Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.6301624_6301640delinsTGCGCTGGTGGACCAAGCA1435774275WFS1c.1865_1881delinsTGCGCTGGTGGACCAAG (p.Leu622=)
c.1806_1822delinsTGCGCTGGTGGACCAAG
c.1829_1845delinsTGCGCTGGTGGACCAAG (p.Leu610=)
c.1580_1596delinsTGCGCTGGTGGACCAAG (p.Leu527=)
c.1488_1504delinsTGCGCTGGTGGACCAAG (n.1488_1504delinsTGCGCTGGTGGACCAAG)
n.2014_2030delinsTGCGCTGGTGGACCAAG
c.1838_1854delinsTGCGCTGGTGGACCAAG (p.Leu613=)
4g.6301627_6301642delCA549707909WFS1c.1868_1883del (p.Arg623ProfsTer9)
c.1809_1824del
c.1832_1847del (p.Arg611ProfsTer9)
c.1583_1598del (p.Arg528ProfsTer9)
c.1491_1506del (n.1491_1506del)
n.2017_2032del
c.1841_1856del (p.Arg614ProfsTer9)
 dbSNP gnomAD v2
4g.6301628_6301653delinsCTGGTGGACCAAGGCCAGCTTCTCTGCA1435774306WFS1c.1869_1894delinsCTGGTGGACCAAGGCCAGCTTCTCTG (p.Arg623=)
c.1810_1835delinsCTGGTGGACCAAGGCCAGCTTCTCTG
c.1833_1858delinsCTGGTGGACCAAGGCCAGCTTCTCTG (p.Arg611=)
c.1584_1609delinsCTGGTGGACCAAGGCCAGCTTCTCTG (p.Arg528=)
c.1492_1517delinsCTGGTGGACCAAGGCCAGCTTCTCTG (n.1492_1517delinsCTGGTGGACCAAGGCCAGCTTCTCTG)
n.2018_2043delinsCTGGTGGACCAAGGCCAGCTTCTCTG
c.1842_1867delinsCTGGTGGACCAAGGCCAGCTTCTCTG (p.Arg614=)
4g.6301635_6301659delCA1058892012WFS1c.1876_1900del (p.Thr626GlyfsTer3)
c.1817_1841del
c.1840_1864del (p.Thr614GlyfsTer3)
c.1591_1615del (p.Thr531GlyfsTer3)
c.1499_1523del (n.1499_1523del)
n.2025_2049del
c.1849_1873del (p.Thr617GlyfsTer3)
 dbSNP gnomAD v3 gnomAD v4
4g.6301633G>ACA2839515WFS1c.1874G>A (p.Trp625Ter)
c.1815G>A
c.1838G>A (p.Trp613Ter)
c.1589G>A (p.Trp530Ter)
c.1497G>A (n.1497G>A)
n.2023G>A
c.1847G>A (p.Trp616Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301633G>CCA356176934WFS1c.1874G>C (p.Trp625Ser)
c.1815G>C
c.1838G>C (p.Trp613Ser)
c.1589G>C (p.Trp530Ser)
c.1497G>C (n.1497G>C)
n.2023G>C
c.1847G>C (p.Trp616Ser)
 dbSNP
4g.6301633G=CA1435771535WFS1c.1874G= (p.Trp625=)
c.1815G=
c.1838G= (p.Trp613=)
c.1589G= (p.Trp530=)
c.1497G= (n.1497G=)
n.2023G=
c.1847G= (p.Trp616=)
4g.6301633G>TCA356176935WFS1c.1874G>T (p.Trp625Leu)
c.1815G>T
c.1838G>T (p.Trp613Leu)
c.1589G>T (p.Trp530Leu)
c.1497G>T (n.1497G>T)
n.2023G>T
c.1847G>T (p.Trp616Leu)
 COSMIC
4g.6301634G>ACA2839516WFS1c.1875G>A (p.Trp625Ter)
c.1816G>A
c.1839G>A (p.Trp613Ter)
c.1590G>A (p.Trp530Ter)
c.1498G>A (n.1498G>A)
n.2024G>A
c.1848G>A (p.Trp616Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301634G>CCA356176936WFS1c.1875G>C (p.Trp625Cys)
c.1816G>C
c.1839G>C (p.Trp613Cys)
c.1590G>C (p.Trp530Cys)
c.1498G>C (n.1498G>C)
n.2024G>C
c.1848G>C (p.Trp616Cys)
4g.6301634G=CA1435771541WFS1c.1875G= (p.Trp625=)
c.1816G=
c.1839G= (p.Trp613=)
c.1590G= (p.Trp530=)
c.1498G= (n.1498G=)
n.2024G=
c.1848G= (p.Trp616=)
4g.6301634G>TCA356176937WFS1c.1875G>T (p.Trp625Cys)
c.1816G>T
c.1839G>T (p.Trp613Cys)
c.1590G>T (p.Trp530Cys)
c.1498G>T (n.1498G>T)
n.2024G>T
c.1848G>T (p.Trp616Cys)
 gnomAD v4 COSMIC
4g.6301635A=CA1435771544WFS1c.1876A= (p.Thr626=)
c.1817A=
c.1840A= (p.Thr614=)
c.1591A= (p.Thr531=)
c.1499A= (n.1499A=)
n.2025A=
c.1849A= (p.Thr617=)
4g.6301635A>CCA356176938WFS1c.1876A>C (p.Thr626Pro)
c.1817A>C
c.1840A>C (p.Thr614Pro)
c.1591A>C (p.Thr531Pro)
c.1499A>C (n.1499A>C)
n.2025A>C
c.1849A>C (p.Thr617Pro)
 dbSNP gnomAD v2 gnomAD v4
4g.6301635A>GCA356176939WFS1c.1876A>G (p.Thr626Ala)
c.1817A>G
c.1840A>G (p.Thr614Ala)
c.1591A>G (p.Thr531Ala)
c.1499A>G (n.1499A>G)
n.2025A>G
c.1849A>G (p.Thr617Ala)
 ClinVar
4g.6301635A>TCA356176940WFS1c.1876A>T (p.Thr626Ser)
c.1817A>T
c.1840A>T (p.Thr614Ser)
c.1591A>T (p.Thr531Ser)
c.1499A>T (n.1499A>T)
n.2025A>T
c.1849A>T (p.Thr617Ser)
4g.6301636C>ACA356176942WFS1c.1877C>A (p.Thr626Asn)
c.1818C>A
c.1841C>A (p.Thr614Asn)
c.1592C>A (p.Thr531Asn)
c.1500C>A (n.1500C>A)
n.2026C>A
c.1850C>A (p.Thr617Asn)
4g.6301636C=CA1435771546WFS1c.1877C= (p.Thr626=)
c.1818C=
c.1841C= (p.Thr614=)
c.1592C= (p.Thr531=)
c.1500C= (n.1500C=)
n.2026C=
c.1850C= (p.Thr617=)
4g.6301636C>GCA2839517WFS1c.1877C>G (p.Thr626Ser)
c.1818C>G
c.1841C>G (p.Thr614Ser)
c.1592C>G (p.Thr531Ser)
c.1500C>G (n.1500C>G)
n.2026C>G
c.1850C>G (p.Thr617Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301636C>TCA356176941WFS1c.1877C>T (p.Thr626Ile)
c.1818C>T
c.1841C>T (p.Thr614Ile)
c.1592C>T (p.Thr531Ile)
c.1500C>T (n.1500C>T)
n.2026C>T
c.1850C>T (p.Thr617Ile)
4g.6301637C>ACA438368477WFS1c.1878C>A (p.Thr626=)
c.1819C>A
c.1842C>A (p.Thr614=)
c.1593C>A (p.Thr531=)
c.1501C>A (n.1501C>A)
n.2027C>A
c.1851C>A (p.Thr617=)
4g.6301637C=CA1435771548WFS1c.1878C= (p.Thr626=)
c.1819C=
c.1842C= (p.Thr614=)
c.1593C= (p.Thr531=)
c.1501C= (n.1501C=)
n.2027C=
c.1851C= (p.Thr617=)
4g.6301637C>GCA438368479WFS1c.1878C>G (p.Thr626=)
c.1819C>G
c.1842C>G (p.Thr614=)
c.1593C>G (p.Thr531=)
c.1501C>G (n.1501C>G)
n.2027C>G
c.1851C>G (p.Thr617=)
 gnomAD v4
4g.6301637C>TCA2839518WFS1c.1878C>T (p.Thr626=)
c.1819C>T
c.1842C>T (p.Thr614=)
c.1593C>T (p.Thr531=)
c.1501C>T (n.1501C>T)
n.2027C>T
c.1851C>T (p.Thr617=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301638A>CCA356176943WFS1c.1879A>C (p.Lys627Gln)
c.1820A>C
c.1843A>C (p.Lys615Gln)
c.1594A>C (p.Lys532Gln)
c.1502A>C (n.1502A>C)
n.2028A>C
c.1852A>C (p.Lys618Gln)
4g.6301638A>GCA356176944WFS1c.1879A>G (p.Lys627Glu)
c.1820A>G
c.1843A>G (p.Lys615Glu)
c.1594A>G (p.Lys532Glu)
c.1502A>G (n.1502A>G)
n.2028A>G
c.1852A>G (p.Lys618Glu)
 gnomAD v4
4g.6301638A>TCA356176945WFS1c.1879A>T (p.Lys627Ter)
c.1820A>T
c.1843A>T (p.Lys615Ter)
c.1594A>T (p.Lys532Ter)
c.1502A>T (n.1502A>T)
n.2028A>T
c.1852A>T (p.Lys618Ter)
4g.6301639A>CCA356176946WFS1c.1880A>C (p.Lys627Thr)
c.1821A>C
c.1844A>C (p.Lys615Thr)
c.1595A>C (p.Lys532Thr)
c.1503A>C (n.1503A>C)
n.2029A>C
c.1853A>C (p.Lys618Thr)
 gnomAD v4
4g.6301639A>GCA356176947WFS1c.1880A>G (p.Lys627Arg)
c.1821A>G
c.1844A>G (p.Lys615Arg)
c.1595A>G (p.Lys532Arg)
c.1503A>G (n.1503A>G)
n.2029A>G
c.1853A>G (p.Lys618Arg)
4g.6301639A>TCA356176948WFS1c.1880A>T (p.Lys627Met)
c.1821A>T
c.1844A>T (p.Lys615Met)
c.1595A>T (p.Lys532Met)
c.1503A>T (n.1503A>T)
n.2029A>T
c.1853A>T (p.Lys618Met)
4g.6301640G>ACA438368489WFS1c.1881G>A (p.Lys627=)
c.1822G>A
c.1845G>A (p.Lys615=)
c.1596G>A (p.Lys532=)
c.1504G>A (n.1504G>A)
n.2030G>A
c.1854G>A (p.Lys618=)
 dbSNP gnomAD v4
4g.6301640G>CCA356176949WFS1c.1881G>C (p.Lys627Asn)
c.1822G>C
c.1845G>C (p.Lys615Asn)
c.1596G>C (p.Lys532Asn)
c.1504G>C (n.1504G>C)
n.2030G>C
c.1854G>C (p.Lys618Asn)
 dbSNP
4g.6301640G=CA1435771550WFS1c.1881G= (p.Lys627=)
c.1822G=
c.1845G= (p.Lys615=)
c.1596G= (p.Lys532=)
c.1504G= (n.1504G=)
n.2030G=
c.1854G= (p.Lys618=)
4g.6301640G>TCA356176950WFS1c.1881G>T (p.Lys627Asn)
c.1822G>T
c.1845G>T (p.Lys615Asn)
c.1596G>T (p.Lys532Asn)
c.1504G>T (n.1504G>T)
n.2030G>T
c.1854G>T (p.Lys618Asn)
4g.6301641dupCA2669843453WFS1c.1882dup (p.Ala628GlyfsTer?)
c.1823dup
c.1846dup (p.Ala616GlyfsTer?)
c.1597dup (p.Ala533GlyfsTer?)
c.1505dup (n.1505dup)
n.2031dup
c.1855dup (p.Ala619GlyfsTer?)
 gnomAD v4
4g.6301641G>ACA356176951WFS1c.1882G>A (p.Ala628Thr)
c.1823G>A
c.1846G>A (p.Ala616Thr)
c.1597G>A (p.Ala533Thr)
c.1505G>A (n.1505G>A)
n.2031G>A
c.1855G>A (p.Ala619Thr)
4g.6301641G>CCA356176952WFS1c.1882G>C (p.Ala628Pro)
c.1823G>C
c.1846G>C (p.Ala616Pro)
c.1597G>C (p.Ala533Pro)
c.1505G>C (n.1505G>C)
n.2031G>C
c.1855G>C (p.Ala619Pro)
 ClinVar dbSNP
4g.6301641G=CA1435771552WFS1c.1882G= (p.Ala628=)
c.1823G=
c.1846G= (p.Ala616=)
c.1597G= (p.Ala533=)
c.1505G= (n.1505G=)
n.2031G=
c.1855G= (p.Ala619=)
4g.6301641G>TCA2839519WFS1c.1882G>T (p.Ala628Ser)
c.1823G>T
c.1846G>T (p.Ala616Ser)
c.1597G>T (p.Ala533Ser)
c.1505G>T (n.1505G>T)
n.2031G>T
c.1855G>T (p.Ala619Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301642C>ACA356176954WFS1c.1883C>A (p.Ala628Asp)
c.1824C>A
c.1847C>A (p.Ala616Asp)
c.1598C>A (p.Ala533Asp)
c.1506C>A (n.1506C>A)
n.2032C>A
c.1856C>A (p.Ala619Asp)
 gnomAD v4
4g.6301642C=CA1435771556WFS1c.1883C= (p.Ala628=)
c.1824C=
c.1847C= (p.Ala616=)
c.1598C= (p.Ala533=)
c.1506C= (n.1506C=)
n.2032C=
c.1856C= (p.Ala619=)
4g.6301642C>GCA356176955WFS1c.1883C>G (p.Ala628Gly)
c.1824C>G
c.1847C>G (p.Ala616Gly)
c.1598C>G (p.Ala533Gly)
c.1506C>G (n.1506C>G)
n.2032C>G
c.1856C>G (p.Ala619Gly)
4g.6301642C>TCA356176953WFS1c.1883C>T (p.Ala628Val)
c.1824C>T
c.1847C>T (p.Ala616Val)
c.1598C>T (p.Ala533Val)
c.1506C>T (n.1506C>T)
n.2032C>T
c.1856C>T (p.Ala619Val)
 dbSNP COSMIC
4g.6301643C>ACA438368491WFS1c.1884C>A (p.Ala628=)
c.1825C>A
c.1848C>A (p.Ala616=)
c.1599C>A (p.Ala533=)
c.1507C>A (n.1507C>A)
n.2033C>A
c.1857C>A (p.Ala619=)
4g.6301643C=CA1435771560WFS1c.1884C= (p.Ala628=)
c.1825C=
c.1848C= (p.Ala616=)
c.1599C= (p.Ala533=)
c.1507C= (n.1507C=)
n.2033C=
c.1857C= (p.Ala619=)
4g.6301643C>GCA438368493WFS1c.1884C>G (p.Ala628=)
c.1825C>G
c.1848C>G (p.Ala616=)
c.1599C>G (p.Ala533=)
c.1507C>G (n.1507C>G)
n.2033C>G
c.1857C>G (p.Ala619=)
 gnomAD v4
4g.6301643C>TCA2839520WFS1c.1884C>T (p.Ala628=)
c.1825C>T
c.1848C>T (p.Ala616=)
c.1599C>T (p.Ala533=)
c.1507C>T (n.1507C>T)
n.2033C>T
c.1857C>T (p.Ala619=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301644A=CA1435771563WFS1c.1885A= (p.Ser629=)
c.1826A=
c.1849A= (p.Ser617=)
c.1600A= (p.Ser534=)
c.1508A= (n.1508A=)
n.2034A=
c.1858A= (p.Ser620=)
4g.6301644A>CCA356176956WFS1c.1885A>C (p.Ser629Arg)
c.1826A>C
c.1849A>C (p.Ser617Arg)
c.1600A>C (p.Ser534Arg)
c.1508A>C (n.1508A>C)
n.2034A>C
c.1858A>C (p.Ser620Arg)
 dbSNP gnomAD v4
4g.6301644A>GCA356176957WFS1c.1885A>G (p.Ser629Gly)
c.1826A>G
c.1849A>G (p.Ser617Gly)
c.1600A>G (p.Ser534Gly)
c.1508A>G (n.1508A>G)
n.2034A>G
c.1858A>G (p.Ser620Gly)
 gnomAD v4
4g.6301644A>TCA356176958WFS1c.1885A>T (p.Ser629Cys)
c.1826A>T
c.1849A>T (p.Ser617Cys)
c.1600A>T (p.Ser534Cys)
c.1508A>T (n.1508A>T)
n.2034A>T
c.1858A>T (p.Ser620Cys)
4g.6301645G>ACA356176959WFS1c.1886G>A (p.Ser629Asn)
c.1827G>A
c.1850G>A (p.Ser617Asn)
c.1601G>A (p.Ser534Asn)
c.1509G>A (n.1509G>A)
n.2035G>A
c.1859G>A (p.Ser620Asn)
 gnomAD v4
4g.6301645G>CCA356176960WFS1c.1886G>C (p.Ser629Thr)
c.1827G>C
c.1850G>C (p.Ser617Thr)
c.1601G>C (p.Ser534Thr)
c.1509G>C (n.1509G>C)
n.2035G>C
c.1859G>C (p.Ser620Thr)
 dbSNP
4g.6301645G>TCA356176961WFS1c.1886G>T (p.Ser629Ile)
c.1827G>T
c.1850G>T (p.Ser617Ile)
c.1601G>T (p.Ser534Ile)
c.1509G>T (n.1509G>T)
n.2035G>T
c.1859G>T (p.Ser620Ile)
4g.6301646C>ACA356176962WFS1c.1887C>A (p.Ser629Arg)
c.1828C>A
c.1851C>A (p.Ser617Arg)
c.1602C>A (p.Ser534Arg)
c.1510C>A (n.1510C>A)
n.2036C>A
c.1860C>A (p.Ser620Arg)
 ClinVar dbSNP gnomAD v4
4g.6301646C=CA1435771571WFS1c.1887C= (p.Ser629=)
c.1828C=
c.1851C= (p.Ser617=)
c.1602C= (p.Ser534=)
c.1510C= (n.1510C=)
n.2036C=
c.1860C= (p.Ser620=)
4g.6301646C>GCA356176963WFS1c.1887C>G (p.Ser629Arg)
c.1828C>G
c.1851C>G (p.Ser617Arg)
c.1602C>G (p.Ser534Arg)
c.1510C>G (n.1510C>G)
n.2036C>G
c.1860C>G (p.Ser620Arg)
4g.6301646C>TCA438368500WFS1c.1887C>T (p.Ser629=)
c.1828C>T
c.1851C>T (p.Ser617=)
c.1602C>T (p.Ser534=)
c.1510C>T (n.1510C>T)
n.2036C>T
c.1860C>T (p.Ser620=)
4g.6301647T>ACA356176964WFS1c.1888T>A (p.Phe630Ile)
c.1829T>A
c.1852T>A (p.Phe618Ile)
c.1603T>A (p.Phe535Ile)
c.1511T>A (n.1511T>A)
n.2037T>A
c.1861T>A (p.Phe621Ile)
4g.6301647T>CCA356176965WFS1c.1888T>C (p.Phe630Leu)
c.1829T>C
c.1852T>C (p.Phe618Leu)
c.1603T>C (p.Phe535Leu)
c.1511T>C (n.1511T>C)
n.2037T>C
c.1861T>C (p.Phe621Leu)
 gnomAD v4
4g.6301647T>GCA356176966WFS1c.1888T>G (p.Phe630Val)
c.1829T>G
c.1852T>G (p.Phe618Val)
c.1603T>G (p.Phe535Val)
c.1511T>G (n.1511T>G)
n.2037T>G
c.1861T>G (p.Phe621Val)
4g.6301648T>ACA356176967WFS1c.1889T>A (p.Phe630Tyr)
c.1830T>A
c.1853T>A (p.Phe618Tyr)
c.1604T>A (p.Phe535Tyr)
c.1512T>A (n.1512T>A)
n.2038T>A
c.1862T>A (p.Phe621Tyr)
 gnomAD v4
4g.6301648T>CCA356176968WFS1c.1889T>C (p.Phe630Ser)
c.1830T>C
c.1853T>C (p.Phe618Ser)
c.1604T>C (p.Phe535Ser)
c.1512T>C (n.1512T>C)
n.2038T>C
c.1862T>C (p.Phe621Ser)
 dbSNP gnomAD v3 gnomAD v4
4g.6301648T>GCA356176969WFS1c.1889T>G (p.Phe630Cys)
c.1830T>G
c.1853T>G (p.Phe618Cys)
c.1604T>G (p.Phe535Cys)
c.1512T>G (n.1512T>G)
n.2038T>G
c.1862T>G (p.Phe621Cys)
 gnomAD v4
4g.6301648T=CA1435771574WFS1c.1889T= (p.Phe630=)
c.1830T=
c.1853T= (p.Phe618=)
c.1604T= (p.Phe535=)
c.1512T= (n.1512T=)
n.2038T=
c.1862T= (p.Phe621=)
4g.6301651_6301652delCA2586973637WFS1c.1892_1893del (p.Ser631CysfsTer?)
c.1833_1834del
c.1856_1857del (p.Ser619CysfsTer?)
c.1607_1608del (p.Ser536CysfsTer?)
c.1515_1516del (n.1515_1516del)
n.2041_2042del
c.1865_1866del (p.Ser622CysfsTer?)
4g.6301649C>ACA356176971WFS1c.1890C>A (p.Phe630Leu)
c.1831C>A
c.1854C>A (p.Phe618Leu)
c.1605C>A (p.Phe535Leu)
c.1513C>A (n.1513C>A)
n.2039C>A
c.1863C>A (p.Phe621Leu)
4g.6301649C=CA1435771577WFS1c.1890C= (p.Phe630=)
c.1831C=
c.1854C= (p.Phe618=)
c.1605C= (p.Phe535=)
c.1513C= (n.1513C=)
n.2039C=
c.1863C= (p.Phe621=)
4g.6301649C>GCA356176970WFS1c.1890C>G (p.Phe630Leu)
c.1831C>G
c.1854C>G (p.Phe618Leu)
c.1605C>G (p.Phe535Leu)
c.1513C>G (n.1513C>G)
n.2039C>G
c.1863C>G (p.Phe621Leu)
4g.6301649C>TCA438368501WFS1c.1890C>T (p.Phe630=)
c.1831C>T
c.1854C>T (p.Phe618=)
c.1605C>T (p.Phe535=)
c.1513C>T (n.1513C>T)
n.2039C>T
c.1863C>T (p.Phe621=)
 dbSNP gnomAD v4
4g.6301650T>ACA356176972WFS1c.1891T>A (p.Ser631Thr)
c.1832T>A
c.1855T>A (p.Ser619Thr)
c.1606T>A (p.Ser536Thr)
c.1514T>A (n.1514T>A)
n.2040T>A
c.1864T>A (p.Ser622Thr)
4g.6301650T>CCA356176973WFS1c.1891T>C (p.Ser631Pro)
c.1832T>C
c.1855T>C (p.Ser619Pro)
c.1606T>C (p.Ser536Pro)
c.1514T>C (n.1514T>C)
n.2040T>C
c.1864T>C (p.Ser622Pro)
4g.6301650T>GCA356176974WFS1c.1891T>G (p.Ser631Ala)
c.1832T>G
c.1855T>G (p.Ser619Ala)
c.1606T>G (p.Ser536Ala)
c.1514T>G (n.1514T>G)
n.2040T>G
c.1864T>G (p.Ser622Ala)
4g.6301651C>ACA356176975WFS1c.1892C>A (p.Ser631Tyr)
c.1833C>A
c.1856C>A (p.Ser619Tyr)
c.1607C>A (p.Ser536Tyr)
c.1515C>A (n.1515C>A)
n.2041C>A
c.1865C>A (p.Ser622Tyr)
4g.6301651C>GCA356176976WFS1c.1892C>G (p.Ser631Cys)
c.1833C>G
c.1856C>G (p.Ser619Cys)
c.1607C>G (p.Ser536Cys)
c.1515C>G (n.1515C>G)
n.2041C>G
c.1865C>G (p.Ser622Cys)
4g.6301651C>TCA356176977WFS1c.1892C>T (p.Ser631Phe)
c.1833C>T
c.1856C>T (p.Ser619Phe)
c.1607C>T (p.Ser536Phe)
c.1515C>T (n.1515C>T)
n.2041C>T
c.1865C>T (p.Ser622Phe)
 ClinVar gnomAD v4
4g.6301652T>ACA438368509WFS1c.1893T>A (p.Ser631=)
c.1834T>A
c.1857T>A (p.Ser619=)
c.1608T>A (p.Ser536=)
c.1516T>A (n.1516T>A)
n.2042T>A
c.1866T>A (p.Ser622=)
4g.6301652T>CCA2839521WFS1c.1893T>C (p.Ser631=)
c.1834T>C
c.1857T>C (p.Ser619=)
c.1608T>C (p.Ser536=)
c.1516T>C (n.1516T>C)
n.2042T>C
c.1866T>C (p.Ser622=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301652T>GCA438368511WFS1c.1893T>G (p.Ser631=)
c.1834T>G
c.1857T>G (p.Ser619=)
c.1608T>G (p.Ser536=)
c.1516T>G (n.1516T>G)
n.2042T>G
c.1866T>G (p.Ser622=)
4g.6301652T=CA1435771579WFS1c.1893T= (p.Ser631=)
c.1834T=
c.1857T= (p.Ser619=)
c.1608T= (p.Ser536=)
c.1516T= (n.1516T=)
n.2042T=
c.1866T= (p.Ser622=)
4g.6301653G>ACA356176978WFS1c.1894G>A (p.Val632Met)
c.1835G>A
c.1858G>A (p.Val620Met)
c.1609G>A (p.Val537Met)
c.1517G>A (n.1517G>A)
n.2043G>A
c.1867G>A (p.Val623Met)
 ClinVar dbSNP gnomAD v4
4g.6301653G>CCA2839522WFS1c.1894G>C (p.Val632Leu)
c.1835G>C
c.1858G>C (p.Val620Leu)
c.1609G>C (p.Val537Leu)
c.1517G>C (n.1517G>C)
n.2043G>C
c.1867G>C (p.Val623Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301653G=CA1435771583WFS1c.1894G= (p.Val632=)
c.1835G=
c.1858G= (p.Val620=)
c.1609G= (p.Val537=)
c.1517G= (n.1517G=)
n.2043G=
c.1867G= (p.Val623=)
4g.6301653G>TCA356176979WFS1c.1894G>T (p.Val632Leu)
c.1835G>T
c.1858G>T (p.Val620Leu)
c.1609G>T (p.Val537Leu)
c.1517G>T (n.1517G>T)
n.2043G>T
c.1867G>T (p.Val623Leu)
 dbSNP
4g.6301654T>ACA356176980WFS1c.1895T>A (p.Val632Glu)
c.1836T>A
c.1859T>A (p.Val620Glu)
c.1610T>A (p.Val537Glu)
c.1518T>A (n.1518T>A)
n.2044T>A
c.1868T>A (p.Val623Glu)
4g.6301654T>CCA2839524WFS1c.1895T>C (p.Val632Ala)
c.1836T>C
c.1859T>C (p.Val620Ala)
c.1610T>C (p.Val537Ala)
c.1518T>C (n.1518T>C)
n.2044T>C
c.1868T>C (p.Val623Ala)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301654T>GCA2839523WFS1c.1895T>G (p.Val632Gly)
c.1836T>G
c.1859T>G (p.Val620Gly)
c.1610T>G (p.Val537Gly)
c.1518T>G (n.1518T>G)
n.2044T>G
c.1868T>G (p.Val623Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301654T=CA1435771587WFS1c.1895T= (p.Val632=)
c.1836T=
c.1859T= (p.Val620=)
c.1610T= (p.Val537=)
c.1518T= (n.1518T=)
n.2044T=
c.1868T= (p.Val623=)
4g.6301655G>ACA438368515WFS1c.1896G>A (p.Val632=)
c.1837G>A
c.1860G>A (p.Val620=)
c.1611G>A (p.Val537=)
c.1519G>A (n.1519G>A)
n.2045G>A
c.1869G>A (p.Val623=)
4g.6301655G>CCA438368516WFS1c.1896G>C (p.Val632=)
c.1837G>C
c.1860G>C (p.Val620=)
c.1611G>C (p.Val537=)
c.1519G>C (n.1519G>C)
n.2045G>C
c.1869G>C (p.Val623=)
4g.6301655G>TCA438368517WFS1c.1896G>T (p.Val632=)
c.1837G>T
c.1860G>T (p.Val620=)
c.1611G>T (p.Val537=)
c.1519G>T (n.1519G>T)
n.2045G>T
c.1869G>T (p.Val623=)
4g.6301656G>ACA356176986WFS1c.1897G>A (p.Val633Met)
c.1838G>A
c.1861G>A (p.Val621Met)
c.1612G>A (p.Val538Met)
c.1520G>A (n.1520G>A)
n.2046G>A
c.1870G>A (p.Val624Met)
4g.6301656G>CCA356176984WFS1c.1897G>C (p.Val633Leu)
c.1838G>C
c.1861G>C (p.Val621Leu)
c.1612G>C (p.Val538Leu)
c.1520G>C (n.1520G>C)
n.2046G>C
c.1870G>C (p.Val624Leu)
4g.6301656G>TCA356176982WFS1c.1897G>T (p.Val633Leu)
c.1838G>T
c.1861G>T (p.Val621Leu)
c.1612G>T (p.Val538Leu)
c.1520G>T (n.1520G>T)
n.2046G>T
c.1870G>T (p.Val624Leu)
4g.6301657T>ACA356176988WFS1c.1898T>A (p.Val633Glu)
c.1839T>A
c.1862T>A (p.Val621Glu)
c.1613T>A (p.Val538Glu)
c.1521T>A (n.1521T>A)
n.2047T>A
c.1871T>A (p.Val624Glu)
 gnomAD v4
4g.6301657T>CCA356176991WFS1c.1898T>C (p.Val633Ala)
c.1839T>C
c.1862T>C (p.Val621Ala)
c.1613T>C (p.Val538Ala)
c.1521T>C (n.1521T>C)
n.2047T>C
c.1871T>C (p.Val624Ala)
 gnomAD v4
4g.6301657T>GCA356176990WFS1c.1898T>G (p.Val633Gly)
c.1839T>G
c.1862T>G (p.Val621Gly)
c.1613T>G (p.Val538Gly)
c.1521T>G (n.1521T>G)
n.2047T>G
c.1871T>G (p.Val624Gly)
4g.6301658G>ACA438368519WFS1c.1899G>A (p.Val633=)
c.1840G>A
c.1863G>A (p.Val621=)
c.1614G>A (p.Val538=)
c.1522G>A (n.1522G>A)
n.2048G>A
c.1872G>A (p.Val624=)
 dbSNP gnomAD v2 gnomAD v4
4g.6301658G>CCA2839525WFS1c.1899G>C (p.Val633=)
c.1840G>C
c.1863G>C (p.Val621=)
c.1614G>C (p.Val538=)
c.1522G>C (n.1522G>C)
n.2048G>C
c.1872G>C (p.Val624=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301658G=CA1435771594WFS1c.1899G= (p.Val633=)
c.1840G=
c.1863G= (p.Val621=)
c.1614G= (p.Val538=)
c.1522G= (n.1522G=)
n.2048G=
c.1872G= (p.Val624=)
4g.6301658G>TCA438368520WFS1c.1899G>T (p.Val633=)
c.1840G>T
c.1863G>T (p.Val621=)
c.1614G>T (p.Val538=)
c.1522G>T (n.1522G>T)
n.2048G>T
c.1872G>T (p.Val624=)
4g.6301659G>ACA356176994WFS1c.1900G>A (p.Gly634Arg)
c.1841G>A
c.1864G>A (p.Gly622Arg)
c.1615G>A (p.Gly539Arg)
c.1523G>A (n.1523G>A)
n.2049G>A
c.1873G>A (p.Gly625Arg)
4g.6301659G>CCA356176996WFS1c.1900G>C (p.Gly634Arg)
c.1841G>C
c.1864G>C (p.Gly622Arg)
c.1615G>C (p.Gly539Arg)
c.1523G>C (n.1523G>C)
n.2049G>C
c.1873G>C (p.Gly625Arg)
4g.6301659G>TCA356176997WFS1c.1900G>T (p.Gly634Trp)
c.1841G>T
c.1864G>T (p.Gly622Trp)
c.1615G>T (p.Gly539Trp)
c.1523G>T (n.1523G>T)
n.2049G>T
c.1873G>T (p.Gly625Trp)
4g.6301660G>ACA356176999WFS1c.1901G>A (p.Gly634Glu)
c.1842G>A
c.1865G>A (p.Gly622Glu)
c.1616G>A (p.Gly539Glu)
c.1524G>A (n.1524G>A)
n.2050G>A
c.1874G>A (p.Gly625Glu)
 gnomAD v4
4g.6301660G>CCA356177000WFS1c.1901G>C (p.Gly634Ala)
c.1842G>C
c.1865G>C (p.Gly622Ala)
c.1616G>C (p.Gly539Ala)
c.1524G>C (n.1524G>C)
n.2050G>C
c.1874G>C (p.Gly625Ala)
 gnomAD v4
4g.6301660G=CA1435771598WFS1c.1901G= (p.Gly634=)
c.1842G=
c.1865G= (p.Gly622=)
c.1616G= (p.Gly539=)
c.1524G= (n.1524G=)
n.2050G=
c.1874G= (p.Gly625=)
4g.6301660G>TCA2839526WFS1c.1901G>T (p.Gly634Val)
c.1842G>T
c.1865G>T (p.Gly622Val)
c.1616G>T (p.Gly539Val)
c.1524G>T (n.1524G>T)
n.2050G>T
c.1874G>T (p.Gly625Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301661G>ACA91796655WFS1c.1902G>A (p.Gly634=)
c.1843G>A
c.1866G>A (p.Gly622=)
c.1617G>A (p.Gly539=)
c.1525G>A (n.1525G>A)
n.2051G>A
c.1875G>A (p.Gly625=)
 dbSNP gnomAD v4
4g.6301661G>CCA438368527WFS1c.1902G>C (p.Gly634=)
c.1843G>C
c.1866G>C (p.Gly622=)
c.1617G>C (p.Gly539=)
c.1525G>C (n.1525G>C)
n.2051G>C
c.1875G>C (p.Gly625=)
4g.6301661G=CA1435771600WFS1c.1902G= (p.Gly634=)
c.1843G=
c.1866G= (p.Gly622=)
c.1617G= (p.Gly539=)
c.1525G= (n.1525G=)
n.2051G=
c.1875G= (p.Gly625=)
4g.6301661G>TCA438368525WFS1c.1902G>T (p.Gly634=)
c.1843G>T
c.1866G>T (p.Gly622=)
c.1617G>T (p.Gly539=)
c.1525G>T (n.1525G>T)
n.2051G>T
c.1875G>T (p.Gly625=)
 dbSNP gnomAD v3 gnomAD v4
4g.6301662delCA2586973638WFS1c.1903del (p.Met635TrpfsTer2)
c.1844del
c.1867del (p.Met623TrpfsTer2)
c.1618del (p.Met540TrpfsTer2)
c.1526del (n.1526del)
n.2052del
c.1876del (p.Met626TrpfsTer2)
4g.6301662A=CA1435771605WFS1c.1903A= (p.Met635=)
c.1844A=
c.1867A= (p.Met623=)
c.1618A= (p.Met540=)
c.1526A= (n.1526A=)
n.2052A=
c.1876A= (p.Met626=)
4g.6301662A>CCA356177002WFS1c.1903A>C (p.Met635Leu)
c.1844A>C
c.1867A>C (p.Met623Leu)
c.1618A>C (p.Met540Leu)
c.1526A>C (n.1526A>C)
n.2052A>C
c.1876A>C (p.Met626Leu)
4g.6301662A>GCA356177003WFS1c.1903A>G (p.Met635Val)
c.1844A>G
c.1867A>G (p.Met623Val)
c.1618A>G (p.Met540Val)
c.1526A>G (n.1526A>G)
n.2052A>G
c.1876A>G (p.Met626Val)
 dbSNP gnomAD v2 gnomAD v4
4g.6301662A>TCA356177004WFS1c.1903A>T (p.Met635Leu)
c.1844A>T
c.1867A>T (p.Met623Leu)
c.1618A>T (p.Met540Leu)
c.1526A>T (n.1526A>T)
n.2052A>T
c.1876A>T (p.Met626Leu)
4g.6301663T>ACA16609252WFS1c.1904T>A (p.Met635Lys)
c.1845T>A
c.1868T>A (p.Met623Lys)
c.1619T>A (p.Met540Lys)
c.1527T>A (n.1527T>A)
n.2053T>A
c.1877T>A (p.Met626Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6301663T>CCA2839527WFS1c.1904T>C (p.Met635Thr)
c.1845T>C
c.1868T>C (p.Met623Thr)
c.1619T>C (p.Met540Thr)
c.1527T>C (n.1527T>C)
n.2053T>C
c.1877T>C (p.Met626Thr)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301663T>GCA356177005WFS1c.1904T>G (p.Met635Arg)
c.1845T>G
c.1868T>G (p.Met623Arg)
c.1619T>G (p.Met540Arg)
c.1527T>G (n.1527T>G)
n.2053T>G
c.1877T>G (p.Met626Arg)
 ClinVar gnomAD v4
4g.6301663T=CA1435771609WFS1c.1904T= (p.Met635=)
c.1845T=
c.1868T= (p.Met623=)
c.1619T= (p.Met540=)
c.1527T= (n.1527T=)
n.2053T=
c.1877T= (p.Met626=)
4g.6301665_6301667delCA2669843455WFS1c.1906_1908del (p.Val636del)
c.1847_1849del
c.1870_1872del (p.Val624del)
c.1621_1623del (p.Val541del)
c.1529_1531del (n.1529_1531del)
n.2055_2057del
c.1879_1881del (p.Val627del)
 gnomAD v4
4g.6301664G>ACA2839528WFS1c.1905G>A (p.Met635Ile)
c.1846G>A
c.1869G>A (p.Met623Ile)
c.1620G>A (p.Met540Ile)
c.1528G>A (n.1528G>A)
n.2054G>A
c.1878G>A (p.Met626Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301664G>CCA356177006WFS1c.1905G>C (p.Met635Ile)
c.1846G>C
c.1869G>C (p.Met623Ile)
c.1620G>C (p.Met540Ile)
c.1528G>C (n.1528G>C)
n.2054G>C
c.1878G>C (p.Met626Ile)
4g.6301664G=CA1435771613WFS1c.1905G= (p.Met635=)
c.1846G=
c.1869G= (p.Met623=)
c.1620G= (p.Met540=)
c.1528G= (n.1528G=)
n.2054G=
c.1878G= (p.Met626=)
4g.6301664G>TCA356177007WFS1c.1905G>T (p.Met635Ile)
c.1846G>T
c.1869G>T (p.Met623Ile)
c.1620G>T (p.Met540Ile)
c.1528G>T (n.1528G>T)
n.2054G>T
c.1878G>T (p.Met626Ile)
4g.6301665G>ACA356177008WFS1c.1906G>A (p.Val636Met)
c.1847G>A
c.1870G>A (p.Val624Met)
c.1621G>A (p.Val541Met)
c.1529G>A (n.1529G>A)
n.2055G>A
c.1879G>A (p.Val627Met)
 gnomAD v4
4g.6301665G>CCA356177009WFS1c.1906G>C (p.Val636Leu)
c.1847G>C
c.1870G>C (p.Val624Leu)
c.1621G>C (p.Val541Leu)
c.1529G>C (n.1529G>C)
n.2055G>C
c.1879G>C (p.Val627Leu)
4g.6301665G>TCA356177010WFS1c.1906G>T (p.Val636Leu)
c.1847G>T
c.1870G>T (p.Val624Leu)
c.1621G>T (p.Val541Leu)
c.1529G>T (n.1529G>T)
n.2055G>T
c.1879G>T (p.Val627Leu)
4g.6301666T>ACA356177011WFS1c.1907T>A (p.Val636Glu)
c.1848T>A
c.1871T>A (p.Val624Glu)
c.1622T>A (p.Val541Glu)
c.1530T>A (n.1530T>A)
n.2056T>A
c.1880T>A (p.Val627Glu)
4g.6301666T>CCA2839529WFS1c.1907T>C (p.Val636Ala)
c.1848T>C
c.1871T>C (p.Val624Ala)
c.1622T>C (p.Val541Ala)
c.1530T>C (n.1530T>C)
n.2056T>C
c.1880T>C (p.Val627Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301666T>GCA356177012WFS1c.1907T>G (p.Val636Gly)
c.1848T>G
c.1871T>G (p.Val624Gly)
c.1622T>G (p.Val541Gly)
c.1530T>G (n.1530T>G)
n.2056T>G
c.1880T>G (p.Val627Gly)
 ClinVar dbSNP
4g.6301666T=CA1435771618WFS1c.1907T= (p.Val636=)
c.1848T=
c.1871T= (p.Val624=)
c.1622T= (p.Val541=)
c.1530T= (n.1530T=)
n.2056T=
c.1880T= (p.Val627=)
4g.6301667G>ACA438368539WFS1c.1908G>A (p.Val636=)
c.1849G>A
c.1872G>A (p.Val624=)
c.1623G>A (p.Val541=)
c.1531G>A (n.1531G>A)
n.2057G>A
c.1881G>A (p.Val627=)
 ClinVar
4g.6301667G>CCA438368540WFS1c.1908G>C (p.Val636=)
c.1849G>C
c.1872G>C (p.Val624=)
c.1623G>C (p.Val541=)
c.1531G>C (n.1531G>C)
n.2057G>C
c.1881G>C (p.Val627=)
4g.6301667G>TCA438368542WFS1c.1908G>T (p.Val636=)
c.1849G>T
c.1872G>T (p.Val624=)
c.1623G>T (p.Val541=)
c.1531G>T (n.1531G>T)
n.2057G>T
c.1881G>T (p.Val627=)
 gnomAD v4
4g.6301668A>CCA356177013WFS1c.1909A>C (p.Lys637Gln)
c.1850A>C
c.1873A>C (p.Lys625Gln)
c.1624A>C (p.Lys542Gln)
c.1532A>C (n.1532A>C)
n.2058A>C
c.1882A>C (p.Lys628Gln)
 gnomAD v4
4g.6301668A>GCA356177014WFS1c.1909A>G (p.Lys637Glu)
c.1850A>G
c.1873A>G (p.Lys625Glu)
c.1624A>G (p.Lys542Glu)
c.1532A>G (n.1532A>G)
n.2058A>G
c.1882A>G (p.Lys628Glu)
4g.6301668A>TCA356177015WFS1c.1909A>T (p.Lys637Ter)
c.1850A>T
c.1873A>T (p.Lys625Ter)
c.1624A>T (p.Lys542Ter)
c.1532A>T (n.1532A>T)
n.2058A>T
c.1882A>T (p.Lys628Ter)
4g.6301669A>CCA356177018WFS1c.1910A>C (p.Lys637Thr)
c.1851A>C
c.1874A>C (p.Lys625Thr)
c.1625A>C (p.Lys542Thr)
c.1533A>C (n.1533A>C)
n.2059A>C
c.1883A>C (p.Lys628Thr)
4g.6301669A>GCA356177017WFS1c.1910A>G (p.Lys637Arg)
c.1851A>G
c.1874A>G (p.Lys625Arg)
c.1625A>G (p.Lys542Arg)
c.1533A>G (n.1533A>G)
n.2059A>G
c.1883A>G (p.Lys628Arg)
4g.6301669A>TCA356177016WFS1c.1910A>T (p.Lys637Met)
c.1851A>T
c.1874A>T (p.Lys625Met)
c.1625A>T (p.Lys542Met)
c.1533A>T (n.1533A>T)
n.2059A>T
c.1883A>T (p.Lys628Met)
4g.6301670G>ACA438368544WFS1c.1911G>A (p.Lys637=)
c.1852G>A
c.1875G>A (p.Lys625=)
c.1626G>A (p.Lys542=)
c.1534G>A (n.1534G>A)
n.2060G>A
c.1884G>A (p.Lys628=)
 ClinVar
4g.6301670G>CCA356177019WFS1c.1911G>C (p.Lys637Asn)
c.1852G>C
c.1875G>C (p.Lys625Asn)
c.1626G>C (p.Lys542Asn)
c.1534G>C (n.1534G>C)
n.2060G>C
c.1884G>C (p.Lys628Asn)
4g.6301670G>TCA356177020WFS1c.1911G>T (p.Lys637Asn)
c.1852G>T
c.1875G>T (p.Lys625Asn)
c.1626G>T (p.Lys542Asn)
c.1534G>T (n.1534G>T)
n.2060G>T
c.1884G>T (p.Lys628Asn)
4g.6301671T>ACA356177021WFS1c.1912T>A (p.Ser638Thr)
c.1853T>A
c.1876T>A (p.Ser626Thr)
c.1627T>A (p.Ser543Thr)
c.1535T>A (n.1535T>A)
n.2061T>A
c.1885T>A (p.Ser629Thr)
4g.6301671T>CCA356177023WFS1c.1912T>C (p.Ser638Pro)
c.1853T>C
c.1876T>C (p.Ser626Pro)
c.1627T>C (p.Ser543Pro)
c.1535T>C (n.1535T>C)
n.2061T>C
c.1885T>C (p.Ser629Pro)
4g.6301671T>GCA356177022WFS1c.1912T>G (p.Ser638Ala)
c.1853T>G
c.1876T>G (p.Ser626Ala)
c.1627T>G (p.Ser543Ala)
c.1535T>G (n.1535T>G)
n.2061T>G
c.1885T>G (p.Ser629Ala)
 dbSNP
4g.6301671T=CA1435771623WFS1c.1912T= (p.Ser638=)
c.1853T=
c.1876T= (p.Ser626=)
c.1627T= (p.Ser543=)
c.1535T= (n.1535T=)
n.2061T=
c.1885T= (p.Ser629=)
4g.6301672C>ACA356177024WFS1c.1913C>A (p.Ser638Tyr)
c.1854C>A
c.1877C>A (p.Ser626Tyr)
c.1628C>A (p.Ser543Tyr)
c.1536C>A (n.1536C>A)
n.2062C>A
c.1886C>A (p.Ser629Tyr)
4g.6301672C=CA1435771627WFS1c.1913C= (p.Ser638=)
c.1854C=
c.1877C= (p.Ser626=)
c.1628C= (p.Ser543=)
c.1536C= (n.1536C=)
n.2062C=
c.1886C= (p.Ser629=)
4g.6301672C>GCA356177025WFS1c.1913C>G (p.Ser638Cys)
c.1854C>G
c.1877C>G (p.Ser626Cys)
c.1628C>G (p.Ser543Cys)
c.1536C>G (n.1536C>G)
n.2062C>G
c.1886C>G (p.Ser629Cys)
4g.6301672C>TCA2839530WFS1c.1913C>T (p.Ser638Phe)
c.1854C>T
c.1877C>T (p.Ser626Phe)
c.1628C>T (p.Ser543Phe)
c.1536C>T (n.1536C>T)
n.2062C>T
c.1886C>T (p.Ser629Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301673C>ACA438368545WFS1c.1914C>A (p.Ser638=)
c.1855C>A
c.1878C>A (p.Ser626=)
c.1629C>A (p.Ser543=)
c.1537C>A (n.1537C>A)
n.2063C>A
c.1887C>A (p.Ser629=)
 gnomAD v4
4g.6301673C>GCA438368548WFS1c.1914C>G (p.Ser638=)
c.1855C>G
c.1878C>G (p.Ser626=)
c.1629C>G (p.Ser543=)
c.1537C>G (n.1537C>G)
n.2063C>G
c.1887C>G (p.Ser629=)
4g.6301673C>TCA438368546WFS1c.1914C>T (p.Ser638=)
c.1855C>T
c.1878C>T (p.Ser626=)
c.1629C>T (p.Ser543=)
c.1537C>T (n.1537C>T)
n.2063C>T
c.1887C>T (p.Ser629=)
 ClinVar dbSNP gnomAD v4
4g.6301674C>ACA356177026WFS1c.1915C>A (p.Leu639Met)
c.1856C>A
c.1879C>A (p.Leu627Met)
c.1630C>A (p.Leu544Met)
c.1538C>A (n.1538C>A)
n.2064C>A
c.1888C>A (p.Leu630Met)
4g.6301674C=CA1435771633WFS1c.1915C= (p.Leu639=)
c.1856C=
c.1879C= (p.Leu627=)
c.1630C= (p.Leu544=)
c.1538C= (n.1538C=)
n.2064C=
c.1888C= (p.Leu630=)
4g.6301674C>GCA2839531WFS1c.1915C>G (p.Leu639Val)
c.1856C>G
c.1879C>G (p.Leu627Val)
c.1630C>G (p.Leu544Val)
c.1538C>G (n.1538C>G)
n.2064C>G
c.1888C>G (p.Leu630Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301674C>TCA438368549WFS1c.1915C>T (p.Leu639=)
c.1856C>T
c.1879C>T (p.Leu627=)
c.1630C>T (p.Leu544=)
c.1538C>T (n.1538C>T)
n.2064C>T
c.1888C>T (p.Leu630=)
 ClinVar dbSNP
4g.6301675T>ACA356177027WFS1c.1916T>A (p.Leu639Gln)
c.1857T>A
c.1880T>A (p.Leu627Gln)
c.1631T>A (p.Leu544Gln)
c.1539T>A (n.1539T>A)
n.2065T>A
c.1889T>A (p.Leu630Gln)
4g.6301675T>CCA356177028WFS1c.1916T>C (p.Leu639Pro)
c.1857T>C
c.1880T>C (p.Leu627Pro)
c.1631T>C (p.Leu544Pro)
c.1539T>C (n.1539T>C)
n.2065T>C
c.1889T>C (p.Leu630Pro)
4g.6301675T>GCA356177029WFS1c.1916T>G (p.Leu639Arg)
c.1857T>G
c.1880T>G (p.Leu627Arg)
c.1631T>G (p.Leu544Arg)
c.1539T>G (n.1539T>G)
n.2065T>G
c.1889T>G (p.Leu630Arg)
4g.6301676G>ACA438368553WFS1c.1917G>A (p.Leu639=)
c.1858G>A
c.1881G>A (p.Leu627=)
c.1632G>A (p.Leu544=)
c.1540G>A (n.1540G>A)
n.2066G>A
c.1890G>A (p.Leu630=)
4g.6301676G>CCA438368557WFS1c.1917G>C (p.Leu639=)
c.1858G>C
c.1881G>C (p.Leu627=)
c.1632G>C (p.Leu544=)
c.1540G>C (n.1540G>C)
n.2066G>C
c.1890G>C (p.Leu630=)
4g.6301676G>TCA438368560WFS1c.1917G>T (p.Leu639=)
c.1858G>T
c.1881G>T (p.Leu627=)
c.1632G>T (p.Leu544=)
c.1540G>T (n.1540G>T)
n.2066G>T
c.1890G>T (p.Leu630=)
4g.6301677A>CCA356177030WFS1c.1918A>C (p.Thr640Pro)
c.1859A>C
c.1882A>C (p.Thr628Pro)
c.1633A>C (p.Thr545Pro)
c.1541A>C (n.1541A>C)
n.2067A>C
c.1891A>C (p.Thr631Pro)
 gnomAD v4
4g.6301677A>GCA356177031WFS1c.1918A>G (p.Thr640Ala)
c.1859A>G
c.1882A>G (p.Thr628Ala)
c.1633A>G (p.Thr545Ala)
c.1541A>G (n.1541A>G)
n.2067A>G
c.1891A>G (p.Thr631Ala)
4g.6301677A>TCA356177032WFS1c.1918A>T (p.Thr640Ser)
c.1859A>T
c.1882A>T (p.Thr628Ser)
c.1633A>T (p.Thr545Ser)
c.1541A>T (n.1541A>T)
n.2067A>T
c.1891A>T (p.Thr631Ser)
4g.6301678C>ACA356177033WFS1c.1919C>A (p.Thr640Lys)
c.1860C>A
c.1883C>A (p.Thr628Lys)
c.1634C>A (p.Thr545Lys)
c.1542C>A (n.1542C>A)
n.2068C>A
c.1892C>A (p.Thr631Lys)
 gnomAD v4
4g.6301678C=CA1435771636WFS1c.1919C= (p.Thr640=)
c.1860C=
c.1883C= (p.Thr628=)
c.1634C= (p.Thr545=)
c.1542C= (n.1542C=)
n.2068C=
c.1892C= (p.Thr631=)
4g.6301678C>GCA2839532WFS1c.1919C>G (p.Thr640Arg)
c.1860C>G
c.1883C>G (p.Thr628Arg)
c.1634C>G (p.Thr545Arg)
c.1542C>G (n.1542C>G)
n.2068C>G
c.1892C>G (p.Thr631Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301678C>TCA2839533WFS1c.1919C>T (p.Thr640Met)
c.1860C>T
c.1883C>T (p.Thr628Met)
c.1634C>T (p.Thr545Met)
c.1542C>T (n.1542C>T)
n.2068C>T
c.1892C>T (p.Thr631Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301679G>ACA2839534WFS1c.1920G>A (p.Thr640=)
c.1861G>A
c.1884G>A (p.Thr628=)
c.1635G>A (p.Thr545=)
c.1543G>A (n.1543G>A)
n.2069G>A
c.1893G>A (p.Thr631=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6301679G>CCA438368563WFS1c.1920G>C (p.Thr640=)
c.1861G>C
c.1884G>C (p.Thr628=)
c.1635G>C (p.Thr545=)
c.1543G>C (n.1543G>C)
n.2069G>C
c.1893G>C (p.Thr631=)
4g.6301679G=CA1435771639WFS1c.1920G= (p.Thr640=)
c.1861G=
c.1884G= (p.Thr628=)
c.1635G= (p.Thr545=)
c.1543G= (n.1543G=)
n.2069G=
c.1893G= (p.Thr631=)
4g.6301679G>TCA91796666WFS1c.1920G>T (p.Thr640=)
c.1861G>T
c.1884G>T (p.Thr628=)
c.1635G>T (p.Thr545=)
c.1543G>T (n.1543G>T)
n.2069G>T
c.1893G>T (p.Thr631=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301680C>ACA438368565WFS1c.1921C>A (p.Arg641=)
c.1862C>A
c.1885C>A (p.Arg629=)
c.1636C>A (p.Arg546=)
c.1544C>A (n.1544C>A)
n.2070C>A
c.1894C>A (p.Arg632=)
4g.6301680C=CA1435771642WFS1c.1921C= (p.Arg641=)
c.1862C=
c.1885C= (p.Arg629=)
c.1636C= (p.Arg546=)
c.1544C= (n.1544C=)
n.2070C=
c.1894C= (p.Arg632=)
4g.6301680C>GCA356177034WFS1c.1921C>G (p.Arg641Gly)
c.1862C>G
c.1885C>G (p.Arg629Gly)
c.1636C>G (p.Arg546Gly)
c.1544C>G (n.1544C>G)
n.2070C>G
c.1894C>G (p.Arg632Gly)
4g.6301680C>TCA2839535WFS1c.1921C>T (p.Arg641Trp)
c.1862C>T
c.1885C>T (p.Arg629Trp)
c.1636C>T (p.Arg546Trp)
c.1544C>T (n.1544C>T)
n.2070C>T
c.1894C>T (p.Arg632Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301680_6301681insTCA2669843456WFS1c.1921_1922insT (p.Arg641LeufsTer?)
c.1862_1863insT
c.1885_1886insT (p.Arg629LeufsTer?)
c.1636_1637insT (p.Arg546LeufsTer?)
c.1544_1545insT (n.1544_1545insT)
n.2070_2071insT
c.1894_1895insT (p.Arg632LeufsTer?)
 gnomAD v4
4g.6301681G>ACA261748WFS1c.1922G>A (p.Arg641Gln)
c.1863G>A
c.1886G>A (p.Arg629Gln)
c.1637G>A (p.Arg546Gln)
c.1545G>A (n.1545G>A)
n.2071G>A
c.1895G>A (p.Arg632Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301681G>CCA356177035WFS1c.1922G>C (p.Arg641Pro)
c.1863G>C
c.1886G>C (p.Arg629Pro)
c.1637G>C (p.Arg546Pro)
c.1545G>C (n.1545G>C)
n.2071G>C
c.1895G>C (p.Arg632Pro)
4g.6301681G=CA1435771649WFS1c.1922G= (p.Arg641=)
c.1863G=
c.1886G= (p.Arg629=)
c.1637G= (p.Arg546=)
c.1545G= (n.1545G=)
n.2071G=
c.1895G= (p.Arg632=)
4g.6301681G>TCA356177036WFS1c.1922G>T (p.Arg641Leu)
c.1863G>T
c.1886G>T (p.Arg629Leu)
c.1637G>T (p.Arg546Leu)
c.1545G>T (n.1545G>T)
n.2071G>T
c.1895G>T (p.Arg632Leu)
4g.6301682G>ACA438368571WFS1c.1923G>A (p.Arg641=)
c.1864G>A
c.1887G>A (p.Arg629=)
c.1638G>A (p.Arg546=)
c.1546G>A (n.1546G>A)
n.2072G>A
c.1896G>A (p.Arg632=)
 gnomAD v4
4g.6301682G>CCA438368570WFS1c.1923G>C (p.Arg641=)
c.1864G>C
c.1887G>C (p.Arg629=)
c.1638G>C (p.Arg546=)
c.1546G>C (n.1546G>C)
n.2072G>C
c.1896G>C (p.Arg632=)
 gnomAD v4
4g.6301682G>TCA438368567WFS1c.1923G>T (p.Arg641=)
c.1864G>T
c.1887G>T (p.Arg629=)
c.1638G>T (p.Arg546=)
c.1546G>T (n.1546G>T)
n.2072G>T
c.1896G>T (p.Arg632=)
 gnomAD v4
4g.6301683A>CCA356177037WFS1c.1924A>C (p.Ser642Arg)
c.1865A>C
c.1888A>C (p.Ser630Arg)
c.1639A>C (p.Ser547Arg)
c.1547A>C (n.1547A>C)
n.2073A>C
c.1897A>C (p.Ser633Arg)
4g.6301683A>GCA356177038WFS1c.1924A>G (p.Ser642Gly)
c.1865A>G
c.1888A>G (p.Ser630Gly)
c.1639A>G (p.Ser547Gly)
c.1547A>G (n.1547A>G)
n.2073A>G
c.1897A>G (p.Ser633Gly)
4g.6301683A>TCA356177039WFS1c.1924A>T (p.Ser642Cys)
c.1865A>T
c.1888A>T (p.Ser630Cys)
c.1639A>T (p.Ser547Cys)
c.1547A>T (n.1547A>T)
n.2073A>T
c.1897A>T (p.Ser633Cys)
 gnomAD v4
4g.6301683_6301685delCA2669843457WFS1c.1924_1926del (p.Ser642del)
c.1865_1867del
c.1888_1890del (p.Ser630del)
c.1639_1641del (p.Ser547del)
c.1547_1549del (n.1547_1549del)
n.2073_2075del
c.1897_1899del (p.Ser633del)
 gnomAD v4
4g.6301684G>ACA356177040WFS1c.1925G>A (p.Ser642Asn)
c.1866G>A
c.1889G>A (p.Ser630Asn)
c.1640G>A (p.Ser547Asn)
c.1548G>A (n.1548G>A)
n.2074G>A
c.1898G>A (p.Ser633Asn)
4g.6301684G>CCA356177041WFS1c.1925G>C (p.Ser642Thr)
c.1866G>C
c.1889G>C (p.Ser630Thr)
c.1640G>C (p.Ser547Thr)
c.1548G>C (n.1548G>C)
n.2074G>C
c.1898G>C (p.Ser633Thr)
4g.6301684G>TCA356177042WFS1c.1925G>T (p.Ser642Ile)
c.1866G>T
c.1889G>T (p.Ser630Ile)
c.1640G>T (p.Ser547Ile)
c.1548G>T (n.1548G>T)
n.2074G>T
c.1898G>T (p.Ser633Ile)
4g.6301685C>ACA356177043WFS1c.1926C>A (p.Ser642Arg)
c.1867C>A
c.1890C>A (p.Ser630Arg)
c.1641C>A (p.Ser547Arg)
c.1549C>A (n.1549C>A)
n.2075C>A
c.1899C>A (p.Ser633Arg)
4g.6301685C>GCA356177044WFS1c.1926C>G (p.Ser642Arg)
c.1867C>G
c.1890C>G (p.Ser630Arg)
c.1641C>G (p.Ser547Arg)
c.1549C>G (n.1549C>G)
n.2075C>G
c.1899C>G (p.Ser633Arg)
4g.6301685C>TCA438368579WFS1c.1926C>T (p.Ser642=)
c.1867C>T
c.1890C>T (p.Ser630=)
c.1641C>T (p.Ser547=)
c.1549C>T (n.1549C>T)
n.2075C>T
c.1899C>T (p.Ser633=)
 gnomAD v4
4g.6301686T>ACA356177047WFS1c.1927T>A (p.Ser643Thr)
c.1868T>A
c.1891T>A (p.Ser631Thr)
c.1642T>A (p.Ser548Thr)
c.1550T>A (n.1550T>A)
n.2076T>A
c.1900T>A (p.Ser634Thr)
4g.6301686T>CCA356177045WFS1c.1927T>C (p.Ser643Pro)
c.1868T>C
c.1891T>C (p.Ser631Pro)
c.1642T>C (p.Ser548Pro)
c.1550T>C (n.1550T>C)
n.2076T>C
c.1900T>C (p.Ser634Pro)
4g.6301686T>GCA356177046WFS1c.1927T>G (p.Ser643Ala)
c.1868T>G
c.1891T>G (p.Ser631Ala)
c.1642T>G (p.Ser548Ala)
c.1550T>G (n.1550T>G)
n.2076T>G
c.1900T>G (p.Ser634Ala)
4g.6301687C>ACA356177048WFS1c.1928C>A (p.Ser643Tyr)
c.1869C>A
c.1892C>A (p.Ser631Tyr)
c.1643C>A (p.Ser548Tyr)
c.1551C>A (n.1551C>A)
n.2077C>A
c.1901C>A (p.Ser634Tyr)
4g.6301687C>GCA356177049WFS1c.1928C>G (p.Ser643Cys)
c.1869C>G
c.1892C>G (p.Ser631Cys)
c.1643C>G (p.Ser548Cys)
c.1551C>G (n.1551C>G)
n.2077C>G
c.1901C>G (p.Ser634Cys)
 ClinVar gnomAD v4
4g.6301687C>TCA356177050WFS1c.1928C>T (p.Ser643Phe)
c.1869C>T
c.1892C>T (p.Ser631Phe)
c.1643C>T (p.Ser548Phe)
c.1551C>T (n.1551C>T)
n.2077C>T
c.1901C>T (p.Ser634Phe)
4g.6301688C>ACA438368634WFS1c.1929C>A (p.Ser643=)
c.1870C>A
c.1893C>A (p.Ser631=)
c.1644C>A (p.Ser548=)
c.1552C>A (n.1552C>A)
n.2078C>A
c.1902C>A (p.Ser634=)
 ClinVar dbSNP
4g.6301688C=CA1435771651WFS1c.1929C= (p.Ser643=)
c.1870C=
c.1893C= (p.Ser631=)
c.1644C= (p.Ser548=)
c.1552C= (n.1552C=)
n.2078C=
c.1902C= (p.Ser634=)
4g.6301688C>GCA438368635WFS1c.1929C>G (p.Ser643=)
c.1870C>G
c.1893C>G (p.Ser631=)
c.1644C>G (p.Ser548=)
c.1552C>G (n.1552C>G)
n.2078C>G
c.1902C>G (p.Ser634=)
4g.6301688C>TCA2839536WFS1c.1929C>T (p.Ser643=)
c.1870C>T
c.1893C>T (p.Ser631=)
c.1644C>T (p.Ser548=)
c.1552C>T (n.1552C>T)
n.2078C>T
c.1902C>T (p.Ser634=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301689A=CA1435771656WFS1c.1930A= (p.Met644=)
c.1871A=
c.1894A= (p.Met632=)
c.1645A= (p.Met549=)
c.1553A= (n.1553A=)
n.2079A=
c.1903A= (p.Met635=)
4g.6301689A>CCA356177051WFS1c.1930A>C (p.Met644Leu)
c.1871A>C
c.1894A>C (p.Met632Leu)
c.1645A>C (p.Met549Leu)
c.1553A>C (n.1553A>C)
n.2079A>C
c.1903A>C (p.Met635Leu)
4g.6301689A>GCA356177052WFS1c.1930A>G (p.Met644Val)
c.1871A>G
c.1894A>G (p.Met632Val)
c.1645A>G (p.Met549Val)
c.1553A>G (n.1553A>G)
n.2079A>G
c.1903A>G (p.Met635Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301689A>TCA356177053WFS1c.1930A>T (p.Met644Leu)
c.1871A>T
c.1894A>T (p.Met632Leu)
c.1645A>T (p.Met549Leu)
c.1553A>T (n.1553A>T)
n.2079A>T
c.1903A>T (p.Met635Leu)
4g.6301690T>ACA356177054WFS1c.1931T>A (p.Met644Lys)
c.1872T>A
c.1895T>A (p.Met632Lys)
c.1646T>A (p.Met549Lys)
c.1554T>A (n.1554T>A)
n.2080T>A
c.1904T>A (p.Met635Lys)
4g.6301690T>CCA356177055WFS1c.1931T>C (p.Met644Thr)
c.1872T>C
c.1895T>C (p.Met632Thr)
c.1646T>C (p.Met549Thr)
c.1554T>C (n.1554T>C)
n.2080T>C
c.1904T>C (p.Met635Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6301690T>GCA356177056WFS1c.1931T>G (p.Met644Arg)
c.1872T>G
c.1895T>G (p.Met632Arg)
c.1646T>G (p.Met549Arg)
c.1554T>G (n.1554T>G)
n.2080T>G
c.1904T>G (p.Met635Arg)
4g.6301690T=CA1435771658WFS1c.1931T= (p.Met644=)
c.1872T=
c.1895T= (p.Met632=)
c.1646T= (p.Met549=)
c.1554T= (n.1554T=)
n.2080T=
c.1904T= (p.Met635=)
4g.6301691G>ACA356177057WFS1c.1932G>A (p.Met644Ile)
c.1873G>A
c.1896G>A (p.Met632Ile)
c.1647G>A (p.Met549Ile)
c.1555G>A (n.1555G>A)
n.2081G>A
c.1905G>A (p.Met635Ile)
 ClinVar dbSNP
4g.6301691G>CCA356177058WFS1c.1932G>C (p.Met644Ile)
c.1873G>C
c.1896G>C (p.Met632Ile)
c.1647G>C (p.Met549Ile)
c.1555G>C (n.1555G>C)
n.2081G>C
c.1905G>C (p.Met635Ile)
 dbSNP
4g.6301691G=CA1435771663WFS1c.1932G= (p.Met644=)
c.1873G=
c.1896G= (p.Met632=)
c.1647G= (p.Met549=)
c.1555G= (n.1555G=)
n.2081G=
c.1905G= (p.Met635=)
4g.6301691G>TCA16609253WFS1c.1932G>T (p.Met644Ile)
c.1873G>T
c.1896G>T (p.Met632Ile)
c.1647G>T (p.Met549Ile)
c.1555G>T (n.1555G>T)
n.2081G>T
c.1905G>T (p.Met635Ile)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301692G>ACA356177061WFS1c.1933G>A (p.Val645Ile)
c.1874G>A
c.1897G>A (p.Val633Ile)
c.1648G>A (p.Val550Ile)
c.1556G>A (n.1556G>A)
n.2082G>A
c.1906G>A (p.Val636Ile)
4g.6301692G>CCA356177059WFS1c.1933G>C (p.Val645Leu)
c.1874G>C
c.1897G>C (p.Val633Leu)
c.1648G>C (p.Val550Leu)
c.1556G>C (n.1556G>C)
n.2082G>C
c.1906G>C (p.Val636Leu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6301692G=CA1435771668WFS1c.1933G= (p.Val645=)
c.1874G=
c.1897G= (p.Val633=)
c.1648G= (p.Val550=)
c.1556G= (n.1556G=)
n.2082G=
c.1906G= (p.Val636=)
4g.6301692G>TCA356177060WFS1c.1933G>T (p.Val645Phe)
c.1874G>T
c.1897G>T (p.Val633Phe)
c.1648G>T (p.Val550Phe)
c.1556G>T (n.1556G>T)
n.2082G>T
c.1906G>T (p.Val636Phe)
4g.6301693T>ACA356177062WFS1c.1934T>A (p.Val645Asp)
c.1875T>A
c.1898T>A (p.Val633Asp)
c.1649T>A (p.Val550Asp)
c.1557T>A (n.1557T>A)
n.2083T>A
c.1907T>A (p.Val636Asp)
4g.6301693T>CCA356177063WFS1c.1934T>C (p.Val645Ala)
c.1875T>C
c.1898T>C (p.Val633Ala)
c.1649T>C (p.Val550Ala)
c.1557T>C (n.1557T>C)
n.2083T>C
c.1907T>C (p.Val636Ala)
4g.6301693T>GCA356177064WFS1c.1934T>G (p.Val645Gly)
c.1875T>G
c.1898T>G (p.Val633Gly)
c.1649T>G (p.Val550Gly)
c.1557T>G (n.1557T>G)
n.2083T>G
c.1907T>G (p.Val636Gly)
4g.6301694C>ACA438368640WFS1c.1935C>A (p.Val645=)
c.1876C>A
c.1899C>A (p.Val633=)
c.1650C>A (p.Val550=)
c.1558C>A (n.1558C>A)
n.2084C>A
c.1908C>A (p.Val636=)
4g.6301694C=CA1435771670WFS1c.1935C= (p.Val645=)
c.1876C=
c.1899C= (p.Val633=)
c.1650C= (p.Val550=)
c.1558C= (n.1558C=)
n.2084C=
c.1908C= (p.Val636=)
4g.6301694C>GCA438368641WFS1c.1935C>G (p.Val645=)
c.1876C>G
c.1899C>G (p.Val633=)
c.1650C>G (p.Val550=)
c.1558C>G (n.1558C>G)
n.2084C>G
c.1908C>G (p.Val636=)
4g.6301694C>TCA2839537WFS1c.1935C>T (p.Val645=)
c.1876C>T
c.1899C>T (p.Val633=)
c.1650C>T (p.Val550=)
c.1558C>T (n.1558C>T)
n.2084C>T
c.1908C>T (p.Val636=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301695A=CA1435771674WFS1c.1936A= (p.Lys646=)
c.1877A=
c.1900A= (p.Lys634=)
c.1651A= (p.Lys551=)
c.1559A= (n.1559A=)
n.2085A=
c.1909A= (p.Lys637=)
4g.6301695A>CCA2839538WFS1c.1936A>C (p.Lys646Gln)
c.1877A>C
c.1900A>C (p.Lys634Gln)
c.1651A>C (p.Lys551Gln)
c.1559A>C (n.1559A>C)
n.2085A>C
c.1909A>C (p.Lys637Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301695A>GCA356177065WFS1c.1936A>G (p.Lys646Glu)
c.1877A>G
c.1900A>G (p.Lys634Glu)
c.1651A>G (p.Lys551Glu)
c.1559A>G (n.1559A>G)
n.2085A>G
c.1909A>G (p.Lys637Glu)
4g.6301695A>TCA356177066WFS1c.1936A>T (p.Lys646Ter)
c.1877A>T
c.1900A>T (p.Lys634Ter)
c.1651A>T (p.Lys551Ter)
c.1559A>T (n.1559A>T)
n.2085A>T
c.1909A>T (p.Lys637Ter)
4g.6301696A=CA1435771680WFS1c.1937A= (p.Lys646=)
c.1878A=
c.1901A= (p.Lys634=)
c.1652A= (p.Lys551=)
c.1560A= (n.1560A=)
n.2086A=
c.1910A= (p.Lys637=)
4g.6301696A>CCA253205WFS1c.1937A>C (p.Lys646Thr)
c.1878A>C
c.1901A>C (p.Lys634Thr)
c.1652A>C (p.Lys551Thr)
c.1560A>C (n.1560A>C)
n.2086A>C
c.1910A>C (p.Lys637Thr)
 ClinVar dbSNP gnomAD v4
4g.6301696A>GCA2839539WFS1c.1937A>G (p.Lys646Arg)
c.1878A>G
c.1901A>G (p.Lys634Arg)
c.1652A>G (p.Lys551Arg)
c.1560A>G (n.1560A>G)
n.2086A>G
c.1910A>G (p.Lys637Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301696A>TCA356177067WFS1c.1937A>T (p.Lys646Met)
c.1878A>T
c.1901A>T (p.Lys634Met)
c.1652A>T (p.Lys551Met)
c.1560A>T (n.1560A>T)
n.2086A>T
c.1910A>T (p.Lys637Met)
4g.6301697G>ACA438368642WFS1c.1938G>A (p.Lys646=)
c.1879G>A
c.1902G>A (p.Lys634=)
c.1653G>A (p.Lys551=)
c.1561G>A (n.1561G>A)
n.2087G>A
c.1911G>A (p.Lys637=)
 dbSNP gnomAD v4
4g.6301697G>CCA356177068WFS1c.1938G>C (p.Lys646Asn)
c.1879G>C
c.1902G>C (p.Lys634Asn)
c.1653G>C (p.Lys551Asn)
c.1561G>C (n.1561G>C)
n.2087G>C
c.1911G>C (p.Lys637Asn)
4g.6301697G=CA1435771684WFS1c.1938G= (p.Lys646=)
c.1879G=
c.1902G= (p.Lys634=)
c.1653G= (p.Lys551=)
c.1561G= (n.1561G=)
n.2087G=
c.1911G= (p.Lys637=)
4g.6301697G>TCA2839540WFS1c.1938G>T (p.Lys646Asn)
c.1879G>T
c.1902G>T (p.Lys634Asn)
c.1653G>T (p.Lys551Asn)
c.1561G>T (n.1561G>T)
n.2087G>T
c.1911G>T (p.Lys637Asn)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301698C>ACA356177069WFS1c.1939C>A (p.Leu647Ile)
c.1880C>A
c.1903C>A (p.Leu635Ile)
c.1654C>A (p.Leu552Ile)
c.1562C>A (n.1562C>A)
n.2088C>A
c.1912C>A (p.Leu638Ile)
4g.6301698C=CA1435771689WFS1c.1939C= (p.Leu647=)
c.1880C=
c.1903C= (p.Leu635=)
c.1654C= (p.Leu552=)
c.1562C= (n.1562C=)
n.2088C=
c.1912C= (p.Leu638=)
4g.6301698C>GCA2839541WFS1c.1939C>G (p.Leu647Val)
c.1880C>G
c.1903C>G (p.Leu635Val)
c.1654C>G (p.Leu552Val)
c.1562C>G (n.1562C>G)
n.2088C>G
c.1912C>G (p.Leu638Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301698C>TCA356177070WFS1c.1939C>T (p.Leu647Phe)
c.1880C>T
c.1903C>T (p.Leu635Phe)
c.1654C>T (p.Leu552Phe)
c.1562C>T (n.1562C>T)
n.2088C>T
c.1912C>T (p.Leu638Phe)
 dbSNP gnomAD v2 gnomAD v4
4g.6301699T>ACA356177071WFS1c.1940T>A (p.Leu647His)
c.1881T>A
c.1904T>A (p.Leu635His)
c.1655T>A (p.Leu552His)
c.1563T>A (n.1563T>A)
n.2089T>A
c.1913T>A (p.Leu638His)
 gnomAD v4
4g.6301699T>CCA356177073WFS1c.1940T>C (p.Leu647Pro)
c.1881T>C
c.1904T>C (p.Leu635Pro)
c.1655T>C (p.Leu552Pro)
c.1563T>C (n.1563T>C)
n.2089T>C
c.1913T>C (p.Leu638Pro)
4g.6301699T>GCA356177072WFS1c.1940T>G (p.Leu647Arg)
c.1881T>G
c.1904T>G (p.Leu635Arg)
c.1655T>G (p.Leu552Arg)
c.1563T>G (n.1563T>G)
n.2089T>G
c.1913T>G (p.Leu638Arg)
4g.6301699_6301702dupCA549707913WFS1c.1940_1943dup (p.Leu649HisfsTer?)
c.1881_1884dup
c.1904_1907dup (p.Leu637HisfsTer?)
c.1655_1658dup (p.Leu554HisfsTer?)
c.1563_1566dup (n.1563_1566dup)
n.2089_2092dup
c.1913_1916dup (p.Leu640HisfsTer?)
 dbSNP gnomAD v2 gnomAD v4
4g.6301700C>ACA438368646WFS1c.1941C>A (p.Leu647=)
c.1882C>A
c.1905C>A (p.Leu635=)
c.1656C>A (p.Leu552=)
c.1564C>A (n.1564C>A)
n.2090C>A
c.1914C>A (p.Leu638=)
4g.6301700C>GCA438368647WFS1c.1941C>G (p.Leu647=)
c.1882C>G
c.1905C>G (p.Leu635=)
c.1656C>G (p.Leu552=)
c.1564C>G (n.1564C>G)
n.2090C>G
c.1914C>G (p.Leu638=)
4g.6301700C>TCA438368648WFS1c.1941C>T (p.Leu647=)
c.1882C>T
c.1905C>T (p.Leu635=)
c.1656C>T (p.Leu552=)
c.1564C>T (n.1564C>T)
n.2090C>T
c.1914C>T (p.Leu638=)
 gnomAD v4
4g.6301701A>CCA356177074WFS1c.1942A>C (p.Ile648Leu)
c.1883A>C
c.1906A>C (p.Ile636Leu)
c.1657A>C (p.Ile553Leu)
c.1565A>C (n.1565A>C)
n.2091A>C
c.1915A>C (p.Ile639Leu)
4g.6301701A>GCA356177075WFS1c.1942A>G (p.Ile648Val)
c.1883A>G
c.1906A>G (p.Ile636Val)
c.1657A>G (p.Ile553Val)
c.1565A>G (n.1565A>G)
n.2091A>G
c.1915A>G (p.Ile639Val)
4g.6301701A>TCA356177076WFS1c.1942A>T (p.Ile648Phe)
c.1883A>T
c.1906A>T (p.Ile636Phe)
c.1657A>T (p.Ile553Phe)
c.1565A>T (n.1565A>T)
n.2091A>T
c.1915A>T (p.Ile639Phe)
4g.6301702T>ACA356177077WFS1c.1943T>A (p.Ile648Asn)
c.1884T>A
c.1907T>A (p.Ile636Asn)
c.1658T>A (p.Ile553Asn)
c.1566T>A (n.1566T>A)
n.2092T>A
c.1916T>A (p.Ile639Asn)
4g.6301702T>CCA356177078WFS1c.1943T>C (p.Ile648Thr)
c.1884T>C
c.1907T>C (p.Ile636Thr)
c.1658T>C (p.Ile553Thr)
c.1566T>C (n.1566T>C)
n.2092T>C
c.1916T>C (p.Ile639Thr)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301702T>GCA356177079WFS1c.1943T>G (p.Ile648Ser)
c.1884T>G
c.1907T>G (p.Ile636Ser)
c.1658T>G (p.Ile553Ser)
c.1566T>G (n.1566T>G)
n.2092T>G
c.1916T>G (p.Ile639Ser)
 gnomAD v4
4g.6301702T=CA1435771691WFS1c.1943T= (p.Ile648=)
c.1884T=
c.1907T= (p.Ile636=)
c.1658T= (p.Ile553=)
c.1566T= (n.1566T=)
n.2092T=
c.1916T= (p.Ile639=)
4g.6301703C>ACA438368649WFS1c.1944C>A (p.Ile648=)
c.1885C>A
c.1908C>A (p.Ile636=)
c.1659C>A (p.Ile553=)
c.1567C>A (n.1567C>A)
n.2093C>A
c.1917C>A (p.Ile639=)
4g.6301703C=CA1435771695WFS1c.1944C= (p.Ile648=)
c.1885C=
c.1908C= (p.Ile636=)
c.1659C= (p.Ile553=)
c.1567C= (n.1567C=)
n.2093C=
c.1917C= (p.Ile639=)
4g.6301703C>GCA2839542WFS1c.1944C>G (p.Ile648Met)
c.1885C>G
c.1908C>G (p.Ile636Met)
c.1659C>G (p.Ile553Met)
c.1567C>G (n.1567C>G)
n.2093C>G
c.1917C>G (p.Ile639Met)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301703C>TCA2839543WFS1c.1944C>T (p.Ile648=)
c.1885C>T
c.1908C>T (p.Ile636=)
c.1659C>T (p.Ile553=)
c.1567C>T (n.1567C>T)
n.2093C>T
c.1917C>T (p.Ile639=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301703_6301727delinsCCTGGTGTGGCTCACGGCCATCGTGCA1435771693WFS1c.1944_1968delinsCCTGGTGTGGCTCACGGCCATCGTG (p.Ile648=)
c.1885_1909delinsCCTGGTGTGGCTCACGGCCATCGTG
c.1908_1932delinsCCTGGTGTGGCTCACGGCCATCGTG (p.Ile636=)
c.1659_1683delinsCCTGGTGTGGCTCACGGCCATCGTG (p.Ile553=)
c.1567_1591delinsCCTGGTGTGGCTCACGGCCATCGTG (n.1567_1591delinsCCTGGTGTGGCTCACGGCCATCGTG)
n.2093_2117delinsCCTGGTGTGGCTCACGGCCATCGTG
c.1917_1941delinsCCTGGTGTGGCTCACGGCCATCGTG (p.Ile639=)
4g.6301704C>ACA356177080WFS1c.1945C>A (p.Leu649Met)
c.1886C>A
c.1909C>A (p.Leu637Met)
c.1660C>A (p.Leu554Met)
c.1568C>A (n.1568C>A)
n.2094C>A
c.1918C>A (p.Leu640Met)
4g.6301704C=CA1435771697WFS1c.1945C= (p.Leu649=)
c.1886C=
c.1909C= (p.Leu637=)
c.1660C= (p.Leu554=)
c.1568C= (n.1568C=)
n.2094C=
c.1918C= (p.Leu640=)
4g.6301704C>GCA356177081WFS1c.1945C>G (p.Leu649Val)
c.1886C>G
c.1909C>G (p.Leu637Val)
c.1660C>G (p.Leu554Val)
c.1568C>G (n.1568C>G)
n.2094C>G
c.1918C>G (p.Leu640Val)
 gnomAD v4
4g.6301704C>TCA438368650WFS1c.1945C>T (p.Leu649=)
c.1886C>T
c.1909C>T (p.Leu637=)
c.1660C>T (p.Leu554=)
c.1568C>T (n.1568C>T)
n.2094C>T
c.1918C>T (p.Leu640=)
 dbSNP
4g.6301707_6301730delCA1435771696WFS1c.1948_1971del (p.Val650_Leu657del)
c.1889_1912del
c.1912_1935del (p.Val638_Leu645del)
c.1663_1686del (p.Val555_Leu562del)
c.1571_1594del (n.1571_1594del)
n.2097_2120del
c.1921_1944del (p.Val641_Leu648del)
 dbSNP
4g.6301705T>ACA356177082WFS1c.1946T>A (p.Leu649Gln)
c.1887T>A
c.1910T>A (p.Leu637Gln)
c.1661T>A (p.Leu554Gln)
c.1569T>A (n.1569T>A)
n.2095T>A
c.1919T>A (p.Leu640Gln)
4g.6301705T>CCA356177083WFS1c.1946T>C (p.Leu649Pro)
c.1887T>C
c.1910T>C (p.Leu637Pro)
c.1661T>C (p.Leu554Pro)
c.1569T>C (n.1569T>C)
n.2095T>C
c.1919T>C (p.Leu640Pro)
 ClinVar dbSNP
4g.6301705T>GCA356177084WFS1c.1946T>G (p.Leu649Arg)
c.1887T>G
c.1910T>G (p.Leu637Arg)
c.1661T>G (p.Leu554Arg)
c.1569T>G (n.1569T>G)
n.2095T>G
c.1919T>G (p.Leu640Arg)
 gnomAD v4
4g.6301706G>ACA438368651WFS1c.1947G>A (p.Leu649=)
c.1888G>A
c.1911G>A (p.Leu637=)
c.1662G>A (p.Leu554=)
c.1570G>A (n.1570G>A)
n.2096G>A
c.1920G>A (p.Leu640=)
 gnomAD v4
4g.6301706G>CCA438368652WFS1c.1947G>C (p.Leu649=)
c.1888G>C
c.1911G>C (p.Leu637=)
c.1662G>C (p.Leu554=)
c.1570G>C (n.1570G>C)
n.2096G>C
c.1920G>C (p.Leu640=)
4g.6301706G=CA1435771699WFS1c.1947G= (p.Leu649=)
c.1888G=
c.1911G= (p.Leu637=)
c.1662G= (p.Leu554=)
c.1570G= (n.1570G=)
n.2096G=
c.1920G= (p.Leu640=)
4g.6301706G>TCA438368653WFS1c.1947G>T (p.Leu649=)
c.1888G>T
c.1911G>T (p.Leu637=)
c.1662G>T (p.Leu554=)
c.1570G>T (n.1570G>T)
n.2096G>T
c.1920G>T (p.Leu640=)
 dbSNP gnomAD v4
4g.6301707delCA645523670WFS1c.1948del (p.Val650CysfsTer20)
c.1889del
c.1912del (p.Val638CysfsTer20)
c.1663del (p.Val555CysfsTer20)
c.1571del (n.1571del)
n.2097del
c.1921del (p.Val641CysfsTer20)
 COSMIC
4g.6301707G>ACA356177085WFS1c.1948G>A (p.Val650Met)
c.1889G>A
c.1912G>A (p.Val638Met)
c.1663G>A (p.Val555Met)
c.1571G>A (n.1571G>A)
n.2097G>A
c.1921G>A (p.Val641Met)
 gnomAD v4
4g.6301707G>CCA356177087WFS1c.1948G>C (p.Val650Leu)
c.1889G>C
c.1912G>C (p.Val638Leu)
c.1663G>C (p.Val555Leu)
c.1571G>C (n.1571G>C)
n.2097G>C
c.1921G>C (p.Val641Leu)
 gnomAD v4
4g.6301707G>TCA356177086WFS1c.1948G>T (p.Val650Leu)
c.1889G>T
c.1912G>T (p.Val638Leu)
c.1663G>T (p.Val555Leu)
c.1571G>T (n.1571G>T)
n.2097G>T
c.1921G>T (p.Val641Leu)
4g.6301708T>ACA356177088WFS1c.1949T>A (p.Val650Glu)
c.1890T>A
c.1913T>A (p.Val638Glu)
c.1664T>A (p.Val555Glu)
c.1572T>A (n.1572T>A)
n.2098T>A
c.1922T>A (p.Val641Glu)
4g.6301708T>CCA356177089WFS1c.1949T>C (p.Val650Ala)
c.1890T>C
c.1913T>C (p.Val638Ala)
c.1664T>C (p.Val555Ala)
c.1572T>C (n.1572T>C)
n.2098T>C
c.1922T>C (p.Val641Ala)
4g.6301708T>GCA356177090WFS1c.1949T>G (p.Val650Gly)
c.1890T>G
c.1913T>G (p.Val638Gly)
c.1664T>G (p.Val555Gly)
c.1572T>G (n.1572T>G)
n.2098T>G
c.1922T>G (p.Val641Gly)
 gnomAD v4
4g.6301709G>ACA438368654WFS1c.1950G>A (p.Val650=)
c.1891G>A
c.1914G>A (p.Val638=)
c.1665G>A (p.Val555=)
c.1573G>A (n.1573G>A)
n.2099G>A
c.1923G>A (p.Val641=)
 dbSNP gnomAD v2 gnomAD v4
4g.6301709G>CCA438368655WFS1c.1950G>C (p.Val650=)
c.1891G>C
c.1914G>C (p.Val638=)
c.1665G>C (p.Val555=)
c.1573G>C (n.1573G>C)
n.2099G>C
c.1923G>C (p.Val641=)
4g.6301709G=CA1435771700WFS1c.1950G= (p.Val650=)
c.1891G=
c.1914G= (p.Val638=)
c.1665G= (p.Val555=)
c.1573G= (n.1573G=)
n.2099G=
c.1923G= (p.Val641=)
4g.6301709G>TCA438368656WFS1c.1950G>T (p.Val650=)
c.1891G>T
c.1914G>T (p.Val638=)
c.1665G>T (p.Val555=)
c.1573G>T (n.1573G>T)
n.2099G>T
c.1923G>T (p.Val641=)
4g.6301710T>ACA356177091WFS1c.1951T>A (p.Trp651Arg)
c.1892T>A
c.1915T>A (p.Trp639Arg)
c.1666T>A (p.Trp556Arg)
c.1574T>A (n.1574T>A)
n.2100T>A
c.1924T>A (p.Trp642Arg)
4g.6301710T>CCA356177092WFS1c.1951T>C (p.Trp651Arg)
c.1892T>C
c.1915T>C (p.Trp639Arg)
c.1666T>C (p.Trp556Arg)
c.1574T>C (n.1574T>C)
n.2100T>C
c.1924T>C (p.Trp642Arg)
4g.6301710T>GCA356177093WFS1c.1951T>G (p.Trp651Gly)
c.1892T>G
c.1915T>G (p.Trp639Gly)
c.1666T>G (p.Trp556Gly)
c.1574T>G (n.1574T>G)
n.2100T>G
c.1924T>G (p.Trp642Gly)
 gnomAD v4
4g.6301711G>ACA356177094WFS1c.1952G>A (p.Trp651Ter)
c.1893G>A
c.1916G>A (p.Trp639Ter)
c.1667G>A (p.Trp556Ter)
c.1575G>A (n.1575G>A)
n.2101G>A
c.1925G>A (p.Trp642Ter)
 gnomAD v4
4g.6301711G>CCA356177095WFS1c.1952G>C (p.Trp651Ser)
c.1893G>C
c.1916G>C (p.Trp639Ser)
c.1667G>C (p.Trp556Ser)
c.1575G>C (n.1575G>C)
n.2101G>C
c.1925G>C (p.Trp642Ser)
4g.6301711G>TCA356177096WFS1c.1952G>T (p.Trp651Leu)
c.1893G>T
c.1916G>T (p.Trp639Leu)
c.1667G>T (p.Trp556Leu)
c.1575G>T (n.1575G>T)
n.2101G>T
c.1925G>T (p.Trp642Leu)
4g.6301712G>ACA356177099WFS1c.1953G>A (p.Trp651Ter)
c.1894G>A
c.1917G>A (p.Trp639Ter)
c.1668G>A (p.Trp556Ter)
c.1576G>A (n.1576G>A)
n.2102G>A
c.1926G>A (p.Trp642Ter)
 ClinVar
4g.6301712G>CCA356177098WFS1c.1953G>C (p.Trp651Cys)
c.1894G>C
c.1917G>C (p.Trp639Cys)
c.1668G>C (p.Trp556Cys)
c.1576G>C (n.1576G>C)
n.2102G>C
c.1926G>C (p.Trp642Cys)
4g.6301712G>TCA356177097WFS1c.1953G>T (p.Trp651Cys)
c.1894G>T
c.1917G>T (p.Trp639Cys)
c.1668G>T (p.Trp556Cys)
c.1576G>T (n.1576G>T)
n.2102G>T
c.1926G>T (p.Trp642Cys)
4g.6301713C>ACA356177100WFS1c.1954C>A (p.Leu652Ile)
c.1895C>A
c.1918C>A (p.Leu640Ile)
c.1669C>A (p.Leu557Ile)
c.1577C>A (n.1577C>A)
n.2103C>A
c.1927C>A (p.Leu643Ile)
4g.6301713C=CA1435771701WFS1c.1954C= (p.Leu652=)
c.1895C=
c.1918C= (p.Leu640=)
c.1669C= (p.Leu557=)
c.1577C= (n.1577C=)
n.2103C=
c.1927C= (p.Leu643=)
4g.6301713C>GCA91796680WFS1c.1954C>G (p.Leu652Val)
c.1895C>G
c.1918C>G (p.Leu640Val)
c.1669C>G (p.Leu557Val)
c.1577C>G (n.1577C>G)
n.2103C>G
c.1927C>G (p.Leu643Val)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6301713C>TCA356177101WFS1c.1954C>T (p.Leu652Phe)
c.1895C>T
c.1918C>T (p.Leu640Phe)
c.1669C>T (p.Leu557Phe)
c.1577C>T (n.1577C>T)
n.2103C>T
c.1927C>T (p.Leu643Phe)
 dbSNP gnomAD v4
4g.6301714_6301724delCA2586973639WFS1c.1955_1965del (p.Leu652ArgfsTer?)
c.1896_1906del
c.1919_1929del (p.Leu640ArgfsTer?)
c.1670_1680del (p.Leu557ArgfsTer?)
c.1578_1588del (n.1578_1588del)
n.2104_2114del
c.1928_1938del (p.Leu643ArgfsTer?)
4g.6301714T>ACA356177102WFS1c.1955T>A (p.Leu652His)
c.1896T>A
c.1919T>A (p.Leu640His)
c.1670T>A (p.Leu557His)
c.1578T>A (n.1578T>A)
n.2104T>A
c.1928T>A (p.Leu643His)
4g.6301714T>CCA356177103WFS1c.1955T>C (p.Leu652Pro)
c.1896T>C
c.1919T>C (p.Leu640Pro)
c.1670T>C (p.Leu557Pro)
c.1578T>C (n.1578T>C)
n.2104T>C
c.1928T>C (p.Leu643Pro)
4g.6301714T>GCA356177104WFS1c.1955T>G (p.Leu652Arg)
c.1896T>G
c.1919T>G (p.Leu640Arg)
c.1670T>G (p.Leu557Arg)
c.1578T>G (n.1578T>G)
n.2104T>G
c.1928T>G (p.Leu643Arg)
4g.6301714_6301723delCA2586973640WFS1c.1955_1964del (p.Leu652ProfsTer15)
c.1896_1905del
c.1919_1928del (p.Leu640ProfsTer15)
c.1670_1679del (p.Leu557ProfsTer15)
c.1578_1587del (n.1578_1587del)
n.2104_2113del
c.1928_1937del (p.Leu643ProfsTer15)
4g.6301715C>ACA438368662WFS1c.1956C>A (p.Leu652=)
c.1897C>A
c.1920C>A (p.Leu640=)
c.1671C>A (p.Leu557=)
c.1579C>A (n.1579C>A)
n.2105C>A
c.1929C>A (p.Leu643=)
4g.6301715C=CA1435771704WFS1c.1956C= (p.Leu652=)
c.1897C=
c.1920C= (p.Leu640=)
c.1671C= (p.Leu557=)
c.1579C= (n.1579C=)
n.2105C=
c.1929C= (p.Leu643=)
4g.6301715C>GCA2839544WFS1c.1956C>G (p.Leu652=)
c.1897C>G
c.1920C>G (p.Leu640=)
c.1671C>G (p.Leu557=)
c.1579C>G (n.1579C>G)
n.2105C>G
c.1929C>G (p.Leu643=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301715C>TCA438368663WFS1c.1956C>T (p.Leu652=)
c.1897C>T
c.1920C>T (p.Leu640=)
c.1671C>T (p.Leu557=)
c.1579C>T (n.1579C>T)
n.2105C>T
c.1929C>T (p.Leu643=)
 dbSNP gnomAD v2 gnomAD v4
4g.6301716A=CA1435771708WFS1c.1957A= (p.Thr653=)
c.1898A=
c.1921A= (p.Thr641=)
c.1672A= (p.Thr558=)
c.1580A= (n.1580A=)
n.2106A=
c.1930A= (p.Thr644=)
4g.6301716A>CCA2839545WFS1c.1957A>C (p.Thr653Pro)
c.1898A>C
c.1921A>C (p.Thr641Pro)
c.1672A>C (p.Thr558Pro)
c.1580A>C (n.1580A>C)
n.2106A>C
c.1930A>C (p.Thr644Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301716A>GCA356177105WFS1c.1957A>G (p.Thr653Ala)
c.1898A>G
c.1921A>G (p.Thr641Ala)
c.1672A>G (p.Thr558Ala)
c.1580A>G (n.1580A>G)
n.2106A>G
c.1930A>G (p.Thr644Ala)
4g.6301716A>TCA356177106WFS1c.1957A>T (p.Thr653Ser)
c.1898A>T
c.1921A>T (p.Thr641Ser)
c.1672A>T (p.Thr558Ser)
c.1580A>T (n.1580A>T)
n.2106A>T
c.1930A>T (p.Thr644Ser)
 dbSNP gnomAD v2 gnomAD v4
4g.6301716dupCA549707915WFS1c.1957dup (p.Thr653AsnfsTer?)
c.1898dup
c.1921dup (p.Thr641AsnfsTer?)
c.1672dup (p.Thr558AsnfsTer?)
c.1580dup (n.1580dup)
n.2106dup
c.1930dup (p.Thr644AsnfsTer?)
 dbSNP gnomAD v2 gnomAD v4
4g.6301716_6301718dupCA1435771707WFS1c.1957_1959dup (p.Thr653_Ala654insThr)
c.1898_1900dup
c.1921_1923dup (p.Thr641_Ala642insThr)
c.1672_1674dup (p.Thr558_Ala559insThr)
c.1580_1582dup (n.1580_1582dup)
n.2106_2108dup
c.1930_1932dup (p.Thr644_Ala645insThr)
 dbSNP gnomAD v4
4g.6301717C>ACA179659WFS1c.1958C>A (p.Thr653Lys)
c.1899C>A
c.1922C>A (p.Thr641Lys)
c.1673C>A (p.Thr558Lys)
c.1581C>A (n.1581C>A)
n.2107C>A
c.1931C>A (p.Thr644Lys)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301717C=CA1435771713WFS1c.1958C= (p.Thr653=)
c.1899C=
c.1922C= (p.Thr641=)
c.1673C= (p.Thr558=)
c.1581C= (n.1581C=)
n.2107C=
c.1931C= (p.Thr644=)
4g.6301717C>GCA356177107WFS1c.1958C>G (p.Thr653Arg)
c.1899C>G
c.1922C>G (p.Thr641Arg)
c.1673C>G (p.Thr558Arg)
c.1581C>G (n.1581C>G)
n.2107C>G
c.1931C>G (p.Thr644Arg)
4g.6301717C>TCA2839546WFS1c.1958C>T (p.Thr653Met)
c.1899C>T
c.1922C>T (p.Thr641Met)
c.1673C>T (p.Thr558Met)
c.1581C>T (n.1581C>T)
n.2107C>T
c.1931C>T (p.Thr644Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301718G>ACA2839547WFS1c.1959G>A (p.Thr653=)
c.1900G>A
c.1923G>A (p.Thr641=)
c.1674G>A (p.Thr558=)
c.1582G>A (n.1582G>A)
n.2108G>A
c.1932G>A (p.Thr644=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6301718G>CCA438368666WFS1c.1959G>C (p.Thr653=)
c.1900G>C
c.1923G>C (p.Thr641=)
c.1674G>C (p.Thr558=)
c.1582G>C (n.1582G>C)
n.2108G>C
c.1932G>C (p.Thr644=)
4g.6301718G=CA1435771718WFS1c.1959G= (p.Thr653=)
c.1900G=
c.1923G= (p.Thr641=)
c.1674G= (p.Thr558=)
c.1582G= (n.1582G=)
n.2108G=
c.1932G= (p.Thr644=)
4g.6301718G>TCA438368667WFS1c.1959G>T (p.Thr653=)
c.1900G>T
c.1923G>T (p.Thr641=)
c.1674G>T (p.Thr558=)
c.1582G>T (n.1582G>T)
n.2108G>T
c.1932G>T (p.Thr644=)
 gnomAD v4
4g.6301719G>ACA356177108WFS1c.1960G>A (p.Ala654Thr)
c.1901G>A
c.1924G>A (p.Ala642Thr)
c.1675G>A (p.Ala559Thr)
c.1583G>A (n.1583G>A)
n.2109G>A
c.1933G>A (p.Ala645Thr)
 gnomAD v4
4g.6301719G>CCA356177109WFS1c.1960G>C (p.Ala654Pro)
c.1901G>C
c.1924G>C (p.Ala642Pro)
c.1675G>C (p.Ala559Pro)
c.1583G>C (n.1583G>C)
n.2109G>C
c.1933G>C (p.Ala645Pro)
 gnomAD v4
4g.6301719G>TCA356177110WFS1c.1960G>T (p.Ala654Ser)
c.1901G>T
c.1924G>T (p.Ala642Ser)
c.1675G>T (p.Ala559Ser)
c.1583G>T (n.1583G>T)
n.2109G>T
c.1933G>T (p.Ala645Ser)
4g.6301720C>ACA356177111WFS1c.1961C>A (p.Ala654Asp)
c.1902C>A
c.1925C>A (p.Ala642Asp)
c.1676C>A (p.Ala559Asp)
c.1584C>A (n.1584C>A)
n.2110C>A
c.1934C>A (p.Ala645Asp)
 gnomAD v4
4g.6301720C>GCA356177112WFS1c.1961C>G (p.Ala654Gly)
c.1902C>G
c.1925C>G (p.Ala642Gly)
c.1676C>G (p.Ala559Gly)
c.1584C>G (n.1584C>G)
n.2110C>G
c.1934C>G (p.Ala645Gly)
4g.6301720C>TCA356177113WFS1c.1961C>T (p.Ala654Val)
c.1902C>T
c.1925C>T (p.Ala642Val)
c.1676C>T (p.Ala559Val)
c.1584C>T (n.1584C>T)
n.2110C>T
c.1934C>T (p.Ala645Val)
 COSMIC
4g.6301721C>ACA438368670WFS1c.1962C>A (p.Ala654=)
c.1903C>A
c.1926C>A (p.Ala642=)
c.1677C>A (p.Ala559=)
c.1585C>A (n.1585C>A)
n.2111C>A
c.1935C>A (p.Ala645=)
4g.6301721C=CA1435771723WFS1c.1962C= (p.Ala654=)
c.1903C=
c.1926C= (p.Ala642=)
c.1677C= (p.Ala559=)
c.1585C= (n.1585C=)
n.2111C=
c.1935C= (p.Ala645=)
4g.6301721C>GCA438368671WFS1c.1962C>G (p.Ala654=)
c.1903C>G
c.1926C>G (p.Ala642=)
c.1677C>G (p.Ala559=)
c.1585C>G (n.1585C>G)
n.2111C>G
c.1935C>G (p.Ala645=)
4g.6301721C>TCA2839548WFS1c.1962C>T (p.Ala654=)
c.1903C>T
c.1926C>T (p.Ala642=)
c.1677C>T (p.Ala559=)
c.1585C>T (n.1585C>T)
n.2111C>T
c.1935C>T (p.Ala645=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6301722A>CCA356177114WFS1c.1963A>C (p.Ile655Leu)
c.1904A>C
c.1927A>C (p.Ile643Leu)
c.1678A>C (p.Ile560Leu)
c.1586A>C (n.1586A>C)
n.2112A>C
c.1936A>C (p.Ile646Leu)
4g.6301722A>GCA356177115WFS1c.1963A>G (p.Ile655Val)
c.1904A>G
c.1927A>G (p.Ile643Val)
c.1678A>G (p.Ile560Val)
c.1586A>G (n.1586A>G)
n.2112A>G
c.1936A>G (p.Ile646Val)
4g.6301722A>TCA356177116WFS1c.1963A>T (p.Ile655Phe)
c.1904A>T
c.1927A>T (p.Ile643Phe)
c.1678A>T (p.Ile560Phe)
c.1586A>T (n.1586A>T)
n.2112A>T
c.1936A>T (p.Ile646Phe)
4g.6301723T>ACA356177117WFS1c.1964T>A (p.Ile655Asn)
c.1905T>A
c.1928T>A (p.Ile643Asn)
c.1679T>A (p.Ile560Asn)
c.1587T>A (n.1587T>A)
n.2113T>A
c.1937T>A (p.Ile646Asn)
4g.6301723T>CCA91796689WFS1c.1964T>C (p.Ile655Thr)
c.1905T>C
c.1928T>C (p.Ile643Thr)
c.1679T>C (p.Ile560Thr)
c.1587T>C (n.1587T>C)
n.2113T>C
c.1937T>C (p.Ile646Thr)
 dbSNP gnomAD v4
4g.6301723T>GCA356177118WFS1c.1964T>G (p.Ile655Ser)
c.1905T>G
c.1928T>G (p.Ile643Ser)
c.1679T>G (p.Ile560Ser)
c.1587T>G (n.1587T>G)
n.2113T>G
c.1937T>G (p.Ile646Ser)
4g.6301723T=CA1435771725WFS1c.1964T= (p.Ile655=)
c.1905T=
c.1928T= (p.Ile643=)
c.1679T= (p.Ile560=)
c.1587T= (n.1587T=)
n.2113T=
c.1937T= (p.Ile646=)
4g.6301724C>ACA438368675WFS1c.1965C>A (p.Ile655=)
c.1906C>A
c.1929C>A (p.Ile643=)
c.1680C>A (p.Ile560=)
c.1588C>A (n.1588C>A)
n.2114C>A
c.1938C>A (p.Ile646=)
4g.6301724C=CA1435771729WFS1c.1965C= (p.Ile655=)
c.1906C=
c.1929C= (p.Ile643=)
c.1680C= (p.Ile560=)
c.1588C= (n.1588C=)
n.2114C=
c.1938C= (p.Ile646=)
4g.6301724C>GCA2839550WFS1c.1965C>G (p.Ile655Met)
c.1906C>G
c.1929C>G (p.Ile643Met)
c.1680C>G (p.Ile560Met)
c.1588C>G (n.1588C>G)
n.2114C>G
c.1938C>G (p.Ile646Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301724C>TCA2839549WFS1c.1965C>T (p.Ile655=)
c.1906C>T
c.1929C>T (p.Ile643=)
c.1680C>T (p.Ile560=)
c.1588C>T (n.1588C>T)
n.2114C>T
c.1938C>T (p.Ile646=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301725G>ACA2839551WFS1c.1966G>A (p.Val656Met)
c.1907G>A
c.1930G>A (p.Val644Met)
c.1681G>A (p.Val561Met)
c.1589G>A (n.1589G>A)
n.2115G>A
c.1939G>A (p.Val647Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301725G>CCA356177119WFS1c.1966G>C (p.Val656Leu)
c.1907G>C
c.1930G>C (p.Val644Leu)
c.1681G>C (p.Val561Leu)
c.1589G>C (n.1589G>C)
n.2115G>C
c.1939G>C (p.Val647Leu)
4g.6301725G=CA1435771734WFS1c.1966G= (p.Val656=)
c.1907G=
c.1930G= (p.Val644=)
c.1681G= (p.Val561=)
c.1589G= (n.1589G=)
n.2115G=
c.1939G= (p.Val647=)
4g.6301725G>TCA324828WFS1c.1966G>T (p.Val656Leu)
c.1907G>T
c.1930G>T (p.Val644Leu)
c.1681G>T (p.Val561Leu)
c.1589G>T (n.1589G>T)
n.2115G>T
c.1939G>T (p.Val647Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6301725_6301733delinsGTGCTGTTCCA1435771733WFS1c.1966_1974delinsGTGCTGTTC (p.Val656=)
c.1907_1915delinsGTGCTGTTC
c.1930_1938delinsGTGCTGTTC (p.Val644=)
c.1681_1689delinsGTGCTGTTC (p.Val561=)
c.1589_1597delinsGTGCTGTTC (n.1589_1597delinsGTGCTGTTC)
n.2115_2123delinsGTGCTGTTC
c.1939_1947delinsGTGCTGTTC (p.Val647=)
4g.6301726T>ACA356177120WFS1c.1967T>A (p.Val656Glu)
c.1908T>A
c.1931T>A (p.Val644Glu)
c.1682T>A (p.Val561Glu)
c.1590T>A (n.1590T>A)
n.2116T>A
c.1940T>A (p.Val647Glu)
4g.6301726T>CCA356177121WFS1c.1967T>C (p.Val656Ala)
c.1908T>C
c.1931T>C (p.Val644Ala)
c.1682T>C (p.Val561Ala)
c.1590T>C (n.1590T>C)
n.2116T>C
c.1940T>C (p.Val647Ala)
4g.6301726T>GCA356177122WFS1c.1967T>G (p.Val656Gly)
c.1908T>G
c.1931T>G (p.Val644Gly)
c.1682T>G (p.Val561Gly)
c.1590T>G (n.1590T>G)
n.2116T>G
c.1940T>G (p.Val647Gly)
 dbSNP gnomAD v2 gnomAD v4
4g.6301726T=CA1435771737WFS1c.1967T= (p.Val656=)
c.1908T=
c.1931T= (p.Val644=)
c.1682T= (p.Val561=)
c.1590T= (n.1590T=)
n.2116T=
c.1940T= (p.Val647=)
4g.6301731_6301738delCA91796697WFS1c.1972_1979del (p.Phe658ValfsTer?)
c.1913_1920del
c.1936_1943del (p.Phe646ValfsTer?)
c.1687_1694del (p.Phe563ValfsTer?)
c.1595_1602del (n.1595_1602del)
n.2121_2128del
c.1945_1952del (p.Phe649ValfsTer?)
 ClinVar dbSNP gnomAD v4
4g.6301727G>ACA438368679WFS1c.1968G>A (p.Val656=)
c.1909G>A
c.1932G>A (p.Val644=)
c.1683G>A (p.Val561=)
c.1591G>A (n.1591G>A)
n.2117G>A
c.1941G>A (p.Val647=)
4g.6301727G>CCA438368681WFS1c.1968G>C (p.Val656=)
c.1909G>C
c.1932G>C (p.Val644=)
c.1683G>C (p.Val561=)
c.1591G>C (n.1591G>C)
n.2117G>C
c.1941G>C (p.Val647=)
4g.6301727G>TCA438368684WFS1c.1968G>T (p.Val656=)
c.1909G>T
c.1932G>T (p.Val644=)
c.1683G>T (p.Val561=)
c.1591G>T (n.1591G>T)
n.2117G>T
c.1941G>T (p.Val647=)
4g.6301728C>ACA356177123WFS1c.1969C>A (p.Leu657Met)
c.1910C>A
c.1933C>A (p.Leu645Met)
c.1684C>A (p.Leu562Met)
c.1592C>A (n.1592C>A)
n.2118C>A
c.1942C>A (p.Leu648Met)
 gnomAD v4 COSMIC
4g.6301728C=CA1435771739WFS1c.1969C= (p.Leu657=)
c.1910C=
c.1933C= (p.Leu645=)
c.1684C= (p.Leu562=)
c.1592C= (n.1592C=)
n.2118C=
c.1942C= (p.Leu648=)
4g.6301728C>GCA356177124WFS1c.1969C>G (p.Leu657Val)
c.1910C>G
c.1933C>G (p.Leu645Val)
c.1684C>G (p.Leu562Val)
c.1592C>G (n.1592C>G)
n.2118C>G
c.1942C>G (p.Leu648Val)
4g.6301728C>TCA438368686WFS1c.1969C>T (p.Leu657=)
c.1910C>T
c.1933C>T (p.Leu645=)
c.1684C>T (p.Leu562=)
c.1592C>T (n.1592C>T)
n.2118C>T
c.1942C>T (p.Leu648=)
 dbSNP gnomAD v4
4g.6301729T>ACA356177125WFS1c.1970T>A (p.Leu657Gln)
c.1911T>A
c.1934T>A (p.Leu645Gln)
c.1685T>A (p.Leu562Gln)
c.1593T>A (n.1593T>A)
n.2119T>A
c.1943T>A (p.Leu648Gln)
4g.6301729T>CCA356177126WFS1c.1970T>C (p.Leu657Pro)
c.1911T>C
c.1934T>C (p.Leu645Pro)
c.1685T>C (p.Leu562Pro)
c.1593T>C (n.1593T>C)
n.2119T>C
c.1943T>C (p.Leu648Pro)
 ClinVar
4g.6301729T>GCA356177127WFS1c.1970T>G (p.Leu657Arg)
c.1911T>G
c.1934T>G (p.Leu645Arg)
c.1685T>G (p.Leu562Arg)
c.1593T>G (n.1593T>G)
n.2119T>G
c.1943T>G (p.Leu648Arg)
4g.6301730G>ACA438368687WFS1c.1971G>A (p.Leu657=)
c.1912G>A
c.1935G>A (p.Leu645=)
c.1686G>A (p.Leu562=)
c.1594G>A (n.1594G>A)
n.2120G>A
c.1944G>A (p.Leu648=)
 dbSNP gnomAD v2 gnomAD v4
4g.6301730G>CCA438368688WFS1c.1971G>C (p.Leu657=)
c.1912G>C
c.1935G>C (p.Leu645=)
c.1686G>C (p.Leu562=)
c.1594G>C (n.1594G>C)
n.2120G>C
c.1944G>C (p.Leu648=)
4g.6301730G=CA1435771741WFS1c.1971G= (p.Leu657=)
c.1912G=
c.1935G= (p.Leu645=)
c.1686G= (p.Leu562=)
c.1594G= (n.1594G=)
n.2120G=
c.1944G= (p.Leu648=)
4g.6301730G>TCA184559WFS1c.1971G>T (p.Leu657=)
c.1912G>T
c.1935G>T (p.Leu645=)
c.1686G>T (p.Leu562=)
c.1594G>T (n.1594G>T)
n.2120G>T
c.1944G>T (p.Leu648=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6301731T>ACA356177128WFS1c.1972T>A (p.Phe658Ile)
c.1913T>A
c.1936T>A (p.Phe646Ile)
c.1687T>A (p.Phe563Ile)
c.1595T>A (n.1595T>A)
n.2121T>A
c.1945T>A (p.Phe649Ile)
4g.6301731T>CCA356177129WFS1c.1972T>C (p.Phe658Leu)
c.1913T>C
c.1936T>C (p.Phe646Leu)
c.1687T>C (p.Phe563Leu)
c.1595T>C (n.1595T>C)
n.2121T>C
c.1945T>C (p.Phe649Leu)
4g.6301731T>GCA356177130WFS1c.1972T>G (p.Phe658Val)
c.1913T>G
c.1936T>G (p.Phe646Val)
c.1687T>G (p.Phe563Val)
c.1595T>G (n.1595T>G)
n.2121T>G
c.1945T>G (p.Phe649Val)
4g.6301732T>ACA356177133WFS1c.1973T>A (p.Phe658Tyr)
c.1914T>A
c.1937T>A (p.Phe646Tyr)
c.1688T>A (p.Phe563Tyr)
c.1596T>A (n.1596T>A)
n.2122T>A
c.1946T>A (p.Phe649Tyr)
4g.6301732T>CCA356177132WFS1c.1973T>C (p.Phe658Ser)
c.1914T>C
c.1937T>C (p.Phe646Ser)
c.1688T>C (p.Phe563Ser)
c.1596T>C (n.1596T>C)
n.2122T>C
c.1946T>C (p.Phe649Ser)
4g.6301732T>GCA356177131WFS1c.1973T>G (p.Phe658Cys)
c.1914T>G
c.1937T>G (p.Phe646Cys)
c.1688T>G (p.Phe563Cys)
c.1596T>G (n.1596T>G)
n.2122T>G
c.1946T>G (p.Phe649Cys)
4g.6301733C>ACA356177134WFS1c.1974C>A (p.Phe658Leu)
c.1915C>A
c.1938C>A (p.Phe646Leu)
c.1689C>A (p.Phe563Leu)
c.1597C>A (n.1597C>A)
n.2123C>A
c.1947C>A (p.Phe649Leu)
4g.6301733C=CA1435771742WFS1c.1974C= (p.Phe658=)
c.1915C=
c.1938C= (p.Phe646=)
c.1689C= (p.Phe563=)
c.1597C= (n.1597C=)
n.2123C=
c.1947C= (p.Phe649=)
4g.6301733C>GCA356177135WFS1c.1974C>G (p.Phe658Leu)
c.1915C>G
c.1938C>G (p.Phe646Leu)
c.1689C>G (p.Phe563Leu)
c.1597C>G (n.1597C>G)
n.2123C>G
c.1947C>G (p.Phe649Leu)
4g.6301733C>TCA438368690WFS1c.1974C>T (p.Phe658=)
c.1915C>T
c.1938C>T (p.Phe646=)
c.1689C>T (p.Phe563=)
c.1597C>T (n.1597C>T)
n.2123C>T
c.1947C>T (p.Phe649=)
 ClinVar dbSNP
4g.6301736_6301738delCA2669843460WFS1c.1977_1979del (p.Cys659del)
c.1918_1920del
c.1941_1943del (p.Cys647del)
c.1692_1694del (p.Cys564del)
c.1600_1602del (n.1600_1602del)
n.2126_2128del
c.1950_1952del (p.Cys650del)
 gnomAD v4

Number of alleles fetched