Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.37739385del | CA2637449170 | HNF1B | c.544+58del (n.544+58del) | gnomAD v4 |
17 | g.37739383G>C | CA2809374064 | HNF1B | c.544+57C>G (n.544+57C>G) | |
17 | g.37739383G>T | CA2576244080 | HNF1B | c.544+57C>A (n.544+57C>A) | gnomAD v4 |
17 | g.37739384G>A | CA2576244081 | HNF1B | c.544+56C>T (n.544+56C>T) | dbSNP gnomAD v4 |
17 | g.37739384G>T | CA290288536 | HNF1B | c.544+56C>A (n.544+56C>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739385G>A | CA2637449172 | HNF1B | c.544+55C>T (n.544+55C>T) | dbSNP gnomAD v4 |
17 | g.37739387G>A | CA2637449174 | HNF1B | c.544+53C>T (n.544+53C>T) | gnomAD v4 |
17 | g.37739387G>T | CA2637449175 | HNF1B | c.544+53C>A (n.544+53C>A) | gnomAD v4 |
17 | g.37739390_37739391del | CA2576244082 | HNF1B | c.544+52_544+53del (n.544+52_544+53del) | |
17 | g.37739388_37739393del | CA2637449173 | HNF1B | c.544+48_544+53del (n.544+48_544+53del) | gnomAD v4 |
17 | g.37739388A>G | CA2637449176 | HNF1B | c.544+52T>C (n.544+52T>C) | gnomAD v4 |
17 | g.37739389G>T | CA8519055 | HNF1B | c.544+51C>A (n.544+51C>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739391G>A | CA626207266 | HNF1B | c.544+49C>T (n.544+49C>T) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739393del | CA2576244083 | HNF1B | c.544+49del (n.544+49del) | |
17 | g.37739392G>A | CA290288541 | HNF1B | c.544+48C>T (n.544+48C>T) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739392G>T | CA2576244084 | HNF1B | c.544+48C>A (n.544+48C>A) | |
17 | g.37739392_37739416dup | CA2637449177 | HNF1B | c.544+24_544+48dup (n.544+24_544+48dup) | gnomAD v4 |
17 | g.37739393G>A | CA8519056 | HNF1B | c.544+47C>T (n.544+47C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37739393G>T | CA2576244085 | HNF1B | c.544+47C>A (n.544+47C>A) | gnomAD v4 |
17 | g.37739396A>G | CA2637449178 | HNF1B | c.544+44T>C (n.544+44T>C) | gnomAD v4 |
17 | g.37739398G>A | CA290288549 | HNF1B | c.544+42C>T (n.544+42C>T) | dbSNP |
17 | g.37739399G>A | CA8519057 | HNF1B | c.544+41C>T (n.544+41C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739401C>A | CA2637449179 | HNF1B | c.544+39G>T (n.544+39G>T) | gnomAD v4 |
17 | g.37739401C>T | CA8519058 | HNF1B | c.544+39G>A (n.544+39G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37739403C>A | CA2809374070 | HNF1B | c.544+37G>T (n.544+37G>T) | |
17 | g.37739403C>T | CA8519059 | HNF1B | c.544+37G>A (n.544+37G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739405T>C | CA2637449180 | HNF1B | c.544+35A>G (n.544+35A>G) | gnomAD v4 |
17 | g.37739406C>A | CA2733206292 | HNF1B | c.544+34G>T (n.544+34G>T) | dbSNP |
17 | g.37739406C>T | CA8519060 | HNF1B | c.544+34G>A (n.544+34G>A) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739408G>A | CA2637449181 | HNF1B | c.544+32C>T (n.544+32C>T) | gnomAD v4 |
17 | g.37739409G>A | CA8519061 | HNF1B | c.544+31C>T (n.544+31C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739409G>T | CA2637449182 | HNF1B | c.544+31C>A (n.544+31C>A) | gnomAD v4 |
17 | g.37739410T>C | CA2733259526 | HNF1B | c.544+30A>G (n.544+30A>G) | dbSNP |
17 | g.37739410T>G | CA626207267 | HNF1B | c.544+30A>C (n.544+30A>C) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739411T>A | CA2637449183 | HNF1B | c.544+29A>T (n.544+29A>T) | gnomAD v4 |
17 | g.37739412G>A | CA8519062 | HNF1B | c.544+28C>T (n.544+28C>T) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739412G>T | CA2637449184 | HNF1B | c.544+28C>A (n.544+28C>A) | gnomAD v4 |
17 | g.37739419_37739424del | CA2637449185 | HNF1B | c.544+23_544+28del (n.544+23_544+28del) | gnomAD v4 |
17 | g.37739414G>T | CA2637449186 | HNF1B | c.544+26C>A (n.544+26C>A) | gnomAD v4 |
17 | g.37739415G>A | CA626207268 | HNF1B | c.544+25C>T (n.544+25C>T) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739415G>T | CA2637449187 | HNF1B | c.544+25C>A (n.544+25C>A) | gnomAD v4 |
17 | g.37739416C>T | CA290288582 | HNF1B | c.544+24G>A (n.544+24G>A) | dbSNP |
17 | g.37739418G>C | CA8519063 | HNF1B | c.544+22C>G (n.544+22C>G) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739420G>A | CA2637449188 | HNF1B | c.544+20C>T (n.544+20C>T) | gnomAD v4 |
17 | g.37739424G>A | CA626207269 | HNF1B | c.544+16C>T (n.544+16C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739427_37739445del | CA2695225790 | HNF1B | c.542_544+16del | |
17 | g.37739425G>A | CA2637449189 | HNF1B | c.544+15C>T (n.544+15C>T) | gnomAD v4 |
17 | g.37739425G>C | CA290288588 | HNF1B | c.544+15C>G (n.544+15C>G) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739425_37739426insT | CA771673892 | HNF1B | c.544+14_544+15insA (n.544+14_544+15insA) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739426A>G | CA8519065 | HNF1B | c.544+14T>C (n.544+14T>C) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739426A>T | CA8519064 | HNF1B | c.544+14T>A (n.544+14T>A) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739426dup | CA2576244086 | HNF1B | c.544+14dup (n.544+14dup) | |
17 | g.37739432del | CA2576244087 | HNF1B | c.544+11del (n.544+11del) | |
17 | g.37739433C>T | CA290288594 | HNF1B | c.544+7G>A (n.544+7G>A) | ClinVar dbSNP |
17 | g.37739436_37739439del | CA913190784 | HNF1B | c.544+3_544+6del (n.544+3_544+6del) | ClinVar dbSNP |
17 | g.37739435C>T | CA2697559834 | HNF1B | c.544+5G>A (n.544+5G>A) | ClinVar |
17 | g.37739436T>G | CA2695225791 | HNF1B | c.544+4A>C (n.544+4A>C) | |
17 | g.37739436_37739437insA | CA913190785 | HNF1B | c.544+3_544+4insT (n.544+3_544+4insT) | ClinVar |
17 | g.37739437_37739438dup | CA913190786 | HNF1B | c.544+2_544+3dup (n.544+2_544+3dup) | ClinVar |
17 | g.37739438A>C | CA398750977 | HNF1B | c.544+2T>G (n.544+2T>G) | |
17 | g.37739438A>G | CA398750980 | HNF1B | c.544+2T>C (n.544+2T>C) | |
17 | g.37739438A>T | CA398750986 | HNF1B | c.544+2T>A (n.544+2T>A) | |
17 | g.37739438dup | CA913190787 | HNF1B | c.544+2dup (n.544+2dup) | ClinVar |
17 | g.37739439C>A | CA398750992 | HNF1B | c.544+1G>T (n.544+1G>T) | ClinVar |
17 | g.37739439C>G | CA398750995 | HNF1B | c.544+1G>C (n.544+1G>C) | ClinVar |
17 | g.37739439C>T | CA398750998 | HNF1B | c.544+1G>A (n.544+1G>A) | ClinVar |
17 | g.37739440G>A | CA398751000 | HNF1B | c.544C>T (p.Gln182Ter) | ClinVar |
17 | g.37739440G>C | CA398751004 | HNF1B | c.544C>G (p.Gln182Glu) | |
17 | g.37739440G>T | CA398751002 | HNF1B | c.544C>A (p.Gln182Lys) | |
17 | g.37739441T>A | CA499603839 | HNF1B | c.543A>T (p.Arg181=) | |
17 | g.37739441T>C | CA499603840 | HNF1B | c.543A>G (p.Arg181=) | gnomAD v4 |
17 | g.37739441T>G | CA499603841 | HNF1B | c.543A>C (p.Arg181=) | |
17 | g.37739442C>A | CA398751006 | HNF1B | c.542G>T (p.Arg181Leu) | gnomAD v4 |
17 | g.37739442C>G | CA398751010 | HNF1B | c.542G>C (p.Arg181Pro) | |
17 | g.37739442C>T | CA8519066 | HNF1B | c.542G>A (p.Arg181Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739443G>A | CA16043028 | HNF1B | c.541C>T (p.Arg181Ter) | ClinVar dbSNP |
17 | g.37739443G>C | CA398751020 | HNF1B | c.541C>G (p.Arg181Gly) | |
17 | g.37739443G>T | CA499603842 | HNF1B | c.541C>A (p.Arg181=) | |
17 | g.37739444G>A | CA499603843 | HNF1B | c.540C>T (p.Leu180=) | |
17 | g.37739444G>C | CA499603844 | HNF1B | c.540C>G (p.Leu180=) | |
17 | g.37739444G>T | CA499603845 | HNF1B | c.540C>A (p.Leu180=) | |
17 | g.37739445A>C | CA398751022 | HNF1B | c.539T>G (p.Leu180Arg) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739445A>G | CA398751025 | HNF1B | c.539T>C (p.Leu180Pro) | |
17 | g.37739445A>T | CA398751027 | HNF1B | c.539T>A (p.Leu180His) | |
17 | g.37739446G>A | CA398751029 | HNF1B | c.538C>T (p.Leu180Phe) | |
17 | g.37739446G>C | CA398751031 | HNF1B | c.538C>G (p.Leu180Val) | |
17 | g.37739446G>T | CA398751032 | HNF1B | c.538C>A (p.Leu180Ile) | |
17 | g.37739447G>A | CA499603847 | HNF1B | c.537C>T (p.Ile179=) | |
17 | g.37739447G>C | CA398751035 | HNF1B | c.537C>G (p.Ile179Met) | |
17 | g.37739447G>T | CA499603846 | HNF1B | c.537C>A (p.Ile179=) | gnomAD v4 |
17 | g.37739448A>C | CA398751040 | HNF1B | c.536T>G (p.Ile179Ser) | |
17 | g.37739448A>G | CA398751037 | HNF1B | c.536T>C (p.Ile179Thr) | dbSNP |
17 | g.37739448A>T | CA398751041 | HNF1B | c.536T>A (p.Ile179Asn) | |
17 | g.37739449T>A | CA398751043 | HNF1B | c.535A>T (p.Ile179Phe) | |
17 | g.37739449T>C | CA398751047 | HNF1B | c.535A>G (p.Ile179Val) | |
17 | g.37739449T>G | CA398751050 | HNF1B | c.535A>C (p.Ile179Leu) | |
17 | g.37739450del | CA913190788 | HNF1B | c.534del (p.Ile179SerfsTer15) c.534del (p.Ile179SerfsTer?) | ClinVar |
17 | g.37739450C>A | CA398751055 | HNF1B | c.534G>T (p.Glu178Asp) | |
17 | g.37739450C>G | CA398751056 | HNF1B | c.534G>C (p.Glu178Asp) | |
17 | g.37739450C>T | CA499603848 | HNF1B | c.534G>A (p.Glu178=) | gnomAD v4 |
17 | g.37739451T>A | CA398751058 | HNF1B | c.533A>T (p.Glu178Val) | |
17 | g.37739451T>C | CA398751060 | HNF1B | c.533A>G (p.Glu178Gly) | ClinVar dbSNP |
17 | g.37739451T>G | CA398751063 | HNF1B | c.533A>C (p.Glu178Ala) | |
17 | g.37739452C>A | CA398751065 | HNF1B | c.532G>T (p.Glu178Ter) | |
17 | g.37739452C>G | CA398751067 | HNF1B | c.532G>C (p.Glu178Gln) | |
17 | g.37739452C>T | CA398751068 | HNF1B | c.532G>A (p.Glu178Lys) | |
17 | g.37739453T>A | CA499603849 | HNF1B | c.531A>T (p.Arg177=) | |
17 | g.37739453T>C | CA499603850 | HNF1B | c.531A>G (p.Arg177=) | |
17 | g.37739453T>G | CA499603851 | HNF1B | c.531A>C (p.Arg177=) | |
17 | g.37739454C>A | CA398751070 | HNF1B | c.530G>T (p.Arg177Leu) | |
17 | g.37739454C>G | CA398751072 | HNF1B | c.530G>C (p.Arg177Pro) | |
17 | g.37739454C>T | CA8519067 | HNF1B | c.530G>A (p.Arg177Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37739455G>A | CA122597 | HNF1B | c.529C>T (p.Arg177Ter) | ClinVar dbSNP |
17 | g.37739455G>C | CA398751075 | HNF1B | c.529C>G (p.Arg177Gly) | gnomAD v4 |
17 | g.37739455G>T | CA499603852 | HNF1B | c.529C>A (p.Arg177=) | dbSNP |
17 | g.37739456T>A | CA398751077 | HNF1B | c.528A>T (p.Gln176His) | |
17 | g.37739456T>C | CA499603853 | HNF1B | c.528A>G (p.Gln176=) | |
17 | g.37739456T>G | CA398751079 | HNF1B | c.528A>C (p.Gln176His) | |
17 | g.37739457T>A | CA398751081 | HNF1B | c.527A>T (p.Gln176Leu) | |
17 | g.37739457T>C | CA398751083 | HNF1B | c.527A>G (p.Gln176Arg) | |
17 | g.37739457T>G | CA398751085 | HNF1B | c.527A>C (p.Gln176Pro) | ClinVar dbSNP |
17 | g.37739458G>A | CA398751087 | HNF1B | c.526C>T (p.Gln176Ter) | ClinVar |
17 | g.37739458G>C | CA398751089 | HNF1B | c.526C>G (p.Gln176Glu) | |
17 | g.37739458G>T | CA398751090 | HNF1B | c.526C>A (p.Gln176Lys) | |
17 | g.37739459C>A | CA398751093 | HNF1B | c.525G>T (p.Lys175Asn) | |
17 | g.37739459C>G | CA398751095 | HNF1B | c.525G>C (p.Lys175Asn) | |
17 | g.37739459C>T | CA499603854 | HNF1B | c.525G>A (p.Lys175=) | |
17 | g.37739461_37739464del | CA913190789 | HNF1B | c.522_525del (p.Arg174SerfsTer19) c.522_525del (p.Arg174SerfsTer?) | ClinVar |
17 | g.37739460T>A | CA398751096 | HNF1B | c.524A>T (p.Lys175Met) | |
17 | g.37739460T>C | CA398751097 | HNF1B | c.524A>G (p.Lys175Arg) | |
17 | g.37739460T>G | CA398751100 | HNF1B | c.524A>C (p.Lys175Thr) | |
17 | g.37739461T>A | CA398751102 | HNF1B | c.523A>T (p.Lys175Ter) | |
17 | g.37739461T>C | CA398751107 | HNF1B | c.523A>G (p.Lys175Glu) | |
17 | g.37739461T>G | CA398751104 | HNF1B | c.523A>C (p.Lys175Gln) | |
17 | g.37739462T>A | CA398751109 | HNF1B | c.522A>T (p.Arg174Ser) | |
17 | g.37739462T>C | CA499603855 | HNF1B | c.522A>G (p.Arg174=) | |
17 | g.37739462T>G | CA398751110 | HNF1B | c.522A>C (p.Arg174Ser) | |
17 | g.37739463C>A | CA398751112 | HNF1B | c.521G>T (p.Arg174Ile) | |
17 | g.37739463C>G | CA398751114 | HNF1B | c.521G>C (p.Arg174Thr) | |
17 | g.37739463C>T | CA398751117 | HNF1B | c.521G>A (p.Arg174Lys) | |
17 | g.37739464T>A | CA398751118 | HNF1B | c.520A>T (p.Arg174Ter) | |
17 | g.37739464T>C | CA398751120 | HNF1B | c.520A>G (p.Arg174Gly) | ClinVar |
17 | g.37739464T>G | CA499603856 | HNF1B | c.520A>C (p.Arg174=) | |
17 | g.37739465G>A | CA499603859 | HNF1B | c.519C>T (p.Val173=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739465G>C | CA499603858 | HNF1B | c.519C>G (p.Val173=) | |
17 | g.37739465G>T | CA499603857 | HNF1B | c.519C>A (p.Val173=) | |
17 | g.37739466A>C | CA398751123 | HNF1B | c.518T>G (p.Val173Gly) | |
17 | g.37739466A>G | CA398751125 | HNF1B | c.518T>C (p.Val173Ala) | dbSNP gnomAD v4 |
17 | g.37739466A>T | CA398751128 | HNF1B | c.518T>A (p.Val173Asp) | |
17 | g.37739467C>A | CA398751129 | HNF1B | c.517G>T (p.Val173Phe) | |
17 | g.37739467C>G | CA398751132 | HNF1B | c.517G>C (p.Val173Leu) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739467C>T | CA290288602 | HNF1B | c.517G>A (p.Val173Ile) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739468G>A | CA8519068 | HNF1B | c.516C>T (p.Tyr172=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739468G>C | CA398751136 | HNF1B | c.516C>G (p.Tyr172Ter) | ClinVar dbSNP |
17 | g.37739468G>T | CA398751139 | HNF1B | c.516C>A (p.Tyr172Ter) | |
17 | g.37739469del | CA2582342165 | HNF1B | c.515del (p.Tyr172SerfsTer22) c.515del (p.Tyr172SerfsTer?) | ClinVar |
17 | g.37739469T>A | CA398751143 | HNF1B | c.515A>T (p.Tyr172Phe) | |
17 | g.37739469T>C | CA398751144 | HNF1B | c.515A>G (p.Tyr172Cys) | |
17 | g.37739469T>G | CA398751146 | HNF1B | c.515A>C (p.Tyr172Ser) | |
17 | g.37739470A>C | CA398751150 | HNF1B | c.514T>G (p.Tyr172Asp) | |
17 | g.37739470A>G | CA398751151 | HNF1B | c.514T>C (p.Tyr172His) | gnomAD v4 |
17 | g.37739470A>T | CA398751154 | HNF1B | c.514T>A (p.Tyr172Asn) | |
17 | g.37739471C>A | CA398751157 | HNF1B | c.513G>T (p.Trp171Cys) | |
17 | g.37739471C>G | CA398751159 | HNF1B | c.513G>C (p.Trp171Cys) | ClinVar |
17 | g.37739471C>T | CA398751161 | HNF1B | c.513G>A (p.Trp171Ter) | ClinVar |
17 | g.37739472C>A | CA398751164 | HNF1B | c.512G>T (p.Trp171Leu) | |
17 | g.37739472C>G | CA398751166 | HNF1B | c.512G>C (p.Trp171Ser) | |
17 | g.37739472C>T | CA398751169 | HNF1B | c.512G>A (p.Trp171Ter) | |
17 | g.37739473A>C | CA398751170 | HNF1B | c.511T>G (p.Trp171Gly) | |
17 | g.37739473A>G | CA214361 | HNF1B | c.511T>C (p.Trp171Arg) | ClinVar dbSNP |
17 | g.37739473A>T | CA398751173 | HNF1B | c.511T>A (p.Trp171Arg) | |
17 | g.37739474G>A | CA499603860 | HNF1B | c.510C>T (p.Thr170=) | dbSNP |
17 | g.37739474G>C | CA499603861 | HNF1B | c.510C>G (p.Thr170=) | gnomAD v4 |
17 | g.37739474G>T | CA499603862 | HNF1B | c.510C>A (p.Thr170=) | |
17 | g.37739475G>A | CA398751178 | HNF1B | c.509C>T (p.Thr170Ile) | gnomAD v4 |
17 | g.37739475G>C | CA398751181 | HNF1B | c.509C>G (p.Thr170Ser) | |
17 | g.37739475G>T | CA398751180 | HNF1B | c.509C>A (p.Thr170Asn) | |
17 | g.37739476T>A | CA398751184 | HNF1B | c.508A>T (p.Thr170Ser) | |
17 | g.37739476T>C | CA398751187 | HNF1B | c.508A>G (p.Thr170Ala) | gnomAD v4 |
17 | g.37739476T>G | CA398751189 | HNF1B | c.508A>C (p.Thr170Pro) | |
17 | g.37739477G>A | CA8519069 | HNF1B | c.507C>T (p.Tyr169=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37739477G>C | CA398751193 | HNF1B | c.507C>G (p.Tyr169Ter) | |
17 | g.37739477G>T | CA398751195 | HNF1B | c.507C>A (p.Tyr169Ter) | |
17 | g.37739478T>A | CA398751198 | HNF1B | c.506A>T (p.Tyr169Phe) | gnomAD v4 |
17 | g.37739478T>C | CA398751200 | HNF1B | c.506A>G (p.Tyr169Cys) | |
17 | g.37739478T>G | CA398751203 | HNF1B | c.506A>C (p.Tyr169Ser) | |
17 | g.37739479A>C | CA398751206 | HNF1B | c.505T>G (p.Tyr169Asp) | |
17 | g.37739479A>G | CA398751208 | HNF1B | c.505T>C (p.Tyr169His) | ClinVar |
17 | g.37739479A>T | CA398751209 | HNF1B | c.505T>A (p.Tyr169Asn) | |
17 | g.37739480C>A | CA499603863 | HNF1B | c.504G>T (p.Leu168=) | |
17 | g.37739480C>G | CA499603864 | HNF1B | c.504G>C (p.Leu168=) | |
17 | g.37739480C>T | CA499603865 | HNF1B | c.504G>A (p.Leu168=) | |
17 | g.37739480_37739485delinsAGGGG | CA913190790 | HNF1B | c.499_504delinsCCCCT (p.Ala167ProfsTer27) c.499_504delinsCCCCT (p.Ala167ProfsTer?) | ClinVar dbSNP |
17 | g.37739481A>C | CA398751212 | HNF1B | c.503T>G (p.Leu168Arg) | |
17 | g.37739481A>G | CA398751217 | HNF1B | c.503T>C (p.Leu168Pro) | |
17 | g.37739481A>T | CA398751214 | HNF1B | c.503T>A (p.Leu168Gln) | |
17 | g.37739482G>A | CA499603866 | HNF1B | c.502C>T (p.Leu168=) | |
17 | g.37739482G>C | CA398751219 | HNF1B | c.502C>G (p.Leu168Val) | |
17 | g.37739482G>T | CA398751220 | HNF1B | c.502C>A (p.Leu168Met) | |
17 | g.37739483A>C | CA499603869 | HNF1B | c.501T>G (p.Ala167=) | |
17 | g.37739483A>G | CA499603868 | HNF1B | c.501T>C (p.Ala167=) | dbSNP |
17 | g.37739483A>T | CA499603867 | HNF1B | c.501T>A (p.Ala167=) |