Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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=) | |
17 | g.37739484G>A | CA398751221 | HNF1B | c.500C>T (p.Ala167Val) | |
17 | g.37739484G>C | CA398751223 | HNF1B | c.500C>G (p.Ala167Gly) | |
17 | g.37739484G>T | CA398751225 | HNF1B | c.500C>A (p.Ala167Asp) | |
17 | g.37739485C>A | CA398751227 | HNF1B | c.499G>T (p.Ala167Ser) | |
17 | g.37739485C>G | CA398751228 | HNF1B | c.499G>C (p.Ala167Pro) | ClinVar dbSNP |
17 | g.37739485C>T | CA8519070 | HNF1B | c.499G>A (p.Ala167Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37739486G>A | CA8519071 | HNF1B | c.498C>T (p.Ala166=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739486G>C | CA499603870 | HNF1B | c.498C>G (p.Ala166=) | |
17 | g.37739486G>T | CA499603871 | HNF1B | c.498C>A (p.Ala166=) | |
17 | g.37739487G>A | CA8519072 | HNF1B | c.497C>T (p.Ala166Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.37739487G>C | CA398751233 | HNF1B | c.497C>G (p.Ala166Gly) | |
17 | g.37739487G>T | CA398751232 | HNF1B | c.497C>A (p.Ala166Asp) | |
17 | g.37739488C>A | CA398751235 | HNF1B | c.496G>T (p.Ala166Ser) | |
17 | g.37739488C>G | CA398751237 | HNF1B | c.496G>C (p.Ala166Pro) | |
17 | g.37739488C>T | CA398751238 | HNF1B | c.496G>A (p.Ala166Thr) | |
17 | g.37739489_37739490del | CA1139665506 | HNF1B | c.495_496del (p.Ala166ArgfsTer?) c.495_496del (p.Ala166ArgfsTer29) | ClinVar dbSNP |
17 | g.37739489A>C | CA499603872 | HNF1B | c.495T>G (p.Arg165=) | |
17 | g.37739489A>G | CA499603873 | HNF1B | c.495T>C (p.Arg165=) | |
17 | g.37739489A>T | CA499603874 | HNF1B | c.495T>A (p.Arg165=) | |
17 | g.37739490C>A | CA398751240 | HNF1B | c.494G>T (p.Arg165Leu) | |
17 | g.37739490C>G | CA398751241 | HNF1B | c.494G>C (p.Arg165Pro) | ClinVar |
17 | g.37739490C>T | CA122605 | HNF1B | c.494G>A (p.Arg165His) | ClinVar dbSNP |
17 | g.37739491G>A | CA398751247 | HNF1B | c.493C>T (p.Arg165Cys) | ClinVar gnomAD v4 |
17 | g.37739491G>C | CA398751244 | HNF1B | c.493C>G (p.Arg165Gly) | |
17 | g.37739491G>T | CA398751245 | HNF1B | c.493C>A (p.Arg165Ser) | |
17 | g.37739492C>A | CA398751248 | HNF1B | c.492G>T (p.Lys164Asn) | |
17 | g.37739492C>G | CA398751250 | HNF1B | c.492G>C (p.Lys164Asn) | |
17 | g.37739492C>T | CA499603879 | HNF1B | c.492G>A (p.Lys164=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739493T>A | CA398751252 | HNF1B | c.491A>T (p.Lys164Met) | |
17 | g.37739493T>C | CA398751253 | HNF1B | c.491A>G (p.Lys164Arg) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739493T>G | CA398751254 | HNF1B | c.491A>C (p.Lys164Thr) | |
17 | g.37739494T>A | CA398751256 | HNF1B | c.490A>T (p.Lys164Ter) | |
17 | g.37739494T>C | CA398751259 | HNF1B | c.490A>G (p.Lys164Glu) | ClinVar |
17 | g.37739494T>G | CA398751258 | HNF1B | c.490A>C (p.Lys164Gln) | ClinVar |
17 | g.37739495C>A | CA398751261 | HNF1B | c.489G>T (p.Gln163His) | dbSNP |
17 | g.37739495C>G | CA398751262 | HNF1B | c.489G>C (p.Gln163His) | |
17 | g.37739495C>T | CA499603883 | HNF1B | c.489G>A (p.Gln163=) | |
17 | g.37739496T>A | CA398751264 | HNF1B | c.488A>T (p.Gln163Leu) | |
17 | g.37739496T>C | CA398751266 | HNF1B | c.488A>G (p.Gln163Arg) | |
17 | g.37739496T>G | CA398751267 | HNF1B | c.488A>C (p.Gln163Pro) | |
17 | g.37739497G>A | CA398751269 | HNF1B | c.487C>T (p.Gln163Ter) | |
17 | g.37739497G>C | CA398751270 | HNF1B | c.487C>G (p.Gln163Glu) | dbSNP gnomAD v4 |
17 | g.37739497G>T | CA398751272 | HNF1B | c.487C>A (p.Gln163Lys) | ClinVar dbSNP |
17 | g.37739499del | CA913190791 | HNF1B | c.487del (p.Gln163ArgfsTer?) | ClinVar |
17 | g.37739498G>A | CA499603887 | HNF1B | c.486C>T (p.Thr162=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739498G>C | CA499603888 | HNF1B | c.486C>G (p.Thr162=) | |
17 | g.37739498G>T | CA499603889 | HNF1B | c.486C>A (p.Thr162=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739499G>A | CA398751274 | HNF1B | c.485C>T (p.Thr162Ile) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739499G>C | CA398751275 | HNF1B | c.485C>G (p.Thr162Ser) | |
17 | g.37739499G>T | CA398751276 | HNF1B | c.485C>A (p.Thr162Asn) | |
17 | g.37739500del | CA913190792 | HNF1B | c.484del (p.Thr162ProfsTer?) | ClinVar |
17 | g.37739500T>A | CA398751282 | HNF1B | c.484A>T (p.Thr162Ser) | |
17 | g.37739500T>C | CA398751280 | HNF1B | c.484A>G (p.Thr162Ala) | |
17 | g.37739500T>G | CA398751279 | HNF1B | c.484A>C (p.Thr162Pro) | |
17 | g.37739503_37739577del | CA913190793 | HNF1B | c.410_484del (p.Arg137_Lys161del) | ClinVar |
17 | g.37739501C>A | CA398751283 | HNF1B | c.483G>T (p.Lys161Asn) | |
17 | g.37739501C>G | CA398751286 | HNF1B | c.483G>C (p.Lys161Asn) | |
17 | g.37739501C>T | CA8519073 | HNF1B | c.483G>A (p.Lys161=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739502T>A | CA398751288 | HNF1B | c.482A>T (p.Lys161Met) | |
17 | g.37739502T>C | CA290288642 | HNF1B | c.482A>G (p.Lys161Arg) | dbSNP |
17 | g.37739502T>G | CA398751289 | HNF1B | c.482A>C (p.Lys161Thr) | |
17 | g.37739503T>A | CA398751292 | HNF1B | c.481A>T (p.Lys161Ter) | ClinVar dbSNP |
17 | g.37739503T>C | CA398751294 | HNF1B | c.481A>G (p.Lys161Glu) | |
17 | g.37739503T>G | CA398751293 | HNF1B | c.481A>C (p.Lys161Gln) | |
17 | g.37739504C>A | CA398751296 | HNF1B | c.480G>T (p.Met160Ile) | |
17 | g.37739504C>G | CA398751300 | HNF1B | c.480G>C (p.Met160Ile) | |
17 | g.37739504C>T | CA398751298 | HNF1B | c.480G>A (p.Met160Ile) | ClinVar |
17 | g.37739505A>C | CA10606095 | HNF1B | c.479T>G (p.Met160Arg) | ClinVar dbSNP |
17 | g.37739505A>G | CA398751302 | HNF1B | c.479T>C (p.Met160Thr) | ClinVar |
17 | g.37739505A>T | CA398751303 | HNF1B | c.479T>A (p.Met160Lys) | |
17 | g.37739506T>A | CA398751305 | HNF1B | c.478A>T (p.Met160Leu) | |
17 | g.37739506T>C | CA398751307 | HNF1B | c.478A>G (p.Met160Val) | ClinVar |
17 | g.37739506T>G | CA398751308 | HNF1B | c.478A>C (p.Met160Leu) | |
17 | g.37739507del | CA214360 | HNF1B | c.477del (p.Met160Ter) | ClinVar dbSNP |
17 | g.37739507A>C | CA499603899 | HNF1B | c.477T>G (p.Pro159=) | |
17 | g.37739507A>G | CA499603900 | HNF1B | c.477T>C (p.Pro159=) | ClinVar dbSNP |
17 | g.37739507A>T | CA499603902 | HNF1B | c.477T>A (p.Pro159=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739508G>A | CA398751311 | HNF1B | c.476C>T (p.Pro159Leu) | ClinVar gnomAD v4 |
17 | g.37739508G>C | CA398751312 | HNF1B | c.476C>G (p.Pro159Arg) | |
17 | g.37739508G>T | CA398751314 | HNF1B | c.476C>A (p.Pro159His) | |
17 | g.37739509G>A | CA398751319 | HNF1B | c.475C>T (p.Pro159Ser) | ClinVar |
17 | g.37739509G>C | CA398751316 | HNF1B | c.475C>G (p.Pro159Ala) | |
17 | g.37739509G>T | CA398751317 | HNF1B | c.475C>A (p.Pro159Thr) | |
17 | g.37739510G>A | CA499603904 | HNF1B | c.474C>T (p.Thr158=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739510G>C | CA499603905 | HNF1B | c.474C>G (p.Thr158=) | |
17 | g.37739510G>T | CA499603906 | HNF1B | c.474C>A (p.Thr158=) | |
17 | g.37739511G>A | CA398751320 | HNF1B | c.473C>T (p.Thr158Ile) | ClinVar dbSNP |
17 | g.37739511G>C | CA398751322 | HNF1B | c.473C>G (p.Thr158Ser) | |
17 | g.37739511G>T | CA398751323 | HNF1B | c.473C>A (p.Thr158Asn) | ClinVar dbSNP |
17 | g.37739511_37739512insGGGCTGCA | CA913190794 | HNF1B | c.472_473insTGCAGCCC (p.Thr158MetfsTer6) | ClinVar |
17 | g.37739512T>A | CA398751324 | HNF1B | c.472A>T (p.Thr158Ser) | |
17 | g.37739512T>C | CA398751325 | HNF1B | c.472A>G (p.Thr158Ala) | |
17 | g.37739512T>G | CA398751327 | HNF1B | c.472A>C (p.Thr158Pro) | |
17 | g.37739513del | CA913190795 | HNF1B | c.471del (p.Thr158ProfsTer3) | ClinVar |
17 | g.37739513G>A | CA499603910 | HNF1B | c.471C>T (p.Gly157=) | |
17 | g.37739513G>C | CA499603911 | HNF1B | c.471C>G (p.Gly157=) | |
17 | g.37739513G>T | CA499603909 | HNF1B | c.471C>A (p.Gly157=) | dbSNP gnomAD v4 |
17 | g.37739514C>A | CA398751329 | HNF1B | c.470G>T (p.Gly157Val) | |
17 | g.37739514C>G | CA398751330 | HNF1B | c.470G>C (p.Gly157Ala) | |
17 | g.37739514C>T | CA398751331 | HNF1B | c.470G>A (p.Gly157Asp) | |
17 | g.37739515C>A | CA398751335 | HNF1B | c.469G>T (p.Gly157Cys) | |
17 | g.37739515C>G | CA398751337 | HNF1B | c.469G>C (p.Gly157Arg) | |
17 | g.37739515C>T | CA398751333 | HNF1B | c.469G>A (p.Gly157Ser) | |
17 | g.37739516C>A | CA398751338 | HNF1B | c.468G>T (p.Lys156Asn) | |
17 | g.37739516C>G | CA398751339 | HNF1B | c.468G>C (p.Lys156Asn) | |
17 | g.37739516C>T | CA499603917 | HNF1B | c.468G>A (p.Lys156=) | gnomAD v4 |
17 | g.37739517T>A | CA398751342 | HNF1B | c.467A>T (p.Lys156Met) | |
17 | g.37739517T>C | CA398751344 | HNF1B | c.467A>G (p.Lys156Arg) | |
17 | g.37739517T>G | CA398751345 | HNF1B | c.467A>C (p.Lys156Thr) | |
17 | g.37739518T>A | CA398751349 | HNF1B | c.466A>T (p.Lys156Ter) | |
17 | g.37739518T>C | CA398751347 | HNF1B | c.466A>G (p.Lys156Glu) | ClinVar |
17 | g.37739518T>G | CA398751348 | HNF1B | c.466A>C (p.Lys156Gln) | |
17 | g.37739519G>A | CA499603923 | HNF1B | c.465C>T (p.Asn155=) | |
17 | g.37739519G>C | CA398751351 | HNF1B | c.465C>G (p.Asn155Lys) | |
17 | g.37739519G>T | CA398751352 | HNF1B | c.465C>A (p.Asn155Lys) | |
17 | g.37739520T>A | CA398751353 | HNF1B | c.464A>T (p.Asn155Ile) | |
17 | g.37739520T>C | CA398751355 | HNF1B | c.464A>G (p.Asn155Ser) | |
17 | g.37739520T>G | CA398751356 | HNF1B | c.464A>C (p.Asn155Thr) | |
17 | g.37739521T>A | CA398751358 | HNF1B | c.463A>T (p.Asn155Tyr) | |
17 | g.37739521T>C | CA398751360 | HNF1B | c.463A>G (p.Asn155Asp) | |
17 | g.37739521T>G | CA398751359 | HNF1B | c.463A>C (p.Asn155His) | dbSNP gnomAD v4 |
17 | g.37739522G>A | CA499603924 | HNF1B | c.462C>T (p.Leu154=) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.37739522G>C | CA499603925 | HNF1B | c.462C>G (p.Leu154=) | |
17 | g.37739522G>T | CA499603926 | HNF1B | c.462C>A (p.Leu154=) | |
17 | g.37739523A>C | CA398751362 | HNF1B | c.461T>G (p.Leu154Arg) | |
17 | g.37739523A>G | CA398751364 | HNF1B | c.461T>C (p.Leu154Pro) | |
17 | g.37739523A>T | CA398751365 | HNF1B | c.461T>A (p.Leu154His) | |
17 | g.37739524G>A | CA398751367 | HNF1B | c.460C>T (p.Leu154Phe) | ClinVar |
17 | g.37739524G>C | CA398751368 | HNF1B | c.460C>G (p.Leu154Val) | |
17 | g.37739524G>T | CA398751370 | HNF1B | c.460C>A (p.Leu154Ile) | |
17 | g.37739525A>C | CA398751371 | HNF1B | c.459T>G (p.His153Gln) | |
17 | g.37739525A>G | CA499603928 | HNF1B | c.459T>C (p.His153=) | |
17 | g.37739525A>T | CA398751373 | HNF1B | c.459T>A (p.His153Gln) | |
17 | g.37739526T>A | CA398751375 | HNF1B | c.458A>T (p.His153Leu) | |
17 | g.37739526T>C | CA398751376 | HNF1B | c.458A>G (p.His153Arg) | ClinVar dbSNP |
17 | g.37739526T>G | CA398751377 | HNF1B | c.458A>C (p.His153Pro) | |
17 | g.37739527G>A | CA398751381 | HNF1B | c.457C>T (p.His153Tyr) | |
17 | g.37739527G>C | CA398751383 | HNF1B | c.457C>G (p.His153Asp) | |
17 | g.37739527G>T | CA398751379 | HNF1B | c.457C>A (p.His153Asn) | ClinVar |
17 | g.37739528C>A | CA398751384 | HNF1B | c.456G>T (p.Gln152His) | |
17 | g.37739528C>G | CA398751385 | HNF1B | c.456G>C (p.Gln152His) | |
17 | g.37739528C>T | CA499603929 | HNF1B | c.456G>A (p.Gln152=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739529T>A | CA398751387 | HNF1B | c.455A>T (p.Gln152Leu) | |
17 | g.37739529T>C | CA398751389 | HNF1B | c.455A>G (p.Gln152Arg) | |
17 | g.37739529T>G | CA398751391 | HNF1B | c.455A>C (p.Gln152Pro) | |
17 | g.37739530G>A | CA398751395 | HNF1B | c.454C>T (p.Gln152Ter) | |
17 | g.37739530G>C | CA398751393 | HNF1B | c.454C>G (p.Gln152Glu) | |
17 | g.37739530G>T | CA398751392 | HNF1B | c.454C>A (p.Gln152Lys) | |
17 | g.37739532del | CA2695225793 | HNF1B | c.454del (p.Gln152SerfsTer9) | |
17 | g.37739531G>A | CA499603930 | HNF1B | c.453C>T (p.Ser151=) | gnomAD v4 |
17 | g.37739531G>C | CA499603931 | HNF1B | c.453C>G (p.Ser151=) | |
17 | g.37739531G>T | CA499603932 | HNF1B | c.453C>A (p.Ser151=) | |
17 | g.37739532G>A | CA398751396 | HNF1B | c.452C>T (p.Ser151Phe) | ClinVar |
17 | g.37739532G>C | CA398751398 | HNF1B | c.452C>G (p.Ser151Cys) | ClinVar |
17 | g.37739532G>T | CA398751400 | HNF1B | c.452C>A (p.Ser151Tyr) | |
17 | g.37739533A>C | CA398751401 | HNF1B | c.451T>G (p.Ser151Ala) | |
17 | g.37739533A>G | CA398751403 | HNF1B | c.451T>C (p.Ser151Pro) | ClinVar |
17 | g.37739533A>T | CA398751404 | HNF1B | c.451T>A (p.Ser151Thr) | |
17 | g.37739534G>A | CA290288657 | HNF1B | c.450C>T (p.Leu150=) | ClinVar dbSNP |
17 | g.37739534G>C | CA499603933 | HNF1B | c.450C>G (p.Leu150=) | |
17 | g.37739534G>T | CA499603934 | HNF1B | c.450C>A (p.Leu150=) | |
17 | g.37739535A>C | CA398751405 | HNF1B | c.449T>G (p.Leu150Arg) | |
17 | g.37739535A>G | CA398751409 | HNF1B | c.449T>C (p.Leu150Pro) | |
17 | g.37739535A>T | CA398751407 | HNF1B | c.449T>A (p.Leu150His) | |
17 | g.37739536G>A | CA398751411 | HNF1B | c.448C>T (p.Leu150Phe) | |
17 | g.37739536G>C | CA398751412 | HNF1B | c.448C>G (p.Leu150Val) | |
17 | g.37739536G>T | CA398751413 | HNF1B | c.448C>A (p.Leu150Ile) | |
17 | g.37739537G>A | CA499603935 | HNF1B | c.447C>T (p.His149=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739537G>C | CA398751415 | HNF1B | c.447C>G (p.His149Gln) | |
17 | g.37739537G>T | CA398751417 | HNF1B | c.447C>A (p.His149Gln) | |
17 | g.37739538T>A | CA398751418 | HNF1B | c.446A>T (p.His149Leu) | |
17 | g.37739538T>C | CA398751420 | HNF1B | c.446A>G (p.His149Arg) | |
17 | g.37739538T>G | CA398751421 | HNF1B | c.446A>C (p.His149Pro) | |
17 | g.37739539G>A | CA398751423 | HNF1B | c.445C>T (p.His149Tyr) | |
17 | g.37739539G>C | CA398751425 | HNF1B | c.445C>G (p.His149Asp) | |
17 | g.37739539G>T | CA398751427 | HNF1B | c.445C>A (p.His149Asn) | |
17 | g.37739540C>A | CA499603936 | HNF1B | c.444G>T (p.Ser148=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739540C>G | CA499603937 | HNF1B | c.444G>C (p.Ser148=) | |
17 | g.37739540C>T | CA8519074 | HNF1B | c.444G>A (p.Ser148=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739541G>A | CA398751429 | HNF1B | c.443C>T (p.Ser148Leu) | ClinVar gnomAD v4 |
17 | g.37739541G>C | CA122604 | HNF1B | c.443C>G (p.Ser148Trp) | ClinVar dbSNP |
17 | g.37739541G>T | CA398751431 | HNF1B | c.443C>A (p.Ser148Ter) | ClinVar |
17 | g.37739542A>C | CA398751434 | HNF1B | c.442T>G (p.Ser148Ala) | |
17 | g.37739542A>G | CA398751435 | HNF1B | c.442T>C (p.Ser148Pro) | |
17 | g.37739542A>T | CA398751437 | HNF1B | c.442T>A (p.Ser148Thr) | |
17 | g.37739543C>A | CA398751439 | HNF1B | c.441G>T (p.Gln147His) | |
17 | g.37739543C>G | CA398751440 | HNF1B | c.441G>C (p.Gln147His) | |
17 | g.37739543C>T | CA499603938 | HNF1B | c.441G>A (p.Gln147=) | dbSNP |
17 | g.37739544T>A | CA398751442 | HNF1B | c.440A>T (p.Gln147Leu) | |
17 | g.37739544T>C | CA398751443 | HNF1B | c.440A>G (p.Gln147Arg) | |
17 | g.37739544T>G | CA398751445 | HNF1B | c.440A>C (p.Gln147Pro) | |
17 | g.37739545G>A | CA398751446 | HNF1B | c.439C>T (p.Gln147Ter) | ClinVar |
17 | g.37739545G>C | CA398751448 | HNF1B | c.439C>G (p.Gln147Glu) | |
17 | g.37739545G>T | CA398751450 | HNF1B | c.439C>A (p.Gln147Lys) | |
17 | g.37739546G>A | CA499603939 | HNF1B | c.438C>T (p.Asn146=) | ClinVar dbSNP gnomAD v4 |
17 | g.37739546G>C | CA398751451 | HNF1B | c.438C>G (p.Asn146Lys) | |
17 | g.37739546G>T | CA398751453 | HNF1B | c.438C>A (p.Asn146Lys) | ClinVar |
17 | g.37739547T>A | CA398751458 | HNF1B | c.437A>T (p.Asn146Ile) | |
17 | g.37739547T>C | CA398751455 | HNF1B | c.437A>G (p.Asn146Ser) | |
17 | g.37739547T>G | CA398751457 | HNF1B | c.437A>C (p.Asn146Thr) | ClinVar |
17 | g.37739548T>A | CA398751460 | HNF1B | c.436A>T (p.Asn146Tyr) | |
17 | g.37739548T>C | CA398751462 | HNF1B | c.436A>G (p.Asn146Asp) | ClinVar |
17 | g.37739548T>G | CA398751464 | HNF1B | c.436A>C (p.Asn146His) | |
17 | g.37739549C>A | CA499603942 | HNF1B | c.435G>T (p.Leu145=) | |
17 | g.37739549C>G | CA499603940 | HNF1B | c.435G>C (p.Leu145=) | |
17 | g.37739549C>T | CA499603941 | HNF1B | c.435G>A (p.Leu145=) | |
17 | g.37739550del | CA2695225794 | HNF1B | c.434del (p.Leu145ArgfsTer16) | |
17 | g.37739550A>C | CA398751465 | HNF1B | c.434T>G (p.Leu145Arg) | |
17 | g.37739550A>G | CA398751466 | HNF1B | c.434T>C (p.Leu145Pro) | |
17 | g.37739550A>T | CA398751468 | HNF1B | c.434T>A (p.Leu145Gln) | ClinVar |
17 | g.37739551G>A | CA499603943 | HNF1B | c.433C>T (p.Leu145=) | |
17 | g.37739551G>C | CA398751470 | HNF1B | c.433C>G (p.Leu145Val) | |
17 | g.37739551G>T | CA398751471 | HNF1B | c.433C>A (p.Leu145Met) | |
17 | g.37739552G>A | CA499603946 | HNF1B | c.432C>T (p.Gly144=) | dbSNP |
17 | g.37739552G>C | CA499603945 | HNF1B | c.432C>G (p.Gly144=) | |
17 | g.37739552G>T | CA499603944 | HNF1B | c.432C>A (p.Gly144=) | |
17 | g.37739553C>A | CA398751472 | HNF1B | c.431G>T (p.Gly144Val) | dbSNP |
17 | g.37739553C>G | CA398751474 | HNF1B | c.431G>C (p.Gly144Ala) | |
17 | g.37739553C>T | CA398751475 | HNF1B | c.431G>A (p.Gly144Asp) | |
17 | g.37739554C>A | CA398751480 | HNF1B | c.430G>T (p.Gly144Cys) | |
17 | g.37739554C>G | CA398751478 | HNF1B | c.430G>C (p.Gly144Arg) | |
17 | g.37739554C>T | CA8519075 | HNF1B | c.430G>A (p.Gly144Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739555G>A | CA8519076 | HNF1B | c.429C>T (p.Thr143=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739555G>C | CA499603947 | HNF1B | c.429C>G (p.Thr143=) | |
17 | g.37739555G>T | CA499603948 | HNF1B | c.429C>A (p.Thr143=) | |
17 | g.37739556G>A | CA398751485 | HNF1B | c.428C>T (p.Thr143Ile) | |
17 | g.37739556G>C | CA398751482 | HNF1B | c.428C>G (p.Thr143Ser) | |
17 | g.37739556G>T | CA398751483 | HNF1B | c.428C>A (p.Thr143Asn) | |
17 | g.37739557T>A | CA398751487 | HNF1B | c.427A>T (p.Thr143Ser) | |
17 | g.37739557T>C | CA398751488 | HNF1B | c.427A>G (p.Thr143Ala) | |
17 | g.37739557T>G | CA398751490 | HNF1B | c.427A>C (p.Thr143Pro) | |
17 | g.37739558G>A | CA499603949 | HNF1B | c.426C>T (p.Val142=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.37739558G>C | CA499603950 | HNF1B | c.426C>G (p.Val142=) | |
17 | g.37739558G>T | CA499603951 | HNF1B | c.426C>A (p.Val142=) | |
17 | g.37739559A>C | CA398751493 | HNF1B | c.425T>G (p.Val142Gly) | |
17 | g.37739559A>G | CA398751494 | HNF1B | c.425T>C (p.Val142Ala) | |
17 | g.37739559A>T | CA398751495 | HNF1B | c.425T>A (p.Val142Asp) | |
17 | g.37739560C>A | CA398751497 | HNF1B | c.424G>T (p.Val142Phe) | |
17 | g.37739560C>G | CA398751499 | HNF1B | c.424G>C (p.Val142Leu) | |
17 | g.37739560C>T | CA398751502 | HNF1B | c.424G>A (p.Val142Ile) | |
17 | g.37739561A>C | CA398751504 | HNF1B | c.423T>G (p.Asp141Glu) | |
17 | g.37739561A>G | CA499603952 | HNF1B | c.423T>C (p.Asp141=) | dbSNP |
17 | g.37739561A>T | CA398751505 | HNF1B | c.423T>A (p.Asp141Glu) | |
17 | g.37739562T>A | CA398751508 | HNF1B | c.422A>T (p.Asp141Val) | |
17 | g.37739562T>C | CA398751507 | HNF1B | c.422A>G (p.Asp141Gly) | |
17 | g.37739562T>G | CA398751506 | HNF1B | c.422A>C (p.Asp141Ala) | |
17 | g.37739563C>A | CA398751510 | HNF1B | c.421G>T (p.Asp141Tyr) | |
17 | g.37739563C>G | CA398751512 | HNF1B | c.421G>C (p.Asp141His) | |
17 | g.37739563C>T | CA290288699 | HNF1B | c.421G>A (p.Asp141Asn) | dbSNP gnomAD v4 |
17 | g.37739564G>A | CA8519077 | HNF1B | c.420C>T (p.Val140=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.37739564G>C | CA499603953 | HNF1B | c.420C>G (p.Val140=) | |
17 | g.37739564G>T | CA499603954 | HNF1B | c.420C>A (p.Val140=) | |
17 | g.37739565A>C | CA398751514 | HNF1B | c.419T>G (p.Val140Gly) | |
17 | g.37739565A>G | CA398751515 | HNF1B | c.419T>C (p.Val140Ala) | |
17 | g.37739565A>T | CA398751516 | HNF1B | c.419T>A (p.Val140Asp) | |
17 | g.37739566C>A | CA398751519 | HNF1B | c.418G>T (p.Val140Phe) | gnomAD v4 |
17 | g.37739566C>G | CA398751520 | HNF1B | c.418G>C (p.Val140Leu) | |
17 | g.37739566C>T | CA398751522 | HNF1B | c.418G>A (p.Val140Ile) | |
17 | g.37739567C>A | CA499603955 | HNF1B | c.417G>T (p.Val139=) | |
17 | g.37739567C>G | CA499603956 | HNF1B | c.417G>C (p.Val139=) | |
17 | g.37739567C>T | CA499603957 | HNF1B | c.417G>A (p.Val139=) | |
17 | g.37739568A>C | CA398751523 | HNF1B | c.416T>G (p.Val139Gly) | ClinVar |
17 | g.37739568A>G | CA398751525 | HNF1B | c.416T>C (p.Val139Ala) | gnomAD v4 |
17 | g.37739568A>T | CA398751528 | HNF1B | c.416T>A (p.Val139Glu) | |
17 | g.37739569C>A | CA398751532 | HNF1B | c.415G>T (p.Val139Leu) | |
17 | g.37739569C>G | CA398751534 | HNF1B | c.415G>C (p.Val139Leu) | |
17 | g.37739569C>T | CA398751530 | HNF1B | c.415G>A (p.Val139Met) | |
17 | g.37739570C>A | CA398751536 | HNF1B | c.414G>T (p.Glu138Asp) | |
17 | g.37739570C>G | CA398751537 | HNF1B | c.414G>C (p.Glu138Asp) | |
17 | g.37739570C>T | CA499603958 | HNF1B | c.414G>A (p.Glu138=) | |
17 | g.37739571T>A | CA398751538 | HNF1B | c.413A>T (p.Glu138Val) | |
17 | g.37739571T>C | CA398751539 | HNF1B | c.413A>G (p.Glu138Gly) | |
17 | g.37739571T>G | CA398751540 | HNF1B | c.413A>C (p.Glu138Ala) |