Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.176093385_176093390delCA2577165627HOXD13c.495_500del (p.Glu165_Tyr167delinsAsp)
c.725-1095_725-1090del (n.725-1095_725-1090del)
2g.176093390A=CA1309431401HOXD13c.500A= (p.Tyr167=)
c.725-1090A= (n.725-1090A=)
2g.176093390A>CCA349352872HOXD13c.500A>C (p.Tyr167Ser)
c.725-1090A>C (n.725-1090A>C)
2g.176093390A>GCA249106HOXD13c.500A>G (p.Tyr167Cys)
c.725-1090A>G (n.725-1090A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093390A>TCA349352873HOXD13c.500A>T (p.Tyr167Phe)
c.725-1090A>T (n.725-1090A>T)
2g.176093391C>ACA349352874HOXD13c.501C>A (p.Tyr167Ter)
c.725-1089C>A (n.725-1089C>A)
2g.176093391C>GCA349352875HOXD13c.501C>G (p.Tyr167Ter)
c.725-1089C>G (n.725-1089C>G)
dbSNP
2g.176093391C>TCA430224522HOXD13c.501C>T (p.Tyr167=)
c.725-1089C>T (n.725-1089C>T)
dbSNP gnomAD v4
2g.176093392A=CA1309431402HOXD13c.502A= (p.Met168=)
c.725-1088A= (n.725-1088A=)
2g.176093392A>CCA349352876HOXD13c.502A>C (p.Met168Leu)
c.725-1088A>C (n.725-1088A>C)
2g.176093392A>GCA1976615HOXD13c.502A>G (p.Met168Val)
c.725-1088A>G (n.725-1088A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093392A>TCA349352877HOXD13c.502A>T (p.Met168Leu)
c.725-1088A>T (n.725-1088A>T)
dbSNP
2g.176093393T>ACA349352878HOXD13c.503T>A (p.Met168Lys)
c.725-1087T>A (n.725-1087T>A)
2g.176093393T>CCA349352879HOXD13c.503T>C (p.Met168Thr)
c.725-1087T>C (n.725-1087T>C)
gnomAD v4
2g.176093393T>GCA349352880HOXD13c.503T>G (p.Met168Arg)
c.725-1087T>G (n.725-1087T>G)
gnomAD v4 COSMIC
2g.176093394G>ACA349352881HOXD13c.504G>A (p.Met168Ile)
c.725-1086G>A (n.725-1086G>A)
dbSNP
2g.176093394G>CCA349352882HOXD13c.504G>C (p.Met168Ile)
c.725-1086G>C (n.725-1086G>C)
dbSNP
2g.176093394G>TCA349352883HOXD13c.504G>T (p.Met168Ile)
c.725-1086G>T (n.725-1086G>T)
dbSNP
2g.176093395G>ACA349352885HOXD13c.505G>A (p.Asp169Asn)
c.725-1085G>A (n.725-1085G>A)
gnomAD v4
2g.176093395G>CCA349352886HOXD13c.505G>C (p.Asp169His)
c.725-1085G>C (n.725-1085G>C)
dbSNP
2g.176093395G>TCA349352884HOXD13c.505G>T (p.Asp169Tyr)
c.725-1085G>T (n.725-1085G>T)
dbSNP
2g.176093396A>CCA349352887HOXD13c.506A>C (p.Asp169Ala)
c.725-1084A>C (n.725-1084A>C)
dbSNP
2g.176093396A>GCA349352888HOXD13c.506A>G (p.Asp169Gly)
c.725-1084A>G (n.725-1084A>G)
dbSNP
2g.176093396A>TCA349352889HOXD13c.506A>T (p.Asp169Val)
c.725-1084A>T (n.725-1084A>T)
dbSNP
2g.176093397C>ACA1976616HOXD13c.507C>A (p.Asp169Glu)
c.725-1083C>A (n.725-1083C>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093397C=CA1309431403HOXD13c.507C= (p.Asp169=)
c.725-1083C= (n.725-1083C=)
2g.176093397C>GCA349352890HOXD13c.507C>G (p.Asp169Glu)
c.725-1083C>G (n.725-1083C>G)
dbSNP
2g.176093397C>TCA430224523HOXD13c.507C>T (p.Asp169=)
c.725-1083C>T (n.725-1083C>T)
dbSNP
2g.176093398G>ACA349352893HOXD13c.508G>A (p.Val170Met)
c.725-1082G>A (n.725-1082G>A)
dbSNP gnomAD v2 gnomAD v4
2g.176093398G>CCA349352892HOXD13c.508G>C (p.Val170Leu)
c.725-1082G>C (n.725-1082G>C)
dbSNP
2g.176093398G=CA1309431404HOXD13c.508G= (p.Val170=)
c.725-1082G= (n.725-1082G=)
2g.176093398G>TCA349352891HOXD13c.508G>T (p.Val170Leu)
c.725-1082G>T (n.725-1082G>T)
dbSNP
2g.176093399T>ACA349352894HOXD13c.509T>A (p.Val170Glu)
c.725-1081T>A (n.725-1081T>A)
dbSNP
2g.176093399T>CCA349352895HOXD13c.509T>C (p.Val170Ala)
c.725-1081T>C (n.725-1081T>C)
dbSNP
2g.176093399T>GCA349352896HOXD13c.509T>G (p.Val170Gly)
c.725-1081T>G (n.725-1081T>G)
dbSNP
2g.176093400G>ACA430224524HOXD13c.510G>A (p.Val170=)
c.725-1080G>A (n.725-1080G>A)
dbSNP gnomAD v3 gnomAD v4
2g.176093400G>CCA430224525HOXD13c.510G>C (p.Val170=)
c.725-1080G>C (n.725-1080G>C)
dbSNP
2g.176093400G=CA1309431405HOXD13c.510G= (p.Val170=)
c.725-1080G= (n.725-1080G=)
2g.176093400G>TCA430224526HOXD13c.510G>T (p.Val170=)
c.725-1080G>T (n.725-1080G>T)
2g.176093401T>ACA349352897HOXD13c.511T>A (p.Ser171Thr)
c.725-1079T>A (n.725-1079T>A)
dbSNP
2g.176093401T>CCA349352898HOXD13c.511T>C (p.Ser171Pro)
c.725-1079T>C (n.725-1079T>C)
dbSNP COSMIC
2g.176093401T>GCA349352899HOXD13c.511T>G (p.Ser171Ala)
c.725-1079T>G (n.725-1079T>G)
dbSNP
2g.176093402C>ACA349352900HOXD13c.512C>A (p.Ser171Ter)
c.725-1078C>A (n.725-1078C>A)
dbSNP
2g.176093402C=CA1309431406HOXD13c.512C= (p.Ser171=)
c.725-1078C= (n.725-1078C=)
2g.176093402C>GCA349352902HOXD13c.512C>G (p.Ser171Ter)
c.725-1078C>G (n.725-1078C>G)
dbSNP
2g.176093402C>TCA349352901HOXD13c.512C>T (p.Ser171Leu)
c.725-1078C>T (n.725-1078C>T)
dbSNP gnomAD v3 gnomAD v4
2g.176093403A=CA1309431407HOXD13c.513A= (p.Ser171=)
c.725-1077A= (n.725-1077A=)
2g.176093403A>CCA430224527HOXD13c.513A>C (p.Ser171=)
c.725-1077A>C (n.725-1077A>C)
2g.176093403A>GCA430224528HOXD13c.513A>G (p.Ser171=)
c.725-1077A>G (n.725-1077A>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093403A>TCA430224529HOXD13c.513A>T (p.Ser171=)
c.725-1077A>T (n.725-1077A>T)
dbSNP
2g.176093404G>ACA349352903HOXD13c.514G>A (p.Gly172Ser)
c.725-1076G>A (n.725-1076G>A)
dbSNP
2g.176093404G>CCA349352904HOXD13c.514G>C (p.Gly172Arg)
c.725-1076G>C (n.725-1076G>C)
dbSNP
2g.176093404G>TCA349352905HOXD13c.514G>T (p.Gly172Cys)
c.725-1076G>T (n.725-1076G>T)
2g.176093405G>ACA349352906HOXD13c.515G>A (p.Gly172Asp)
c.725-1075G>A (n.725-1075G>A)
dbSNP
2g.176093405G>CCA349352907HOXD13c.515G>C (p.Gly172Ala)
c.725-1075G>C (n.725-1075G>C)
dbSNP
2g.176093405G>TCA349352908HOXD13c.515G>T (p.Gly172Val)
c.725-1075G>T (n.725-1075G>T)
2g.176093406C>ACA430224530HOXD13c.516C>A (p.Gly172=)
c.725-1074C>A (n.725-1074C>A)
dbSNP gnomAD v4
2g.176093406C>GCA430224531HOXD13c.516C>G (p.Gly172=)
c.725-1074C>G (n.725-1074C>G)
dbSNP
2g.176093406C>TCA430224532HOXD13c.516C>T (p.Gly172=)
c.725-1074C>T (n.725-1074C>T)
dbSNP
2g.176093407C>ACA349352909HOXD13c.517C>A (p.Leu173Met)
c.725-1073C>A (n.725-1073C>A)
dbSNP
2g.176093407C>GCA349352910HOXD13c.517C>G (p.Leu173Val)
c.725-1073C>G (n.725-1073C>G)
dbSNP
2g.176093407C>TCA430224533HOXD13c.517C>T (p.Leu173=)
c.725-1073C>T (n.725-1073C>T)
dbSNP
2g.176093408T>ACA349352911HOXD13c.518T>A (p.Leu173Gln)
c.725-1072T>A (n.725-1072T>A)
2g.176093408T>CCA349352912HOXD13c.518T>C (p.Leu173Pro)
c.725-1072T>C (n.725-1072T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.176093408T>GCA349352913HOXD13c.518T>G (p.Leu173Arg)
c.725-1072T>G (n.725-1072T>G)
2g.176093408T=CA1309431408HOXD13c.518T= (p.Leu173=)
c.725-1072T= (n.725-1072T=)
2g.176093409G>ACA430224534HOXD13c.519G>A (p.Leu173=)
c.725-1071G>A (n.725-1071G>A)
dbSNP gnomAD v4
2g.176093409G>CCA430224536HOXD13c.519G>C (p.Leu173=)
c.725-1071G>C (n.725-1071G>C)
dbSNP
2g.176093409G=CA1309431409HOXD13c.519G= (p.Leu173=)
c.725-1071G= (n.725-1071G=)
2g.176093409G>TCA430224535HOXD13c.519G>T (p.Leu173=)
c.725-1071G>T (n.725-1071G>T)
dbSNP gnomAD v4
2g.176093410G>ACA1976617HOXD13c.520G>A (p.Ala174Thr)
c.725-1070G>A (n.725-1070G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093410G>CCA349352915HOXD13c.520G>C (p.Ala174Pro)
c.725-1070G>C (n.725-1070G>C)
dbSNP
2g.176093410G=CA1309431410HOXD13c.520G= (p.Ala174=)
c.725-1070G= (n.725-1070G=)
2g.176093410G>TCA349352914HOXD13c.520G>T (p.Ala174Ser)
c.725-1070G>T (n.725-1070G>T)
dbSNP
2g.176093411C>ACA1976618HOXD13c.521C>A (p.Ala174Glu)
c.725-1069C>A (n.725-1069C>A)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.176093411C=CA1309431411HOXD13c.521C= (p.Ala174=)
c.725-1069C= (n.725-1069C=)
2g.176093411C>GCA349352917HOXD13c.521C>G (p.Ala174Gly)
c.725-1069C>G (n.725-1069C>G)
dbSNP
2g.176093411C>TCA349352916HOXD13c.521C>T (p.Ala174Val)
c.725-1069C>T (n.725-1069C>T)
dbSNP gnomAD v4
2g.176093412G>ACA430224537HOXD13c.522G>A (p.Ala174=)
c.725-1068G>A (n.725-1068G>A)
dbSNP gnomAD v4
2g.176093412G>CCA430224538HOXD13c.522G>C (p.Ala174=)
c.725-1068G>C (n.725-1068G>C)
dbSNP gnomAD v4
2g.176093412G>TCA430224539HOXD13c.522G>T (p.Ala174=)
c.725-1068G>T (n.725-1068G>T)
2g.176093413A>CCA349352918HOXD13c.523A>C (p.Ser175Arg)
c.725-1067A>C (n.725-1067A>C)
2g.176093413A>GCA349352920HOXD13c.523A>G (p.Ser175Gly)
c.725-1067A>G (n.725-1067A>G)
dbSNP
2g.176093413A>TCA349352919HOXD13c.523A>T (p.Ser175Cys)
c.725-1067A>T (n.725-1067A>T)
dbSNP
2g.176093414G>ACA349352921HOXD13c.524G>A (p.Ser175Asn)
c.725-1066G>A (n.725-1066G>A)
dbSNP
2g.176093414G>CCA349352922HOXD13c.524G>C (p.Ser175Thr)
c.725-1066G>C (n.725-1066G>C)
dbSNP
2g.176093414G>TCA349352923HOXD13c.524G>T (p.Ser175Ile)
c.725-1066G>T (n.725-1066G>T)
gnomAD v4
2g.176093415C>ACA349352924HOXD13c.525C>A (p.Ser175Arg)
c.725-1065C>A (n.725-1065C>A)
dbSNP
2g.176093415C>GCA349352925HOXD13c.525C>G (p.Ser175Arg)
c.725-1065C>G (n.725-1065C>G)
dbSNP
2g.176093415C>TCA430224540HOXD13c.525C>T (p.Ser175=)
c.725-1065C>T (n.725-1065C>T)
dbSNP gnomAD v4
2g.176093416A>CCA349352926HOXD13c.526A>C (p.Ser176Arg)
c.725-1064A>C (n.725-1064A>C)
2g.176093416A>GCA349352927HOXD13c.526A>G (p.Ser176Gly)
c.725-1064A>G (n.725-1064A>G)
2g.176093416A>TCA349352928HOXD13c.526A>T (p.Ser176Cys)
c.725-1064A>T (n.725-1064A>T)
dbSNP
2g.176093417G>ACA1976619HOXD13c.527G>A (p.Ser176Asn)
c.725-1063G>A (n.725-1063G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093417G>CCA349352929HOXD13c.527G>C (p.Ser176Thr)
c.725-1063G>C (n.725-1063G>C)
dbSNP
2g.176093417G=CA1309431412HOXD13c.527G= (p.Ser176=)
c.725-1063G= (n.725-1063G=)
2g.176093417G>TCA349352930HOXD13c.527G>T (p.Ser176Ile)
c.725-1063G>T (n.725-1063G>T)
dbSNP
2g.176093418C>ACA349352932HOXD13c.528C>A (p.Ser176Arg)
c.725-1062C>A (n.725-1062C>A)
2g.176093418C>GCA349352931HOXD13c.528C>G (p.Ser176Arg)
c.725-1062C>G (n.725-1062C>G)
2g.176093418C>TCA430224541HOXD13c.528C>T (p.Ser176=)
c.725-1062C>T (n.725-1062C>T)
COSMIC
2g.176093419A>CCA349352933HOXD13c.529A>C (p.Ser177Arg)
c.725-1061A>C (n.725-1061A>C)
2g.176093419A>GCA349352934HOXD13c.529A>G (p.Ser177Gly)
c.725-1061A>G (n.725-1061A>G)
dbSNP
2g.176093419A>TCA349352935HOXD13c.529A>T (p.Ser177Cys)
c.725-1061A>T (n.725-1061A>T)
dbSNP
2g.176093420G>ACA349352936HOXD13c.530G>A (p.Ser177Asn)
c.725-1060G>A (n.725-1060G>A)
dbSNP
2g.176093420G>CCA349352937HOXD13c.530G>C (p.Ser177Thr)
c.725-1060G>C (n.725-1060G>C)
dbSNP
2g.176093420G>TCA349352938HOXD13c.530G>T (p.Ser177Ile)
c.725-1060G>T (n.725-1060G>T)
dbSNP
2g.176093421delCA2577165628HOXD13c.531del (p.Ser177ArgfsTer?)
c.725-1059del (n.725-1059del)
2g.176093421C>ACA349352939HOXD13c.531C>A (p.Ser177Arg)
c.725-1059C>A (n.725-1059C>A)
2g.176093421C>GCA349352940HOXD13c.531C>G (p.Ser177Arg)
c.725-1059C>G (n.725-1059C>G)
dbSNP
2g.176093421C>TCA430224542HOXD13c.531C>T (p.Ser177=)
c.725-1059C>T (n.725-1059C>T)
dbSNP gnomAD v4
2g.176093422G>ACA349352941HOXD13c.532G>A (p.Val178Ile)
c.725-1058G>A (n.725-1058G>A)
dbSNP gnomAD v4 COSMIC
2g.176093422G>CCA349352942HOXD13c.532G>C (p.Val178Leu)
c.725-1058G>C (n.725-1058G>C)
dbSNP gnomAD v4
2g.176093422G>TCA349352943HOXD13c.532G>T (p.Val178Leu)
c.725-1058G>T (n.725-1058G>T)
2g.176093423T>ACA349352945HOXD13c.533T>A (p.Val178Glu)
c.725-1057T>A (n.725-1057T>A)
dbSNP
2g.176093423T>CCA1976620HOXD13c.533T>C (p.Val178Ala)
c.725-1057T>C (n.725-1057T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093423T>GCA349352944HOXD13c.533T>G (p.Val178Gly)
c.725-1057T>G (n.725-1057T>G)
dbSNP
2g.176093423T=CA1309431413HOXD13c.533T= (p.Val178=)
c.725-1057T= (n.725-1057T=)
2g.176093424A=CA1309431414HOXD13c.534A= (p.Val178=)
c.725-1056A= (n.725-1056A=)
2g.176093424A>CCA430224543HOXD13c.534A>C (p.Val178=)
c.725-1056A>C (n.725-1056A>C)
dbSNP gnomAD v4
2g.176093424A>GCA430224544HOXD13c.534A>G (p.Val178=)
c.725-1056A>G (n.725-1056A>G)
dbSNP gnomAD v4
2g.176093424A>TCA430224545HOXD13c.534A>T (p.Val178=)
c.725-1056A>T (n.725-1056A>T)
gnomAD v4
2g.176093425C>ACA349352946HOXD13c.535C>A (p.Pro179Thr)
c.725-1055C>A (n.725-1055C>A)
dbSNP gnomAD v2 gnomAD v4
2g.176093425C=CA1309431415HOXD13c.535C= (p.Pro179=)
c.725-1055C= (n.725-1055C=)
2g.176093425C>GCA349352947HOXD13c.535C>G (p.Pro179Ala)
c.725-1055C>G (n.725-1055C>G)
dbSNP
2g.176093425C>TCA349352948HOXD13c.535C>T (p.Pro179Ser)
c.725-1055C>T (n.725-1055C>T)
dbSNP COSMIC
2g.176093426C>ACA349352949HOXD13c.536C>A (p.Pro179Gln)
c.725-1054C>A (n.725-1054C>A)
dbSNP
2g.176093426C=CA1309431416HOXD13c.536C= (p.Pro179=)
c.725-1054C= (n.725-1054C=)
2g.176093426C>GCA349352950HOXD13c.536C>G (p.Pro179Arg)
c.725-1054C>G (n.725-1054C>G)
dbSNP gnomAD v4
2g.176093426C>TCA349352951HOXD13c.536C>T (p.Pro179Leu)
c.725-1054C>T (n.725-1054C>T)
ClinVar dbSNP
2g.176093427G>ACA430224546HOXD13c.537G>A (p.Pro179=)
c.725-1053G>A (n.725-1053G>A)
dbSNP COSMIC
2g.176093427G>CCA430224547HOXD13c.537G>C (p.Pro179=)
c.725-1053G>C (n.725-1053G>C)
dbSNP
2g.176093427G>TCA430224548HOXD13c.537G>T (p.Pro179=)
c.725-1053G>T (n.725-1053G>T)
dbSNP COSMIC
2g.176093428G>ACA349352952HOXD13c.538G>A (p.Ala180Thr)
c.725-1052G>A (n.725-1052G>A)
dbSNP
2g.176093428G>CCA349352953HOXD13c.538G>C (p.Ala180Pro)
c.725-1052G>C (n.725-1052G>C)
2g.176093428G>TCA349352954HOXD13c.538G>T (p.Ala180Ser)
c.725-1052G>T (n.725-1052G>T)
2g.176093432_176093442delCA2573134022HOXD13c.542_552del (p.Asn181SerfsTer?)
c.725-1048_725-1038del (n.725-1048_725-1038del)
ClinVar dbSNP
2g.176093429C>ACA349352955HOXD13c.539C>A (p.Ala180Asp)
c.725-1051C>A (n.725-1051C>A)
dbSNP
2g.176093429C=CA1309431417HOXD13c.539C= (p.Ala180=)
c.725-1051C= (n.725-1051C=)
2g.176093429C>GCA349352956HOXD13c.539C>G (p.Ala180Gly)
c.725-1051C>G (n.725-1051C>G)
dbSNP
2g.176093429C>TCA349352957HOXD13c.539C>T (p.Ala180Val)
c.725-1051C>T (n.725-1051C>T)
dbSNP gnomAD v2 gnomAD v4
2g.176093430C>ACA430224549HOXD13c.540C>A (p.Ala180=)
c.725-1050C>A (n.725-1050C>A)
dbSNP
2g.176093430C>GCA430224550HOXD13c.540C>G (p.Ala180=)
c.725-1050C>G (n.725-1050C>G)
2g.176093430C>TCA430224551HOXD13c.540C>T (p.Ala180=)
c.725-1050C>T (n.725-1050C>T)
dbSNP COSMIC COSMIC
2g.176093431_176093433delCA2577165629HOXD13c.541_543del (p.Asn181del)
c.725-1049_725-1047del (n.725-1049_725-1047del)
2g.176093431A=CA1309431418HOXD13c.541A= (p.Asn181=)
c.725-1049A= (n.725-1049A=)
2g.176093431A>CCA349352959HOXD13c.541A>C (p.Asn181His)
c.725-1049A>C (n.725-1049A>C)
gnomAD v4
2g.176093431A>GCA1976621HOXD13c.541A>G (p.Asn181Asp)
c.725-1049A>G (n.725-1049A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093431A>TCA349352958HOXD13c.541A>T (p.Asn181Tyr)
c.725-1049A>T (n.725-1049A>T)
dbSNP
2g.176093432A>CCA349352960HOXD13c.542A>C (p.Asn181Thr)
c.725-1048A>C (n.725-1048A>C)
dbSNP
2g.176093432A>GCA349352961HOXD13c.542A>G (p.Asn181Ser)
c.725-1048A>G (n.725-1048A>G)
dbSNP gnomAD v4
2g.176093432A>TCA349352962HOXD13c.542A>T (p.Asn181Ile)
c.725-1048A>T (n.725-1048A>T)
dbSNP
2g.176093433C>ACA60846401HOXD13c.543C>A (p.Asn181Lys)
c.725-1047C>A (n.725-1047C>A)
dbSNP gnomAD v4
2g.176093433C=CA1309431419HOXD13c.543C= (p.Asn181=)
c.725-1047C= (n.725-1047C=)
2g.176093433C>GCA349352963HOXD13c.543C>G (p.Asn181Lys)
c.725-1047C>G (n.725-1047C>G)
dbSNP
2g.176093433C>TCA430224552HOXD13c.543C>T (p.Asn181=)
c.725-1047C>T (n.725-1047C>T)
dbSNP gnomAD v4
2g.176093434G>ACA1976622HOXD13c.544G>A (p.Glu182Lys)
c.725-1046G>A (n.725-1046G>A)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.176093434G>CCA349352964HOXD13c.544G>C (p.Glu182Gln)
c.725-1046G>C (n.725-1046G>C)
dbSNP
2g.176093434G=CA1309431420HOXD13c.544G= (p.Glu182=)
c.725-1046G= (n.725-1046G=)
2g.176093434G>TCA349352965HOXD13c.544G>T (p.Glu182Ter)
c.725-1046G>T (n.725-1046G>T)
2g.176093435A>CCA349352966HOXD13c.545A>C (p.Glu182Ala)
c.725-1045A>C (n.725-1045A>C)
2g.176093435A>GCA349352967HOXD13c.545A>G (p.Glu182Gly)
c.725-1045A>G (n.725-1045A>G)
dbSNP
2g.176093435A>TCA349352968HOXD13c.545A>T (p.Glu182Val)
c.725-1045A>T (n.725-1045A>T)
dbSNP
2g.176093436G>ACA430224553HOXD13c.546G>A (p.Glu182=)
c.725-1044G>A (n.725-1044G>A)
dbSNP
2g.176093436G>CCA349352969HOXD13c.546G>C (p.Glu182Asp)
c.725-1044G>C (n.725-1044G>C)
dbSNP gnomAD v2 gnomAD v4
2g.176093436G=CA1309431421HOXD13c.546G= (p.Glu182=)
c.725-1044G= (n.725-1044G=)
2g.176093436G>TCA349352970HOXD13c.546G>T (p.Glu182Asp)
c.725-1044G>T (n.725-1044G>T)
2g.176093437G>ACA349352973HOXD13c.547G>A (p.Val183Met)
c.725-1043G>A (n.725-1043G>A)
dbSNP
2g.176093437G>CCA349352972HOXD13c.547G>C (p.Val183Leu)
c.725-1043G>C (n.725-1043G>C)
dbSNP
2g.176093437G>TCA349352971HOXD13c.547G>T (p.Val183Leu)
c.725-1043G>T (n.725-1043G>T)
gnomAD v4
2g.176093438T>ACA349352974HOXD13c.548T>A (p.Val183Glu)
c.725-1042T>A (n.725-1042T>A)
dbSNP
2g.176093438T>CCA349352976HOXD13c.548T>C (p.Val183Ala)
c.725-1042T>C (n.725-1042T>C)
2g.176093438T>GCA349352975HOXD13c.548T>G (p.Val183Gly)
c.725-1042T>G (n.725-1042T>G)
dbSNP
2g.176093438T=CA1309431422HOXD13c.548T= (p.Val183=)
c.725-1042T= (n.725-1042T=)
2g.176093439G>ACA430224555HOXD13c.549G>A (p.Val183=)
c.725-1041G>A (n.725-1041G>A)
2g.176093439G>CCA430224556HOXD13c.549G>C (p.Val183=)
c.725-1041G>C (n.725-1041G>C)
2g.176093439G>TCA430224554HOXD13c.549G>T (p.Val183=)
c.725-1041G>T (n.725-1041G>T)
2g.176093440C>ACA349352977HOXD13c.550C>A (p.Pro184Thr)
c.725-1040C>A (n.725-1040C>A)
dbSNP
2g.176093440C>GCA349352978HOXD13c.550C>G (p.Pro184Ala)
c.725-1040C>G (n.725-1040C>G)
dbSNP
2g.176093440C>TCA349352979HOXD13c.550C>T (p.Pro184Ser)
c.725-1040C>T (n.725-1040C>T)
dbSNP COSMIC
2g.176093441C>ACA349352980HOXD13c.551C>A (p.Pro184Gln)
c.725-1039C>A (n.725-1039C>A)
2g.176093441C>GCA349352981HOXD13c.551C>G (p.Pro184Arg)
c.725-1039C>G (n.725-1039C>G)
dbSNP
2g.176093441C>TCA349352982HOXD13c.551C>T (p.Pro184Leu)
c.725-1039C>T (n.725-1039C>T)
dbSNP gnomAD v4
2g.176093442A=CA1309431423HOXD13c.552A= (p.Pro184=)
c.725-1038A= (n.725-1038A=)
2g.176093442A>CCA430224557HOXD13c.552A>C (p.Pro184=)
c.725-1038A>C (n.725-1038A>C)
2g.176093442A>GCA430224558HOXD13c.552A>G (p.Pro184=)
c.725-1038A>G (n.725-1038A>G)
dbSNP gnomAD v4
2g.176093442A>TCA430224559HOXD13c.552A>T (p.Pro184=)
c.725-1038A>T (n.725-1038A>T)
dbSNP gnomAD v2 gnomAD v4
2g.176093443G>ACA349352983HOXD13c.553G>A (p.Ala185Thr)
c.725-1037G>A (n.725-1037G>A)
dbSNP gnomAD v4
2g.176093443G>CCA349352984HOXD13c.553G>C (p.Ala185Pro)
c.725-1037G>C (n.725-1037G>C)
dbSNP
2g.176093443G=CA1309431424HOXD13c.553G= (p.Ala185=)
c.725-1037G= (n.725-1037G=)
2g.176093443G>TCA349352985HOXD13c.553G>T (p.Ala185Ser)
c.725-1037G>T (n.725-1037G>T)
dbSNP gnomAD v2 gnomAD v4
2g.176093444C>ACA349352986HOXD13c.554C>A (p.Ala185Glu)
c.725-1036C>A (n.725-1036C>A)
dbSNP
2g.176093444C>GCA349352987HOXD13c.554C>G (p.Ala185Gly)
c.725-1036C>G (n.725-1036C>G)
dbSNP
2g.176093444C>TCA349352988HOXD13c.554C>T (p.Ala185Val)
c.725-1036C>T (n.725-1036C>T)
dbSNP gnomAD v4
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

Number of alleles fetched