Chr Mutation (hg38) CAid Gene Transcript Linkouts
17g.37739453T>ACA499603849HNF1Bc.531A>T (p.Arg177=)
17g.37739453T>CCA499603850HNF1Bc.531A>G (p.Arg177=)
17g.37739453T>GCA499603851HNF1Bc.531A>C (p.Arg177=)
17g.37739454C>ACA398751070HNF1Bc.530G>T (p.Arg177Leu)
17g.37739454C>GCA398751072HNF1Bc.530G>C (p.Arg177Pro)
17g.37739454C>TCA8519067HNF1Bc.530G>A (p.Arg177Gln)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.37739455G>ACA122597HNF1Bc.529C>T (p.Arg177Ter)
ClinVar dbSNP
17g.37739455G>CCA398751075HNF1Bc.529C>G (p.Arg177Gly)
gnomAD v4
17g.37739455G>TCA499603852HNF1Bc.529C>A (p.Arg177=)
dbSNP
17g.37739456T>ACA398751077HNF1Bc.528A>T (p.Gln176His)
17g.37739456T>CCA499603853HNF1Bc.528A>G (p.Gln176=)
17g.37739456T>GCA398751079HNF1Bc.528A>C (p.Gln176His)
17g.37739457T>ACA398751081HNF1Bc.527A>T (p.Gln176Leu)
17g.37739457T>CCA398751083HNF1Bc.527A>G (p.Gln176Arg)
17g.37739457T>GCA398751085HNF1Bc.527A>C (p.Gln176Pro)
ClinVar dbSNP
17g.37739458G>ACA398751087HNF1Bc.526C>T (p.Gln176Ter)
ClinVar
17g.37739458G>CCA398751089HNF1Bc.526C>G (p.Gln176Glu)
17g.37739458G>TCA398751090HNF1Bc.526C>A (p.Gln176Lys)
17g.37739459C>ACA398751093HNF1Bc.525G>T (p.Lys175Asn)
17g.37739459C>GCA398751095HNF1Bc.525G>C (p.Lys175Asn)
17g.37739459C>TCA499603854HNF1Bc.525G>A (p.Lys175=)
17g.37739461_37739464delCA913190789HNF1Bc.522_525del (p.Arg174SerfsTer19)
c.522_525del (p.Arg174SerfsTer?)
ClinVar
17g.37739460T>ACA398751096HNF1Bc.524A>T (p.Lys175Met)
17g.37739460T>CCA398751097HNF1Bc.524A>G (p.Lys175Arg)
17g.37739460T>GCA398751100HNF1Bc.524A>C (p.Lys175Thr)
17g.37739461T>ACA398751102HNF1Bc.523A>T (p.Lys175Ter)
17g.37739461T>CCA398751107HNF1Bc.523A>G (p.Lys175Glu)
17g.37739461T>GCA398751104HNF1Bc.523A>C (p.Lys175Gln)
17g.37739462T>ACA398751109HNF1Bc.522A>T (p.Arg174Ser)
17g.37739462T>CCA499603855HNF1Bc.522A>G (p.Arg174=)
17g.37739462T>GCA398751110HNF1Bc.522A>C (p.Arg174Ser)
17g.37739463C>ACA398751112HNF1Bc.521G>T (p.Arg174Ile)
17g.37739463C>GCA398751114HNF1Bc.521G>C (p.Arg174Thr)
17g.37739463C>TCA398751117HNF1Bc.521G>A (p.Arg174Lys)
17g.37739464T>ACA398751118HNF1Bc.520A>T (p.Arg174Ter)
17g.37739464T>CCA398751120HNF1Bc.520A>G (p.Arg174Gly)
ClinVar
17g.37739464T>GCA499603856HNF1Bc.520A>C (p.Arg174=)
17g.37739465G>ACA499603859HNF1Bc.519C>T (p.Val173=)
dbSNP gnomAD v2 gnomAD v4
17g.37739465G>CCA499603858HNF1Bc.519C>G (p.Val173=)
17g.37739465G>TCA499603857HNF1Bc.519C>A (p.Val173=)
17g.37739466A>CCA398751123HNF1Bc.518T>G (p.Val173Gly)
17g.37739466A>GCA398751125HNF1Bc.518T>C (p.Val173Ala)
dbSNP gnomAD v4
17g.37739466A>TCA398751128HNF1Bc.518T>A (p.Val173Asp)
17g.37739467C>ACA398751129HNF1Bc.517G>T (p.Val173Phe)
17g.37739467C>GCA398751132HNF1Bc.517G>C (p.Val173Leu)
ClinVar dbSNP gnomAD v2 gnomAD v4
17g.37739467C>TCA290288602HNF1Bc.517G>A (p.Val173Ile)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37739468G>ACA8519068HNF1Bc.516C>T (p.Tyr172=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37739468G>CCA398751136HNF1Bc.516C>G (p.Tyr172Ter)
ClinVar dbSNP
17g.37739468G>TCA398751139HNF1Bc.516C>A (p.Tyr172Ter)
17g.37739469delCA2582342165HNF1Bc.515del (p.Tyr172SerfsTer22)
c.515del (p.Tyr172SerfsTer?)
ClinVar
17g.37739469T>ACA398751143HNF1Bc.515A>T (p.Tyr172Phe)
17g.37739469T>CCA398751144HNF1Bc.515A>G (p.Tyr172Cys)
17g.37739469T>GCA398751146HNF1Bc.515A>C (p.Tyr172Ser)
17g.37739470A>CCA398751150HNF1Bc.514T>G (p.Tyr172Asp)
17g.37739470A>GCA398751151HNF1Bc.514T>C (p.Tyr172His)
gnomAD v4
17g.37739470A>TCA398751154HNF1Bc.514T>A (p.Tyr172Asn)
17g.37739471C>ACA398751157HNF1Bc.513G>T (p.Trp171Cys)
17g.37739471C>GCA398751159HNF1Bc.513G>C (p.Trp171Cys)
ClinVar
17g.37739471C>TCA398751161HNF1Bc.513G>A (p.Trp171Ter)
ClinVar
17g.37739472C>ACA398751164HNF1Bc.512G>T (p.Trp171Leu)
17g.37739472C>GCA398751166HNF1Bc.512G>C (p.Trp171Ser)
17g.37739472C>TCA398751169HNF1Bc.512G>A (p.Trp171Ter)
17g.37739473A>CCA398751170HNF1Bc.511T>G (p.Trp171Gly)
17g.37739473A>GCA214361HNF1Bc.511T>C (p.Trp171Arg)
ClinVar dbSNP
17g.37739473A>TCA398751173HNF1Bc.511T>A (p.Trp171Arg)
17g.37739474G>ACA499603860HNF1Bc.510C>T (p.Thr170=)
dbSNP
17g.37739474G>CCA499603861HNF1Bc.510C>G (p.Thr170=)
gnomAD v4
17g.37739474G>TCA499603862HNF1Bc.510C>A (p.Thr170=)
17g.37739475G>ACA398751178HNF1Bc.509C>T (p.Thr170Ile)
gnomAD v4
17g.37739475G>CCA398751181HNF1Bc.509C>G (p.Thr170Ser)
17g.37739475G>TCA398751180HNF1Bc.509C>A (p.Thr170Asn)
17g.37739476T>ACA398751184HNF1Bc.508A>T (p.Thr170Ser)
17g.37739476T>CCA398751187HNF1Bc.508A>G (p.Thr170Ala)
gnomAD v4
17g.37739476T>GCA398751189HNF1Bc.508A>C (p.Thr170Pro)
17g.37739477G>ACA8519069HNF1Bc.507C>T (p.Tyr169=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.37739477G>CCA398751193HNF1Bc.507C>G (p.Tyr169Ter)
17g.37739477G>TCA398751195HNF1Bc.507C>A (p.Tyr169Ter)
17g.37739478T>ACA398751198HNF1Bc.506A>T (p.Tyr169Phe)
gnomAD v4
17g.37739478T>CCA398751200HNF1Bc.506A>G (p.Tyr169Cys)
17g.37739478T>GCA398751203HNF1Bc.506A>C (p.Tyr169Ser)
17g.37739479A>CCA398751206HNF1Bc.505T>G (p.Tyr169Asp)
17g.37739479A>GCA398751208HNF1Bc.505T>C (p.Tyr169His)
ClinVar
17g.37739479A>TCA398751209HNF1Bc.505T>A (p.Tyr169Asn)
17g.37739480C>ACA499603863HNF1Bc.504G>T (p.Leu168=)
17g.37739480C>GCA499603864HNF1Bc.504G>C (p.Leu168=)
17g.37739480C>TCA499603865HNF1Bc.504G>A (p.Leu168=)
17g.37739480_37739485delinsAGGGGCA913190790HNF1Bc.499_504delinsCCCCT (p.Ala167ProfsTer27)
c.499_504delinsCCCCT (p.Ala167ProfsTer?)
ClinVar dbSNP
17g.37739481A>CCA398751212HNF1Bc.503T>G (p.Leu168Arg)
17g.37739481A>GCA398751217HNF1Bc.503T>C (p.Leu168Pro)
17g.37739481A>TCA398751214HNF1Bc.503T>A (p.Leu168Gln)
17g.37739482G>ACA499603866HNF1Bc.502C>T (p.Leu168=)
17g.37739482G>CCA398751219HNF1Bc.502C>G (p.Leu168Val)
17g.37739482G>TCA398751220HNF1Bc.502C>A (p.Leu168Met)
17g.37739483A>CCA499603869HNF1Bc.501T>G (p.Ala167=)
17g.37739483A>GCA499603868HNF1Bc.501T>C (p.Ala167=)
dbSNP
17g.37739483A>TCA499603867HNF1Bc.501T>A (p.Ala167=)
17g.37739484G>ACA398751221HNF1Bc.500C>T (p.Ala167Val)
17g.37739484G>CCA398751223HNF1Bc.500C>G (p.Ala167Gly)
17g.37739484G>TCA398751225HNF1Bc.500C>A (p.Ala167Asp)
17g.37739485C>ACA398751227HNF1Bc.499G>T (p.Ala167Ser)
17g.37739485C>GCA398751228HNF1Bc.499G>C (p.Ala167Pro)
ClinVar dbSNP
17g.37739485C>TCA8519070HNF1Bc.499G>A (p.Ala167Thr)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
17g.37739486G>ACA8519071HNF1Bc.498C>T (p.Ala166=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37739486G>CCA499603870HNF1Bc.498C>G (p.Ala166=)
17g.37739486G>TCA499603871HNF1Bc.498C>A (p.Ala166=)
17g.37739487G>ACA8519072HNF1Bc.497C>T (p.Ala166Val)
dbSNP ExAC gnomAD v2 gnomAD v4
17g.37739487G>CCA398751233HNF1Bc.497C>G (p.Ala166Gly)
17g.37739487G>TCA398751232HNF1Bc.497C>A (p.Ala166Asp)
17g.37739488C>ACA398751235HNF1Bc.496G>T (p.Ala166Ser)
17g.37739488C>GCA398751237HNF1Bc.496G>C (p.Ala166Pro)
17g.37739488C>TCA398751238HNF1Bc.496G>A (p.Ala166Thr)
17g.37739489_37739490delCA1139665506HNF1Bc.495_496del (p.Ala166ArgfsTer?)
c.495_496del (p.Ala166ArgfsTer29)
ClinVar dbSNP
17g.37739489A>CCA499603872HNF1Bc.495T>G (p.Arg165=)
17g.37739489A>GCA499603873HNF1Bc.495T>C (p.Arg165=)
17g.37739489A>TCA499603874HNF1Bc.495T>A (p.Arg165=)
17g.37739490C>ACA398751240HNF1Bc.494G>T (p.Arg165Leu)
17g.37739490C>GCA398751241HNF1Bc.494G>C (p.Arg165Pro)
ClinVar
17g.37739490C>TCA122605HNF1Bc.494G>A (p.Arg165His)
ClinVar dbSNP
17g.37739491G>ACA398751247HNF1Bc.493C>T (p.Arg165Cys)
ClinVar gnomAD v4
17g.37739491G>CCA398751244HNF1Bc.493C>G (p.Arg165Gly)
17g.37739491G>TCA398751245HNF1Bc.493C>A (p.Arg165Ser)
17g.37739492C>ACA398751248HNF1Bc.492G>T (p.Lys164Asn)
17g.37739492C>GCA398751250HNF1Bc.492G>C (p.Lys164Asn)
17g.37739492C>TCA499603879HNF1Bc.492G>A (p.Lys164=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37739493T>ACA398751252HNF1Bc.491A>T (p.Lys164Met)
17g.37739493T>CCA398751253HNF1Bc.491A>G (p.Lys164Arg)
dbSNP gnomAD v2 gnomAD v4
17g.37739493T>GCA398751254HNF1Bc.491A>C (p.Lys164Thr)
17g.37739494T>ACA398751256HNF1Bc.490A>T (p.Lys164Ter)
17g.37739494T>CCA398751259HNF1Bc.490A>G (p.Lys164Glu)
ClinVar
17g.37739494T>GCA398751258HNF1Bc.490A>C (p.Lys164Gln)
ClinVar
17g.37739495C>ACA398751261HNF1Bc.489G>T (p.Gln163His)
dbSNP
17g.37739495C>GCA398751262HNF1Bc.489G>C (p.Gln163His)
17g.37739495C>TCA499603883HNF1Bc.489G>A (p.Gln163=)
17g.37739496T>ACA398751264HNF1Bc.488A>T (p.Gln163Leu)
17g.37739496T>CCA398751266HNF1Bc.488A>G (p.Gln163Arg)
17g.37739496T>GCA398751267HNF1Bc.488A>C (p.Gln163Pro)
17g.37739497G>ACA398751269HNF1Bc.487C>T (p.Gln163Ter)
17g.37739497G>CCA398751270HNF1Bc.487C>G (p.Gln163Glu)
dbSNP gnomAD v4
17g.37739497G>TCA398751272HNF1Bc.487C>A (p.Gln163Lys)
ClinVar dbSNP
17g.37739499delCA913190791HNF1Bc.487del (p.Gln163ArgfsTer?)
ClinVar
17g.37739498G>ACA499603887HNF1Bc.486C>T (p.Thr162=)
dbSNP gnomAD v2 gnomAD v4
17g.37739498G>CCA499603888HNF1Bc.486C>G (p.Thr162=)
17g.37739498G>TCA499603889HNF1Bc.486C>A (p.Thr162=)
ClinVar dbSNP gnomAD v3 gnomAD v4
17g.37739499G>ACA398751274HNF1Bc.485C>T (p.Thr162Ile)
dbSNP gnomAD v3 gnomAD v4
17g.37739499G>CCA398751275HNF1Bc.485C>G (p.Thr162Ser)
17g.37739499G>TCA398751276HNF1Bc.485C>A (p.Thr162Asn)
17g.37739500delCA913190792HNF1Bc.484del (p.Thr162ProfsTer?)
ClinVar
17g.37739500T>ACA398751282HNF1Bc.484A>T (p.Thr162Ser)
17g.37739500T>CCA398751280HNF1Bc.484A>G (p.Thr162Ala)
17g.37739500T>GCA398751279HNF1Bc.484A>C (p.Thr162Pro)
17g.37739503_37739577delCA913190793HNF1Bc.410_484del (p.Arg137_Lys161del)
ClinVar
17g.37739501C>ACA398751283HNF1Bc.483G>T (p.Lys161Asn)
17g.37739501C>GCA398751286HNF1Bc.483G>C (p.Lys161Asn)
17g.37739501C>TCA8519073HNF1Bc.483G>A (p.Lys161=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37739502T>ACA398751288HNF1Bc.482A>T (p.Lys161Met)
17g.37739502T>CCA290288642HNF1Bc.482A>G (p.Lys161Arg)
dbSNP
17g.37739502T>GCA398751289HNF1Bc.482A>C (p.Lys161Thr)
17g.37739503T>ACA398751292HNF1Bc.481A>T (p.Lys161Ter)
ClinVar dbSNP
17g.37739503T>CCA398751294HNF1Bc.481A>G (p.Lys161Glu)
17g.37739503T>GCA398751293HNF1Bc.481A>C (p.Lys161Gln)
17g.37739504C>ACA398751296HNF1Bc.480G>T (p.Met160Ile)
17g.37739504C>GCA398751300HNF1Bc.480G>C (p.Met160Ile)
17g.37739504C>TCA398751298HNF1Bc.480G>A (p.Met160Ile)
ClinVar
17g.37739505A>CCA10606095HNF1Bc.479T>G (p.Met160Arg)
ClinVar dbSNP
17g.37739505A>GCA398751302HNF1Bc.479T>C (p.Met160Thr)
ClinVar
17g.37739505A>TCA398751303HNF1Bc.479T>A (p.Met160Lys)
17g.37739506T>ACA398751305HNF1Bc.478A>T (p.Met160Leu)
17g.37739506T>CCA398751307HNF1Bc.478A>G (p.Met160Val)
ClinVar
17g.37739506T>GCA398751308HNF1Bc.478A>C (p.Met160Leu)
17g.37739507delCA214360HNF1Bc.477del (p.Met160Ter)
ClinVar dbSNP
17g.37739507A>CCA499603899HNF1Bc.477T>G (p.Pro159=)
17g.37739507A>GCA499603900HNF1Bc.477T>C (p.Pro159=)
ClinVar dbSNP
17g.37739507A>TCA499603902HNF1Bc.477T>A (p.Pro159=)
dbSNP gnomAD v2 gnomAD v4
17g.37739508G>ACA398751311HNF1Bc.476C>T (p.Pro159Leu)
ClinVar gnomAD v4
17g.37739508G>CCA398751312HNF1Bc.476C>G (p.Pro159Arg)
17g.37739508G>TCA398751314HNF1Bc.476C>A (p.Pro159His)
17g.37739509G>ACA398751319HNF1Bc.475C>T (p.Pro159Ser)
ClinVar
17g.37739509G>CCA398751316HNF1Bc.475C>G (p.Pro159Ala)
17g.37739509G>TCA398751317HNF1Bc.475C>A (p.Pro159Thr)
17g.37739510G>ACA499603904HNF1Bc.474C>T (p.Thr158=)
dbSNP gnomAD v2 gnomAD v4
17g.37739510G>CCA499603905HNF1Bc.474C>G (p.Thr158=)
17g.37739510G>TCA499603906HNF1Bc.474C>A (p.Thr158=)
17g.37739511G>ACA398751320HNF1Bc.473C>T (p.Thr158Ile)
ClinVar dbSNP
17g.37739511G>CCA398751322HNF1Bc.473C>G (p.Thr158Ser)
17g.37739511G>TCA398751323HNF1Bc.473C>A (p.Thr158Asn)
ClinVar dbSNP
17g.37739511_37739512insGGGCTGCACA913190794HNF1Bc.472_473insTGCAGCCC (p.Thr158MetfsTer6)
ClinVar
17g.37739512T>ACA398751324HNF1Bc.472A>T (p.Thr158Ser)
17g.37739512T>CCA398751325HNF1Bc.472A>G (p.Thr158Ala)
17g.37739512T>GCA398751327HNF1Bc.472A>C (p.Thr158Pro)
17g.37739513delCA913190795HNF1Bc.471del (p.Thr158ProfsTer3)
ClinVar
17g.37739513G>ACA499603910HNF1Bc.471C>T (p.Gly157=)
17g.37739513G>CCA499603911HNF1Bc.471C>G (p.Gly157=)
17g.37739513G>TCA499603909HNF1Bc.471C>A (p.Gly157=)
dbSNP gnomAD v4
17g.37739514C>ACA398751329HNF1Bc.470G>T (p.Gly157Val)
17g.37739514C>GCA398751330HNF1Bc.470G>C (p.Gly157Ala)
17g.37739514C>TCA398751331HNF1Bc.470G>A (p.Gly157Asp)
17g.37739515C>ACA398751335HNF1Bc.469G>T (p.Gly157Cys)
17g.37739515C>GCA398751337HNF1Bc.469G>C (p.Gly157Arg)
17g.37739515C>TCA398751333HNF1Bc.469G>A (p.Gly157Ser)
17g.37739516C>ACA398751338HNF1Bc.468G>T (p.Lys156Asn)
17g.37739516C>GCA398751339HNF1Bc.468G>C (p.Lys156Asn)
17g.37739516C>TCA499603917HNF1Bc.468G>A (p.Lys156=)
gnomAD v4
17g.37739517T>ACA398751342HNF1Bc.467A>T (p.Lys156Met)
17g.37739517T>CCA398751344HNF1Bc.467A>G (p.Lys156Arg)
17g.37739517T>GCA398751345HNF1Bc.467A>C (p.Lys156Thr)
17g.37739518T>ACA398751349HNF1Bc.466A>T (p.Lys156Ter)
17g.37739518T>CCA398751347HNF1Bc.466A>G (p.Lys156Glu)
ClinVar
17g.37739518T>GCA398751348HNF1Bc.466A>C (p.Lys156Gln)
17g.37739519G>ACA499603923HNF1Bc.465C>T (p.Asn155=)
17g.37739519G>CCA398751351HNF1Bc.465C>G (p.Asn155Lys)
17g.37739519G>TCA398751352HNF1Bc.465C>A (p.Asn155Lys)
17g.37739520T>ACA398751353HNF1Bc.464A>T (p.Asn155Ile)
17g.37739520T>CCA398751355HNF1Bc.464A>G (p.Asn155Ser)
17g.37739520T>GCA398751356HNF1Bc.464A>C (p.Asn155Thr)
17g.37739521T>ACA398751358HNF1Bc.463A>T (p.Asn155Tyr)
17g.37739521T>CCA398751360HNF1Bc.463A>G (p.Asn155Asp)
17g.37739521T>GCA398751359HNF1Bc.463A>C (p.Asn155His)
dbSNP gnomAD v4
17g.37739522G>ACA499603924HNF1Bc.462C>T (p.Leu154=)
dbSNP gnomAD v3 gnomAD v4
17g.37739522G>CCA499603925HNF1Bc.462C>G (p.Leu154=)
17g.37739522G>TCA499603926HNF1Bc.462C>A (p.Leu154=)
17g.37739523A>CCA398751362HNF1Bc.461T>G (p.Leu154Arg)
17g.37739523A>GCA398751364HNF1Bc.461T>C (p.Leu154Pro)
17g.37739523A>TCA398751365HNF1Bc.461T>A (p.Leu154His)
17g.37739524G>ACA398751367HNF1Bc.460C>T (p.Leu154Phe)
ClinVar
17g.37739524G>CCA398751368HNF1Bc.460C>G (p.Leu154Val)
17g.37739524G>TCA398751370HNF1Bc.460C>A (p.Leu154Ile)
17g.37739525A>CCA398751371HNF1Bc.459T>G (p.His153Gln)
17g.37739525A>GCA499603928HNF1Bc.459T>C (p.His153=)
17g.37739525A>TCA398751373HNF1Bc.459T>A (p.His153Gln)
17g.37739526T>ACA398751375HNF1Bc.458A>T (p.His153Leu)
17g.37739526T>CCA398751376HNF1Bc.458A>G (p.His153Arg)
ClinVar dbSNP
17g.37739526T>GCA398751377HNF1Bc.458A>C (p.His153Pro)
17g.37739527G>ACA398751381HNF1Bc.457C>T (p.His153Tyr)
17g.37739527G>CCA398751383HNF1Bc.457C>G (p.His153Asp)
17g.37739527G>TCA398751379HNF1Bc.457C>A (p.His153Asn)
ClinVar
17g.37739528C>ACA398751384HNF1Bc.456G>T (p.Gln152His)
17g.37739528C>GCA398751385HNF1Bc.456G>C (p.Gln152His)
17g.37739528C>TCA499603929HNF1Bc.456G>A (p.Gln152=)
dbSNP gnomAD v2 gnomAD v4
17g.37739529T>ACA398751387HNF1Bc.455A>T (p.Gln152Leu)
17g.37739529T>CCA398751389HNF1Bc.455A>G (p.Gln152Arg)
17g.37739529T>GCA398751391HNF1Bc.455A>C (p.Gln152Pro)
17g.37739530G>ACA398751395HNF1Bc.454C>T (p.Gln152Ter)
17g.37739530G>CCA398751393HNF1Bc.454C>G (p.Gln152Glu)
17g.37739530G>TCA398751392HNF1Bc.454C>A (p.Gln152Lys)
17g.37739532delCA2695225793HNF1Bc.454del (p.Gln152SerfsTer9)
17g.37739531G>ACA499603930HNF1Bc.453C>T (p.Ser151=)
gnomAD v4
17g.37739531G>CCA499603931HNF1Bc.453C>G (p.Ser151=)
17g.37739531G>TCA499603932HNF1Bc.453C>A (p.Ser151=)
17g.37739532G>ACA398751396HNF1Bc.452C>T (p.Ser151Phe)
ClinVar
17g.37739532G>CCA398751398HNF1Bc.452C>G (p.Ser151Cys)
ClinVar
17g.37739532G>TCA398751400HNF1Bc.452C>A (p.Ser151Tyr)
17g.37739533A>CCA398751401HNF1Bc.451T>G (p.Ser151Ala)
17g.37739533A>GCA398751403HNF1Bc.451T>C (p.Ser151Pro)
ClinVar
17g.37739533A>TCA398751404HNF1Bc.451T>A (p.Ser151Thr)
17g.37739534G>ACA290288657HNF1Bc.450C>T (p.Leu150=)
ClinVar dbSNP
17g.37739534G>CCA499603933HNF1Bc.450C>G (p.Leu150=)
17g.37739534G>TCA499603934HNF1Bc.450C>A (p.Leu150=)
17g.37739535A>CCA398751405HNF1Bc.449T>G (p.Leu150Arg)
17g.37739535A>GCA398751409HNF1Bc.449T>C (p.Leu150Pro)
17g.37739535A>TCA398751407HNF1Bc.449T>A (p.Leu150His)
17g.37739536G>ACA398751411HNF1Bc.448C>T (p.Leu150Phe)
17g.37739536G>CCA398751412HNF1Bc.448C>G (p.Leu150Val)
17g.37739536G>TCA398751413HNF1Bc.448C>A (p.Leu150Ile)
17g.37739537G>ACA499603935HNF1Bc.447C>T (p.His149=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
17g.37739537G>CCA398751415HNF1Bc.447C>G (p.His149Gln)
17g.37739537G>TCA398751417HNF1Bc.447C>A (p.His149Gln)
17g.37739538T>ACA398751418HNF1Bc.446A>T (p.His149Leu)
17g.37739538T>CCA398751420HNF1Bc.446A>G (p.His149Arg)
17g.37739538T>GCA398751421HNF1Bc.446A>C (p.His149Pro)
17g.37739539G>ACA398751423HNF1Bc.445C>T (p.His149Tyr)
17g.37739539G>CCA398751425HNF1Bc.445C>G (p.His149Asp)
17g.37739539G>TCA398751427HNF1Bc.445C>A (p.His149Asn)
17g.37739540C>ACA499603936HNF1Bc.444G>T (p.Ser148=)
dbSNP gnomAD v2 gnomAD v4
17g.37739540C>GCA499603937HNF1Bc.444G>C (p.Ser148=)
17g.37739540C>TCA8519074HNF1Bc.444G>A (p.Ser148=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
17g.37739541G>ACA398751429HNF1Bc.443C>T (p.Ser148Leu)
ClinVar gnomAD v4
17g.37739541G>CCA122604HNF1Bc.443C>G (p.Ser148Trp)
ClinVar dbSNP
17g.37739541G>TCA398751431HNF1Bc.443C>A (p.Ser148Ter)
ClinVar
17g.37739542A>CCA398751434HNF1Bc.442T>G (p.Ser148Ala)
17g.37739542A>GCA398751435HNF1Bc.442T>C (p.Ser148Pro)
17g.37739542A>TCA398751437HNF1Bc.442T>A (p.Ser148Thr)
17g.37739543C>ACA398751439HNF1Bc.441G>T (p.Gln147His)
17g.37739543C>GCA398751440HNF1Bc.441G>C (p.Gln147His)
17g.37739543C>TCA499603938HNF1Bc.441G>A (p.Gln147=)
dbSNP
17g.37739544T>ACA398751442HNF1Bc.440A>T (p.Gln147Leu)
17g.37739544T>CCA398751443HNF1Bc.440A>G (p.Gln147Arg)
17g.37739544T>GCA398751445HNF1Bc.440A>C (p.Gln147Pro)
17g.37739545G>ACA398751446HNF1Bc.439C>T (p.Gln147Ter)
ClinVar
17g.37739545G>CCA398751448HNF1Bc.439C>G (p.Gln147Glu)
17g.37739545G>TCA398751450HNF1Bc.439C>A (p.Gln147Lys)
17g.37739546G>ACA499603939HNF1Bc.438C>T (p.Asn146=)
ClinVar dbSNP gnomAD v4
17g.37739546G>CCA398751451HNF1Bc.438C>G (p.Asn146Lys)
17g.37739546G>TCA398751453HNF1Bc.438C>A (p.Asn146Lys)
ClinVar
17g.37739547T>ACA398751458HNF1Bc.437A>T (p.Asn146Ile)
17g.37739547T>CCA398751455HNF1Bc.437A>G (p.Asn146Ser)
17g.37739547T>GCA398751457HNF1Bc.437A>C (p.Asn146Thr)
ClinVar
17g.37739548T>ACA398751460HNF1Bc.436A>T (p.Asn146Tyr)
17g.37739548T>CCA398751462HNF1Bc.436A>G (p.Asn146Asp)
ClinVar
17g.37739548T>GCA398751464HNF1Bc.436A>C (p.Asn146His)
17g.37739549C>ACA499603942HNF1Bc.435G>T (p.Leu145=)
17g.37739549C>GCA499603940HNF1Bc.435G>C (p.Leu145=)
17g.37739549C>TCA499603941HNF1Bc.435G>A (p.Leu145=)
17g.37739550delCA2695225794HNF1Bc.434del (p.Leu145ArgfsTer16)
17g.37739550A>CCA398751465HNF1Bc.434T>G (p.Leu145Arg)
17g.37739550A>GCA398751466HNF1Bc.434T>C (p.Leu145Pro)
17g.37739550A>TCA398751468HNF1Bc.434T>A (p.Leu145Gln)
ClinVar
17g.37739551G>ACA499603943HNF1Bc.433C>T (p.Leu145=)
17g.37739551G>CCA398751470HNF1Bc.433C>G (p.Leu145Val)
17g.37739551G>TCA398751471HNF1Bc.433C>A (p.Leu145Met)
17g.37739552G>ACA499603946HNF1Bc.432C>T (p.Gly144=)
dbSNP
17g.37739552G>CCA499603945HNF1Bc.432C>G (p.Gly144=)
17g.37739552G>TCA499603944HNF1Bc.432C>A (p.Gly144=)
17g.37739553C>ACA398751472HNF1Bc.431G>T (p.Gly144Val)
dbSNP
17g.37739553C>GCA398751474HNF1Bc.431G>C (p.Gly144Ala)
17g.37739553C>TCA398751475HNF1Bc.431G>A (p.Gly144Asp)

Number of alleles fetched