNP
2g.176093454G=CA1309431433HOXD13c.564G= (p.Lys188=)
c.725-1026G= (n.725-1026G=)
2g.176093454G>TCA349353001HOXD13c.564G>T (p.Lys188Asn)
c.725-1026G>T (n.725-1026G>T)
2g.176093455G>ACA1976628HOXD13c.565G>A (p.Glu189Lys)
c.725-1025G>A (n.725-1025G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093455G>CCA349353002HOXD13c.565G>C (p.Glu189Gln)
c.725-1025G>C (n.725-1025G>C)
 dbSNP
2g.176093455G=CA1309431434HOXD13c.565G= (p.Glu189=)
c.725-1025G= (n.725-1025G=)
2g.176093455G>TCA349353003HOXD13c.565G>T (p.Glu189Ter)
c.725-1025G>T (n.725-1025G>T)
2g.176093456A>CCA349353004HOXD13c.566A>C (p.Glu189Ala)
c.725-1024A>C (n.725-1024A>C)
 gnomAD v4
2g.176093456A>GCA349353005HOXD13c.566A>G (p.Glu189Gly)
c.725-1024A>G (n.725-1024A>G)
2g.176093456A>TCA349353006HOXD13c.566A>T (p.Glu189Val)
c.725-1024A>T (n.725-1024A>T)
 gnomAD v4
2g.176093456_176093457insCCA2701095682HOXD13c.566_567insC (p.Glu189AspfsTer?)
c.725-1024_725-1023insC (n.725-1024_725-1023insC)
 dbSNP
2g.176093457G>ACA430224571HOXD13c.567G>A (p.Glu189=)
c.725-1023G>A (n.725-1023G>A)
 dbSNP gnomAD v3 gnomAD v4
2g.176093457G>CCA349353007HOXD13c.567G>C (p.Glu189Asp)
c.725-1023G>C (n.725-1023G>C)
2g.176093457G=CA1309431435HOXD13c.567G= (p.Glu189=)
c.725-1023G= (n.725-1023G=)
2g.176093457G>TCA349353008HOXD13c.567G>T (p.Glu189Asp)
c.725-1023G>T (n.725-1023G>T)
 dbSNP gnomAD v4
2g.176093458G>ACA349353009HOXD13c.568G>A (p.Val190Ile)
c.725-1022G>A (n.725-1022G>A)
2g.176093458G>CCA349353010HOXD13c.568G>C (p.Val190Leu)
c.725-1022G>C (n.725-1022G>C)
2g.176093458G=CA1309431436HOXD13c.568G= (p.Val190=)
c.725-1022G= (n.725-1022G=)
2g.176093458G>TCA1976629HOXD13c.568G>T (p.Val190Leu)
c.725-1022G>T (n.725-1022G>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093459T>ACA349353013HOXD13c.569T>A (p.Val190Glu)
c.725-1021T>A (n.725-1021T>A)
2g.176093459T>CCA349353011HOXD13c.569T>C (p.Val190Ala)
c.725-1021T>C (n.725-1021T>C)
2g.176093459T>GCA349353012HOXD13c.569T>G (p.Val190Gly)
c.725-1021T>G (n.725-1021T>G)
 dbSNP
2g.176093459T=CA1309431437HOXD13c.569T= (p.Val190=)
c.725-1021T= (n.725-1021T=)
2g.176093460A=CA1309431438HOXD13c.570A= (p.Val190=)
c.725-1020A= (n.725-1020A=)
2g.176093460A>CCA430224573HOXD13c.570A>C (p.Val190=)
c.725-1020A>C (n.725-1020A>C)
 dbSNP
2g.176093460A>GCA430224572HOXD13c.570A>G (p.Val190=)
c.725-1020A>G (n.725-1020A>G)
 gnomAD v3 gnomAD v4
2g.176093460A>TCA1976630HOXD13c.570A>T (p.Val190=)
c.725-1020A>T (n.725-1020A>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093461T>ACA349353014HOXD13c.571T>A (p.Ser191Thr)
c.725-1019T>A (n.725-1019T>A)
 dbSNP
2g.176093461T>CCA349353015HOXD13c.571T>C (p.Ser191Pro)
c.725-1019T>C (n.725-1019T>C)
2g.176093461T>GCA349353016HOXD13c.571T>G (p.Ser191Ala)
c.725-1019T>G (n.725-1019T>G)
2g.176093462C>ACA349353017HOXD13c.572C>A (p.Ser191Tyr)
c.725-1018C>A (n.725-1018C>A)
 dbSNP gnomAD v3 gnomAD v4
2g.176093462C=CA1309431439HOXD13c.572C= (p.Ser191=)
c.725-1018C= (n.725-1018C=)
2g.176093462C>GCA349353018HOXD13c.572C>G (p.Ser191Cys)
c.725-1018C>G (n.725-1018C>G)
 dbSNP
2g.176093462C>TCA349353019HOXD13c.572C>T (p.Ser191Phe)
c.725-1018C>T (n.725-1018C>T)
 dbSNP
2g.176093462_176093465delinsCCTTCA1309431440HOXD13c.572_575delinsCCTT (p.Ser191=)
c.725-1018_725-1015delinsCCTT (n.725-1018_725-1015delinsCCTT)
2g.176093463C>ACA430224576HOXD13c.573C>A (p.Ser191=)
c.725-1017C>A (n.725-1017C>A)
 COSMIC COSMIC
2g.176093463C>GCA430224575HOXD13c.573C>G (p.Ser191=)
c.725-1017C>G (n.725-1017C>G)
2g.176093463C>TCA430224574HOXD13c.573C>T (p.Ser191=)
c.725-1017C>T (n.725-1017C>T)
2g.176093465_176093467delCA891862724HOXD13c.575_577del (p.Phe192del)
c.725-1015_725-1013del (n.725-1015_725-1013del)
 ClinVar dbSNP
2g.176093464T>ACA349353020HOXD13c.574T>A (p.Phe192Ile)
c.725-1016T>A (n.725-1016T>A)
2g.176093464T>CCA349353021HOXD13c.574T>C (p.Phe192Leu)
c.725-1016T>C (n.725-1016T>C)
 dbSNP
2g.176093464T>GCA349353022HOXD13c.574T>G (p.Phe192Val)
c.725-1016T>G (n.725-1016T>G)
2g.176093465T>ACA349353023HOXD13c.575T>A (p.Phe192Tyr)
c.725-1015T>A (n.725-1015T>A)
2g.176093465T>CCA349353024HOXD13c.575T>C (p.Phe192Ser)
c.725-1015T>C (n.725-1015T>C)
2g.176093465T>GCA349353025HOXD13c.575T>G (p.Phe192Cys)
c.725-1015T>G (n.725-1015T>G)
 dbSNP
2g.176093465T=CA1309431441HOXD13c.575T= (p.Phe192=)
c.725-1015T= (n.725-1015T=)
2g.176093466C>ACA349353026HOXD13c.576C>A (p.Phe192Leu)
c.725-1014C>A (n.725-1014C>A)
2g.176093466C=CA1309431442HOXD13c.576C= (p.Phe192=)
c.725-1014C= (n.725-1014C=)
2g.176093466C>GCA349353027HOXD13c.576C>G (p.Phe192Leu)
c.725-1014C>G (n.725-1014C>G)
 dbSNP
2g.176093466C>TCA1976631HOXD13c.576C>T (p.Phe192=)
c.725-1014C>T (n.725-1014C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093467T>ACA349353029HOXD13c.577T>A (p.Tyr193Asn)
c.725-1013T>A (n.725-1013T>A)
 dbSNP
2g.176093467T>CCA349353028HOXD13c.577T>C (p.Tyr193His)
c.725-1013T>C (n.725-1013T>C)
 gnomAD v4
2g.176093467T>GCA349353030HOXD13c.577T>G (p.Tyr193Asp)
c.725-1013T>G (n.725-1013T>G)
2g.176093468A>CCA349353031HOXD13c.578A>C (p.Tyr193Ser)
c.725-1012A>C (n.725-1012A>C)
2g.176093468A>GCA349353033HOXD13c.578A>G (p.Tyr193Cys)
c.725-1012A>G (n.725-1012A>G)
 gnomAD v4 COSMIC
2g.176093468A>TCA349353032HOXD13c.578A>T (p.Tyr193Phe)
c.725-1012A>T (n.725-1012A>T)
 dbSNP
2g.176093469C>ACA349353034HOXD13c.579C>A (p.Tyr193Ter)
c.725-1011C>A (n.725-1011C>A)
2g.176093469C=CA1309431443HOXD13c.579C= (p.Tyr193=)
c.725-1011C= (n.725-1011C=)
2g.176093469C>GCA349353035HOXD13c.579C>G (p.Tyr193Ter)
c.725-1011C>G (n.725-1011C>G)
 dbSNP gnomAD v4
2g.176093469C>TCA1976632HOXD13c.579C>T (p.Tyr193=)
c.725-1011C>T (n.725-1011C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093470C>ACA349353036HOXD13c.580C>A (p.Gln194Lys)
c.725-1010C>A (n.725-1010C>A)
2g.176093470C=CA1309431444HOXD13c.580C= (p.Gln194=)
c.725-1010C= (n.725-1010C=)
2g.176093470C>GCA349353038HOXD13c.580C>G (p.Gln194Glu)
c.725-1010C>G (n.725-1010C>G)
 dbSNP gnomAD v2 gnomAD v4
2g.176093470C>TCA349353037HOXD13c.580C>T (p.Gln194Ter)
c.725-1010C>T (n.725-1010C>T)
2g.176093471A=CA1309431445HOXD13c.581A= (p.Gln194=)
c.725-1009A= (n.725-1009A=)
2g.176093471A>CCA349353039HOXD13c.581A>C (p.Gln194Pro)
c.725-1009A>C (n.725-1009A>C)
 dbSNP
2g.176093471A>GCA349353041HOXD13c.581A>G (p.Gln194Arg)
c.725-1009A>G (n.725-1009A>G)
 dbSNP gnomAD v4
2g.176093471A>TCA349353040HOXD13c.581A>T (p.Gln194Leu)
c.725-1009A>T (n.725-1009A>T)
 dbSNP
2g.176093472G>ACA430224577HOXD13c.582G>A (p.Gln194=)
c.725-1008G>A (n.725-1008G>A)
2g.176093472G>CCA349353042HOXD13c.582G>C (p.Gln194His)
c.725-1008G>C (n.725-1008G>C)
2g.176093472G>TCA349353043HOXD13c.582G>T (p.Gln194His)
c.725-1008G>T (n.725-1008G>T)
2g.176093473G>ACA349353044HOXD13c.583G>A (p.Gly195Ser)
c.725-1007G>A (n.725-1007G>A)
 dbSNP gnomAD v4 COSMIC COSMIC
2g.176093473G>CCA349353045HOXD13c.583G>C (p.Gly195Arg)
c.725-1007G>C (n.725-1007G>C)
 dbSNP
2g.176093473G>TCA349353046HOXD13c.583G>T (p.Gly195Cys)
c.725-1007G>T (n.725-1007G>T)
 COSMIC
2g.176093474G>ACA349353047HOXD13c.584G>A (p.Gly195Asp)
c.725-1006G>A (n.725-1006G>A)
 dbSNP
2g.176093474G>CCA349353048HOXD13c.584G>C (p.Gly195Ala)
c.725-1006G>C (n.725-1006G>C)
 dbSNP
2g.176093474G=CA1309431446HOXD13c.584G= (p.Gly195=)
c.725-1006G= (n.725-1006G=)
2g.176093474G>TCA349353049HOXD13c.584G>T (p.Gly195Val)
c.725-1006G>T (n.725-1006G>T)
 dbSNP
2g.176093475C>ACA430224578HOXD13c.585C>A (p.Gly195=)
c.725-1005C>A (n.725-1005C>A)
 dbSNP gnomAD v4
2g.176093475C>GCA430224579HOXD13c.585C>G (p.Gly195=)
c.725-1005C>G (n.725-1005C>G)
 dbSNP
2g.176093475C>TCA430224580HOXD13c.585C>T (p.Gly195=)
c.725-1005C>T (n.725-1005C>T)
 dbSNP gnomAD v3 gnomAD v4
2g.176093476T>ACA349353050HOXD13c.586T>A (p.Tyr196Asn)
c.725-1004T>A (n.725-1004T>A)
 dbSNP
2g.176093476T>CCA349353051HOXD13c.586T>C (p.Tyr196His)
c.725-1004T>C (n.725-1004T>C)
2g.176093476T>GCA349353052HOXD13c.586T>G (p.Tyr196Asp)
c.725-1004T>G (n.725-1004T>G)
2g.176093477A>CCA349353053HOXD13c.587A>C (p.Tyr196Ser)
c.725-1003A>C (n.725-1003A>C)
 dbSNP gnomAD v4
2g.176093477A>GCA349353055HOXD13c.587A>G (p.Tyr196Cys)
c.725-1003A>G (n.725-1003A>G)
 dbSNP
2g.176093477A>TCA349353054HOXD13c.587A>T (p.Tyr196Phe)
c.725-1003A>T (n.725-1003A>T)
 dbSNP
2g.176093478T>ACA349353056HOXD13c.588T>A (p.Tyr196Ter)
c.725-1002T>A (n.725-1002T>A)
 dbSNP
2g.176093478T>CCA430224581HOXD13c.588T>C (p.Tyr196=)
c.725-1002T>C (n.725-1002T>C)
 dbSNP gnomAD v2 gnomAD v4
2g.176093478T>GCA349353057HOXD13c.588T>G (p.Tyr196Ter)
c.725-1002T>G (n.725-1002T>G)
2g.176093478T=CA1309431447HOXD13c.588T= (p.Tyr196=)
c.725-1002T= (n.725-1002T=)
2g.176093479A=CA1309431448HOXD13c.589A= (p.Thr197=)
c.725-1001A= (n.725-1001A=)
2g.176093479A>CCA349353058HOXD13c.589A>C (p.Thr197Pro)
c.725-1001A>C (n.725-1001A>C)
 dbSNP
2g.176093479A>GCA349353059HOXD13c.589A>G (p.Thr197Ala)
c.725-1001A>G (n.725-1001A>G)
 dbSNP gnomAD v4
2g.176093479A>TCA1976633HOXD13c.589A>T (p.Thr197Ser)
c.725-1001A>T (n.725-1001A>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093480C>ACA349353060HOXD13c.590C>A (p.Thr197Lys)
c.725-1000C>A (n.725-1000C>A)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
2g.176093480C=CA1309431449HOXD13c.590C= (p.Thr197=)
c.725-1000C= (n.725-1000C=)
2g.176093480C>GCA349353061HOXD13c.590C>G (p.Thr197Arg)
c.725-1000C>G (n.725-1000C>G)
 dbSNP
2g.176093480C>TCA349353062HOXD13c.590C>T (p.Thr197Met)
c.725-1000C>T (n.725-1000C>T)
 dbSNP COSMIC
2g.176093481G>ACA430224584HOXD13c.591G>A (p.Thr197=)
c.725-999G>A (n.725-999G>A)
 dbSNP
2g.176093481G>CCA430224583HOXD13c.591G>C (p.Thr197=)
c.725-999G>C (n.725-999G>C)
 dbSNP COSMIC
2g.176093481G=CA1309431450HOXD13c.591G= (p.Thr197=)
c.725-999G= (n.725-999G=)
2g.176093481G>TCA430224582HOXD13c.591G>T (p.Thr197=)
c.725-999G>T (n.725-999G>T)
 dbSNP
2g.176093482A=CA1309431451HOXD13c.592A= (p.Ser198=)
c.725-998A= (n.725-998A=)
2g.176093482A>CCA349353064HOXD13c.592A>C (p.Ser198Arg)
c.725-998A>C (n.725-998A>C)
2g.176093482A>GCA349353065HOXD13c.592A>G (p.Ser198Gly)
c.725-998A>G (n.725-998A>G)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093482A>TCA349353063HOXD13c.592A>T (p.Ser198Cys)
c.725-998A>T (n.725-998A>T)
 dbSNP
2g.176093483G>ACA349353066HOXD13c.593G>A (p.Ser198Asn)
c.725-997G>A (n.725-997G>A)
2g.176093483G>CCA349353067HOXD13c.593G>C (p.Ser198Thr)
c.725-997G>C (n.725-997G>C)
2g.176093483G>TCA349353068HOXD13c.593G>T (p.Ser198Ile)
c.725-997G>T (n.725-997G>T)
2g.176093484C>ACA349353069HOXD13c.594C>A (p.Ser198Arg)
c.725-996C>A (n.725-996C>A)
 dbSNP
2g.176093484C>GCA349353070HOXD13c.594C>G (p.Ser198Arg)
c.725-996C>G (n.725-996C>G)
 dbSNP
2g.176093484C>TCA430224585HOXD13c.594C>T (p.Ser198=)
c.725-996C>T (n.725-996C>T)
 dbSNP
2g.176093485C>ACA349353071HOXD13c.595C>A (p.Pro199Thr)
c.725-995C>A (n.725-995C>A)
2g.176093485C>GCA349353072HOXD13c.595C>G (p.Pro199Ala)
c.725-995C>G (n.725-995C>G)
2g.176093485C>TCA349353073HOXD13c.595C>T (p.Pro199Ser)
c.725-995C>T (n.725-995C>T)
2g.176093486C>ACA349353074HOXD13c.596C>A (p.Pro199His)
c.725-994C>A (n.725-994C>A)
2g.176093486C=CA1309431452HOXD13c.596C= (p.Pro199=)
c.725-994C= (n.725-994C=)
2g.176093486C>GCA349353075HOXD13c.596C>G (p.Pro199Arg)
c.725-994C>G (n.725-994C>G)
2g.176093486C>TCA349353076HOXD13c.596C>T (p.Pro199Leu)
c.725-994C>T (n.725-994C>T)
 dbSNP
2g.176093487T>ACA430224588HOXD13c.597T>A (p.Pro199=)
c.725-993T>A (n.725-993T>A)
2g.176093487T>CCA430224586HOXD13c.597T>C (p.Pro199=)
c.725-993T>C (n.725-993T>C)
 dbSNP
2g.176093487T>GCA430224587HOXD13c.597T>G (p.Pro199=)
c.725-993T>G (n.725-993T>G)
2g.176093488dupCA2662046506HOXD13c.598dup (p.Tyr200LeufsTer?)
c.725-992dup (n.725-992dup)
 gnomAD v4
2g.176093488T>ACA349353079HOXD13c.598T>A (p.Tyr200Asn)
c.725-992T>A (n.725-992T>A)
 dbSNP
2g.176093488T>CCA349353078HOXD13c.598T>C (p.Tyr200His)
c.725-992T>C (n.725-992T>C)
2g.176093488T>GCA349353077HOXD13c.598T>G (p.Tyr200Asp)
c.725-992T>G (n.725-992T>G)
2g.176093489A=CA1309431453HOXD13c.599A= (p.Tyr200=)
c.725-991A= (n.725-991A=)
2g.176093489A>CCA1976634HOXD13c.599A>C (p.Tyr200Ser)
c.725-991A>C (n.725-991A>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093489A>GCA349353080HOXD13c.599A>G (p.Tyr200Cys)
c.725-991A>G (n.725-991A>G)
 gnomAD v4
2g.176093489A>TCA349353081HOXD13c.599A>T (p.Tyr200Phe)
c.725-991A>T (n.725-991A>T)
2g.176093490C>ACA349353082HOXD13c.600C>A (p.Tyr200Ter)
c.725-990C>A (n.725-990C>A)
 dbSNP
2g.176093490C=CA1309431454HOXD13c.600C= (p.Tyr200=)
c.725-990C= (n.725-990C=)
2g.176093490C>GCA349353083HOXD13c.600C>G (p.Tyr200Ter)
c.725-990C>G (n.725-990C>G)
 dbSNP
2g.176093490C>TCA430224589HOXD13c.600C>T (p.Tyr200=)
c.725-990C>T (n.725-990C>T)
 dbSNP
2g.176093490_176093491insTCA1309431455HOXD13c.600_601insT (p.Gln201SerfsTer?)
c.725-990_725-989insT (n.725-990_725-989insT)
 dbSNP
2g.176093491C>ACA349353084HOXD13c.601C>A (p.Gln201Lys)
c.725-989C>A (n.725-989C>A)
 dbSNP gnomAD v2 gnomAD v4
2g.176093491C=CA1309431456HOXD13c.601C= (p.Gln201=)
c.725-989C= (n.725-989C=)
2g.176093491C>GCA349353085HOXD13c.601C>G (p.Gln201Glu)
c.725-989C>G (n.725-989C>G)
2g.176093491C>TCA349353086HOXD13c.601C>T (p.Gln201Ter)
c.725-989C>T (n.725-989C>T)
 dbSNP
2g.176093492A=CA1309431457HOXD13c.602A= (p.Gln201=)
c.725-988A= (n.725-988A=)
2g.176093492A>CCA349353087HOXD13c.602A>C (p.Gln201Pro)
c.725-988A>C (n.725-988A>C)
2g.176093492A>GCA1976635HOXD13c.602A>G (p.Gln201Arg)
c.725-988A>G (n.725-988A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093492A>TCA349353088HOXD13c.602A>T (p.Gln201Leu)
c.725-988A>T (n.725-988A>T)
 dbSNP
2g.176093493G>ACA430224590HOXD13c.603G>A (p.Gln201=)
c.725-987G>A (n.725-987G>A)
 dbSNP COSMIC
2g.176093493G>CCA349353089HOXD13c.603G>C (p.Gln201His)
c.725-987G>C (n.725-987G>C)
 dbSNP
2g.176093493G>TCA349353090HOXD13c.603G>T (p.Gln201His)
c.725-987G>T (n.725-987G>T)
 dbSNP
2g.176093494C>ACA349353092HOXD13c.604C>A (p.His202Asn)
c.725-986C>A (n.725-986C>A)
2g.176093494C>GCA349353093HOXD13c.604C>G (p.His202Asp)
c.725-986C>G (n.725-986C>G)
 dbSNP
2g.176093494C>TCA349353091HOXD13c.604C>T (p.His202Tyr)
c.725-986C>T (n.725-986C>T)
 dbSNP
2g.176093495A=CA1309431458HOXD13c.605A= (p.His202=)
c.725-985A= (n.725-985A=)
2g.176093495A>CCA1976636HOXD13c.605A>C (p.His202Pro)
c.725-985A>C (n.725-985A>C)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093495A>GCA349353094HOXD13c.605A>G (p.His202Arg)
c.725-985A>G (n.725-985A>G)
2g.176093495A>TCA349353095HOXD13c.605A>T (p.His202Leu)
c.725-985A>T (n.725-985A>T)
 dbSNP
2g.176093496C>ACA349353096HOXD13c.606C>A (p.His202Gln)
c.725-984C>A (n.725-984C>A)
 dbSNP
2g.176093496C=CA1309431459HOXD13c.606C= (p.His202=)
c.725-984C= (n.725-984C=)
2g.176093496C>GCA349353097HOXD13c.606C>G (p.His202Gln)
c.725-984C>G (n.725-984C>G)
 dbSNP
2g.176093496C>TCA430224591HOXD13c.606C>T (p.His202=)
c.725-984C>T (n.725-984C>T)
 dbSNP gnomAD v2 gnomAD v4
2g.176093497delCA430224592HOXD13c.607del (p.Val203CysfsTer?)
c.725-983del (n.725-983del)
 COSMIC
2g.176093497G>ACA349353098HOXD13c.607G>A (p.Val203Met)
c.725-983G>A (n.725-983G>A)
 ClinVar dbSNP gnomAD v2 gnomAD v4
2g.176093497G>CCA349353099HOXD13c.607G>C (p.Val203Leu)
c.725-983G>C (n.725-983G>C)
 dbSNP gnomAD v4
2g.176093497G=CA1309431460HOXD13c.607G= (p.Val203=)
c.725-983G= (n.725-983G=)
2g.176093497G>TCA349353100HOXD13c.607G>T (p.Val203Leu)
c.725-983G>T (n.725-983G>T)
2g.176093498T>ACA349353101HOXD13c.608T>A (p.Val203Glu)
c.725-982T>A (n.725-982T>A)
 dbSNP
2g.176093498T>CCA349353102HOXD13c.608T>C (p.Val203Ala)
c.725-982T>C (n.725-982T>C)
2g.176093498T>GCA349353103HOXD13c.608T>G (p.Val203Gly)
c.725-982T>G (n.725-982T>G)
2g.176093499G>ACA430224593HOXD13c.609G>A (p.Val203=)
c.725-981G>A (n.725-981G>A)
 dbSNP
2g.176093499G>CCA430224594HOXD13c.609G>C (p.Val203=)
c.725-981G>C (n.725-981G>C)
 dbSNP
2g.176093499G=CA1309431461HOXD13c.609G= (p.Val203=)
c.725-981G= (n.725-981G=)
2g.176093499G>TCA430224595HOXD13c.609G>T (p.Val203=)
c.725-981G>T (n.725-981G>T)
 dbSNP gnomAD v2
2g.176093500C>ACA349353104HOXD13c.610C>A (p.Pro204Thr)
c.725-980C>A (n.725-980C>A)
 dbSNP
2g.176093500C=CA1309431462HOXD13c.610C= (p.Pro204=)
c.725-980C= (n.725-980C=)
2g.176093500C>GCA349353105HOXD13c.610C>G (p.Pro204Ala)
c.725-980C>G (n.725-980C>G)
 dbSNP gnomAD v3 gnomAD v4
2g.176093500C>TCA60846486HOXD13c.610C>T (p.Pro204Ser)
c.725-980C>T (n.725-980C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093502delCA2586965142HOXD13c.612del (p.Gly205AlafsTer?)
c.725-978del (n.725-978del)
2g.176093501C>ACA349353106HOXD13c.611C>A (p.Pro204His)
c.725-979C>A (n.725-979C>A)
 gnomAD v4
2g.176093501C>GCA349353108HOXD13c.611C>G (p.Pro204Arg)
c.725-979C>G (n.725-979C>G)
 dbSNP
2g.176093501C>TCA349353107HOXD13c.611C>T (p.Pro204Leu)
c.725-979C>T (n.725-979C>T)
 COSMIC COSMIC
2g.176093502C>ACA430224596HOXD13c.612C>A (p.Pro204=)
c.725-978C>A (n.725-978C>A)
 COSMIC COSMIC
2g.176093502C>GCA430224597HOXD13c.612C>G (p.Pro204=)
c.725-978C>G (n.725-978C>G)
2g.176093502C>TCA430224598HOXD13c.612C>T (p.Pro204=)
c.725-978C>T (n.725-978C>T)
 gnomAD v4
2g.176093503G>ACA1976637HOXD13c.613G>A (p.Gly205Ser)
c.725-977G>A (n.725-977G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093503G>CCA349353109HOXD13c.613G>C (p.Gly205Arg)
c.725-977G>C (n.725-977G>C)
2g.176093503G=CA1309431463HOXD13c.613G= (p.Gly205=)
c.725-977G= (n.725-977G=)
2g.176093503G>TCA349353110HOXD13c.613G>T (p.Gly205Cys)
c.725-977G>T (n.725-977G>T)
2g.176093504G>ACA349353111HOXD13c.614G>A (p.Gly205Asp)
c.725-976G>A (n.725-976G>A)
 dbSNP COSMIC COSMIC
2g.176093504G>CCA349353112HOXD13c.614G>C (p.Gly205Ala)
c.725-976G>C (n.725-976G>C)
 dbSNP gnomAD v4
2g.176093504G>TCA349353113HOXD13c.614G>T (p.Gly205Val)
c.725-976G>T (n.725-976G>T)
2g.176093505C>ACA430224599HOXD13c.615C>A (p.Gly205=)
c.725-975C>A (n.725-975C>A)
2g.176093505C=CA1309431464HOXD13c.615C= (p.Gly205=)
c.725-975C= (n.725-975C=)
2g.176093505C>GCA430224600HOXD13c.615C>G (p.Gly205=)
c.725-975C>G (n.725-975C>G)
2g.176093505C>TCA60846502HOXD13c.615C>T (p.Gly205=)
c.725-975C>T (n.725-975C>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093506T>ACA349353114HOXD13c.616T>A (p.Tyr206Asn)
c.725-974T>A (n.725-974T>A)
 dbSNP
2g.176093506T>CCA349353115HOXD13c.616T>C (p.Tyr206His)
c.725-974T>C (n.725-974T>C)
2g.176093506T>GCA349353116HOXD13c.616T>G (p.Tyr206Asp)
c.725-974T>G (n.725-974T>G)
2g.176093507A=CA1309431465HOXD13c.617A= (p.Tyr206=)
c.725-973A= (n.725-973A=)
2g.176093507A>CCA349353118HOXD13c.617A>C (p.Tyr206Ser)
c.725-973A>C (n.725-973A>C)
2g.176093507A>GCA1976638HOXD13c.617A>G (p.Tyr206Cys)
c.725-973A>G (n.725-973A>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093507A>TCA349353117HOXD13c.617A>T (p.Tyr206Phe)
c.725-973A>T (n.725-973A>T)
 dbSNP
2g.176093508T>ACA349353119HOXD13c.618T>A (p.Tyr206Ter)
c.725-972T>A (n.725-972T>A)
 dbSNP
2g.176093508T>CCA430224601HOXD13c.618T>C (p.Tyr206=)
c.725-972T>C (n.725-972T>C)
2g.176093508T>GCA349353120HOXD13c.618T>G (p.Tyr206Ter)
c.725-972T>G (n.725-972T>G)
2g.176093509A=CA1309431466HOXD13c.619A= (p.Ile207=)
c.725-971A= (n.725-971A=)
2g.176093509A>CCA349353121HOXD13c.619A>C (p.Ile207Leu)
c.725-971A>C (n.725-971A>C)
 dbSNP
2g.176093509A>GCA1976639HOXD13c.619A>G (p.Ile207Val)
c.725-971A>G (n.725-971A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093509A>TCA349353122HOXD13c.619A>T (p.Ile207Phe)
c.725-971A>T (n.725-971A>T)
 dbSNP
2g.176093510T>ACA349353123HOXD13c.620T>A (p.Ile207Asn)
c.725-970T>A (n.725-970T>A)
 gnomAD v4
2g.176093510T>CCA349353124HOXD13c.620T>C (p.Ile207Thr)
c.725-970T>C (n.725-970T>C)
 dbSNP gnomAD v4
2g.176093510T>GCA349353125HOXD13c.620T>G (p.Ile207Ser)
c.725-970T>G (n.725-970T>G)
2g.176093511C>ACA430224602HOXD13c.621C>A (p.Ile207=)
c.725-969C>A (n.725-969C>A)
 dbSNP
2g.176093511C>GCA349353126HOXD13c.621C>G (p.Ile207Met)
c.725-969C>G (n.725-969C>G)
 dbSNP
2g.176093511C>TCA430224603HOXD13c.621C>T (p.Ile207=)
c.725-969C>T (n.725-969C>T)
 dbSNP gnomAD v4
2g.176093512G>ACA349353127HOXD13c.622G>A (p.Asp208Asn)
c.725-968G>A (n.725-968G>A)
 dbSNP COSMIC
2g.176093512G>CCA349353128HOXD13c.622G>C (p.Asp208His)
c.725-968G>C (n.725-968G>C)
 dbSNP
2g.176093512G>TCA349353129HOXD13c.622G>T (p.Asp208Tyr)
c.725-968G>T (n.725-968G>T)
2g.176093513A>CCA349353131HOXD13c.623A>C (p.Asp208Ala)
c.725-967A>C (n.725-967A>C)
 dbSNP
2g.176093513A>GCA349353132HOXD13c.623A>G (p.Asp208Gly)
c.725-967A>G (n.725-967A>G)
 dbSNP
2g.176093513A>TCA349353130HOXD13c.623A>T (p.Asp208Val)
c.725-967A>T (n.725-967A>T)
 ClinVar dbSNP
2g.176093514C>ACA349353133HOXD13c.624C>A (p.Asp208Glu)
c.725-966C>A (n.725-966C>A)
 dbSNP
2g.176093514C>GCA349353134HOXD13c.624C>G (p.Asp208Glu)
c.725-966C>G (n.725-966C>G)
 dbSNP
2g.176093514C>TCA430224604HOXD13c.624C>T (p.Asp208=)
c.725-966C>T (n.725-966C>T)
2g.176093515A=CA1309431467HOXD13c.625A= (p.Met209=)
c.725-965A= (n.725-965A=)
2g.176093515A>CCA349353135HOXD13c.625A>C (p.Met209Leu)
c.725-965A>C (n.725-965A>C)
 dbSNP gnomAD v4
2g.176093515A>GCA1976640HOXD13c.625A>G (p.Met209Val)
c.725-965A>G (n.725-965A>G)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093515A>TCA349353136HOXD13c.625A>T (p.Met209Leu)
c.725-965A>T (n.725-965A>T)
 dbSNP
2g.176093515_176093518delinsATGGCA1309431468HOXD13c.625_628delinsATGG (p.Met209=)
c.725-965_725-962delinsATGG (n.725-965_725-962delinsATGG)
2g.176093516T>ACA349353139HOXD13c.626T>A (p.Met209Lys)
c.725-964T>A (n.725-964T>A)
 dbSNP
2g.176093516T>CCA349353137HOXD13c.626T>C (p.Met209Thr)
c.725-964T>C (n.725-964T>C)
2g.176093516T>GCA349353138HOXD13c.626T>G (p.Met209Arg)
c.725-964T>G (n.725-964T>G)
2g.176093518_176093520delCA537975473HOXD13c.628_630del (p.Val210del)
c.725-962_725-960del (n.725-962_725-960del)
 dbSNP gnomAD v2 gnomAD v4
2g.176093517G>ACA349353140HOXD13c.627G>A (p.Met209Ile)
c.725-963G>A (n.725-963G>A)
 dbSNP gnomAD v2 gnomAD v4
2g.176093517G>CCA349353141HOXD13c.627G>C (p.Met209Ile)
c.725-963G>C (n.725-963G>C)
 dbSNP
2g.176093517G=CA1309431469HOXD13c.627G= (p.Met209=)
c.725-963G= (n.725-963G=)
2g.176093517G>TCA349353142HOXD13c.627G>T (p.Met209Ile)
c.725-963G>T (n.725-963G>T)
2g.176093518G>ACA349353143HOXD13c.628G>A (p.Val210Met)
c.725-962G>A (n.725-962G>A)
2g.176093518G>CCA349353144HOXD13c.628G>C (p.Val210Leu)
c.725-962G>C (n.725-962G>C)
 dbSNP
2g.176093518G>TCA349353145HOXD13c.628G>T (p.Val210Leu)
c.725-962G>T (n.725-962G>T)
2g.176093519T>ACA349353147HOXD13c.629T>A (p.Val210Glu)
c.725-961T>A (n.725-961T>A)
2g.176093519T>CCA60846528HOXD13c.629T>C (p.Val210Ala)
c.725-961T>C (n.725-961T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093519T>GCA349353146HOXD13c.629T>G (p.Val210Gly)
c.725-961T>G (n.725-961T>G)
2g.176093519T=CA1309431470HOXD13c.629T= (p.Val210=)
c.725-961T= (n.725-961T=)
2g.176093520G>ACA430224605HOXD13c.630G>A (p.Val210=)
c.725-960G>A (n.725-960G>A)
 dbSNP
2g.176093520G>CCA430224606HOXD13c.630G>C (p.Val210=)
c.725-960G>C (n.725-960G>C)
 dbSNP
2g.176093520G>TCA430224607HOXD13c.630G>T (p.Val210=)
c.725-960G>T (n.725-960G>T)
2g.176093521T>ACA349353149HOXD13c.631T>A (p.Ser211Thr)
c.725-959T>A (n.725-959T>A)
2g.176093521T>CCA349353148HOXD13c.631T>C (p.Ser211Pro)
c.725-959T>C (n.725-959T>C)
2g.176093521T>GCA349353150HOXD13c.631T>G (p.Ser211Ala)
c.725-959T>G (n.725-959T>G)
2g.176093522C>ACA349353151HOXD13c.632C>A (p.Ser211Tyr)
c.725-958C>A (n.725-958C>A)
2g.176093522C>GCA349353152HOXD13c.632C>G (p.Ser211Cys)
c.725-958C>G (n.725-958C>G)
 gnomAD v4
2g.176093522C>TCA349353153HOXD13c.632C>T (p.Ser211Phe)
c.725-958C>T (n.725-958C>T)
2g.176093523delCA2701097024HOXD13c.633del (p.Thr212LeufsTer?)
c.725-957del (n.725-957del)
 dbSNP
2g.176093523C>ACA430224608HOXD13c.633C>A (p.Ser211=)
c.725-957C>A (n.725-957C>A)
2g.176093523C=CA1309431471HOXD13c.633C= (p.Ser211=)
c.725-957C= (n.725-957C=)
2g.176093523C>GCA430224609HOXD13c.633C>G (p.Ser211=)
c.725-957C>G (n.725-957C>G)
2g.176093523C>TCA430224610HOXD13c.633C>T (p.Ser211=)
c.725-957C>T (n.725-957C>T)
 dbSNP gnomAD v4
2g.176093523_176093524insGGGGCTATATCGCA2662046507HOXD13c.633_634insGGGGCTATATCG (p.Ser211_Thr212insGlyAlaIleSer)
c.725-957_725-956insGGGGCTATATCG (n.725-957_725-956insGGGGCTATATCG)
 gnomAD v4
2g.176093524delCA2701097050HOXD13c.634del (p.Thr212LeufsTer?)
c.725-956del (n.725-956del)
 dbSNP
2g.176093524A>CCA349353154HOXD13c.634A>C (p.Thr212Pro)
c.725-956A>C (n.725-956A>C)
 dbSNP
2g.176093524A>GCA349353155HOXD13c.634A>G (p.Thr212Ala)
c.725-956A>G (n.725-956A>G)
 dbSNP
2g.176093524A>TCA349353156HOXD13c.634A>T (p.Thr212Ser)
c.725-956A>T (n.725-956A>T)
 dbSNP
2g.176093525C>ACA349353157HOXD13c.635C>A (p.Thr212Asn)
c.725-955C>A (n.725-955C>A)
2g.176093525C>GCA349353158HOXD13c.635C>G (p.Thr212Ser)
c.725-955C>G (n.725-955C>G)
2g.176093525C>TCA349353159HOXD13c.635C>T (p.Thr212Ile)
c.725-955C>T (n.725-955C>T)
2g.176093526T>ACA430224611HOXD13c.636T>A (p.Thr212=)
c.725-954T>A (n.725-954T>A)
2g.176093526T>CCA430224613HOXD13c.636T>C (p.Thr212=)
c.725-954T>C (n.725-954T>C)
2g.176093526T>GCA430224612HOXD13c.636T>G (p.Thr212=)
c.725-954T>G (n.725-954T>G)
2g.176093527T>ACA349353160HOXD13c.637T>A (p.Phe213Ile)
c.725-953T>A (n.725-953T>A)
 dbSNP
2g.176093527T>CCA349353161HOXD13c.637T>C (p.Phe213Leu)
c.725-953T>C (n.725-953T>C)
 dbSNP
2g.176093527T>GCA349353162HOXD13c.637T>G (p.Phe213Val)
c.725-953T>G (n.725-953T>G)
2g.176093528T>ACA349353164HOXD13c.638T>A (p.Phe213Tyr)
c.725-952T>A (n.725-952T>A)
 gnomAD v4
2g.176093528T>CCA60846553HOXD13c.638T>C (p.Phe213Ser)
c.725-952T>C (n.725-952T>C)
 dbSNP
2g.176093528T>GCA349353163HOXD13c.638T>G (p.Phe213Cys)
c.725-952T>G (n.725-952T>G)
2g.176093528T=CA1309431472HOXD13c.638T= (p.Phe213=)
c.725-952T= (n.725-952T=)
2g.176093529C>ACA349353165HOXD13c.639C>A (p.Phe213Leu)
c.725-951C>A (n.725-951C>A)
 dbSNP
2g.176093529C>GCA349353166HOXD13c.639C>G (p.Phe213Leu)
c.725-951C>G (n.725-951C>G)
 dbSNP gnomAD v4
2g.176093529C>TCA430224614HOXD13c.639C>T (p.Phe213=)
c.725-951C>T (n.725-951C>T)
 dbSNP gnomAD v4 COSMIC
2g.176093531_176093551delCA2701097511HOXD13c.641_661del (p.Gly214_His220del)
c.725-949_725-929del (n.725-949_725-929del)
 dbSNP
2g.176093530G>ACA349353167HOXD13c.640G>A (p.Gly214Ser)
c.725-950G>A (n.725-950G>A)
 dbSNP
2g.176093530G>CCA349353168HOXD13c.640G>C (p.Gly214Arg)
c.725-950G>C (n.725-950G>C)
2g.176093530G=CA1309431473HOXD13c.640G= (p.Gly214=)
c.725-950G= (n.725-950G=)
2g.176093530G>TCA349353169HOXD13c.640G>T (p.Gly214Cys)
c.725-950G>T (n.725-950G>T)
2g.176093531G>ACA349353170HOXD13c.641G>A (p.Gly214Asp)
c.725-949G>A (n.725-949G>A)
 dbSNP
2g.176093531G>CCA349353171HOXD13c.641G>C (p.Gly214Ala)
c.725-949G>C (n.725-949G>C)
2g.176093531G>TCA349353172HOXD13c.641G>T (p.Gly214Val)
c.725-949G>T (n.725-949G>T)
2g.176093532C>ACA430224615HOXD13c.642C>A (p.Gly214=)
c.725-948C>A (n.725-948C>A)
 dbSNP
2g.176093532C=CA1309431474HOXD13c.642C= (p.Gly214=)
c.725-948C= (n.725-948C=)
2g.176093532C>GCA430224616HOXD13c.642C>G (p.Gly214=)
c.725-948C>G (n.725-948C>G)
 dbSNP
2g.176093532C>TCA1976641HOXD13c.642C>T (p.Gly214=)
c.725-948C>T (n.725-948C>T)
 dbSNP ExAC gnomAD v2
2g.176093533T>ACA349353173HOXD13c.643T>A (p.Ser215Thr)
c.725-947T>A (n.725-947T>A)
2g.176093533T>CCA349353174HOXD13c.643T>C (p.Ser215Pro)
c.725-947T>C (n.725-947T>C)
 dbSNP
2g.176093533T>GCA349353175HOXD13c.643T>G (p.Ser215Ala)
c.725-947T>G (n.725-947T>G)
2g.176093534C>ACA349353178HOXD13c.644C>A (p.Ser215Tyr)
c.725-946C>A (n.725-946C>A)
2g.176093534C=CA1309431475HOXD13c.644C= (p.Ser215=)
c.725-946C= (n.725-946C=)
2g.176093534C>GCA349353177HOXD13c.644C>G (p.Ser215Cys)
c.725-946C>G (n.725-946C>G)
 dbSNP
2g.176093534C>TCA349353176HOXD13c.644C>T (p.Ser215Phe)
c.725-946C>T (n.725-946C>T)
 dbSNP gnomAD v3 gnomAD v4
2g.176093535C>ACA430224619HOXD13c.645C>A (p.Ser215=)
c.725-945C>A (n.725-945C>A)
2g.176093535C>GCA430224618HOXD13c.645C>G (p.Ser215=)
c.725-945C>G (n.725-945C>G)
2g.176093535C>TCA430224617HOXD13c.645C>T (p.Ser215=)
c.725-945C>T (n.725-945C>T)
2g.176093536G>ACA349353179HOXD13c.646G>A (p.Gly216Arg)
c.725-944G>A (n.725-944G>A)
 gnomAD v4
2g.176093536G>CCA349353180HOXD13c.646G>C (p.Gly216Arg)
c.725-944G>C (n.725-944G>C)
2g.176093536G>TCA349353181HOXD13c.646G>T (p.Gly216Trp)
c.725-944G>T (n.725-944G>T)
 gnomAD v4
2g.176093537G>ACA349353182HOXD13c.647G>A (p.Gly216Glu)
c.725-943G>A (n.725-943G>A)
2g.176093537G>CCA349353183HOXD13c.647G>C (p.Gly216Ala)
c.725-943G>C (n.725-943G>C)
2g.176093537G>TCA349353184HOXD13c.647G>T (p.Gly216Val)
c.725-943G>T (n.725-943G>T)
2g.176093538G>ACA430224620HOXD13c.648G>A (p.Gly216=)
c.725-942G>A (n.725-942G>A)
 dbSNP gnomAD v4
2g.176093538G>CCA430224621HOXD13c.648G>C (p.Gly216=)
c.725-942G>C (n.725-942G>C)
 dbSNP
2g.176093538G=CA1309431476HOXD13c.648G= (p.Gly216=)
c.725-942G= (n.725-942G=)
2g.176093538G>TCA430224622HOXD13c.648G>T (p.Gly216=)
c.725-942G>T (n.725-942G>T)
 dbSNP gnomAD v2 gnomAD v4
2g.176093539G>ACA349353187HOXD13c.649G>A (p.Glu217Lys)
c.725-941G>A (n.725-941G>A)
 dbSNP COSMIC COSMIC
2g.176093539G>CCA349353185HOXD13c.649G>C (p.Glu217Gln)
c.725-941G>C (n.725-941G>C)
2g.176093539G=CA1309431477HOXD13c.649G= (p.Glu217=)
c.725-941G= (n.725-941G=)
2g.176093539G>TCA349353186HOXD13c.649G>T (p.Glu217Ter)
c.725-941G>T (n.725-941G>T)
2g.176093540A>CCA349353188HOXD13c.650A>C (p.Glu217Ala)
c.725-940A>C (n.725-940A>C)
2g.176093540A>GCA349353189HOXD13c.650A>G (p.Glu217Gly)
c.725-940A>G (n.725-940A>G)
 dbSNP
2g.176093540A>TCA349353190HOXD13c.650A>T (p.Glu217Val)
c.725-940A>T (n.725-940A>T)
2g.176093541G>ACA430224623HOXD13c.651G>A (p.Glu217=)
c.725-939G>A (n.725-939G>A)
 dbSNP gnomAD v4
2g.176093541G>CCA349353191HOXD13c.651G>C (p.Glu217Asp)
c.725-939G>C (n.725-939G>C)
 dbSNP gnomAD v2
2g.176093541G=CA1309431478HOXD13c.651G= (p.Glu217=)
c.725-939G= (n.725-939G=)
2g.176093541G>TCA349353192HOXD13c.651G>T (p.Glu217Asp)
c.725-939G>T (n.725-939G>T)
2g.176093542C>ACA349353193HOXD13c.652C>A (p.Pro218Thr)
c.725-938C>A (n.725-938C>A)
2g.176093542C=CA1309431479HOXD13c.652C= (p.Pro218=)
c.725-938C= (n.725-938C=)
2g.176093542C>GCA349353195HOXD13c.652C>G (p.Pro218Ala)
c.725-938C>G (n.725-938C>G)
2g.176093542C>TCA349353194HOXD13c.652C>T (p.Pro218Ser)
c.725-938C>T (n.725-938C>T)
 dbSNP
2g.176093543delCA2577165630HOXD13c.653del (p.Pro218LeufsTer?)
c.725-937del (n.725-937del)
2g.176093543C>ACA349353196HOXD13c.653C>A (p.Pro218His)
c.725-937C>A (n.725-937C>A)
 dbSNP
2g.176093543C>GCA349353197HOXD13c.653C>G (p.Pro218Arg)
c.725-937C>G (n.725-937C>G)
2g.176093543C>TCA349353198HOXD13c.653C>T (p.Pro218Leu)
c.725-937C>T (n.725-937C>T)
 dbSNP gnomAD v4
2g.176093544T>ACA430224624HOXD13c.654T>A (p.Pro218=)
c.725-936T>A (n.725-936T>A)
2g.176093544T>CCA430224625HOXD13c.654T>C (p.Pro218=)
c.725-936T>C (n.725-936T>C)
2g.176093544T>GCA430224626HOXD13c.654T>G (p.Pro218=)
c.725-936T>G (n.725-936T>G)
2g.176093545C>ACA430224627HOXD13c.655C>A (p.Arg219=)
c.725-935C>A (n.725-935C>A)
2g.176093545C=CA1309431480HOXD13c.655C= (p.Arg219=)
c.725-935C= (n.725-935C=)
2g.176093545C>GCA349353199HOXD13c.655C>G (p.Arg219Gly)
c.725-935C>G (n.725-935C>G)
2g.176093545C>TCA349353200HOXD13c.655C>T (p.Arg219Trp)
c.725-935C>T (n.725-935C>T)
 dbSNP

Number of alleles fetched