Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.6301907C>ACA356177748WFS1c.2148C>A (p.Phe716Leu)
c.2089C>A
c.2112C>A (p.Phe704Leu)
c.1863C>A (p.Phe621Leu)
c.1771C>A (n.1771C>A)
n.2297C>A
c.2121C>A (p.Phe707Leu)
4g.6301907C>GCA356177750WFS1c.2148C>G (p.Phe716Leu)
c.2089C>G
c.2112C>G (p.Phe704Leu)
c.1863C>G (p.Phe621Leu)
c.1771C>G (n.1771C>G)
n.2297C>G
c.2121C>G (p.Phe707Leu)
4g.6301907C>TCA438368541WFS1c.2148C>T (p.Phe716=)
c.2089C>T
c.2112C>T (p.Phe704=)
c.1863C>T (p.Phe621=)
c.1771C>T (n.1771C>T)
n.2297C>T
c.2121C>T (p.Phe707=)
 COSMIC
4g.6301908A>CCA356177752WFS1c.2149A>C (p.Lys717Gln)
c.2090A>C
c.2113A>C (p.Lys705Gln)
c.1864A>C (p.Lys622Gln)
c.1772A>C (n.1772A>C)
n.2298A>C
c.2122A>C (p.Lys708Gln)
4g.6301908A>GCA356177753WFS1c.2149A>G (p.Lys717Glu)
c.2090A>G
c.2113A>G (p.Lys705Glu)
c.1864A>G (p.Lys622Glu)
c.1772A>G (n.1772A>G)
n.2298A>G
c.2122A>G (p.Lys708Glu)
 ClinVar dbSNP
4g.6301908A>TCA356177755WFS1c.2149A>T (p.Lys717Ter)
c.2090A>T
c.2113A>T (p.Lys705Ter)
c.1864A>T (p.Lys622Ter)
c.1772A>T (n.1772A>T)
n.2298A>T
c.2122A>T (p.Lys708Ter)
4g.6301909A>CCA356177757WFS1c.2150A>C (p.Lys717Thr)
c.2091A>C
c.2114A>C (p.Lys705Thr)
c.1865A>C (p.Lys622Thr)
c.1773A>C (n.1773A>C)
n.2299A>C
c.2123A>C (p.Lys708Thr)
4g.6301909A>GCA356177758WFS1c.2150A>G (p.Lys717Arg)
c.2091A>G
c.2114A>G (p.Lys705Arg)
c.1865A>G (p.Lys622Arg)
c.1773A>G (n.1773A>G)
n.2299A>G
c.2123A>G (p.Lys708Arg)
 gnomAD v4
4g.6301909A>TCA356177759WFS1c.2150A>T (p.Lys717Met)
c.2091A>T
c.2114A>T (p.Lys705Met)
c.1865A>T (p.Lys622Met)
c.1773A>T (n.1773A>T)
n.2299A>T
c.2123A>T (p.Lys708Met)
4g.6301910G>ACA438368543WFS1c.2151G>A (p.Lys717=)
c.2092G>A
c.2115G>A (p.Lys705=)
c.1866G>A (p.Lys622=)
c.1774G>A (n.1774G>A)
n.2300G>A
c.2124G>A (p.Lys708=)
 gnomAD v4
4g.6301910G>CCA356177762WFS1c.2151G>C (p.Lys717Asn)
c.2092G>C
c.2115G>C (p.Lys705Asn)
c.1866G>C (p.Lys622Asn)
c.1774G>C (n.1774G>C)
n.2300G>C
c.2124G>C (p.Lys708Asn)
 ClinVar dbSNP
4g.6301910G>TCA356177763WFS1c.2151G>T (p.Lys717Asn)
c.2092G>T
c.2115G>T (p.Lys705Asn)
c.1866G>T (p.Lys622Asn)
c.1774G>T (n.1774G>T)
n.2300G>T
c.2124G>T (p.Lys708Asn)
4g.6301911T>ACA356177765WFS1c.2152T>A (p.Tyr718Asn)
c.2093T>A
c.2116T>A (p.Tyr706Asn)
c.1867T>A (p.Tyr623Asn)
c.1775T>A (n.1775T>A)
n.2301T>A
c.2125T>A (p.Tyr709Asn)
4g.6301911T>CCA356177766WFS1c.2152T>C (p.Tyr718His)
c.2093T>C
c.2116T>C (p.Tyr706His)
c.1867T>C (p.Tyr623His)
c.1775T>C (n.1775T>C)
n.2301T>C
c.2125T>C (p.Tyr709His)
4g.6301911T>GCA356177768WFS1c.2152T>G (p.Tyr718Asp)
c.2093T>G
c.2116T>G (p.Tyr706Asp)
c.1867T>G (p.Tyr623Asp)
c.1775T>G (n.1775T>G)
n.2301T>G
c.2125T>G (p.Tyr709Asp)
4g.6301912A>CCA356177772WFS1c.2153A>C (p.Tyr718Ser)
c.2094A>C
c.2117A>C (p.Tyr706Ser)
c.1868A>C (p.Tyr623Ser)
c.1776A>C (n.1776A>C)
n.2302A>C
c.2126A>C (p.Tyr709Ser)
4g.6301912A>GCA356177771WFS1c.2153A>G (p.Tyr718Cys)
c.2094A>G
c.2117A>G (p.Tyr706Cys)
c.1868A>G (p.Tyr623Cys)
c.1776A>G (n.1776A>G)
n.2302A>G
c.2126A>G (p.Tyr709Cys)
4g.6301912A>TCA356177770WFS1c.2153A>T (p.Tyr718Phe)
c.2094A>T
c.2117A>T (p.Tyr706Phe)
c.1868A>T (p.Tyr623Phe)
c.1776A>T (n.1776A>T)
n.2302A>T
c.2126A>T (p.Tyr709Phe)
4g.6301913C>ACA356177774WFS1c.2154C>A (p.Tyr718Ter)
c.2095C>A
c.2118C>A (p.Tyr706Ter)
c.1869C>A (p.Tyr623Ter)
c.1777C>A (n.1777C>A)
n.2303C>A
c.2127C>A (p.Tyr709Ter)
4g.6301913C=CA1435772039WFS1c.2154C= (p.Tyr718=)
c.2095C=
c.2118C= (p.Tyr706=)
c.1869C= (p.Tyr623=)
c.1777C= (n.1777C=)
n.2303C=
c.2127C= (p.Tyr709=)
4g.6301913C>GCA356177775WFS1c.2154C>G (p.Tyr718Ter)
c.2095C>G
c.2118C>G (p.Tyr706Ter)
c.1869C>G (p.Tyr623Ter)
c.1777C>G (n.1777C>G)
n.2303C>G
c.2127C>G (p.Tyr709Ter)
4g.6301913C>TCA2839604WFS1c.2154C>T (p.Tyr718=)
c.2095C>T
c.2118C>T (p.Tyr706=)
c.1869C>T (p.Tyr623=)
c.1777C>T (n.1777C>T)
n.2303C>T
c.2127C>T (p.Tyr709=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6301914G>ACA325333WFS1c.2155G>A (p.Val719Ile)
c.2096G>A
c.2119G>A (p.Val707Ile)
c.1870G>A (p.Val624Ile)
c.1778G>A (n.1778G>A)
n.2304G>A
c.2128G>A (p.Val710Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301914G>CCA356177779WFS1c.2155G>C (p.Val719Leu)
c.2096G>C
c.2119G>C (p.Val707Leu)
c.1870G>C (p.Val624Leu)
c.1778G>C (n.1778G>C)
n.2304G>C
c.2128G>C (p.Val710Leu)
 gnomAD v4
4g.6301914G=CA1435772042WFS1c.2155G= (p.Val719=)
c.2096G=
c.2119G= (p.Val707=)
c.1870G= (p.Val624=)
c.1778G= (n.1778G=)
n.2304G=
c.2128G= (p.Val710=)
4g.6301914G>TCA259830WFS1c.2155G>T (p.Val719Phe)
c.2096G>T
c.2119G>T (p.Val707Phe)
c.1870G>T (p.Val624Phe)
c.1778G>T (n.1778G>T)
n.2304G>T
c.2128G>T (p.Val710Phe)
 ClinVar dbSNP
4g.[6301914G>T;6302444del]CA2742038358WFS1c.[2155G>T;2685del] (p.[Val719Phe;Phe896SerfsTer?])
c.[2096G>T;2626del]
c.[2119G>T;2649del] (p.[Val707Phe;Phe884SerfsTer?])
c.[1870G>T;2400del] (p.[Val624Phe;Phe801SerfsTer?])
n.[2304G>T;2834del]
c.[2128G>T;2658del] (p.[Val710Phe;Phe887SerfsTer?])
4g.6301915T>ACA356177782WFS1c.2156T>A (p.Val719Asp)
c.2097T>A
c.2120T>A (p.Val707Asp)
c.1871T>A (p.Val624Asp)
c.1779T>A (n.1779T>A)
n.2305T>A
c.2129T>A (p.Val710Asp)
4g.6301915T>CCA356177784WFS1c.2156T>C (p.Val719Ala)
c.2097T>C
c.2120T>C (p.Val707Ala)
c.1871T>C (p.Val624Ala)
c.1779T>C (n.1779T>C)
n.2305T>C
c.2129T>C (p.Val710Ala)
 dbSNP
4g.6301915T>GCA356177785WFS1c.2156T>G (p.Val719Gly)
c.2097T>G
c.2120T>G (p.Val707Gly)
c.1871T>G (p.Val624Gly)
c.1779T>G (n.1779T>G)
n.2305T>G
c.2129T>G (p.Val710Gly)
4g.6301915T=CA1435772044WFS1c.2156T= (p.Val719=)
c.2097T=
c.2120T= (p.Val707=)
c.1871T= (p.Val624=)
c.1779T= (n.1779T=)
n.2305T=
c.2129T= (p.Val710=)
4g.6301916C>ACA438368555WFS1c.2157C>A (p.Val719=)
c.2098C>A
c.2121C>A (p.Val707=)
c.1872C>A (p.Val624=)
c.1780C>A (n.1780C>A)
n.2306C>A
c.2130C>A (p.Val710=)
 ClinVar
4g.6301916C>GCA438368558WFS1c.2157C>G (p.Val719=)
c.2098C>G
c.2121C>G (p.Val707=)
c.1872C>G (p.Val624=)
c.1780C>G (n.1780C>G)
n.2306C>G
c.2130C>G (p.Val710=)
4g.6301916C>TCA438368561WFS1c.2157C>T (p.Val719=)
c.2098C>T
c.2121C>T (p.Val707=)
c.1872C>T (p.Val624=)
c.1780C>T (n.1780C>T)
n.2306C>T
c.2130C>T (p.Val710=)
 gnomAD v4
4g.6301917C>ACA356177786WFS1c.2158C>A (p.Arg720Ser)
c.2099C>A
c.2122C>A (p.Arg708Ser)
c.1873C>A (p.Arg625Ser)
c.1781C>A (n.1781C>A)
n.2307C>A
c.2131C>A (p.Arg711Ser)
4g.6301917C=CA1435772045WFS1c.2158C= (p.Arg720=)
c.2099C=
c.2122C= (p.Arg708=)
c.1873C= (p.Arg625=)
c.1781C= (n.1781C=)
n.2307C=
c.2131C= (p.Arg711=)
4g.6301917C>GCA356177787WFS1c.2158C>G (p.Arg720Gly)
c.2099C>G
c.2122C>G (p.Arg708Gly)
c.1873C>G (p.Arg625Gly)
c.1781C>G (n.1781C>G)
n.2307C>G
c.2131C>G (p.Arg711Gly)
4g.6301917C>TCA2839605WFS1c.2158C>T (p.Arg720Cys)
c.2099C>T
c.2122C>T (p.Arg708Cys)
c.1873C>T (p.Arg625Cys)
c.1781C>T (n.1781C>T)
n.2307C>T
c.2131C>T (p.Arg711Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301918G>ACA2839606WFS1c.2159G>A (p.Arg720His)
c.2100G>A
c.2123G>A (p.Arg708His)
c.1874G>A (p.Arg625His)
c.1782G>A (n.1782G>A)
n.2308G>A
c.2132G>A (p.Arg711His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301918G>CCA356177790WFS1c.2159G>C (p.Arg720Pro)
c.2100G>C
c.2123G>C (p.Arg708Pro)
c.1874G>C (p.Arg625Pro)
c.1782G>C (n.1782G>C)
n.2308G>C
c.2132G>C (p.Arg711Pro)
4g.6301918G=CA1435772046WFS1c.2159G= (p.Arg720=)
c.2100G=
c.2123G= (p.Arg708=)
c.1874G= (p.Arg625=)
c.1782G= (n.1782G=)
n.2308G=
c.2132G= (p.Arg711=)
4g.6301918G>TCA356177789WFS1c.2159G>T (p.Arg720Leu)
c.2100G>T
c.2123G>T (p.Arg708Leu)
c.1874G>T (p.Arg625Leu)
c.1782G>T (n.1782G>T)
n.2308G>T
c.2132G>T (p.Arg711Leu)
 ClinVar gnomAD v4
4g.6301919C>ACA438368562WFS1c.2160C>A (p.Arg720=)
c.2101C>A
c.2124C>A (p.Arg708=)
c.1875C>A (p.Arg625=)
c.1783C>A (n.1783C>A)
n.2309C>A
c.2133C>A (p.Arg711=)
4g.6301919C=CA1435772047WFS1c.2160C= (p.Arg720=)
c.2101C=
c.2124C= (p.Arg708=)
c.1875C= (p.Arg625=)
c.1783C= (n.1783C=)
n.2309C=
c.2133C= (p.Arg711=)
4g.6301919C>GCA438368564WFS1c.2160C>G (p.Arg720=)
c.2101C>G
c.2124C>G (p.Arg708=)
c.1875C>G (p.Arg625=)
c.1783C>G (n.1783C>G)
n.2309C>G
c.2133C>G (p.Arg711=)
4g.6301919C>TCA295793WFS1c.2160C>T (p.Arg720=)
c.2101C>T
c.2124C>T (p.Arg708=)
c.1875C>T (p.Arg625=)
c.1783C>T (n.1783C>T)
n.2309C>T
c.2133C>T (p.Arg711=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301920G>ACA2839607WFS1c.2161G>A (p.Val721Met)
c.2102G>A
c.2125G>A (p.Val709Met)
c.1876G>A (p.Val626Met)
c.1784G>A (n.1784G>A)
n.2310G>A
c.2134G>A (p.Val712Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301920G>CCA356177793WFS1c.2161G>C (p.Val721Leu)
c.2102G>C
c.2125G>C (p.Val709Leu)
c.1876G>C (p.Val626Leu)
c.1784G>C (n.1784G>C)
n.2310G>C
c.2134G>C (p.Val712Leu)
4g.6301920G=CA1435772048WFS1c.2161G= (p.Val721=)
c.2102G=
c.2125G= (p.Val709=)
c.1876G= (p.Val626=)
c.1784G= (n.1784G=)
n.2310G=
c.2134G= (p.Val712=)
4g.6301920G>TCA356177797WFS1c.2161G>T (p.Val721Leu)
c.2102G>T
c.2125G>T (p.Val709Leu)
c.1876G>T (p.Val626Leu)
c.1784G>T (n.1784G>T)
n.2310G>T
c.2134G>T (p.Val712Leu)
4g.6301921_6301922delCA2669843472WFS1c.2162_2163del (p.Val721AspfsTer2)
c.2103_2104del
c.2126_2127del (p.Val709AspfsTer2)
c.1877_1878del (p.Val626AspfsTer2)
c.1785_1786del (n.1785_1786del)
n.2311_2312del
c.2135_2136del (p.Val712AspfsTer2)
 gnomAD v4
4g.6301921T>ACA356177799WFS1c.2162T>A (p.Val721Glu)
c.2103T>A
c.2126T>A (p.Val709Glu)
c.1877T>A (p.Val626Glu)
c.1785T>A (n.1785T>A)
n.2311T>A
c.2135T>A (p.Val712Glu)
4g.6301921T>CCA356177801WFS1c.2162T>C (p.Val721Ala)
c.2103T>C
c.2126T>C (p.Val709Ala)
c.1877T>C (p.Val626Ala)
c.1785T>C (n.1785T>C)
n.2311T>C
c.2135T>C (p.Val712Ala)
4g.6301921T>GCA356177804WFS1c.2162T>G (p.Val721Gly)
c.2103T>G
c.2126T>G (p.Val709Gly)
c.1877T>G (p.Val626Gly)
c.1785T>G (n.1785T>G)
n.2311T>G
c.2135T>G (p.Val712Gly)
 gnomAD v4
4g.6301922G>ACA438368568WFS1c.2163G>A (p.Val721=)
c.2104G>A
c.2127G>A (p.Val709=)
c.1878G>A (p.Val626=)
c.1786G>A (n.1786G>A)
n.2312G>A
c.2136G>A (p.Val712=)
4g.6301922G>CCA2839608WFS1c.2163G>C (p.Val721=)
c.2104G>C
c.2127G>C (p.Val709=)
c.1878G>C (p.Val626=)
c.1786G>C (n.1786G>C)
n.2312G>C
c.2136G>C (p.Val712=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301922G=CA1435772050WFS1c.2163G= (p.Val721=)
c.2104G=
c.2127G= (p.Val709=)
c.1878G= (p.Val626=)
c.1786G= (n.1786G=)
n.2312G=
c.2136G= (p.Val712=)
4g.6301922G>TCA438368572WFS1c.2163G>T (p.Val721=)
c.2104G>T
c.2127G>T (p.Val709=)
c.1878G>T (p.Val626=)
c.1786G>T (n.1786G>T)
n.2312G>T
c.2136G>T (p.Val712=)
 dbSNP
4g.6301923A=CA1435772051WFS1c.2164A= (p.Thr722=)
c.2105A=
c.2128A= (p.Thr710=)
c.1879A= (p.Thr627=)
c.1787A= (n.1787A=)
n.2313A=
c.2137A= (p.Thr713=)
4g.6301923A>CCA356177805WFS1c.2164A>C (p.Thr722Pro)
c.2105A>C
c.2128A>C (p.Thr710Pro)
c.1879A>C (p.Thr627Pro)
c.1787A>C (n.1787A>C)
n.2313A>C
c.2137A>C (p.Thr713Pro)
 COSMIC
4g.6301923A>GCA356177806WFS1c.2164A>G (p.Thr722Ala)
c.2105A>G
c.2128A>G (p.Thr710Ala)
c.1879A>G (p.Thr627Ala)
c.1787A>G (n.1787A>G)
n.2313A>G
c.2137A>G (p.Thr713Ala)
4g.6301923A>TCA356177807WFS1c.2164A>T (p.Thr722Ser)
c.2105A>T
c.2128A>T (p.Thr710Ser)
c.1879A>T (p.Thr627Ser)
c.1787A>T (n.1787A>T)
n.2313A>T
c.2137A>T (p.Thr713Ser)
4g.6301923_6301924insTCA1435772054WFS1c.2164_2165insT (p.Thr722IlefsTer2)
c.2105_2106insT
c.2128_2129insT (p.Thr710IlefsTer2)
c.1879_1880insT (p.Thr627IlefsTer2)
c.1787_1788insT (n.1787_1788insT)
n.2313_2314insT
c.2137_2138insT (p.Thr713IlefsTer2)
 dbSNP
4g.6301924C>ACA356177810WFS1c.2165C>A (p.Thr722Asn)
c.2106C>A
c.2129C>A (p.Thr710Asn)
c.1880C>A (p.Thr627Asn)
c.1788C>A (n.1788C>A)
n.2314C>A
c.2138C>A (p.Thr713Asn)
4g.6301924C=CA1435772055WFS1c.2165C= (p.Thr722=)
c.2106C=
c.2129C= (p.Thr710=)
c.1880C= (p.Thr627=)
c.1788C= (n.1788C=)
n.2314C=
c.2138C= (p.Thr713=)
4g.6301924C>GCA2839609WFS1c.2165C>G (p.Thr722Ser)
c.2106C>G
c.2129C>G (p.Thr710Ser)
c.1880C>G (p.Thr627Ser)
c.1788C>G (n.1788C>G)
n.2314C>G
c.2138C>G (p.Thr713Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301924C>TCA356177812WFS1c.2165C>T (p.Thr722Ile)
c.2106C>T
c.2129C>T (p.Thr710Ile)
c.1880C>T (p.Thr627Ile)
c.1788C>T (n.1788C>T)
n.2314C>T
c.2138C>T (p.Thr713Ile)
 gnomAD v4
4g.6301925T>ACA438368580WFS1c.2166T>A (p.Thr722=)
c.2107T>A
c.2130T>A (p.Thr710=)
c.1881T>A (p.Thr627=)
c.1789T>A (n.1789T>A)
n.2315T>A
c.2139T>A (p.Thr713=)
4g.6301925T>CCA91796850WFS1c.2166T>C (p.Thr722=)
c.2107T>C
c.2130T>C (p.Thr710=)
c.1881T>C (p.Thr627=)
c.1789T>C (n.1789T>C)
n.2315T>C
c.2139T>C (p.Thr713=)
 dbSNP
4g.6301925T>GCA438368582WFS1c.2166T>G (p.Thr722=)
c.2107T>G
c.2130T>G (p.Thr710=)
c.1881T>G (p.Thr627=)
c.1789T>G (n.1789T>G)
n.2315T>G
c.2139T>G (p.Thr713=)
4g.6301925T=CA1435772057WFS1c.2166T= (p.Thr722=)
c.2107T=
c.2130T= (p.Thr710=)
c.1881T= (p.Thr627=)
c.1789T= (n.1789T=)
n.2315T=
c.2139T= (p.Thr713=)
4g.6301925_6301931delinsTGACATCCA1435772058WFS1c.2166_2172delinsTGACATC (p.Thr722=)
c.2107_2113delinsTGACATC
c.2130_2136delinsTGACATC (p.Thr710=)
c.1881_1887delinsTGACATC (p.Thr627=)
c.1789_1795delinsTGACATC (n.1789_1795delinsTGACATC)
n.2315_2321delinsTGACATC
c.2139_2145delinsTGACATC (p.Thr713=)
4g.6301926G>ACA2839610WFS1c.2167G>A (p.Asp723Asn)
c.2108G>A
c.2131G>A (p.Asp711Asn)
c.1882G>A (p.Asp628Asn)
c.1790G>A (n.1790G>A)
n.2316G>A
c.2140G>A (p.Asp714Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301926G>CCA356177815WFS1c.2167G>C (p.Asp723His)
c.2108G>C
c.2131G>C (p.Asp711His)
c.1882G>C (p.Asp628His)
c.1790G>C (n.1790G>C)
n.2316G>C
c.2140G>C (p.Asp714His)
 gnomAD v4
4g.6301926G=CA1435772061WFS1c.2167G= (p.Asp723=)
c.2108G=
c.2131G= (p.Asp711=)
c.1882G= (p.Asp628=)
c.1790G= (n.1790G=)
n.2316G=
c.2140G= (p.Asp714=)
4g.6301926G>TCA356177814WFS1c.2167G>T (p.Asp723Tyr)
c.2108G>T
c.2131G>T (p.Asp711Tyr)
c.1882G>T (p.Asp628Tyr)
c.1790G>T (n.1790G>T)
n.2316G>T
c.2140G>T (p.Asp714Tyr)
4g.6301930_6301935delCA1435772060WFS1c.2171_2176del (p.Ile724_Asp725del)
c.2112_2117del
c.2135_2140del (p.Ile712_Asp713del)
c.1886_1891del (p.Ile629_Asp630del)
c.1794_1799del (n.1794_1799del)
n.2320_2325del
c.2144_2149del (p.Ile715_Asp716del)
 dbSNP
4g.6301927A>CCA356177817WFS1c.2168A>C (p.Asp723Ala)
c.2109A>C
c.2132A>C (p.Asp711Ala)
c.1883A>C (p.Asp628Ala)
c.1791A>C (n.1791A>C)
n.2317A>C
c.2141A>C (p.Asp714Ala)
4g.6301927A>GCA356177819WFS1c.2168A>G (p.Asp723Gly)
c.2109A>G
c.2132A>G (p.Asp711Gly)
c.1883A>G (p.Asp628Gly)
c.1791A>G (n.1791A>G)
n.2317A>G
c.2141A>G (p.Asp714Gly)
4g.6301927A>TCA356177821WFS1c.2168A>T (p.Asp723Val)
c.2109A>T
c.2132A>T (p.Asp711Val)
c.1883A>T (p.Asp628Val)
c.1791A>T (n.1791A>T)
n.2317A>T
c.2141A>T (p.Asp714Val)
4g.6301928C>ACA356177823WFS1c.2169C>A (p.Asp723Glu)
c.2110C>A
c.2133C>A (p.Asp711Glu)
c.1884C>A (p.Asp628Glu)
c.1792C>A (n.1792C>A)
n.2318C>A
c.2142C>A (p.Asp714Glu)
4g.6301928C=CA1435772063WFS1c.2169C= (p.Asp723=)
c.2110C=
c.2133C= (p.Asp711=)
c.1884C= (p.Asp628=)
c.1792C= (n.1792C=)
n.2318C=
c.2142C= (p.Asp714=)
4g.6301928C>GCA356177825WFS1c.2169C>G (p.Asp723Glu)
c.2110C>G
c.2133C>G (p.Asp711Glu)
c.1884C>G (p.Asp628Glu)
c.1792C>G (n.1792C>G)
n.2318C>G
c.2142C>G (p.Asp714Glu)
4g.6301928C>TCA438368587WFS1c.2169C>T (p.Asp723=)
c.2110C>T
c.2133C>T (p.Asp711=)
c.1884C>T (p.Asp628=)
c.1792C>T (n.1792C>T)
n.2318C>T
c.2142C>T (p.Asp714=)
 dbSNP gnomAD v3 gnomAD v4
4g.6301929A=CA1435772064WFS1c.2170A= (p.Ile724=)
c.2111A=
c.2134A= (p.Ile712=)
c.1885A= (p.Ile629=)
c.1793A= (n.1793A=)
n.2319A=
c.2143A= (p.Ile715=)
4g.6301929A>CCA356177827WFS1c.2170A>C (p.Ile724Leu)
c.2111A>C
c.2134A>C (p.Ile712Leu)
c.1885A>C (p.Ile629Leu)
c.1793A>C (n.1793A>C)
n.2319A>C
c.2143A>C (p.Ile715Leu)
 gnomAD v4
4g.6301929A>GCA2839611WFS1c.2170A>G (p.Ile724Val)
c.2111A>G
c.2134A>G (p.Ile712Val)
c.1885A>G (p.Ile629Val)
c.1793A>G (n.1793A>G)
n.2319A>G
c.2143A>G (p.Ile715Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301929A>TCA356177830WFS1c.2170A>T (p.Ile724Phe)
c.2111A>T
c.2134A>T (p.Ile712Phe)
c.1885A>T (p.Ile629Phe)
c.1793A>T (n.1793A>T)
n.2319A>T
c.2143A>T (p.Ile715Phe)
4g.6301930T>ACA356177832WFS1c.2171T>A (p.Ile724Asn)
c.2112T>A
c.2135T>A (p.Ile712Asn)
c.1886T>A (p.Ile629Asn)
c.1794T>A (n.1794T>A)
n.2320T>A
c.2144T>A (p.Ile715Asn)
4g.6301930T>CCA356177834WFS1c.2171T>C (p.Ile724Thr)
c.2112T>C
c.2135T>C (p.Ile712Thr)
c.1886T>C (p.Ile629Thr)
c.1794T>C (n.1794T>C)
n.2320T>C
c.2144T>C (p.Ile715Thr)
 ClinVar dbSNP
4g.6301930T>GCA356177835WFS1c.2171T>G (p.Ile724Ser)
c.2112T>G
c.2135T>G (p.Ile712Ser)
c.1886T>G (p.Ile629Ser)
c.1794T>G (n.1794T>G)
n.2320T>G
c.2144T>G (p.Ile715Ser)
 ClinVar
4g.6301930T=CA1435772065WFS1c.2171T= (p.Ile724=)
c.2112T=
c.2135T= (p.Ile712=)
c.1886T= (p.Ile629=)
c.1794T= (n.1794T=)
n.2320T=
c.2144T= (p.Ile715=)
4g.6301931C>ACA2839613WFS1c.2172C>A (p.Ile724=)
c.2113C>A
c.2136C>A (p.Ile712=)
c.1887C>A (p.Ile629=)
c.1795C>A (n.1795C>A)
n.2321C>A
c.2145C>A (p.Ile715=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301931C=CA1435772068WFS1c.2172C= (p.Ile724=)
c.2113C=
c.2136C= (p.Ile712=)
c.1887C= (p.Ile629=)
c.1795C= (n.1795C=)
n.2321C=
c.2145C= (p.Ile715=)
4g.6301931C>GCA356177838WFS1c.2172C>G (p.Ile724Met)
c.2113C>G
c.2136C>G (p.Ile712Met)
c.1887C>G (p.Ile629Met)
c.1795C>G (n.1795C>G)
n.2321C>G
c.2145C>G (p.Ile715Met)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301931C>TCA2839612WFS1c.2172C>T (p.Ile724=)
c.2113C>T
c.2136C>T (p.Ile712=)
c.1887C>T (p.Ile629=)
c.1795C>T (n.1795C>T)
n.2321C>T
c.2145C>T (p.Ile715=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301932_6301934delCA2586973644WFS1c.2173_2175del (p.Asp725del)
c.2114_2116del
c.2137_2139del (p.Asp713del)
c.1888_1890del (p.Asp630del)
c.1796_1798del (n.1796_1798del)
n.2322_2324del
c.2146_2148del (p.Asp716del)
4g.6301932G>ACA2839614WFS1c.2173G>A (p.Asp725Asn)
c.2114G>A
c.2137G>A (p.Asp713Asn)
c.1888G>A (p.Asp630Asn)
c.1796G>A (n.1796G>A)
n.2322G>A
c.2146G>A (p.Asp716Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301932G>CCA356177841WFS1c.2173G>C (p.Asp725His)
c.2114G>C
c.2137G>C (p.Asp713His)
c.1888G>C (p.Asp630His)
c.1796G>C (n.1796G>C)
n.2322G>C
c.2146G>C (p.Asp716His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301932G=CA1435772071WFS1c.2173G= (p.Asp725=)
c.2114G=
c.2137G= (p.Asp713=)
c.1888G= (p.Asp630=)
c.1796G= (n.1796G=)
n.2322G=
c.2146G= (p.Asp716=)
4g.6301932G>TCA356177844WFS1c.2173G>T (p.Asp725Tyr)
c.2114G>T
c.2137G>T (p.Asp713Tyr)
c.1888G>T (p.Asp630Tyr)
c.1796G>T (n.1796G>T)
n.2322G>T
c.2146G>T (p.Asp716Tyr)
 gnomAD v4
4g.6301932_6301956delinsGACAACAGCGCCGAGTCTGCCATCACA1435772070WFS1c.2173_2197delinsGACAACAGCGCCGAGTCTGCCATCA (p.Asp725=)
c.2114_2138delinsGACAACAGCGCCGAGTCTGCCATCA
c.2137_2161delinsGACAACAGCGCCGAGTCTGCCATCA (p.Asp713=)
c.1888_1912delinsGACAACAGCGCCGAGTCTGCCATCA (p.Asp630=)
c.1796_1820delinsGACAACAGCGCCGAGTCTGCCATCA (n.1796_1820delinsGACAACAGCGCCGAGTCTGCCATCA)
n.2322_2346delinsGACAACAGCGCCGAGTCTGCCATCA
c.2146_2170delinsGACAACAGCGCCGAGTCTGCCATCA (p.Asp716=)
4g.6301933A=CA1435772074WFS1c.2174A= (p.Asp725=)
c.2115A=
c.2138A= (p.Asp713=)
c.1889A= (p.Asp630=)
c.1797A= (n.1797A=)
n.2323A=
c.2147A= (p.Asp716=)
4g.6301933A>CCA356177847WFS1c.2174A>C (p.Asp725Ala)
c.2115A>C
c.2138A>C (p.Asp713Ala)
c.1889A>C (p.Asp630Ala)
c.1797A>C (n.1797A>C)
n.2323A>C
c.2147A>C (p.Asp716Ala)
4g.6301933A>GCA2839616WFS1c.2174A>G (p.Asp725Gly)
c.2115A>G
c.2138A>G (p.Asp713Gly)
c.1889A>G (p.Asp630Gly)
c.1797A>G (n.1797A>G)
n.2323A>G
c.2147A>G (p.Asp716Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301933A>TCA356177849WFS1c.2174A>T (p.Asp725Val)
c.2115A>T
c.2138A>T (p.Asp713Val)
c.1889A>T (p.Asp630Val)
c.1797A>T (n.1797A>T)
n.2323A>T
c.2147A>T (p.Asp716Val)
 gnomAD v4
4g.6301936_6301959dupCA549707912WFS1c.2177_2200dup (p.Asn733_Met734insAsnSerAlaGluSerAlaIleAsn)
c.2118_2141dup
c.2141_2164dup (p.Asn721_Met722insAsnSerAlaGluSerAlaIleAsn)
c.1892_1915dup (p.Asn638_Met639insAsnSerAlaGluSerAlaIleAsn)
c.1800_1823dup (n.1800_1823dup)
n.2326_2349dup
c.2150_2173dup (p.Asn724_Met725insAsnSerAlaGluSerAlaIleAsn)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6301936_6301959delCA2839615WFS1c.2177_2200del (p.Asn726_Asn733del)
c.2118_2141del
c.2141_2164del (p.Asn714_Asn721del)
c.1892_1915del (p.Asn631_Asn638del)
c.1800_1823del (n.1800_1823del)
n.2326_2349del
c.2150_2173del (p.Asn717_Asn724del)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301934C>ACA356177852WFS1c.2175C>A (p.Asp725Glu)
c.2116C>A
c.2139C>A (p.Asp713Glu)
c.1890C>A (p.Asp630Glu)
c.1798C>A (n.1798C>A)
n.2324C>A
c.2148C>A (p.Asp716Glu)
4g.6301934C>GCA356177853WFS1c.2175C>G (p.Asp725Glu)
c.2116C>G
c.2139C>G (p.Asp713Glu)
c.1890C>G (p.Asp630Glu)
c.1798C>G (n.1798C>G)
n.2324C>G
c.2148C>G (p.Asp716Glu)
4g.6301934C>TCA438368591WFS1c.2175C>T (p.Asp725=)
c.2116C>T
c.2139C>T (p.Asp713=)
c.1890C>T (p.Asp630=)
c.1798C>T (n.1798C>T)
n.2324C>T
c.2148C>T (p.Asp716=)
 gnomAD v4
4g.6301935A>CCA356177859WFS1c.2176A>C (p.Asn726His)
c.2117A>C
c.2140A>C (p.Asn714His)
c.1891A>C (p.Asn631His)
c.1799A>C (n.1799A>C)
n.2325A>C
c.2149A>C (p.Asn717His)
4g.6301935A>GCA356177855WFS1c.2176A>G (p.Asn726Asp)
c.2117A>G
c.2140A>G (p.Asn714Asp)
c.1891A>G (p.Asn631Asp)
c.1799A>G (n.1799A>G)
n.2325A>G
c.2149A>G (p.Asn717Asp)
 ClinVar dbSNP
4g.6301935A>TCA356177857WFS1c.2176A>T (p.Asn726Tyr)
c.2117A>T
c.2140A>T (p.Asn714Tyr)
c.1891A>T (p.Asn631Tyr)
c.1799A>T (n.1799A>T)
n.2325A>T
c.2149A>T (p.Asn717Tyr)
4g.6301936A=CA1435772076WFS1c.2177A= (p.Asn726=)
c.2118A=
c.2141A= (p.Asn714=)
c.1892A= (p.Asn631=)
c.1800A= (n.1800A=)
n.2326A=
c.2150A= (p.Asn717=)
4g.6301936A>CCA261752WFS1c.2177A>C (p.Asn726Thr)
c.2118A>C
c.2141A>C (p.Asn714Thr)
c.1892A>C (p.Asn631Thr)
c.1800A>C (n.1800A>C)
n.2326A>C
c.2150A>C (p.Asn717Thr)
 ClinVar dbSNP
4g.6301936A>GCA356177861WFS1c.2177A>G (p.Asn726Ser)
c.2118A>G
c.2141A>G (p.Asn714Ser)
c.1892A>G (p.Asn631Ser)
c.1800A>G (n.1800A>G)
n.2326A>G
c.2150A>G (p.Asn717Ser)
4g.6301936A>TCA356177863WFS1c.2177A>T (p.Asn726Ile)
c.2118A>T
c.2141A>T (p.Asn714Ile)
c.1892A>T (p.Asn631Ile)
c.1800A>T (n.1800A>T)
n.2326A>T
c.2150A>T (p.Asn717Ile)
4g.6301937C>ACA356177865WFS1c.2178C>A (p.Asn726Lys)
c.2119C>A
c.2142C>A (p.Asn714Lys)
c.1893C>A (p.Asn631Lys)
c.1801C>A (n.1801C>A)
n.2327C>A
c.2151C>A (p.Asn717Lys)
 gnomAD v4 COSMIC
4g.6301937C=CA1435772078WFS1c.2178C= (p.Asn726=)
c.2119C=
c.2142C= (p.Asn714=)
c.1893C= (p.Asn631=)
c.1801C= (n.1801C=)
n.2327C=
c.2151C= (p.Asn717=)
4g.6301937C>GCA356177866WFS1c.2178C>G (p.Asn726Lys)
c.2119C>G
c.2142C>G (p.Asn714Lys)
c.1893C>G (p.Asn631Lys)
c.1801C>G (n.1801C>G)
n.2327C>G
c.2151C>G (p.Asn717Lys)
 ClinVar
4g.6301937C>TCA438368594WFS1c.2178C>T (p.Asn726=)
c.2119C>T
c.2142C>T (p.Asn714=)
c.1893C>T (p.Asn631=)
c.1801C>T (n.1801C>T)
n.2327C>T
c.2151C>T (p.Asn717=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6301938A=CA1435772080WFS1c.2179A= (p.Ser727=)
c.2120A=
c.2143A= (p.Ser715=)
c.1894A= (p.Ser632=)
c.1802A= (n.1802A=)
n.2328A=
c.2152A= (p.Ser718=)
4g.6301938A>CCA356177870WFS1c.2179A>C (p.Ser727Arg)
c.2120A>C
c.2143A>C (p.Ser715Arg)
c.1894A>C (p.Ser632Arg)
c.1802A>C (n.1802A>C)
n.2328A>C
c.2152A>C (p.Ser718Arg)
4g.6301938A>GCA2839617WFS1c.2179A>G (p.Ser727Gly)
c.2120A>G
c.2143A>G (p.Ser715Gly)
c.1894A>G (p.Ser632Gly)
c.1802A>G (n.1802A>G)
n.2328A>G
c.2152A>G (p.Ser718Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301938A>TCA356177869WFS1c.2179A>T (p.Ser727Cys)
c.2120A>T
c.2143A>T (p.Ser715Cys)
c.1894A>T (p.Ser632Cys)
c.1802A>T (n.1802A>T)
n.2328A>T
c.2152A>T (p.Ser718Cys)
4g.6301939G>ACA356177875WFS1c.2180G>A (p.Ser727Asn)
c.2121G>A
c.2144G>A (p.Ser715Asn)
c.1895G>A (p.Ser632Asn)
c.1803G>A (n.1803G>A)
n.2329G>A
c.2153G>A (p.Ser718Asn)
 ClinVar
4g.6301939G>CCA356177876WFS1c.2180G>C (p.Ser727Thr)
c.2121G>C
c.2144G>C (p.Ser715Thr)
c.1895G>C (p.Ser632Thr)
c.1803G>C (n.1803G>C)
n.2329G>C
c.2153G>C (p.Ser718Thr)
4g.6301939G=CA1435772082WFS1c.2180G= (p.Ser727=)
c.2121G=
c.2144G= (p.Ser715=)
c.1895G= (p.Ser632=)
c.1803G= (n.1803G=)
n.2329G=
c.2153G= (p.Ser718=)
4g.6301939G>TCA2839618WFS1c.2180G>T (p.Ser727Ile)
c.2121G>T
c.2144G>T (p.Ser715Ile)
c.1895G>T (p.Ser632Ile)
c.1803G>T (n.1803G>T)
n.2329G>T
c.2153G>T (p.Ser718Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301939_6301942delinsGCGCCA1435772083WFS1c.2180_2183delinsGCGC (p.Ser727=)
c.2121_2124delinsGCGC
c.2144_2147delinsGCGC (p.Ser715=)
c.1895_1898delinsGCGC (p.Ser632=)
c.1803_1806delinsGCGC (n.1803_1806delinsGCGC)
n.2329_2332delinsGCGC
c.2153_2156delinsGCGC (p.Ser718=)
4g.6301940C>ACA356177879WFS1c.2181C>A (p.Ser727Arg)
c.2122C>A
c.2145C>A (p.Ser715Arg)
c.1896C>A (p.Ser632Arg)
c.1804C>A (n.1804C>A)
n.2330C>A
c.2154C>A (p.Ser718Arg)
4g.6301940C=CA1435772087WFS1c.2181C= (p.Ser727=)
c.2122C=
c.2145C= (p.Ser715=)
c.1896C= (p.Ser632=)
c.1804C= (n.1804C=)
n.2330C=
c.2154C= (p.Ser718=)
4g.6301940C>GCA2839620WFS1c.2181C>G (p.Ser727Arg)
c.2122C>G
c.2145C>G (p.Ser715Arg)
c.1896C>G (p.Ser632Arg)
c.1804C>G (n.1804C>G)
n.2330C>G
c.2154C>G (p.Ser718Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301940C>TCA2839619WFS1c.2181C>T (p.Ser727=)
c.2122C>T
c.2145C>T (p.Ser715=)
c.1896C>T (p.Ser632=)
c.1804C>T (n.1804C>T)
n.2330C>T
c.2154C>T (p.Ser718=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301942_6301944delCA1435772086WFS1c.2183_2185del (p.Ala728del)
c.2124_2126del
c.2147_2149del (p.Ala716del)
c.1898_1900del (p.Ala633del)
c.1806_1808del (n.1806_1808del)
n.2332_2334del
c.2156_2158del (p.Ala719del)
 dbSNP
4g.6301941G>ACA253197WFS1c.2182G>A (p.Ala728Thr)
c.2123G>A
c.2146G>A (p.Ala716Thr)
c.1897G>A (p.Ala633Thr)
c.1805G>A (n.1805G>A)
n.2331G>A
c.2155G>A (p.Ala719Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301941G>CCA356177886WFS1c.2182G>C (p.Ala728Pro)
c.2123G>C
c.2146G>C (p.Ala716Pro)
c.1897G>C (p.Ala633Pro)
c.1805G>C (n.1805G>C)
n.2331G>C
c.2155G>C (p.Ala719Pro)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301941G=CA1435772089WFS1c.2182G= (p.Ala728=)
c.2123G=
c.2146G= (p.Ala716=)
c.1897G= (p.Ala633=)
c.1805G= (n.1805G=)
n.2331G=
c.2155G= (p.Ala719=)
4g.6301941G>TCA356177887WFS1c.2182G>T (p.Ala728Ser)
c.2123G>T
c.2146G>T (p.Ala716Ser)
c.1897G>T (p.Ala633Ser)
c.1805G>T (n.1805G>T)
n.2331G>T
c.2155G>T (p.Ala719Ser)
4g.6301942C>ACA356177889WFS1c.2183C>A (p.Ala728Asp)
c.2124C>A
c.2147C>A (p.Ala716Asp)
c.1898C>A (p.Ala633Asp)
c.1806C>A (n.1806C>A)
n.2332C>A
c.2156C>A (p.Ala719Asp)
4g.6301942C=CA1435772091WFS1c.2183C= (p.Ala728=)
c.2124C=
c.2147C= (p.Ala716=)
c.1898C= (p.Ala633=)
c.1806C= (n.1806C=)
n.2332C=
c.2156C= (p.Ala719=)
4g.6301942C>GCA356177890WFS1c.2183C>G (p.Ala728Gly)
c.2124C>G
c.2147C>G (p.Ala716Gly)
c.1898C>G (p.Ala633Gly)
c.1806C>G (n.1806C>G)
n.2332C>G
c.2156C>G (p.Ala719Gly)
 dbSNP gnomAD v3 gnomAD v4
4g.6301942C>TCA356177892WFS1c.2183C>T (p.Ala728Val)
c.2124C>T
c.2147C>T (p.Ala716Val)
c.1898C>T (p.Ala633Val)
c.1806C>T (n.1806C>T)
n.2332C>T
c.2156C>T (p.Ala719Val)
 gnomAD v4
4g.6301943C>ACA438368598WFS1c.2184C>A (p.Ala728=)
c.2125C>A
c.2148C>A (p.Ala716=)
c.1899C>A (p.Ala633=)
c.1807C>A (n.1807C>A)
n.2333C>A
c.2157C>A (p.Ala719=)
 gnomAD v4
4g.6301943C=CA1435772093WFS1c.2184C= (p.Ala728=)
c.2125C=
c.2148C= (p.Ala716=)
c.1899C= (p.Ala633=)
c.1807C= (n.1807C=)
n.2333C=
c.2157C= (p.Ala719=)
4g.6301943C>GCA438368600WFS1c.2184C>G (p.Ala728=)
c.2125C>G
c.2148C>G (p.Ala716=)
c.1899C>G (p.Ala633=)
c.1807C>G (n.1807C>G)
n.2333C>G
c.2157C>G (p.Ala719=)
 gnomAD v4
4g.6301943C>TCA2839621WFS1c.2184C>T (p.Ala728=)
c.2125C>T
c.2148C>T (p.Ala716=)
c.1899C>T (p.Ala633=)
c.1807C>T (n.1807C>T)
n.2333C>T
c.2157C>T (p.Ala719=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6301944G>ACA2839622WFS1c.2185G>A (p.Glu729Lys)
c.2126G>A
c.2149G>A (p.Glu717Lys)
c.1900G>A (p.Glu634Lys)
c.1808G>A (n.1808G>A)
n.2334G>A
c.2158G>A (p.Glu720Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301944G>CCA356177897WFS1c.2185G>C (p.Glu729Gln)
c.2126G>C
c.2149G>C (p.Glu717Gln)
c.1900G>C (p.Glu634Gln)
c.1808G>C (n.1808G>C)
n.2334G>C
c.2158G>C (p.Glu720Gln)
 COSMIC
4g.6301944G=CA1435772096WFS1c.2185G= (p.Glu729=)
c.2126G=
c.2149G= (p.Glu717=)
c.1900G= (p.Glu634=)
c.1808G= (n.1808G=)
n.2334G=
c.2158G= (p.Glu720=)
4g.6301944G>TCA91796872WFS1c.2185G>T (p.Glu729Ter)
c.2126G>T
c.2149G>T (p.Glu717Ter)
c.1900G>T (p.Glu634Ter)
c.1808G>T (n.1808G>T)
n.2334G>T
c.2158G>T (p.Glu720Ter)
 dbSNP
4g.6301945A>CCA356177899WFS1c.2186A>C (p.Glu729Ala)
c.2127A>C
c.2150A>C (p.Glu717Ala)
c.1901A>C (p.Glu634Ala)
c.1809A>C (n.1809A>C)
n.2335A>C
c.2159A>C (p.Glu720Ala)
4g.6301945A>GCA356177901WFS1c.2186A>G (p.Glu729Gly)
c.2127A>G
c.2150A>G (p.Glu717Gly)
c.1901A>G (p.Glu634Gly)
c.1809A>G (n.1809A>G)
n.2335A>G
c.2159A>G (p.Glu720Gly)
 dbSNP
4g.6301945A>TCA356177903WFS1c.2186A>T (p.Glu729Val)
c.2127A>T
c.2150A>T (p.Glu717Val)
c.1901A>T (p.Glu634Val)
c.1809A>T (n.1809A>T)
n.2335A>T
c.2159A>T (p.Glu720Val)
4g.6301945dupCA2586973645WFS1c.2186dup (p.Ser730ValfsTer?)
c.2127dup
c.2150dup (p.Ser718ValfsTer?)
c.1901dup (p.Ser635ValfsTer?)
c.1809dup (n.1809dup)
n.2335dup
c.2159dup (p.Ser721ValfsTer?)
4g.6301946G>ACA2839623WFS1c.2187G>A (p.Glu729=)
c.2128G>A
c.2151G>A (p.Glu717=)
c.1902G>A (p.Glu634=)
c.1810G>A (n.1810G>A)
n.2336G>A
c.2160G>A (p.Glu720=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301946G>CCA356177906WFS1c.2187G>C (p.Glu729Asp)
c.2128G>C
c.2151G>C (p.Glu717Asp)
c.1902G>C (p.Glu634Asp)
c.1810G>C (n.1810G>C)
n.2336G>C
c.2160G>C (p.Glu720Asp)
4g.6301946G=CA1435772098WFS1c.2187G= (p.Glu729=)
c.2128G=
c.2151G= (p.Glu717=)
c.1902G= (p.Glu634=)
c.1810G= (n.1810G=)
n.2336G=
c.2160G= (p.Glu720=)
4g.6301946G>TCA356177908WFS1c.2187G>T (p.Glu729Asp)
c.2128G>T
c.2151G>T (p.Glu717Asp)
c.1902G>T (p.Glu634Asp)
c.1810G>T (n.1810G>T)
n.2336G>T
c.2160G>T (p.Glu720Asp)
4g.6301947T>ACA356177910WFS1c.2188T>A (p.Ser730Thr)
c.2129T>A
c.2152T>A (p.Ser718Thr)
c.1903T>A (p.Ser635Thr)
c.1811T>A (n.1811T>A)
n.2337T>A
c.2161T>A (p.Ser721Thr)
4g.6301947T>CCA356177912WFS1c.2188T>C (p.Ser730Pro)
c.2129T>C
c.2152T>C (p.Ser718Pro)
c.1903T>C (p.Ser635Pro)
c.1811T>C (n.1811T>C)
n.2337T>C
c.2161T>C (p.Ser721Pro)
4g.6301947T>GCA356177914WFS1c.2188T>G (p.Ser730Ala)
c.2129T>G
c.2152T>G (p.Ser718Ala)
c.1903T>G (p.Ser635Ala)
c.1811T>G (n.1811T>G)
n.2337T>G
c.2161T>G (p.Ser721Ala)
 dbSNP gnomAD v2 gnomAD v4
4g.6301947T=CA1435772099WFS1c.2188T= (p.Ser730=)
c.2129T=
c.2152T= (p.Ser718=)
c.1903T= (p.Ser635=)
c.1811T= (n.1811T=)
n.2337T=
c.2161T= (p.Ser721=)
4g.6301948C>ACA356177916WFS1c.2189C>A (p.Ser730Tyr)
c.2130C>A
c.2153C>A (p.Ser718Tyr)
c.1904C>A (p.Ser635Tyr)
c.1812C>A (n.1812C>A)
n.2338C>A
c.2162C>A (p.Ser721Tyr)
4g.6301948C=CA1435772101WFS1c.2189C= (p.Ser730=)
c.2130C=
c.2153C= (p.Ser718=)
c.1904C= (p.Ser635=)
c.1812C= (n.1812C=)
n.2338C=
c.2162C= (p.Ser721=)
4g.6301948C>GCA356177917WFS1c.2189C>G (p.Ser730Cys)
c.2130C>G
c.2153C>G (p.Ser718Cys)
c.1904C>G (p.Ser635Cys)
c.1812C>G (n.1812C>G)
n.2338C>G
c.2162C>G (p.Ser721Cys)
4g.6301948C>TCA356177922WFS1c.2189C>T (p.Ser730Phe)
c.2130C>T
c.2153C>T (p.Ser718Phe)
c.1904C>T (p.Ser635Phe)
c.1812C>T (n.1812C>T)
n.2338C>T
c.2162C>T (p.Ser721Phe)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301950_6301963dupCA2586973646WFS1c.2191_2204dup (p.Phe737SerfsTer?)
c.2132_2145dup
c.2155_2168dup (p.Phe725SerfsTer?)
c.1906_1919dup (p.Phe642SerfsTer?)
c.1814_1827dup (n.1814_1827dup)
n.2340_2353dup
c.2164_2177dup (p.Phe728SerfsTer?)
4g.6301949T>ACA438368658WFS1c.2190T>A (p.Ser730=)
c.2131T>A
c.2154T>A (p.Ser718=)
c.1905T>A (p.Ser635=)
c.1813T>A (n.1813T>A)
n.2339T>A
c.2163T>A (p.Ser721=)
4g.6301949T>CCA2839624WFS1c.2190T>C (p.Ser730=)
c.2131T>C
c.2154T>C (p.Ser718=)
c.1905T>C (p.Ser635=)
c.1813T>C (n.1813T>C)
n.2339T>C
c.2163T>C (p.Ser721=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301949T>GCA438368660WFS1c.2190T>G (p.Ser730=)
c.2131T>G
c.2154T>G (p.Ser718=)
c.1905T>G (p.Ser635=)
c.1813T>G (n.1813T>G)
n.2339T>G
c.2163T>G (p.Ser721=)
 dbSNP gnomAD v4
4g.6301949T=CA1435772103WFS1c.2190T= (p.Ser730=)
c.2131T=
c.2154T= (p.Ser718=)
c.1905T= (p.Ser635=)
c.1813T= (n.1813T=)
n.2339T=
c.2163T= (p.Ser721=)
4g.6301950G>ACA356177926WFS1c.2191G>A (p.Ala731Thr)
c.2132G>A
c.2155G>A (p.Ala719Thr)
c.1906G>A (p.Ala636Thr)
c.1814G>A (n.1814G>A)
n.2340G>A
c.2164G>A (p.Ala722Thr)
 dbSNP gnomAD v3 gnomAD v4
4g.6301950G>CCA356177928WFS1c.2191G>C (p.Ala731Pro)
c.2132G>C
c.2155G>C (p.Ala719Pro)
c.1906G>C (p.Ala636Pro)
c.1814G>C (n.1814G>C)
n.2340G>C
c.2164G>C (p.Ala722Pro)
4g.6301950G=CA1435772104WFS1c.2191G= (p.Ala731=)
c.2132G=
c.2155G= (p.Ala719=)
c.1906G= (p.Ala636=)
c.1814G= (n.1814G=)
n.2340G=
c.2164G= (p.Ala722=)
4g.6301950G>TCA356177927WFS1c.2191G>T (p.Ala731Ser)
c.2132G>T
c.2155G>T (p.Ala719Ser)
c.1906G>T (p.Ala636Ser)
c.1814G>T (n.1814G>T)
n.2340G>T
c.2164G>T (p.Ala722Ser)
4g.6301951C>ACA356177929WFS1c.2192C>A (p.Ala731Asp)
c.2133C>A
c.2156C>A (p.Ala719Asp)
c.1907C>A (p.Ala636Asp)
c.1815C>A (n.1815C>A)
n.2341C>A
c.2165C>A (p.Ala722Asp)
4g.6301951C=CA1435772106WFS1c.2192C= (p.Ala731=)
c.2133C=
c.2156C= (p.Ala719=)
c.1907C= (p.Ala636=)
c.1815C= (n.1815C=)
n.2341C=
c.2165C= (p.Ala722=)
4g.6301951C>GCA356177930WFS1c.2192C>G (p.Ala731Gly)
c.2133C>G
c.2156C>G (p.Ala719Gly)
c.1907C>G (p.Ala636Gly)
c.1815C>G (n.1815C>G)
n.2341C>G
c.2165C>G (p.Ala722Gly)
4g.6301951C>TCA2839625WFS1c.2192C>T (p.Ala731Val)
c.2133C>T
c.2156C>T (p.Ala719Val)
c.1907C>T (p.Ala636Val)
c.1815C>T (n.1815C>T)
n.2341C>T
c.2165C>T (p.Ala722Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301952C>ACA438368661WFS1c.2193C>A (p.Ala731=)
c.2134C>A
c.2157C>A (p.Ala719=)
c.1908C>A (p.Ala636=)
c.1816C>A (n.1816C>A)
n.2342C>A
c.2166C>A (p.Ala722=)
4g.6301952C=CA1435772107WFS1c.2193C= (p.Ala731=)
c.2134C=
c.2157C= (p.Ala719=)
c.1908C= (p.Ala636=)
c.1816C= (n.1816C=)
n.2342C=
c.2166C= (p.Ala722=)
4g.6301952C>GCA2839626WFS1c.2193C>G (p.Ala731=)
c.2134C>G
c.2157C>G (p.Ala719=)
c.1908C>G (p.Ala636=)
c.1816C>G (n.1816C>G)
n.2342C>G
c.2166C>G (p.Ala722=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301952C>TCA10621440WFS1c.2193C>T (p.Ala731=)
c.2134C>T
c.2157C>T (p.Ala719=)
c.1908C>T (p.Ala636=)
c.1816C>T (n.1816C>T)
n.2342C>T
c.2166C>T (p.Ala722=)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6301953A=CA1435772110WFS1c.2194A= (p.Ile732=)
c.2135A=
c.2158A= (p.Ile720=)
c.1909A= (p.Ile637=)
c.1817A= (n.1817A=)
n.2343A=
c.2167A= (p.Ile723=)
4g.6301953A>CCA2839627WFS1c.2194A>C (p.Ile732Leu)
c.2135A>C
c.2158A>C (p.Ile720Leu)
c.1909A>C (p.Ile637Leu)
c.1817A>C (n.1817A>C)
n.2343A>C
c.2167A>C (p.Ile723Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301953A>GCA295580WFS1c.2194A>G (p.Ile732Val)
c.2135A>G
c.2158A>G (p.Ile720Val)
c.1909A>G (p.Ile637Val)
c.1817A>G (n.1817A>G)
n.2343A>G
c.2167A>G (p.Ile723Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301953A>TCA356177931WFS1c.2194A>T (p.Ile732Phe)
c.2135A>T
c.2158A>T (p.Ile720Phe)
c.1909A>T (p.Ile637Phe)
c.1817A>T (n.1817A>T)
n.2343A>T
c.2167A>T (p.Ile723Phe)
4g.6301954T>ACA356177933WFS1c.2195T>A (p.Ile732Asn)
c.2136T>A
c.2159T>A (p.Ile720Asn)
c.1910T>A (p.Ile637Asn)
c.1818T>A (n.1818T>A)
n.2344T>A
c.2168T>A (p.Ile723Asn)
 dbSNP gnomAD v2 gnomAD v4
4g.6301954T>CCA356177934WFS1c.2195T>C (p.Ile732Thr)
c.2136T>C
c.2159T>C (p.Ile720Thr)
c.1910T>C (p.Ile637Thr)
c.1818T>C (n.1818T>C)
n.2344T>C
c.2168T>C (p.Ile723Thr)
 dbSNP gnomAD v4
4g.6301954T>GCA356177935WFS1c.2195T>G (p.Ile732Ser)
c.2136T>G
c.2159T>G (p.Ile720Ser)
c.1910T>G (p.Ile637Ser)
c.1818T>G (n.1818T>G)
n.2344T>G
c.2168T>G (p.Ile723Ser)
4g.6301954T=CA1435772113WFS1c.2195T= (p.Ile732=)
c.2136T=
c.2159T= (p.Ile720=)
c.1910T= (p.Ile637=)
c.1818T= (n.1818T=)
n.2344T=
c.2168T= (p.Ile723=)
4g.6301955C>ACA438368665WFS1c.2196C>A (p.Ile732=)
c.2137C>A
c.2160C>A (p.Ile720=)
c.1911C>A (p.Ile637=)
c.1819C>A (n.1819C>A)
n.2345C>A
c.2169C>A (p.Ile723=)
4g.6301955C=CA1435772114WFS1c.2196C= (p.Ile732=)
c.2137C=
c.2160C= (p.Ile720=)
c.1911C= (p.Ile637=)
c.1819C= (n.1819C=)
n.2345C=
c.2169C= (p.Ile723=)
4g.6301955C>GCA356177937WFS1c.2196C>G (p.Ile732Met)
c.2137C>G
c.2160C>G (p.Ile720Met)
c.1911C>G (p.Ile637Met)
c.1819C>G (n.1819C>G)
n.2345C>G
c.2169C>G (p.Ile723Met)
 ClinVar dbSNP gnomAD v4
4g.6301955C>TCA2839628WFS1c.2196C>T (p.Ile732=)
c.2137C>T
c.2160C>T (p.Ile720=)
c.1911C>T (p.Ile637=)
c.1819C>T (n.1819C>T)
n.2345C>T
c.2169C>T (p.Ile723=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301956A>CCA356177939WFS1c.2197A>C (p.Asn733His)
c.2138A>C
c.2161A>C (p.Asn721His)
c.1912A>C (p.Asn638His)
c.1820A>C (n.1820A>C)
n.2346A>C
c.2170A>C (p.Asn724His)
4g.6301956A>GCA356177941WFS1c.2197A>G (p.Asn733Asp)
c.2138A>G
c.2161A>G (p.Asn721Asp)
c.1912A>G (p.Asn638Asp)
c.1820A>G (n.1820A>G)
n.2346A>G
c.2170A>G (p.Asn724Asp)
4g.6301956A>TCA356177942WFS1c.2197A>T (p.Asn733Tyr)
c.2138A>T
c.2161A>T (p.Asn721Tyr)
c.1912A>T (p.Asn638Tyr)
c.1820A>T (n.1820A>T)
n.2346A>T
c.2170A>T (p.Asn724Tyr)
4g.6301957A=CA1435772116WFS1c.2198A= (p.Asn733=)
c.2139A=
c.2162A= (p.Asn721=)
c.1913A= (p.Asn638=)
c.1821A= (n.1821A=)
n.2347A=
c.2171A= (p.Asn724=)
4g.6301957A>CCA356177943WFS1c.2198A>C (p.Asn733Thr)
c.2139A>C
c.2162A>C (p.Asn721Thr)
c.1913A>C (p.Asn638Thr)
c.1821A>C (n.1821A>C)
n.2347A>C
c.2171A>C (p.Asn724Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301957A>GCA2839630WFS1c.2198A>G (p.Asn733Ser)
c.2139A>G
c.2162A>G (p.Asn721Ser)
c.1913A>G (p.Asn638Ser)
c.1821A>G (n.1821A>G)
n.2347A>G
c.2171A>G (p.Asn724Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301957A>TCA2839629WFS1c.2198A>T (p.Asn733Ile)
c.2139A>T
c.2162A>T (p.Asn721Ile)
c.1913A>T (p.Asn638Ile)
c.1821A>T (n.1821A>T)
n.2347A>T
c.2171A>T (p.Asn724Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301958C>ACA356177948WFS1c.2199C>A (p.Asn733Lys)
c.2140C>A
c.2163C>A (p.Asn721Lys)
c.1914C>A (p.Asn638Lys)
c.1822C>A (n.1822C>A)
n.2348C>A
c.2172C>A (p.Asn724Lys)
4g.6301958C>GCA356177947WFS1c.2199C>G (p.Asn733Lys)
c.2140C>G
c.2163C>G (p.Asn721Lys)
c.1914C>G (p.Asn638Lys)
c.1822C>G (n.1822C>G)
n.2348C>G
c.2172C>G (p.Asn724Lys)
 ClinVar dbSNP
4g.6301958C>TCA438368668WFS1c.2199C>T (p.Asn733=)
c.2140C>T
c.2163C>T (p.Asn721=)
c.1914C>T (p.Asn638=)
c.1822C>T (n.1822C>T)
n.2348C>T
c.2172C>T (p.Asn724=)
 gnomAD v4
4g.6301959A=CA1435772119WFS1c.2200A= (p.Met734=)
c.2141A=
c.2164A= (p.Met722=)
c.1915A= (p.Met639=)
c.1823A= (n.1823A=)
n.2349A=
c.2173A= (p.Met725=)
4g.6301959A>CCA2839631WFS1c.2200A>C (p.Met734Leu)
c.2141A>C
c.2164A>C (p.Met722Leu)
c.1915A>C (p.Met639Leu)
c.1823A>C (n.1823A>C)
n.2349A>C
c.2173A>C (p.Met725Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301959A>GCA321222WFS1c.2200A>G (p.Met734Val)
c.2141A>G
c.2164A>G (p.Met722Val)
c.1915A>G (p.Met639Val)
c.1823A>G (n.1823A>G)
n.2349A>G
c.2173A>G (p.Met725Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301959A>TCA356177951WFS1c.2200A>T (p.Met734Leu)
c.2141A>T
c.2164A>T (p.Met722Leu)
c.1915A>T (p.Met639Leu)
c.1823A>T (n.1823A>T)
n.2349A>T
c.2173A>T (p.Met725Leu)
 dbSNP gnomAD v3 gnomAD v4
4g.6301960T>ACA356177953WFS1c.2201T>A (p.Met734Lys)
c.2142T>A
c.2165T>A (p.Met722Lys)
c.1916T>A (p.Met639Lys)
c.1824T>A (n.1824T>A)
n.2350T>A
c.2174T>A (p.Met725Lys)
4g.6301960T>CCA356177956WFS1c.2201T>C (p.Met734Thr)
c.2142T>C
c.2165T>C (p.Met722Thr)
c.1916T>C (p.Met639Thr)
c.1824T>C (n.1824T>C)
n.2350T>C
c.2174T>C (p.Met725Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6301960T>GCA356177957WFS1c.2201T>G (p.Met734Arg)
c.2142T>G
c.2165T>G (p.Met722Arg)
c.1916T>G (p.Met639Arg)
c.1824T>G (n.1824T>G)
n.2350T>G
c.2174T>G (p.Met725Arg)
4g.6301960T=CA1435772121WFS1c.2201T= (p.Met734=)
c.2142T=
c.2165T= (p.Met722=)
c.1916T= (p.Met639=)
c.1824T= (n.1824T=)
n.2350T=
c.2174T= (p.Met725=)
4g.6301961G>ACA2839632WFS1c.2202G>A (p.Met734Ile)
c.2143G>A
c.2166G>A (p.Met722Ile)
c.1917G>A (p.Met639Ile)
c.1825G>A (n.1825G>A)
n.2351G>A
c.2175G>A (p.Met725Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301961G>CCA356177959WFS1c.2202G>C (p.Met734Ile)
c.2143G>C
c.2166G>C (p.Met722Ile)
c.1917G>C (p.Met639Ile)
c.1825G>C (n.1825G>C)
n.2351G>C
c.2175G>C (p.Met725Ile)
 dbSNP gnomAD v2 gnomAD v4
4g.6301961G=CA1435772123WFS1c.2202G= (p.Met734=)
c.2143G=
c.2166G= (p.Met722=)
c.1917G= (p.Met639=)
c.1825G= (n.1825G=)
n.2351G=
c.2175G= (p.Met725=)
4g.6301961G>TCA356177960WFS1c.2202G>T (p.Met734Ile)
c.2143G>T
c.2166G>T (p.Met722Ile)
c.1917G>T (p.Met639Ile)
c.1825G>T (n.1825G>T)
n.2351G>T
c.2175G>T (p.Met725Ile)
4g.6301961_6301963delinsGCTCA1435772124WFS1c.2202_2204delinsGCT (p.Met734=)
c.2143_2145delinsGCT
c.2166_2168delinsGCT (p.Met722=)
c.1917_1919delinsGCT (p.Met639=)
c.1825_1827delinsGCT (n.1825_1827delinsGCT)
n.2351_2353delinsGCT
c.2175_2177delinsGCT (p.Met725=)
4g.6301962C>ACA356177962WFS1c.2203C>A (p.Leu735Ile)
c.2144C>A
c.2167C>A (p.Leu723Ile)
c.1918C>A (p.Leu640Ile)
c.1826C>A (n.1826C>A)
n.2352C>A
c.2176C>A (p.Leu726Ile)
 gnomAD v4
4g.6301962C=CA1435772125WFS1c.2203C= (p.Leu735=)
c.2144C=
c.2167C= (p.Leu723=)
c.1918C= (p.Leu640=)
c.1826C= (n.1826C=)
n.2352C=
c.2176C= (p.Leu726=)
4g.6301962C>GCA356177963WFS1c.2203C>G (p.Leu735Val)
c.2144C>G
c.2167C>G (p.Leu723Val)
c.1918C>G (p.Leu640Val)
c.1826C>G (n.1826C>G)
n.2352C>G
c.2176C>G (p.Leu726Val)
4g.6301962C>TCA356177965WFS1c.2203C>T (p.Leu735Phe)
c.2144C>T
c.2167C>T (p.Leu723Phe)
c.1918C>T (p.Leu640Phe)
c.1826C>T (n.1826C>T)
n.2352C>T
c.2176C>T (p.Leu726Phe)
 dbSNP gnomAD v3 gnomAD v4
4g.6301963_6301964delCA549707921WFS1c.2204_2205del (p.Leu735ProfsTer?)
c.2145_2146del
c.2168_2169del (p.Leu723ProfsTer?)
c.1919_1920del (p.Leu640ProfsTer?)
c.1827_1828del (n.1827_1828del)
n.2353_2354del
c.2177_2178del (p.Leu726ProfsTer?)
 dbSNP gnomAD v2 gnomAD v4
4g.6301963T>ACA356177967WFS1c.2204T>A (p.Leu735His)
c.2145T>A
c.2168T>A (p.Leu723His)
c.1919T>A (p.Leu640His)
c.1827T>A (n.1827T>A)
n.2353T>A
c.2177T>A (p.Leu726His)
4g.6301963T>CCA356177968WFS1c.2204T>C (p.Leu735Pro)
c.2145T>C
c.2168T>C (p.Leu723Pro)
c.1919T>C (p.Leu640Pro)
c.1827T>C (n.1827T>C)
n.2353T>C
c.2177T>C (p.Leu726Pro)
 ClinVar
4g.6301963T>GCA356177970WFS1c.2204T>G (p.Leu735Arg)
c.2145T>G
c.2168T>G (p.Leu723Arg)
c.1919T>G (p.Leu640Arg)
c.1827T>G (n.1827T>G)
n.2353T>G
c.2177T>G (p.Leu726Arg)
4g.6301964C>ACA438368676WFS1c.2205C>A (p.Leu735=)
c.2146C>A
c.2169C>A (p.Leu723=)
c.1920C>A (p.Leu640=)
c.1828C>A (n.1828C>A)
n.2354C>A
c.2178C>A (p.Leu726=)
4g.6301964C=CA1435772127WFS1c.2205C= (p.Leu735=)
c.2146C=
c.2169C= (p.Leu723=)
c.1920C= (p.Leu640=)
c.1828C= (n.1828C=)
n.2354C=
c.2178C= (p.Leu726=)
4g.6301964C>GCA438368677WFS1c.2205C>G (p.Leu735=)
c.2146C>G
c.2169C>G (p.Leu723=)
c.1920C>G (p.Leu640=)
c.1828C>G (n.1828C>G)
n.2354C>G
c.2178C>G (p.Leu726=)
 gnomAD v4
4g.6301964C>TCA438368678WFS1c.2205C>T (p.Leu735=)
c.2146C>T
c.2169C>T (p.Leu723=)
c.1920C>T (p.Leu640=)
c.1828C>T (n.1828C>T)
n.2354C>T
c.2178C>T (p.Leu726=)
 gnomAD v4
4g.6301964_6301965insGAGCA549707922WFS1c.2205_2206insGAG (p.Leu735_Pro736insGlu)
c.2146_2147insGAG
c.2169_2170insGAG (p.Leu723_Pro724insGlu)
c.1920_1921insGAG (p.Leu640_Pro641insGlu)
c.1828_1829insGAG (n.1828_1829insGAG)
n.2354_2355insGAG
c.2178_2179insGAG (p.Leu726_Pro727insGlu)
 dbSNP gnomAD v2 gnomAD v4
4g.6301965C>ACA356177973WFS1c.2206C>A (p.Pro736Thr)
c.2147C>A
c.2170C>A (p.Pro724Thr)
c.1921C>A (p.Pro641Thr)
c.1829C>A (n.1829C>A)
n.2355C>A
c.2179C>A (p.Pro727Thr)
4g.6301965C=CA1435772128WFS1c.2206C= (p.Pro736=)
c.2147C=
c.2170C= (p.Pro724=)
c.1921C= (p.Pro641=)
c.1829C= (n.1829C=)
n.2355C=
c.2179C= (p.Pro727=)
4g.6301965C>GCA356177974WFS1c.2206C>G (p.Pro736Ala)
c.2147C>G
c.2170C>G (p.Pro724Ala)
c.1921C>G (p.Pro641Ala)
c.1829C>G (n.1829C>G)
n.2355C>G
c.2179C>G (p.Pro727Ala)
4g.6301965C>TCA2839633WFS1c.2206C>T (p.Pro736Ser)
c.2147C>T
c.2170C>T (p.Pro724Ser)
c.1921C>T (p.Pro641Ser)
c.1829C>T (n.1829C>T)
n.2355C>T
c.2179C>T (p.Pro727Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301966C>ACA356177976WFS1c.2207C>A (p.Pro736Gln)
c.2148C>A
c.2171C>A (p.Pro724Gln)
c.1922C>A (p.Pro641Gln)
c.1830C>A (n.1830C>A)
n.2356C>A
c.2180C>A (p.Pro727Gln)
4g.6301966C=CA1435772130WFS1c.2207C= (p.Pro736=)
c.2148C=
c.2171C= (p.Pro724=)
c.1922C= (p.Pro641=)
c.1830C= (n.1830C=)
n.2356C=
c.2180C= (p.Pro727=)
4g.6301966C>GCA356177977WFS1c.2207C>G (p.Pro736Arg)
c.2148C>G
c.2171C>G (p.Pro724Arg)
c.1922C>G (p.Pro641Arg)
c.1830C>G (n.1830C>G)
n.2356C>G
c.2180C>G (p.Pro727Arg)
 gnomAD v4
4g.6301966C>TCA253184WFS1c.2207C>T (p.Pro736Leu)
c.2148C>T
c.2171C>T (p.Pro724Leu)
c.1922C>T (p.Pro641Leu)
c.1830C>T (n.1830C>T)
n.2356C>T
c.2180C>T (p.Pro727Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301967G>ACA91796896WFS1c.2208G>A (p.Pro736=)
c.2149G>A
c.2172G>A (p.Pro724=)
c.1923G>A (p.Pro641=)
c.1831G>A (n.1831G>A)
n.2357G>A
c.2181G>A (p.Pro727=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301967G>CCA438368682WFS1c.2208G>C (p.Pro736=)
c.2149G>C
c.2172G>C (p.Pro724=)
c.1923G>C (p.Pro641=)
c.1831G>C (n.1831G>C)
n.2357G>C
c.2181G>C (p.Pro727=)
4g.6301967G=CA1435772132WFS1c.2208G= (p.Pro736=)
c.2149G=
c.2172G= (p.Pro724=)
c.1923G= (p.Pro641=)
c.1831G= (n.1831G=)
n.2357G=
c.2181G= (p.Pro727=)
4g.6301967G>TCA2839634WFS1c.2208G>T (p.Pro736=)
c.2149G>T
c.2172G>T (p.Pro724=)
c.1923G>T (p.Pro641=)
c.1831G>T (n.1831G>T)
n.2357G>T
c.2181G>T (p.Pro727=)
 dbSNP ExAC gnomAD v2
4g.6301967_6301970delinsGTTCCA1435772133WFS1c.2208_2211delinsGTTC (p.Pro736=)
c.2149_2152delinsGTTC
c.2172_2175delinsGTTC (p.Pro724=)
c.1923_1926delinsGTTC (p.Pro641=)
c.1831_1834delinsGTTC (n.1831_1834delinsGTTC)
n.2357_2360delinsGTTC
c.2181_2184delinsGTTC (p.Pro727=)
4g.6301968T>ACA356177980WFS1c.2209T>A (p.Phe737Ile)
c.2150T>A
c.2173T>A (p.Phe725Ile)
c.1924T>A (p.Phe642Ile)
c.1832T>A (n.1832T>A)
n.2358T>A
c.2182T>A (p.Phe728Ile)
4g.6301968T>CCA356177982WFS1c.2209T>C (p.Phe737Leu)
c.2150T>C
c.2173T>C (p.Phe725Leu)
c.1924T>C (p.Phe642Leu)
c.1832T>C (n.1832T>C)
n.2358T>C
c.2182T>C (p.Phe728Leu)
4g.6301968T>GCA356177981WFS1c.2209T>G (p.Phe737Val)
c.2150T>G
c.2173T>G (p.Phe725Val)
c.1924T>G (p.Phe642Val)
c.1832T>G (n.1832T>G)
n.2358T>G
c.2182T>G (p.Phe728Val)
4g.6301971_6301973delCA797209926WFS1c.2212_2214del (p.Phe738del)
c.2153_2155del
c.2176_2178del (p.Phe726del)
c.1927_1929del (p.Phe643del)
c.1835_1837del (n.1835_1837del)
n.2361_2363del
c.2185_2187del (p.Phe729del)
 dbSNP gnomAD v4
4g.6301969T>ACA356177983WFS1c.2210T>A (p.Phe737Tyr)
c.2151T>A
c.2174T>A (p.Phe725Tyr)
c.1925T>A (p.Phe642Tyr)
c.1833T>A (n.1833T>A)
n.2359T>A
c.2183T>A (p.Phe728Tyr)
4g.6301969T>CCA356177984WFS1c.2210T>C (p.Phe737Ser)
c.2151T>C
c.2174T>C (p.Phe725Ser)
c.1925T>C (p.Phe642Ser)
c.1833T>C (n.1833T>C)
n.2359T>C
c.2183T>C (p.Phe728Ser)
4g.6301969T>GCA356177985WFS1c.2210T>G (p.Phe737Cys)
c.2151T>G
c.2174T>G (p.Phe725Cys)
c.1925T>G (p.Phe642Cys)
c.1833T>G (n.1833T>G)
n.2359T>G
c.2183T>G (p.Phe728Cys)
4g.6301969_6301973dupCA2586973647WFS1c.2210_2214dup (p.Ile739SerfsTer?)
c.2151_2155dup
c.2174_2178dup (p.Ile727SerfsTer?)
c.1925_1929dup (p.Ile644SerfsTer?)
c.1833_1837dup (n.1833_1837dup)
n.2359_2363dup
c.2183_2187dup (p.Ile730SerfsTer?)
4g.6301970C>ACA356177986WFS1c.2211C>A (p.Phe737Leu)
c.2152C>A
c.2175C>A (p.Phe725Leu)
c.1926C>A (p.Phe642Leu)
c.1834C>A (n.1834C>A)
n.2360C>A
c.2184C>A (p.Phe728Leu)
4g.6301970C=CA1435772135WFS1c.2211C= (p.Phe737=)
c.2152C=
c.2175C= (p.Phe725=)
c.1926C= (p.Phe642=)
c.1834C= (n.1834C=)
n.2360C=
c.2184C= (p.Phe728=)
4g.6301970C>GCA2839635WFS1c.2211C>G (p.Phe737Leu)
c.2152C>G
c.2175C>G (p.Phe725Leu)
c.1926C>G (p.Phe642Leu)
c.1834C>G (n.1834C>G)
n.2360C>G
c.2184C>G (p.Phe728Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301970C>TCA91796902WFS1c.2211C>T (p.Phe737=)
c.2152C>T
c.2175C>T (p.Phe725=)
c.1926C>T (p.Phe642=)
c.1834C>T (n.1834C>T)
n.2360C>T
c.2184C>T (p.Phe728=)
 dbSNP gnomAD v2 gnomAD v4
4g.6301971T>ACA356177988WFS1c.2212T>A (p.Phe738Ile)
c.2153T>A
c.2176T>A (p.Phe726Ile)
c.1927T>A (p.Phe643Ile)
c.1835T>A (n.1835T>A)
n.2361T>A
c.2185T>A (p.Phe729Ile)
4g.6301971T>CCA356177990WFS1c.2212T>C (p.Phe738Leu)
c.2153T>C
c.2176T>C (p.Phe726Leu)
c.1927T>C (p.Phe643Leu)
c.1835T>C (n.1835T>C)
n.2361T>C
c.2185T>C (p.Phe729Leu)
4g.6301971T>GCA356177992WFS1c.2212T>G (p.Phe738Val)
c.2153T>G
c.2176T>G (p.Phe726Val)
c.1927T>G (p.Phe643Val)
c.1835T>G (n.1835T>G)
n.2361T>G
c.2185T>G (p.Phe729Val)
4g.6301972T>ACA356177994WFS1c.2213T>A (p.Phe738Tyr)
c.2154T>A
c.2177T>A (p.Phe726Tyr)
c.1928T>A (p.Phe643Tyr)
c.1836T>A (n.1836T>A)
n.2362T>A
c.2186T>A (p.Phe729Tyr)
4g.6301972T>CCA356177996WFS1c.2213T>C (p.Phe738Ser)
c.2154T>C
c.2177T>C (p.Phe726Ser)
c.1928T>C (p.Phe643Ser)
c.1836T>C (n.1836T>C)
n.2362T>C
c.2186T>C (p.Phe729Ser)
4g.6301972T>GCA356177998WFS1c.2213T>G (p.Phe738Cys)
c.2154T>G
c.2177T>G (p.Phe726Cys)
c.1928T>G (p.Phe643Cys)
c.1836T>G (n.1836T>G)
n.2362T>G
c.2186T>G (p.Phe729Cys)
4g.6301974_6301976delCA2669843474WFS1c.2215_2217del (p.Ile739del)
c.2156_2158del
c.2179_2181del (p.Ile727del)
c.1930_1932del (p.Ile644del)
c.1838_1840del (n.1838_1840del)
n.2364_2366del
c.2188_2190del (p.Ile730del)
 gnomAD v4
4g.6301973C>ACA356178000WFS1c.2214C>A (p.Phe738Leu)
c.2155C>A
c.2178C>A (p.Phe726Leu)
c.1929C>A (p.Phe643Leu)
c.1837C>A (n.1837C>A)
n.2363C>A
c.2187C>A (p.Phe729Leu)
4g.6301973C=CA1435772138WFS1c.2214C= (p.Phe738=)
c.2155C=
c.2178C= (p.Phe726=)
c.1929C= (p.Phe643=)
c.1837C= (n.1837C=)
n.2363C=
c.2187C= (p.Phe729=)
4g.6301973C>GCA356178002WFS1c.2214C>G (p.Phe738Leu)
c.2155C>G
c.2178C>G (p.Phe726Leu)
c.1929C>G (p.Phe643Leu)
c.1837C>G (n.1837C>G)
n.2363C>G
c.2187C>G (p.Phe729Leu)
4g.6301973C>TCA91796904WFS1c.2214C>T (p.Phe738=)
c.2155C>T
c.2178C>T (p.Phe726=)
c.1929C>T (p.Phe643=)
c.1837C>T (n.1837C>T)
n.2363C>T
c.2187C>T (p.Phe729=)
 ClinVar dbSNP gnomAD v4
4g.6301974A=CA1435772139WFS1c.2215A= (p.Ile739=)
c.2156A=
c.2179A= (p.Ile727=)
c.1930A= (p.Ile644=)
c.1838A= (n.1838A=)
n.2364A=
c.2188A= (p.Ile730=)
4g.6301974A>CCA356178007WFS1c.2215A>C (p.Ile739Leu)
c.2156A>C
c.2179A>C (p.Ile727Leu)
c.1930A>C (p.Ile644Leu)
c.1838A>C (n.1838A>C)
n.2364A>C
c.2188A>C (p.Ile730Leu)
4g.6301974A>GCA356178003WFS1c.2215A>G (p.Ile739Val)
c.2156A>G
c.2179A>G (p.Ile727Val)
c.1930A>G (p.Ile644Val)
c.1838A>G (n.1838A>G)
n.2364A>G
c.2188A>G (p.Ile730Val)
 ClinVar gnomAD v4
4g.6301974A>TCA356178005WFS1c.2215A>T (p.Ile739Phe)
c.2156A>T
c.2179A>T (p.Ile727Phe)
c.1930A>T (p.Ile644Phe)
c.1838A>T (n.1838A>T)
n.2364A>T
c.2188A>T (p.Ile730Phe)
 dbSNP gnomAD v3 gnomAD v4
4g.6301975T>ACA356178009WFS1c.2216T>A (p.Ile739Asn)
c.2157T>A
c.2180T>A (p.Ile727Asn)
c.1931T>A (p.Ile644Asn)
c.1839T>A (n.1839T>A)
n.2365T>A
c.2189T>A (p.Ile730Asn)
4g.6301975T>CCA356178011WFS1c.2216T>C (p.Ile739Thr)
c.2157T>C
c.2180T>C (p.Ile727Thr)
c.1931T>C (p.Ile644Thr)
c.1839T>C (n.1839T>C)
n.2365T>C
c.2189T>C (p.Ile730Thr)
4g.6301975T>GCA356178013WFS1c.2216T>G (p.Ile739Ser)
c.2157T>G
c.2180T>G (p.Ile727Ser)
c.1931T>G (p.Ile644Ser)
c.1839T>G (n.1839T>G)
n.2365T>G
c.2189T>G (p.Ile730Ser)
 gnomAD v4
4g.6301976C>ACA438368691WFS1c.2217C>A (p.Ile739=)
c.2158C>A
c.2181C>A (p.Ile727=)
c.1932C>A (p.Ile644=)
c.1840C>A (n.1840C>A)
n.2366C>A
c.2190C>A (p.Ile730=)
4g.6301976C=CA1435772141WFS1c.2217C= (p.Ile739=)
c.2158C=
c.2181C= (p.Ile727=)
c.1932C= (p.Ile644=)
c.1840C= (n.1840C=)
n.2366C=
c.2190C= (p.Ile730=)
4g.6301976C>GCA356178015WFS1c.2217C>G (p.Ile739Met)
c.2158C>G
c.2181C>G (p.Ile727Met)
c.1932C>G (p.Ile644Met)
c.1840C>G (n.1840C>G)
n.2366C>G
c.2190C>G (p.Ile730Met)
4g.6301976C>TCA247677WFS1c.2217C>T (p.Ile739=)
c.2158C>T
c.2181C>T (p.Ile727=)
c.1932C>T (p.Ile644=)
c.1840C>T (n.1840C>T)
n.2366C>T
c.2190C>T (p.Ile730=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301977G>ACA179669WFS1c.2218G>A (p.Gly740Ser)
c.2159G>A
c.2182G>A (p.Gly728Ser)
c.1933G>A (p.Gly645Ser)
c.1841G>A (n.1841G>A)
n.2367G>A
c.2191G>A (p.Gly731Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301977G>CCA356178019WFS1c.2218G>C (p.Gly740Arg)
c.2159G>C
c.2182G>C (p.Gly728Arg)
c.1933G>C (p.Gly645Arg)
c.1841G>C (n.1841G>C)
n.2367G>C
c.2191G>C (p.Gly731Arg)
4g.6301977G=CA1435772144WFS1c.2218G= (p.Gly740=)
c.2159G=
c.2182G= (p.Gly728=)
c.1933G= (p.Gly645=)
c.1841G= (n.1841G=)
n.2367G=
c.2191G= (p.Gly731=)
4g.6301977G>TCA356178021WFS1c.2218G>T (p.Gly740Cys)
c.2159G>T
c.2182G>T (p.Gly728Cys)
c.1933G>T (p.Gly645Cys)
c.1841G>T (n.1841G>T)
n.2367G>T
c.2191G>T (p.Gly731Cys)
 gnomAD v4
4g.6301978G>ACA356178023WFS1c.2219G>A (p.Gly740Asp)
c.2160G>A
c.2183G>A (p.Gly728Asp)
c.1934G>A (p.Gly645Asp)
c.1842G>A (n.1842G>A)
n.2368G>A
c.2192G>A (p.Gly731Asp)
 ClinVar dbSNP
4g.6301978G>CCA356178025WFS1c.2219G>C (p.Gly740Ala)
c.2160G>C
c.2183G>C (p.Gly728Ala)
c.1934G>C (p.Gly645Ala)
c.1842G>C (n.1842G>C)
n.2368G>C
c.2192G>C (p.Gly731Ala)
4g.6301978G=CA1435772146WFS1c.2219G= (p.Gly740=)
c.2160G=
c.2183G= (p.Gly728=)
c.1934G= (p.Gly645=)
c.1842G= (n.1842G=)
n.2368G=
c.2192G= (p.Gly731=)
4g.6301978G>TCA356178026WFS1c.2219G>T (p.Gly740Val)
c.2160G>T
c.2183G>T (p.Gly728Val)
c.1934G>T (p.Gly645Val)
c.1842G>T (n.1842G>T)
n.2368G>T
c.2192G>T (p.Gly731Val)
 gnomAD v4
4g.6301979C>ACA438368696WFS1c.2220C>A (p.Gly740=)
c.2161C>A
c.2184C>A (p.Gly728=)
c.1935C>A (p.Gly645=)
c.1843C>A (n.1843C>A)
n.2369C>A
c.2193C>A (p.Gly731=)
4g.6301979C=CA1435772147WFS1c.2220C= (p.Gly740=)
c.2161C=
c.2184C= (p.Gly728=)
c.1935C= (p.Gly645=)
c.1843C= (n.1843C=)
n.2369C=
c.2193C= (p.Gly731=)
4g.6301979C>GCA438368697WFS1c.2220C>G (p.Gly740=)
c.2161C>G
c.2184C>G (p.Gly728=)
c.1935C>G (p.Gly645=)
c.1843C>G (n.1843C>G)
n.2369C>G
c.2193C>G (p.Gly731=)
 gnomAD v4
4g.6301979C>TCA136346WFS1c.2220C>T (p.Gly740=)
c.2161C>T
c.2184C>T (p.Gly728=)
c.1935C>T (p.Gly645=)
c.1843C>T (n.1843C>T)
n.2369C>T
c.2193C>T (p.Gly731=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301980G>ACA205181WFS1c.2221G>A (p.Asp741Asn)
c.2162G>A
c.2185G>A (p.Asp729Asn)
c.1936G>A (p.Asp646Asn)
c.1844G>A (n.1844G>A)
n.2370G>A
c.2194G>A (p.Asp732Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301980G>CCA356178031WFS1c.2221G>C (p.Asp741His)
c.2162G>C
c.2185G>C (p.Asp729His)
c.1936G>C (p.Asp646His)
c.1844G>C (n.1844G>C)
n.2370G>C
c.2194G>C (p.Asp732His)
4g.6301980G=CA1435772149WFS1c.2221G= (p.Asp741=)
c.2162G=
c.2185G= (p.Asp729=)
c.1936G= (p.Asp646=)
c.1844G= (n.1844G=)
n.2370G=
c.2194G= (p.Asp732=)
4g.6301980G>TCA356178029WFS1c.2221G>T (p.Asp741Tyr)
c.2162G>T
c.2185G>T (p.Asp729Tyr)
c.1936G>T (p.Asp646Tyr)
c.1844G>T (n.1844G>T)
n.2370G>T
c.2194G>T (p.Asp732Tyr)
 dbSNP gnomAD v4
4g.6301981A=CA1435772151WFS1c.2222A= (p.Asp741=)
c.2163A=
c.2186A= (p.Asp729=)
c.1937A= (p.Asp646=)
c.1845A= (n.1845A=)
n.2371A=
c.2195A= (p.Asp732=)
4g.6301981A>CCA356178033WFS1c.2222A>C (p.Asp741Ala)
c.2163A>C
c.2186A>C (p.Asp729Ala)
c.1937A>C (p.Asp646Ala)
c.1845A>C (n.1845A>C)
n.2371A>C
c.2195A>C (p.Asp732Ala)
 dbSNP
4g.6301981A>GCA356178035WFS1c.2222A>G (p.Asp741Gly)
c.2163A>G
c.2186A>G (p.Asp729Gly)
c.1937A>G (p.Asp646Gly)
c.1845A>G (n.1845A>G)
n.2371A>G
c.2195A>G (p.Asp732Gly)
4g.6301981A>TCA356178036WFS1c.2222A>T (p.Asp741Val)
c.2163A>T
c.2186A>T (p.Asp729Val)
c.1937A>T (p.Asp646Val)
c.1845A>T (n.1845A>T)
n.2371A>T
c.2195A>T (p.Asp732Val)
4g.6301982C>ACA356178038WFS1c.2223C>A (p.Asp741Glu)
c.2164C>A
c.2187C>A (p.Asp729Glu)
c.1938C>A (p.Asp646Glu)
c.1846C>A (n.1846C>A)
n.2372C>A
c.2196C>A (p.Asp732Glu)
4g.6301982C=CA1435772152WFS1c.2223C= (p.Asp741=)
c.2164C=
c.2187C= (p.Asp729=)
c.1938C= (p.Asp646=)
c.1846C= (n.1846C=)
n.2372C=
c.2196C= (p.Asp732=)
4g.6301982C>GCA356178040WFS1c.2223C>G (p.Asp741Glu)
c.2164C>G
c.2187C>G (p.Asp729Glu)
c.1938C>G (p.Asp646Glu)
c.1846C>G (n.1846C>G)
n.2372C>G
c.2196C>G (p.Asp732Glu)
4g.6301982C>TCA2839636WFS1c.2223C>T (p.Asp741=)
c.2164C>T
c.2187C>T (p.Asp729=)
c.1938C>T (p.Asp646=)
c.1846C>T (n.1846C>T)
n.2372C>T
c.2196C>T (p.Asp732=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301983T>ACA356178045WFS1c.2224T>A (p.Trp742Arg)
c.2165T>A
c.2188T>A (p.Trp730Arg)
c.1939T>A (p.Trp647Arg)
c.1847T>A (n.1847T>A)
n.2373T>A
c.2197T>A (p.Trp733Arg)
 gnomAD v4
4g.6301983T>CCA356178043WFS1c.2224T>C (p.Trp742Arg)
c.2165T>C
c.2188T>C (p.Trp730Arg)
c.1939T>C (p.Trp647Arg)
c.1847T>C (n.1847T>C)
n.2373T>C
c.2197T>C (p.Trp733Arg)
 gnomAD v4
4g.6301983T>GCA2839637WFS1c.2224T>G (p.Trp742Gly)
c.2165T>G
c.2188T>G (p.Trp730Gly)
c.1939T>G (p.Trp647Gly)
c.1847T>G (n.1847T>G)
n.2373T>G
c.2197T>G (p.Trp733Gly)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301983T=CA1435772154WFS1c.2224T= (p.Trp742=)
c.2165T=
c.2188T= (p.Trp730=)
c.1939T= (p.Trp647=)
c.1847T= (n.1847T=)
n.2373T=
c.2197T= (p.Trp733=)
4g.6301984G>ACA2839638WFS1c.2225G>A (p.Trp742Ter)
c.2166G>A
c.2189G>A (p.Trp730Ter)
c.1940G>A (p.Trp647Ter)
c.1848G>A (n.1848G>A)
n.2374G>A
c.2198G>A (p.Trp733Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301984G>CCA356178048WFS1c.2225G>C (p.Trp742Ser)
c.2166G>C
c.2189G>C (p.Trp730Ser)
c.1940G>C (p.Trp647Ser)
c.1848G>C (n.1848G>C)
n.2374G>C
c.2198G>C (p.Trp733Ser)
 dbSNP gnomAD v2 gnomAD v4
4g.6301984G=CA1435772155WFS1c.2225G= (p.Trp742=)
c.2166G=
c.2189G= (p.Trp730=)
c.1940G= (p.Trp647=)
c.1848G= (n.1848G=)
n.2374G=
c.2198G= (p.Trp733=)
4g.6301984G>TCA356178050WFS1c.2225G>T (p.Trp742Leu)
c.2166G>T
c.2189G>T (p.Trp730Leu)
c.1940G>T (p.Trp647Leu)
c.1848G>T (n.1848G>T)
n.2374G>T
c.2198G>T (p.Trp733Leu)
 dbSNP gnomAD v2
4g.6301985G>ACA356178052WFS1c.2226G>A (p.Trp742Ter)
c.2167G>A
c.2190G>A (p.Trp730Ter)
c.1941G>A (p.Trp647Ter)
c.1849G>A (n.1849G>A)
n.2375G>A
c.2199G>A (p.Trp733Ter)
4g.6301985G>CCA356178054WFS1c.2226G>C (p.Trp742Cys)
c.2167G>C
c.2190G>C (p.Trp730Cys)
c.1941G>C (p.Trp647Cys)
c.1849G>C (n.1849G>C)
n.2375G>C
c.2199G>C (p.Trp733Cys)
 dbSNP
4g.6301985G=CA1435772157WFS1c.2226G= (p.Trp742=)
c.2167G=
c.2190G= (p.Trp730=)
c.1941G= (p.Trp647=)
c.1849G= (n.1849G=)
n.2375G=
c.2199G= (p.Trp733=)
4g.6301985G>TCA2839639WFS1c.2226G>T (p.Trp742Cys)
c.2167G>T
c.2190G>T (p.Trp730Cys)
c.1941G>T (p.Trp647Cys)
c.1849G>T (n.1849G>T)
n.2375G>T
c.2199G>T (p.Trp733Cys)
 dbSNP ExAC gnomAD v2
4g.6301986A=CA1435772160WFS1c.2227A= (p.Met743=)
c.2168A=
c.2191A= (p.Met731=)
c.1942A= (p.Met648=)
c.1850A= (n.1850A=)
n.2376A=
c.2200A= (p.Met734=)
4g.6301986A>CCA2839641WFS1c.2227A>C (p.Met743Leu)
c.2168A>C
c.2191A>C (p.Met731Leu)
c.1942A>C (p.Met648Leu)
c.1850A>C (n.1850A>C)
n.2376A>C
c.2200A>C (p.Met734Leu)
 dbSNP ExAC gnomAD v4
4g.6301986A>GCA2839640WFS1c.2227A>G (p.Met743Val)
c.2168A>G
c.2191A>G (p.Met731Val)
c.1942A>G (p.Met648Val)
c.1850A>G (n.1850A>G)
n.2376A>G
c.2200A>G (p.Met734Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301986A>TCA356178058WFS1c.2227A>T (p.Met743Leu)
c.2168A>T
c.2191A>T (p.Met731Leu)
c.1942A>T (p.Met648Leu)
c.1850A>T (n.1850A>T)
n.2376A>T
c.2200A>T (p.Met734Leu)
4g.6301987T>ACA91796920WFS1c.2228T>A (p.Met743Lys)
c.2169T>A
c.2192T>A (p.Met731Lys)
c.1943T>A (p.Met648Lys)
c.1851T>A (n.1851T>A)
n.2377T>A
c.2201T>A (p.Met734Lys)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6301987T>CCA91796922WFS1c.2228T>C (p.Met743Thr)
c.2169T>C
c.2192T>C (p.Met731Thr)
c.1943T>C (p.Met648Thr)
c.1851T>C (n.1851T>C)
n.2377T>C
c.2201T>C (p.Met734Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301987T>GCA356178062WFS1c.2228T>G (p.Met743Arg)
c.2169T>G
c.2192T>G (p.Met731Arg)
c.1943T>G (p.Met648Arg)
c.1851T>G (n.1851T>G)
n.2377T>G
c.2201T>G (p.Met734Arg)
 gnomAD v4
4g.6301987T=CA1435772162WFS1c.2228T= (p.Met743=)
c.2169T=
c.2192T= (p.Met731=)
c.1943T= (p.Met648=)
c.1851T= (n.1851T=)
n.2377T=
c.2201T= (p.Met734=)
4g.6301988G>ACA356178065WFS1c.2229G>A (p.Met743Ile)
c.2170G>A
c.2193G>A (p.Met731Ile)
c.1944G>A (p.Met648Ile)
c.1852G>A (n.1852G>A)
n.2378G>A
c.2202G>A (p.Met734Ile)
 gnomAD v4 COSMIC
4g.6301988G>CCA356178066WFS1c.2229G>C (p.Met743Ile)
c.2170G>C
c.2193G>C (p.Met731Ile)
c.1944G>C (p.Met648Ile)
c.1852G>C (n.1852G>C)
n.2378G>C
c.2202G>C (p.Met734Ile)
 dbSNP gnomAD v2 gnomAD v4
4g.6301988G=CA1435772164WFS1c.2229G= (p.Met743=)
c.2170G=
c.2193G= (p.Met731=)
c.1944G= (p.Met648=)
c.1852G= (n.1852G=)
n.2378G=
c.2202G= (p.Met734=)
4g.6301988G>TCA356178068WFS1c.2229G>T (p.Met743Ile)
c.2170G>T
c.2193G>T (p.Met731Ile)
c.1944G>T (p.Met648Ile)
c.1852G>T (n.1852G>T)
n.2378G>T
c.2202G>T (p.Met734Ile)
 gnomAD v4
4g.6301989C>ACA356178069WFS1c.2230C>A (p.Arg744Ser)
c.2171C>A
c.2194C>A (p.Arg732Ser)
c.1945C>A (p.Arg649Ser)
c.1853C>A (n.1853C>A)
n.2379C>A
c.2203C>A (p.Arg735Ser)
 gnomAD v4
4g.6301989C=CA1435772166WFS1c.2230C= (p.Arg744=)
c.2171C=
c.2194C= (p.Arg732=)
c.1945C= (p.Arg649=)
c.1853C= (n.1853C=)
n.2379C=
c.2203C= (p.Arg735=)
4g.6301989C>GCA356178071WFS1c.2230C>G (p.Arg744Gly)
c.2171C>G
c.2194C>G (p.Arg732Gly)
c.1945C>G (p.Arg649Gly)
c.1853C>G (n.1853C>G)
n.2379C>G
c.2203C>G (p.Arg735Gly)
 dbSNP
4g.6301989C>TCA325020WFS1c.2230C>T (p.Arg744Cys)
c.2171C>T
c.2194C>T (p.Arg732Cys)
c.1945C>T (p.Arg649Cys)
c.1853C>T (n.1853C>T)
n.2379C>T
c.2203C>T (p.Arg735Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301990_6302012dupCA797210000WFS1c.2231_2253dup (p.Pro752AlafsTer?)
c.2172_2194dup
c.2195_2217dup (p.Pro740AlafsTer?)
c.1946_1968dup (p.Pro657AlafsTer?)
c.1854_1876dup (n.1854_1876dup)
n.2380_2402dup
c.2204_2226dup (p.Pro743AlafsTer?)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6301990G>ACA321654WFS1c.2231G>A (p.Arg744His)
c.2172G>A
c.2195G>A (p.Arg732His)
c.1946G>A (p.Arg649His)
c.1854G>A (n.1854G>A)
n.2380G>A
c.2204G>A (p.Arg735His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301990G>CCA356178075WFS1c.2231G>C (p.Arg744Pro)
c.2172G>C
c.2195G>C (p.Arg732Pro)
c.1946G>C (p.Arg649Pro)
c.1854G>C (n.1854G>C)
n.2380G>C
c.2204G>C (p.Arg735Pro)
 dbSNP gnomAD v2 gnomAD v4
4g.6301990G=CA1435772168WFS1c.2231G= (p.Arg744=)
c.2172G=
c.2195G= (p.Arg732=)
c.1946G= (p.Arg649=)
c.1854G= (n.1854G=)
n.2380G=
c.2204G= (p.Arg735=)
4g.6301990G>TCA356178076WFS1c.2231G>T (p.Arg744Leu)
c.2172G>T
c.2195G>T (p.Arg732Leu)
c.1946G>T (p.Arg649Leu)
c.1854G>T (n.1854G>T)
n.2380G>T
c.2204G>T (p.Arg735Leu)
 gnomAD v4
4g.6301991C>ACA2839642WFS1c.2232C>A (p.Arg744=)
c.2173C>A
c.2196C>A (p.Arg732=)
c.1947C>A (p.Arg649=)
c.1855C>A (n.1855C>A)
n.2381C>A
c.2205C>A (p.Arg735=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301991C=CA1435772170WFS1c.2232C= (p.Arg744=)
c.2173C=
c.2196C= (p.Arg732=)
c.1947C= (p.Arg649=)
c.1855C= (n.1855C=)
n.2381C=
c.2205C= (p.Arg735=)
4g.6301991C>GCA438368706WFS1c.2232C>G (p.Arg744=)
c.2173C>G
c.2196C>G (p.Arg732=)
c.1947C>G (p.Arg649=)
c.1855C>G (n.1855C>G)
n.2381C>G
c.2205C>G (p.Arg735=)
4g.6301991C>TCA438368708WFS1c.2232C>T (p.Arg744=)
c.2173C>T
c.2196C>T (p.Arg732=)
c.1947C>T (p.Arg649=)
c.1855C>T (n.1855C>T)
n.2381C>T
c.2205C>T (p.Arg735=)
 gnomAD v4
4g.6301992T>ACA356178082WFS1c.2233T>A (p.Cys745Ser)
c.2174T>A
c.2197T>A (p.Cys733Ser)
c.1948T>A (p.Cys650Ser)
c.1856T>A (n.1856T>A)
n.2382T>A
c.2206T>A (p.Cys736Ser)
4g.6301992T>CCA356178079WFS1c.2233T>C (p.Cys745Arg)
c.2174T>C
c.2197T>C (p.Cys733Arg)
c.1948T>C (p.Cys650Arg)
c.1856T>C (n.1856T>C)
n.2382T>C
c.2206T>C (p.Cys736Arg)
4g.6301992T>GCA356178081WFS1c.2233T>G (p.Cys745Gly)
c.2174T>G
c.2197T>G (p.Cys733Gly)
c.1948T>G (p.Cys650Gly)
c.1856T>G (n.1856T>G)
n.2382T>G
c.2206T>G (p.Cys736Gly)
 ClinVar dbSNP gnomAD v4
4g.6301993G>ACA91796929WFS1c.2234G>A (p.Cys745Tyr)
c.2175G>A
c.2198G>A (p.Cys733Tyr)
c.1949G>A (p.Cys650Tyr)
c.1857G>A (n.1857G>A)
n.2383G>A
c.2207G>A (p.Cys736Tyr)
 dbSNP gnomAD v4
4g.6301993G>CCA356178085WFS1c.2234G>C (p.Cys745Ser)
c.2175G>C
c.2198G>C (p.Cys733Ser)
c.1949G>C (p.Cys650Ser)
c.1857G>C (n.1857G>C)
n.2383G>C
c.2207G>C (p.Cys736Ser)
4g.6301993G=CA1435772172WFS1c.2234G= (p.Cys745=)
c.2175G=
c.2198G= (p.Cys733=)
c.1949G= (p.Cys650=)
c.1857G= (n.1857G=)
n.2383G=
c.2207G= (p.Cys736=)
4g.6301993G>TCA356178086WFS1c.2234G>T (p.Cys745Phe)
c.2175G>T
c.2198G>T (p.Cys733Phe)
c.1949G>T (p.Cys650Phe)
c.1857G>T (n.1857G>T)
n.2383G>T
c.2207G>T (p.Cys736Phe)
 gnomAD v4
4g.6301994C>ACA356178087WFS1c.2235C>A (p.Cys745Ter)
c.2176C>A
c.2199C>A (p.Cys733Ter)
c.1950C>A (p.Cys650Ter)
c.1858C>A (n.1858C>A)
n.2384C>A
c.2208C>A (p.Cys736Ter)
 dbSNP
4g.6301994C=CA1435772173WFS1c.2235C= (p.Cys745=)
c.2176C=
c.2199C= (p.Cys733=)
c.1950C= (p.Cys650=)
c.1858C= (n.1858C=)
n.2384C=
c.2208C= (p.Cys736=)
4g.6301994C>GCA356178088WFS1c.2235C>G (p.Cys745Trp)
c.2176C>G
c.2199C>G (p.Cys733Trp)
c.1950C>G (p.Cys650Trp)
c.1858C>G (n.1858C>G)
n.2384C>G
c.2208C>G (p.Cys736Trp)
 gnomAD v4
4g.6301994C>TCA91796932WFS1c.2235C>T (p.Cys745=)
c.2176C>T
c.2199C>T (p.Cys733=)
c.1950C>T (p.Cys650=)
c.1858C>T (n.1858C>T)
n.2384C>T
c.2208C>T (p.Cys736=)
 dbSNP gnomAD v3 gnomAD v4
4g.6301995C>ACA356178089WFS1c.2236C>A (p.Leu746Ile)
c.2177C>A
c.2200C>A (p.Leu734Ile)
c.1951C>A (p.Leu651Ile)
c.1859C>A (n.1859C>A)
n.2385C>A
c.2209C>A (p.Leu737Ile)
 dbSNP gnomAD v3 gnomAD v4
4g.6301995C=CA1435772175WFS1c.2236C= (p.Leu746=)
c.2177C=
c.2200C= (p.Leu734=)
c.1951C= (p.Leu651=)
c.1859C= (n.1859C=)
n.2385C=
c.2209C= (p.Leu737=)
4g.6301995C>GCA356178090WFS1c.2236C>G (p.Leu746Val)
c.2177C>G
c.2200C>G (p.Leu734Val)
c.1951C>G (p.Leu651Val)
c.1859C>G (n.1859C>G)
n.2385C>G
c.2209C>G (p.Leu737Val)
4g.6301995C>TCA2839643WFS1c.2236C>T (p.Leu746Phe)
c.2177C>T
c.2200C>T (p.Leu734Phe)
c.1951C>T (p.Leu651Phe)
c.1859C>T (n.1859C>T)
n.2385C>T
c.2209C>T (p.Leu737Phe)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301996T>ACA356178091WFS1c.2237T>A (p.Leu746His)
c.2178T>A
c.2201T>A (p.Leu734His)
c.1952T>A (p.Leu651His)
c.1860T>A (n.1860T>A)
n.2386T>A
c.2210T>A (p.Leu737His)
 ClinVar dbSNP
4g.6301996T>CCA356178093WFS1c.2237T>C (p.Leu746Pro)
c.2178T>C
c.2201T>C (p.Leu734Pro)
c.1952T>C (p.Leu651Pro)
c.1860T>C (n.1860T>C)
n.2386T>C
c.2210T>C (p.Leu737Pro)
4g.6301996T>GCA356178094WFS1c.2237T>G (p.Leu746Arg)
c.2178T>G
c.2201T>G (p.Leu734Arg)
c.1952T>G (p.Leu651Arg)
c.1860T>G (n.1860T>G)
n.2386T>G
c.2210T>G (p.Leu737Arg)
 dbSNP
4g.6301996T=CA1435772177WFS1c.2237T= (p.Leu746=)
c.2178T=
c.2201T= (p.Leu734=)
c.1952T= (p.Leu651=)
c.1860T= (n.1860T=)
n.2386T=
c.2210T= (p.Leu737=)
4g.6301997C>ACA438368710WFS1c.2238C>A (p.Leu746=)
c.2179C>A
c.2202C>A (p.Leu734=)
c.1953C>A (p.Leu651=)
c.1861C>A (n.1861C>A)
n.2387C>A
c.2211C>A (p.Leu737=)
4g.6301997C=CA1435772179WFS1c.2238C= (p.Leu746=)
c.2179C=
c.2202C= (p.Leu734=)
c.1953C= (p.Leu651=)
c.1861C= (n.1861C=)
n.2387C=
c.2211C= (p.Leu737=)
4g.6301997C>GCA438368711WFS1c.2238C>G (p.Leu746=)
c.2179C>G
c.2202C>G (p.Leu734=)
c.1953C>G (p.Leu651=)
c.1861C>G (n.1861C>G)
n.2387C>G
c.2211C>G (p.Leu737=)
 ClinVar dbSNP gnomAD v2
4g.6301997C>TCA136350WFS1c.2238C>T (p.Leu746=)
c.2179C>T
c.2202C>T (p.Leu734=)
c.1953C>T (p.Leu651=)
c.1861C>T (n.1861C>T)
n.2387C>T
c.2211C>T (p.Leu737=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301998T>ACA356178101WFS1c.2239T>A (p.Tyr747Asn)
c.2180T>A
c.2203T>A (p.Tyr735Asn)
c.1954T>A (p.Tyr652Asn)
c.1862T>A (n.1862T>A)
n.2388T>A
c.2212T>A (p.Tyr738Asn)
 dbSNP gnomAD v4
4g.6301998T>CCA356178099WFS1c.2239T>C (p.Tyr747His)
c.2180T>C
c.2203T>C (p.Tyr735His)
c.1954T>C (p.Tyr652His)
c.1862T>C (n.1862T>C)
n.2388T>C
c.2212T>C (p.Tyr738His)
 gnomAD v4
4g.6301998T>GCA356178098WFS1c.2239T>G (p.Tyr747Asp)
c.2180T>G
c.2203T>G (p.Tyr735Asp)
c.1954T>G (p.Tyr652Asp)
c.1862T>G (n.1862T>G)
n.2388T>G
c.2212T>G (p.Tyr738Asp)
4g.6301998T=CA1435772181WFS1c.2239T= (p.Tyr747=)
c.2180T=
c.2203T= (p.Tyr735=)
c.1954T= (p.Tyr652=)
c.1862T= (n.1862T=)
n.2388T=
c.2212T= (p.Tyr738=)
4g.6301998_6302011delCA2669843451WFS1c.2239_2252del (p.Tyr747ProfsTer19)
c.2180_2193del
c.2203_2216del (p.Tyr735ProfsTer19)
c.1954_1967del (p.Tyr652ProfsTer19)
c.1862_1875del (n.1862_1875del)
n.2388_2401del
c.2212_2225del (p.Tyr738ProfsTer19)
 gnomAD v4
4g.6301999A=CA1435772182WFS1c.2240A= (p.Tyr747=)
c.2181A=
c.2204A= (p.Tyr735=)
c.1955A= (p.Tyr652=)
c.1863A= (n.1863A=)
n.2389A=
c.2213A= (p.Tyr738=)
4g.6301999A>CCA356178103WFS1c.2240A>C (p.Tyr747Ser)
c.2181A>C
c.2204A>C (p.Tyr735Ser)
c.1955A>C (p.Tyr652Ser)
c.1863A>C (n.1863A>C)
n.2389A>C
c.2213A>C (p.Tyr738Ser)
4g.6301999A>GCA356178104WFS1c.2240A>G (p.Tyr747Cys)
c.2181A>G
c.2204A>G (p.Tyr735Cys)
c.1955A>G (p.Tyr652Cys)
c.1863A>G (n.1863A>G)
n.2389A>G
c.2213A>G (p.Tyr738Cys)
 dbSNP gnomAD v4
4g.6301999A>TCA356178105WFS1c.2240A>T (p.Tyr747Phe)
c.2181A>T
c.2204A>T (p.Tyr735Phe)
c.1955A>T (p.Tyr652Phe)
c.1863A>T (n.1863A>T)
n.2389A>T
c.2213A>T (p.Tyr738Phe)
4g.6302000C>ACA356178107WFS1c.2241C>A (p.Tyr747Ter)
c.2182C>A
c.2205C>A (p.Tyr735Ter)
c.1956C>A (p.Tyr652Ter)
c.1864C>A (n.1864C>A)
n.2390C>A
c.2214C>A (p.Tyr738Ter)
 dbSNP gnomAD v2
4g.6302000C=CA1435772185WFS1c.2241C= (p.Tyr747=)
c.2182C=
c.2205C= (p.Tyr735=)
c.1956C= (p.Tyr652=)
c.1864C= (n.1864C=)
n.2390C=
c.2214C= (p.Tyr738=)
4g.6302000C>GCA356178109WFS1c.2241C>G (p.Tyr747Ter)
c.2182C>G
c.2205C>G (p.Tyr735Ter)
c.1956C>G (p.Tyr652Ter)
c.1864C>G (n.1864C>G)
n.2390C>G
c.2214C>G (p.Tyr738Ter)
 ClinVar dbSNP
4g.6302000C>TCA295795WFS1c.2241C>T (p.Tyr747=)
c.2182C>T
c.2205C>T (p.Tyr735=)
c.1956C>T (p.Tyr652=)
c.1864C>T (n.1864C>T)
n.2390C>T
c.2214C>T (p.Tyr738=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6302000_6302001delinsCGCA1435772183WFS1c.2241_2242delinsCG (p.Tyr747=)
c.2182_2183delinsCG
c.2205_2206delinsCG (p.Tyr735=)
c.1956_1957delinsCG (p.Tyr652=)
c.1864_1865delinsCG (n.1864_1865delinsCG)
n.2390_2391delinsCG
c.2214_2215delinsCG (p.Tyr738=)
4g.6302001G>ACA2839644WFS1c.2242G>A (p.Gly748Ser)
c.2183G>A
c.2206G>A (p.Gly736Ser)
c.1957G>A (p.Gly653Ser)
c.1865G>A (n.1865G>A)
n.2391G>A
c.2215G>A (p.Gly739Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302001G>CCA91796940WFS1c.2242G>C (p.Gly748Arg)
c.2183G>C
c.2206G>C (p.Gly736Arg)
c.1957G>C (p.Gly653Arg)
c.1865G>C (n.1865G>C)
n.2391G>C
c.2215G>C (p.Gly739Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302001G=CA1435772187WFS1c.2242G= (p.Gly748=)
c.2183G=
c.2206G= (p.Gly736=)
c.1957G= (p.Gly653=)
c.1865G= (n.1865G=)
n.2391G=
c.2215G= (p.Gly739=)
4g.6302001G>TCA356178113WFS1c.2242G>T (p.Gly748Cys)
c.2183G>T
c.2206G>T (p.Gly736Cys)
c.1957G>T (p.Gly653Cys)
c.1865G>T (n.1865G>T)
n.2391G>T
c.2215G>T (p.Gly739Cys)
4g.6302002delCA1435772186WFS1c.2243del (p.Gly748AlafsTer?)
c.2184del
c.2207del (p.Gly736AlafsTer?)
c.1958del (p.Gly653AlafsTer?)
c.1866del (n.1866del)
n.2392del
c.2216del (p.Gly739AlafsTer?)
 dbSNP
4g.6302001_6302005delinsGGCGACA1435772188WFS1c.2242_2246delinsGGCGA (p.Gly748=)
c.2183_2187delinsGGCGA
c.2206_2210delinsGGCGA (p.Gly736=)
c.1957_1961delinsGGCGA (p.Gly653=)
c.1865_1869delinsGGCGA (n.1865_1869delinsGGCGA)
n.2391_2395delinsGGCGA
c.2215_2219delinsGGCGA (p.Gly739=)
4g.6302002G>ACA91796942WFS1c.2243G>A (p.Gly748Asp)
c.2184G>A
c.2207G>A (p.Gly736Asp)
c.1958G>A (p.Gly653Asp)
c.1866G>A (n.1866G>A)
n.2392G>A
c.2216G>A (p.Gly739Asp)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6302002G>CCA356178116WFS1c.2243G>C (p.Gly748Ala)
c.2184G>C
c.2207G>C (p.Gly736Ala)
c.1958G>C (p.Gly653Ala)
c.1866G>C (n.1866G>C)
n.2392G>C
c.2216G>C (p.Gly739Ala)
 dbSNP gnomAD v3 gnomAD v4
4g.6302002G=CA1435772191WFS1c.2243G= (p.Gly748=)
c.2184G=
c.2207G= (p.Gly736=)
c.1958G= (p.Gly653=)
c.1866G= (n.1866G=)
n.2392G=
c.2216G= (p.Gly739=)
4g.6302002G>TCA356178118WFS1c.2243G>T (p.Gly748Val)
c.2184G>T
c.2207G>T (p.Gly736Val)
c.1958G>T (p.Gly653Val)
c.1866G>T (n.1866G>T)
n.2392G>T
c.2216G>T (p.Gly739Val)
 dbSNP gnomAD v3 gnomAD v4
4g.6302003_6302006delCA16621816WFS1c.2244_2247del (p.Glu749ProfsTer?)
c.2185_2188del
c.2208_2211del (p.Glu737ProfsTer?)
c.1959_1962del (p.Glu654ProfsTer?)
c.1867_1870del (n.1867_1870del)
n.2393_2396del
c.2217_2220del (p.Glu740ProfsTer?)
 ClinVar dbSNP gnomAD v2
4g.6302003C>ACA438368719WFS1c.2244C>A (p.Gly748=)
c.2185C>A
c.2208C>A (p.Gly736=)
c.1959C>A (p.Gly653=)
c.1867C>A (n.1867C>A)
n.2393C>A
c.2217C>A (p.Gly739=)
4g.6302003C=CA1435772195WFS1c.2244C= (p.Gly748=)
c.2185C=
c.2208C= (p.Gly736=)
c.1959C= (p.Gly653=)
c.1867C= (n.1867C=)
n.2393C=
c.2217C= (p.Gly739=)
4g.6302003C>GCA438368721WFS1c.2244C>G (p.Gly748=)
c.2185C>G
c.2208C>G (p.Gly736=)
c.1959C>G (p.Gly653=)
c.1867C>G (n.1867C>G)
n.2393C>G
c.2217C>G (p.Gly739=)
 gnomAD v4
4g.6302003C>TCA2839645WFS1c.2244C>T (p.Gly748=)
c.2185C>T
c.2208C>T (p.Gly736=)
c.1959C>T (p.Gly653=)
c.1867C>T (n.1867C>T)
n.2393C>T
c.2217C>T (p.Gly739=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302004G>ACA232844WFS1c.2245G>A (p.Glu749Lys)
c.2186G>A
c.2209G>A (p.Glu737Lys)
c.1960G>A (p.Glu654Lys)
c.1868G>A (n.1868G>A)
n.2394G>A
c.2218G>A (p.Glu740Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302004G>CCA356178122WFS1c.2245G>C (p.Glu749Gln)
c.2186G>C
c.2209G>C (p.Glu737Gln)
c.1960G>C (p.Glu654Gln)
c.1868G>C (n.1868G>C)
n.2394G>C
c.2218G>C (p.Glu740Gln)
 gnomAD v4
4g.6302004G=CA1435772198WFS1c.2245G= (p.Glu749=)
c.2186G=
c.2209G= (p.Glu737=)
c.1960G= (p.Glu654=)
c.1868G= (n.1868G=)
n.2394G=
c.2218G= (p.Glu740=)
4g.6302004G>TCA356178120WFS1c.2245G>T (p.Glu749Ter)
c.2186G>T
c.2209G>T (p.Glu737Ter)
c.1960G>T (p.Glu654Ter)
c.1868G>T (n.1868G>T)
n.2394G>T
c.2218G>T (p.Glu740Ter)
4g.6302005A>CCA356178123WFS1c.2246A>C (p.Glu749Ala)
c.2187A>C
c.2210A>C (p.Glu737Ala)
c.1961A>C (p.Glu654Ala)
c.1869A>C (n.1869A>C)
n.2395A>C
c.2219A>C (p.Glu740Ala)
4g.6302005A>GCA356178127WFS1c.2246A>G (p.Glu749Gly)
c.2187A>G
c.2210A>G (p.Glu737Gly)
c.1961A>G (p.Glu654Gly)
c.1869A>G (n.1869A>G)
n.2395A>G
c.2219A>G (p.Glu740Gly)
 gnomAD v4
4g.6302005A>TCA356178125WFS1c.2246A>T (p.Glu749Val)
c.2187A>T
c.2210A>T (p.Glu737Val)
c.1961A>T (p.Glu654Val)
c.1869A>T (n.1869A>T)
n.2395A>T
c.2219A>T (p.Glu740Val)
4g.6302006G>ACA438368722WFS1c.2247G>A (p.Glu749=)
c.2188G>A
c.2211G>A (p.Glu737=)
c.1962G>A (p.Glu654=)
c.1870G>A (n.1870G>A)
n.2396G>A
c.2220G>A (p.Glu740=)
4g.6302006G>CCA356178128WFS1c.2247G>C (p.Glu749Asp)
c.2188G>C
c.2211G>C (p.Glu737Asp)
c.1962G>C (p.Glu654Asp)
c.1870G>C (n.1870G>C)
n.2396G>C
c.2220G>C (p.Glu740Asp)
4g.6302006G>TCA356178129WFS1c.2247G>T (p.Glu749Asp)
c.2188G>T
c.2211G>T (p.Glu737Asp)
c.1962G>T (p.Glu654Asp)
c.1870G>T (n.1870G>T)
n.2396G>T
c.2220G>T (p.Glu740Asp)
4g.6302007G>ACA2839646WFS1c.2248G>A (p.Ala750Thr)
c.2189G>A
c.2212G>A (p.Ala738Thr)
c.1963G>A (p.Ala655Thr)
c.1871G>A (n.1871G>A)
n.2397G>A
c.2221G>A (p.Ala741Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302007G>CCA356178132WFS1c.2248G>C (p.Ala750Pro)
c.2189G>C
c.2212G>C (p.Ala738Pro)
c.1963G>C (p.Ala655Pro)
c.1871G>C (n.1871G>C)
n.2397G>C
c.2221G>C (p.Ala741Pro)
4g.6302007G=CA1435772201WFS1c.2248G= (p.Ala750=)
c.2189G=
c.2212G= (p.Ala738=)
c.1963G= (p.Ala655=)
c.1871G= (n.1871G=)
n.2397G=
c.2221G= (p.Ala741=)
4g.6302007G>TCA356178134WFS1c.2248G>T (p.Ala750Ser)
c.2189G>T
c.2212G>T (p.Ala738Ser)
c.1963G>T (p.Ala655Ser)
c.1871G>T (n.1871G>T)
n.2397G>T
c.2221G>T (p.Ala741Ser)

Number of alleles fetched