Chr Mutation (hg38) CAid Gene Transcript Linkouts
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.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.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)
4g.6302008C>ACA2839647WFS1c.2249C>A (p.Ala750Asp)
c.2190C>A
c.2213C>A (p.Ala738Asp)
c.1964C>A (p.Ala655Asp)
c.1872C>A (n.1872C>A)
n.2398C>A
c.2222C>A (p.Ala741Asp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302008C=CA1435772203WFS1c.2249C= (p.Ala750=)
c.2190C=
c.2213C= (p.Ala738=)
c.1964C= (p.Ala655=)
c.1872C= (n.1872C=)
n.2398C=
c.2222C= (p.Ala741=)
4g.6302008C>GCA356178137WFS1c.2249C>G (p.Ala750Gly)
c.2190C>G
c.2213C>G (p.Ala738Gly)
c.1964C>G (p.Ala655Gly)
c.1872C>G (n.1872C>G)
n.2398C>G
c.2222C>G (p.Ala741Gly)
 gnomAD v4
4g.6302008C>TCA356178139WFS1c.2249C>T (p.Ala750Val)
c.2190C>T
c.2213C>T (p.Ala738Val)
c.1964C>T (p.Ala655Val)
c.1872C>T (n.1872C>T)
n.2398C>T
c.2222C>T (p.Ala741Val)
 gnomAD v4 COSMIC
4g.6302009C>ACA438368730WFS1c.2250C>A (p.Ala750=)
c.2191C>A
c.2214C>A (p.Ala738=)
c.1965C>A (p.Ala655=)
c.1873C>A (n.1873C>A)
n.2399C>A
c.2223C>A (p.Ala741=)
4g.6302009C=CA1435772205WFS1c.2250C= (p.Ala750=)
c.2191C=
c.2214C= (p.Ala738=)
c.1965C= (p.Ala655=)
c.1873C= (n.1873C=)
n.2399C=
c.2223C= (p.Ala741=)
4g.6302009C>GCA438368729WFS1c.2250C>G (p.Ala750=)
c.2191C>G
c.2214C>G (p.Ala738=)
c.1965C>G (p.Ala655=)
c.1873C>G (n.1873C>G)
n.2399C>G
c.2223C>G (p.Ala741=)
4g.6302009C>TCA438368728WFS1c.2250C>T (p.Ala750=)
c.2191C>T
c.2214C>T (p.Ala738=)
c.1965C>T (p.Ala655=)
c.1873C>T (n.1873C>T)
n.2399C>T
c.2223C>T (p.Ala741=)
 dbSNP gnomAD v4
4g.6302010T>ACA356178141WFS1c.2251T>A (p.Tyr751Asn)
c.2192T>A
c.2215T>A (p.Tyr739Asn)
c.1966T>A (p.Tyr656Asn)
c.1874T>A (n.1874T>A)
n.2400T>A
c.2224T>A (p.Tyr742Asn)
4g.6302010T>CCA356178143WFS1c.2251T>C (p.Tyr751His)
c.2192T>C
c.2215T>C (p.Tyr739His)
c.1966T>C (p.Tyr656His)
c.1874T>C (n.1874T>C)
n.2400T>C
c.2224T>C (p.Tyr742His)
4g.6302010T>GCA91796952WFS1c.2251T>G (p.Tyr751Asp)
c.2192T>G
c.2215T>G (p.Tyr739Asp)
c.1966T>G (p.Tyr656Asp)
c.1874T>G (n.1874T>G)
n.2400T>G
c.2224T>G (p.Tyr742Asp)
 dbSNP
4g.6302010T=CA1435772207WFS1c.2251T= (p.Tyr751=)
c.2192T=
c.2215T= (p.Tyr739=)
c.1966T= (p.Tyr656=)
c.1874T= (n.1874T=)
n.2400T=
c.2224T= (p.Tyr742=)
4g.6302011A=CA1435772208WFS1c.2252A= (p.Tyr751=)
c.2193A=
c.2216A= (p.Tyr739=)
c.1967A= (p.Tyr656=)
c.1875A= (n.1875A=)
n.2401A=
c.2225A= (p.Tyr742=)
4g.6302011A>CCA356178149WFS1c.2252A>C (p.Tyr751Ser)
c.2193A>C
c.2216A>C (p.Tyr739Ser)
c.1967A>C (p.Tyr656Ser)
c.1875A>C (n.1875A>C)
n.2401A>C
c.2225A>C (p.Tyr742Ser)
 dbSNP
4g.6302011A>GCA356178146WFS1c.2252A>G (p.Tyr751Cys)
c.2193A>G
c.2216A>G (p.Tyr739Cys)
c.1967A>G (p.Tyr656Cys)
c.1875A>G (n.1875A>G)
n.2401A>G
c.2225A>G (p.Tyr742Cys)
 COSMIC
4g.6302011A>TCA356178148WFS1c.2252A>T (p.Tyr751Phe)
c.2193A>T
c.2216A>T (p.Tyr739Phe)
c.1967A>T (p.Tyr656Phe)
c.1875A>T (n.1875A>T)
n.2401A>T
c.2225A>T (p.Tyr742Phe)
4g.6302012C>ACA356178151WFS1c.2253C>A (p.Tyr751Ter)
c.2194C>A
c.2217C>A (p.Tyr739Ter)
c.1968C>A (p.Tyr656Ter)
c.1876C>A (n.1876C>A)
n.2402C>A
c.2226C>A (p.Tyr742Ter)
4g.6302012C>GCA356178153WFS1c.2253C>G (p.Tyr751Ter)
c.2194C>G
c.2217C>G (p.Tyr739Ter)
c.1968C>G (p.Tyr656Ter)
c.1876C>G (n.1876C>G)
n.2402C>G
c.2226C>G (p.Tyr742Ter)
4g.6302012C>TCA438368732WFS1c.2253C>T (p.Tyr751=)
c.2194C>T
c.2217C>T (p.Tyr739=)
c.1968C>T (p.Tyr656=)
c.1876C>T (n.1876C>T)
n.2402C>T
c.2226C>T (p.Tyr742=)
 ClinVar dbSNP gnomAD v4
4g.6302013C>ACA356178155WFS1c.2254C>A (p.Pro752Thr)
c.2195C>A
c.2218C>A (p.Pro740Thr)
c.1969C>A (p.Pro657Thr)
c.1877C>A (n.1877C>A)
n.2403C>A
c.2227C>A (p.Pro743Thr)
 gnomAD v4
4g.6302013C=CA1435772211WFS1c.2254C= (p.Pro752=)
c.2195C=
c.2218C= (p.Pro740=)
c.1969C= (p.Pro657=)
c.1877C= (n.1877C=)
n.2403C=
c.2227C= (p.Pro743=)
4g.6302013C>GCA356178157WFS1c.2254C>G (p.Pro752Ala)
c.2195C>G
c.2218C>G (p.Pro740Ala)
c.1969C>G (p.Pro657Ala)
c.1877C>G (n.1877C>G)
n.2403C>G
c.2227C>G (p.Pro743Ala)
4g.6302013C>TCA2839648WFS1c.2254C>T (p.Pro752Ser)
c.2195C>T
c.2218C>T (p.Pro740Ser)
c.1969C>T (p.Pro657Ser)
c.1877C>T (n.1877C>T)
n.2403C>T
c.2227C>T (p.Pro743Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302014C>ACA2839650WFS1c.2255C>A (p.Pro752His)
c.2196C>A
c.2219C>A (p.Pro740His)
c.1970C>A (p.Pro657His)
c.1878C>A (n.1878C>A)
n.2404C>A
c.2228C>A (p.Pro743His)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302014C=CA1435772213WFS1c.2255C= (p.Pro752=)
c.2196C=
c.2219C= (p.Pro740=)
c.1970C= (p.Pro657=)
c.1878C= (n.1878C=)
n.2404C=
c.2228C= (p.Pro743=)
4g.6302014C>GCA356178160WFS1c.2255C>G (p.Pro752Arg)
c.2196C>G
c.2219C>G (p.Pro740Arg)
c.1970C>G (p.Pro657Arg)
c.1878C>G (n.1878C>G)
n.2404C>G
c.2228C>G (p.Pro743Arg)
4g.6302014C>TCA2839649WFS1c.2255C>T (p.Pro752Leu)
c.2196C>T
c.2219C>T (p.Pro740Leu)
c.1970C>T (p.Pro657Leu)
c.1878C>T (n.1878C>T)
n.2404C>T
c.2228C>T (p.Pro743Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302015T>ACA438368736WFS1c.2256T>A (p.Pro752=)
c.2197T>A
c.2220T>A (p.Pro740=)
c.1971T>A (p.Pro657=)
c.1879T>A (n.1879T>A)
n.2405T>A
c.2229T>A (p.Pro743=)
4g.6302015T>CCA438368737WFS1c.2256T>C (p.Pro752=)
c.2197T>C
c.2220T>C (p.Pro740=)
c.1971T>C (p.Pro657=)
c.1879T>C (n.1879T>C)
n.2405T>C
c.2229T>C (p.Pro743=)
4g.6302015T>GCA438368738WFS1c.2256T>G (p.Pro752=)
c.2197T>G
c.2220T>G (p.Pro740=)
c.1971T>G (p.Pro657=)
c.1879T>G (n.1879T>G)
n.2405T>G
c.2229T>G (p.Pro743=)
4g.6302016G>ACA356178162WFS1c.2257G>A (p.Ala753Thr)
c.2198G>A
c.2221G>A (p.Ala741Thr)
c.1972G>A (p.Ala658Thr)
c.1880G>A (n.1880G>A)
n.2406G>A
c.2230G>A (p.Ala744Thr)
4g.6302016G>CCA356178164WFS1c.2257G>C (p.Ala753Pro)
c.2198G>C
c.2221G>C (p.Ala741Pro)
c.1972G>C (p.Ala658Pro)
c.1880G>C (n.1880G>C)
n.2406G>C
c.2230G>C (p.Ala744Pro)
 gnomAD v4
4g.6302016G>TCA356178166WFS1c.2257G>T (p.Ala753Ser)
c.2198G>T
c.2221G>T (p.Ala741Ser)
c.1972G>T (p.Ala658Ser)
c.1880G>T (n.1880G>T)
n.2406G>T
c.2230G>T (p.Ala744Ser)
4g.6302017C>ACA356178167WFS1c.2258C>A (p.Ala753Asp)
c.2199C>A
c.2222C>A (p.Ala741Asp)
c.1973C>A (p.Ala658Asp)
c.1881C>A (n.1881C>A)
n.2407C>A
c.2231C>A (p.Ala744Asp)
 COSMIC
4g.6302017C=CA1435772214WFS1c.2258C= (p.Ala753=)
c.2199C=
c.2222C= (p.Ala741=)
c.1973C= (p.Ala658=)
c.1881C= (n.1881C=)
n.2407C=
c.2231C= (p.Ala744=)
4g.6302017C>GCA2839651WFS1c.2258C>G (p.Ala753Gly)
c.2199C>G
c.2222C>G (p.Ala741Gly)
c.1973C>G (p.Ala658Gly)
c.1881C>G (n.1881C>G)
n.2407C>G
c.2231C>G (p.Ala744Gly)
 dbSNP ExAC gnomAD v2
4g.6302017C>TCA323939WFS1c.2258C>T (p.Ala753Val)
c.2199C>T
c.2222C>T (p.Ala741Val)
c.1973C>T (p.Ala658Val)
c.1881C>T (n.1881C>T)
n.2407C>T
c.2231C>T (p.Ala744Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302018C>ACA2839653WFS1c.2259C>A (p.Ala753=)
c.2200C>A
c.2223C>A (p.Ala741=)
c.1974C>A (p.Ala658=)
c.1882C>A (n.1882C>A)
n.2408C>A
c.2232C>A (p.Ala744=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302018C=CA1435772216WFS1c.2259C= (p.Ala753=)
c.2200C=
c.2223C= (p.Ala741=)
c.1974C= (p.Ala658=)
c.1882C= (n.1882C=)
n.2408C=
c.2232C= (p.Ala744=)
4g.6302018C>GCA438368741WFS1c.2259C>G (p.Ala753=)
c.2200C>G
c.2223C>G (p.Ala741=)
c.1974C>G (p.Ala658=)
c.1882C>G (n.1882C>G)
n.2408C>G
c.2232C>G (p.Ala744=)
4g.6302018C>TCA2839652WFS1c.2259C>T (p.Ala753=)
c.2200C>T
c.2223C>T (p.Ala741=)
c.1974C>T (p.Ala658=)
c.1882C>T (n.1882C>T)
n.2408C>T
c.2232C>T (p.Ala744=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302019T>ACA356178168WFS1c.2260T>A (p.Cys754Ser)
c.2201T>A
c.2224T>A (p.Cys742Ser)
c.1975T>A (p.Cys659Ser)
c.1883T>A (n.1883T>A)
n.2409T>A
c.2233T>A (p.Cys745Ser)
4g.6302019T>CCA91796965WFS1c.2260T>C (p.Cys754Arg)
c.2201T>C
c.2224T>C (p.Cys742Arg)
c.1975T>C (p.Cys659Arg)
c.1883T>C (n.1883T>C)
n.2409T>C
c.2233T>C (p.Cys745Arg)
 ClinVar dbSNP
4g.6302019T>GCA356178169WFS1c.2260T>G (p.Cys754Gly)
c.2201T>G
c.2224T>G (p.Cys742Gly)
c.1975T>G (p.Cys659Gly)
c.1883T>G (n.1883T>G)
n.2409T>G
c.2233T>G (p.Cys745Gly)
 dbSNP gnomAD v2 gnomAD v4
4g.6302019T=CA1435772218WFS1c.2260T= (p.Cys754=)
c.2201T=
c.2224T= (p.Cys742=)
c.1975T= (p.Cys659=)
c.1883T= (n.1883T=)
n.2409T=
c.2233T= (p.Cys745=)
4g.6302019dupCA915944126WFS1c.2260dup (p.Cys754LeufsTer17)
c.2201dup
c.2224dup (p.Cys742LeufsTer17)
c.1975dup (p.Cys659LeufsTer17)
c.1883dup (n.1883dup)
n.2409dup
c.2233dup (p.Cys745LeufsTer17)
 ClinVar dbSNP
4g.6302019_6302042delinsTGCAGCCCTGGCAACACCTCCACGCA1435772217WFS1c.2260_2283delinsTGCAGCCCTGGCAACACCTCCACG (p.Cys754=)
c.2201_2224delinsTGCAGCCCTGGCAACACCTCCACG
c.2224_2247delinsTGCAGCCCTGGCAACACCTCCACG (p.Cys742=)
c.1975_1998delinsTGCAGCCCTGGCAACACCTCCACG (p.Cys659=)
c.1883_1906delinsTGCAGCCCTGGCAACACCTCCACG (n.1883_1906delinsTGCAGCCCTGGCAACACCTCCACG)
n.2409_2432delinsTGCAGCCCTGGCAACACCTCCACG
c.2233_2256delinsTGCAGCCCTGGCAACACCTCCACG (p.Cys745=)
4g.6302020G>ACA2839654WFS1c.2261G>A (p.Cys754Tyr)
c.2202G>A
c.2225G>A (p.Cys742Tyr)
c.1976G>A (p.Cys659Tyr)
c.1884G>A (n.1884G>A)
n.2410G>A
c.2234G>A (p.Cys745Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302020G>CCA356178170WFS1c.2261G>C (p.Cys754Ser)
c.2202G>C
c.2225G>C (p.Cys742Ser)
c.1976G>C (p.Cys659Ser)
c.1884G>C (n.1884G>C)
n.2410G>C
c.2234G>C (p.Cys745Ser)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6302020G=CA1435772222WFS1c.2261G= (p.Cys754=)
c.2202G=
c.2225G= (p.Cys742=)
c.1976G= (p.Cys659=)
c.1884G= (n.1884G=)
n.2410G=
c.2234G= (p.Cys745=)
4g.6302020G>TCA356178171WFS1c.2261G>T (p.Cys754Phe)
c.2202G>T
c.2225G>T (p.Cys742Phe)
c.1976G>T (p.Cys659Phe)
c.1884G>T (n.1884G>T)
n.2410G>T
c.2234G>T (p.Cys745Phe)
4g.6302022_6302044delCA1435772220WFS1c.2263_2285del (p.Ser755ArgfsTer8)
c.2204_2226del
c.2227_2249del (p.Ser743ArgfsTer8)
c.1978_2000del (p.Ser660ArgfsTer8)
c.1886_1908del (n.1886_1908del)
n.2412_2434del
c.2236_2258del (p.Ser746ArgfsTer8)
 dbSNP
4g.6302021C>ACA356178172WFS1c.2262C>A (p.Cys754Ter)
c.2203C>A
c.2226C>A (p.Cys742Ter)
c.1977C>A (p.Cys659Ter)
c.1885C>A (n.1885C>A)
n.2411C>A
c.2235C>A (p.Cys745Ter)
4g.6302021C=CA1435772223WFS1c.2262C= (p.Cys754=)
c.2203C=
c.2226C= (p.Cys742=)
c.1977C= (p.Cys659=)
c.1885C= (n.1885C=)
n.2411C=
c.2235C= (p.Cys745=)
4g.6302021C>GCA91796971WFS1c.2262C>G (p.Cys754Trp)
c.2203C>G
c.2226C>G (p.Cys742Trp)
c.1977C>G (p.Cys659Trp)
c.1885C>G (n.1885C>G)
n.2411C>G
c.2235C>G (p.Cys745Trp)
 dbSNP
4g.6302021C>TCA438368744WFS1c.2262C>T (p.Cys754=)
c.2203C>T
c.2226C>T (p.Cys742=)
c.1977C>T (p.Cys659=)
c.1885C>T (n.1885C>T)
n.2411C>T
c.2235C>T (p.Cys745=)
 gnomAD v4
4g.6302022A>CCA356178173WFS1c.2263A>C (p.Ser755Arg)
c.2204A>C
c.2227A>C (p.Ser743Arg)
c.1978A>C (p.Ser660Arg)
c.1886A>C (n.1886A>C)
n.2412A>C
c.2236A>C (p.Ser746Arg)
4g.6302022A>GCA356178174WFS1c.2263A>G (p.Ser755Gly)
c.2204A>G
c.2227A>G (p.Ser743Gly)
c.1978A>G (p.Ser660Gly)
c.1886A>G (n.1886A>G)
n.2412A>G
c.2236A>G (p.Ser746Gly)
 gnomAD v4
4g.6302022A>TCA356178175WFS1c.2263A>T (p.Ser755Cys)
c.2204A>T
c.2227A>T (p.Ser743Cys)
c.1978A>T (p.Ser660Cys)
c.1886A>T (n.1886A>T)
n.2412A>T
c.2236A>T (p.Ser746Cys)
4g.6302023G>ACA356178178WFS1c.2264G>A (p.Ser755Asn)
c.2205G>A
c.2228G>A (p.Ser743Asn)
c.1979G>A (p.Ser660Asn)
c.1887G>A (n.1887G>A)
n.2413G>A
c.2237G>A (p.Ser746Asn)
4g.6302023G>CCA356178177WFS1c.2264G>C (p.Ser755Thr)
c.2205G>C
c.2228G>C (p.Ser743Thr)
c.1979G>C (p.Ser660Thr)
c.1887G>C (n.1887G>C)
n.2413G>C
c.2237G>C (p.Ser746Thr)
4g.6302023G>TCA356178176WFS1c.2264G>T (p.Ser755Ile)
c.2205G>T
c.2228G>T (p.Ser743Ile)
c.1979G>T (p.Ser660Ile)
c.1887G>T (n.1887G>T)
n.2413G>T
c.2237G>T (p.Ser746Ile)
4g.6302024C>ACA356178179WFS1c.2265C>A (p.Ser755Arg)
c.2206C>A
c.2229C>A (p.Ser743Arg)
c.1980C>A (p.Ser660Arg)
c.1888C>A (n.1888C>A)
n.2414C>A
c.2238C>A (p.Ser746Arg)
4g.6302024C=CA1435772226WFS1c.2265C= (p.Ser755=)
c.2206C=
c.2229C= (p.Ser743=)
c.1980C= (p.Ser660=)
c.1888C= (n.1888C=)
n.2414C=
c.2238C= (p.Ser746=)
4g.6302024C>GCA356178180WFS1c.2265C>G (p.Ser755Arg)
c.2206C>G
c.2229C>G (p.Ser743Arg)
c.1980C>G (p.Ser660Arg)
c.1888C>G (n.1888C>G)
n.2414C>G
c.2238C>G (p.Ser746Arg)
4g.6302024C>TCA2839655WFS1c.2265C>T (p.Ser755=)
c.2206C>T
c.2229C>T (p.Ser743=)
c.1980C>T (p.Ser660=)
c.1888C>T (n.1888C>T)
n.2414C>T
c.2238C>T (p.Ser746=)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
4g.6302025C>ACA356178181WFS1c.2266C>A (p.Pro756Thr)
c.2207C>A
c.2230C>A (p.Pro744Thr)
c.1981C>A (p.Pro661Thr)
c.1889C>A (n.1889C>A)
n.2415C>A
c.2239C>A (p.Pro747Thr)
4g.6302025C=CA1435772227WFS1c.2266C= (p.Pro756=)
c.2207C=
c.2230C= (p.Pro744=)
c.1981C= (p.Pro661=)
c.1889C= (n.1889C=)
n.2415C=
c.2239C= (p.Pro747=)
4g.6302025C>GCA356178182WFS1c.2266C>G (p.Pro756Ala)
c.2207C>G
c.2230C>G (p.Pro744Ala)
c.1981C>G (p.Pro661Ala)
c.1889C>G (n.1889C>G)
n.2415C>G
c.2239C>G (p.Pro747Ala)
4g.6302025C>TCA356178183WFS1c.2266C>T (p.Pro756Ser)
c.2207C>T
c.2230C>T (p.Pro744Ser)
c.1981C>T (p.Pro661Ser)
c.1889C>T (n.1889C>T)
n.2415C>T
c.2239C>T (p.Pro747Ser)
 dbSNP gnomAD v4
4g.6302026C>ACA356178184WFS1c.2267C>A (p.Pro756His)
c.2208C>A
c.2231C>A (p.Pro744His)
c.1982C>A (p.Pro661His)
c.1890C>A (n.1890C>A)
n.2416C>A
c.2240C>A (p.Pro747His)
4g.6302026C=CA1435772230WFS1c.2267C= (p.Pro756=)
c.2208C=
c.2231C= (p.Pro744=)
c.1982C= (p.Pro661=)
c.1890C= (n.1890C=)
n.2416C=
c.2240C= (p.Pro747=)
4g.6302026C>GCA356178185WFS1c.2267C>G (p.Pro756Arg)
c.2208C>G
c.2231C>G (p.Pro744Arg)
c.1982C>G (p.Pro661Arg)
c.1890C>G (n.1890C>G)
n.2416C>G
c.2240C>G (p.Pro747Arg)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302026C>TCA356178186WFS1c.2267C>T (p.Pro756Leu)
c.2208C>T
c.2231C>T (p.Pro744Leu)
c.1982C>T (p.Pro661Leu)
c.1890C>T (n.1890C>T)
n.2416C>T
c.2240C>T (p.Pro747Leu)
 gnomAD v4
4g.6302027T>ACA438368750WFS1c.2268T>A (p.Pro756=)
c.2209T>A
c.2232T>A (p.Pro744=)
c.1983T>A (p.Pro661=)
c.1891T>A (n.1891T>A)
n.2417T>A
c.2241T>A (p.Pro747=)
4g.6302027T>CCA438368752WFS1c.2268T>C (p.Pro756=)
c.2209T>C
c.2232T>C (p.Pro744=)
c.1983T>C (p.Pro661=)
c.1891T>C (n.1891T>C)
n.2417T>C
c.2241T>C (p.Pro747=)
4g.6302027T>GCA2839656WFS1c.2268T>G (p.Pro756=)
c.2209T>G
c.2232T>G (p.Pro744=)
c.1983T>G (p.Pro661=)
c.1891T>G (n.1891T>G)
n.2417T>G
c.2241T>G (p.Pro747=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302027T=CA1435772233WFS1c.2268T= (p.Pro756=)
c.2209T=
c.2232T= (p.Pro744=)
c.1983T= (p.Pro661=)
c.1891T= (n.1891T=)
n.2417T=
c.2241T= (p.Pro747=)
4g.6302028G>ACA325142WFS1c.2269G>A (p.Gly757Ser)
c.2210G>A
c.2233G>A (p.Gly745Ser)
c.1984G>A (p.Gly662Ser)
c.1892G>A (n.1892G>A)
n.2418G>A
c.2242G>A (p.Gly748Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302028G>CCA356178187WFS1c.2269G>C (p.Gly757Arg)
c.2210G>C
c.2233G>C (p.Gly745Arg)
c.1984G>C (p.Gly662Arg)
c.1892G>C (n.1892G>C)
n.2418G>C
c.2242G>C (p.Gly748Arg)
 gnomAD v4
4g.6302028G=CA1435772236WFS1c.2269G= (p.Gly757=)
c.2210G=
c.2233G= (p.Gly745=)
c.1984G= (p.Gly662=)
c.1892G= (n.1892G=)
n.2418G=
c.2242G= (p.Gly748=)
4g.6302028G>TCA356178188WFS1c.2269G>T (p.Gly757Cys)
c.2210G>T
c.2233G>T (p.Gly745Cys)
c.1984G>T (p.Gly662Cys)
c.1892G>T (n.1892G>T)
n.2418G>T
c.2242G>T (p.Gly748Cys)
4g.6302029G>ACA356178191WFS1c.2270G>A (p.Gly757Asp)
c.2211G>A
c.2234G>A (p.Gly745Asp)
c.1985G>A (p.Gly662Asp)
c.1893G>A (n.1893G>A)
n.2419G>A
c.2243G>A (p.Gly748Asp)
 dbSNP gnomAD v2 gnomAD v4
4g.6302029G>CCA356178189WFS1c.2270G>C (p.Gly757Ala)
c.2211G>C
c.2234G>C (p.Gly745Ala)
c.1985G>C (p.Gly662Ala)
c.1893G>C (n.1893G>C)
n.2419G>C
c.2243G>C (p.Gly748Ala)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302029G=CA1435772238WFS1c.2270G= (p.Gly757=)
c.2211G=
c.2234G= (p.Gly745=)
c.1985G= (p.Gly662=)
c.1893G= (n.1893G=)
n.2419G=
c.2243G= (p.Gly748=)
4g.6302029G>TCA356178190WFS1c.2270G>T (p.Gly757Val)
c.2211G>T
c.2234G>T (p.Gly745Val)
c.1985G>T (p.Gly662Val)
c.1893G>T (n.1893G>T)
n.2419G>T
c.2243G>T (p.Gly748Val)
4g.6302030C>ACA438368763WFS1c.2271C>A (p.Gly757=)
c.2212C>A
c.2235C>A (p.Gly745=)
c.1986C>A (p.Gly662=)
c.1894C>A (n.1894C>A)
n.2420C>A
c.2244C>A (p.Gly748=)
4g.6302030C=CA1435772240WFS1c.2271C= (p.Gly757=)
c.2212C=
c.2235C= (p.Gly745=)
c.1986C= (p.Gly662=)
c.1894C= (n.1894C=)
n.2420C=
c.2244C= (p.Gly748=)
4g.6302030C>GCA438368761WFS1c.2271C>G (p.Gly757=)
c.2212C>G
c.2235C>G (p.Gly745=)
c.1986C>G (p.Gly662=)
c.1894C>G (n.1894C>G)
n.2420C>G
c.2244C>G (p.Gly748=)
 gnomAD v4
4g.6302030C>TCA2839657WFS1c.2271C>T (p.Gly757=)
c.2212C>T
c.2235C>T (p.Gly745=)
c.1986C>T (p.Gly662=)
c.1894C>T (n.1894C>T)
n.2420C>T
c.2244C>T (p.Gly748=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302031A>CCA356178194WFS1c.2272A>C (p.Asn758His)
c.2213A>C
c.2236A>C (p.Asn746His)
c.1987A>C (p.Asn663His)
c.1895A>C (n.1895A>C)
n.2421A>C
c.2245A>C (p.Asn749His)
4g.6302031A>GCA356178192WFS1c.2272A>G (p.Asn758Asp)
c.2213A>G
c.2236A>G (p.Asn746Asp)
c.1987A>G (p.Asn663Asp)
c.1895A>G (n.1895A>G)
n.2421A>G
c.2245A>G (p.Asn749Asp)
4g.6302031A>TCA356178193WFS1c.2272A>T (p.Asn758Tyr)
c.2213A>T
c.2236A>T (p.Asn746Tyr)
c.1987A>T (p.Asn663Tyr)
c.1895A>T (n.1895A>T)
n.2421A>T
c.2245A>T (p.Asn749Tyr)
4g.6302032A>CCA356178195WFS1c.2273A>C (p.Asn758Thr)
c.2214A>C
c.2237A>C (p.Asn746Thr)
c.1988A>C (p.Asn663Thr)
c.1896A>C (n.1896A>C)
n.2422A>C
c.2246A>C (p.Asn749Thr)
4g.6302032A>GCA356178196WFS1c.2273A>G (p.Asn758Ser)
c.2214A>G
c.2237A>G (p.Asn746Ser)
c.1988A>G (p.Asn663Ser)
c.1896A>G (n.1896A>G)
n.2422A>G
c.2246A>G (p.Asn749Ser)
 ClinVar dbSNP gnomAD v4
4g.6302032A>TCA356178197WFS1c.2273A>T (p.Asn758Ile)
c.2214A>T
c.2237A>T (p.Asn746Ile)
c.1988A>T (p.Asn663Ile)
c.1896A>T (n.1896A>T)
n.2422A>T
c.2246A>T (p.Asn749Ile)
4g.6302033C>ACA356178198WFS1c.2274C>A (p.Asn758Lys)
c.2215C>A
c.2238C>A (p.Asn746Lys)
c.1989C>A (p.Asn663Lys)
c.1897C>A (n.1897C>A)
n.2423C>A
c.2247C>A (p.Asn749Lys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302033C=CA1435772241WFS1c.2274C= (p.Asn758=)
c.2215C=
c.2238C= (p.Asn746=)
c.1989C= (p.Asn663=)
c.1897C= (n.1897C=)
n.2423C=
c.2247C= (p.Asn749=)
4g.6302033C>GCA356178199WFS1c.2274C>G (p.Asn758Lys)
c.2215C>G
c.2238C>G (p.Asn746Lys)
c.1989C>G (p.Asn663Lys)
c.1897C>G (n.1897C>G)
n.2423C>G
c.2247C>G (p.Asn749Lys)
4g.6302033C>TCA438368767WFS1c.2274C>T (p.Asn758=)
c.2215C>T
c.2238C>T (p.Asn746=)
c.1989C>T (p.Asn663=)
c.1897C>T (n.1897C>T)
n.2423C>T
c.2247C>T (p.Asn749=)
 gnomAD v4
4g.6302034A=CA1435772243WFS1c.2275A= (p.Thr759=)
c.2216A=
c.2239A= (p.Thr747=)
c.1990A= (p.Thr664=)
c.1898A= (n.1898A=)
n.2424A=
c.2248A= (p.Thr750=)
4g.6302034A>CCA356178200WFS1c.2275A>C (p.Thr759Pro)
c.2216A>C
c.2239A>C (p.Thr747Pro)
c.1990A>C (p.Thr664Pro)
c.1898A>C (n.1898A>C)
n.2424A>C
c.2248A>C (p.Thr750Pro)
 dbSNP
4g.6302034A>GCA356178201WFS1c.2275A>G (p.Thr759Ala)
c.2216A>G
c.2239A>G (p.Thr747Ala)
c.1990A>G (p.Thr664Ala)
c.1898A>G (n.1898A>G)
n.2424A>G
c.2248A>G (p.Thr750Ala)
 gnomAD v4
4g.6302034A>TCA356178202WFS1c.2275A>T (p.Thr759Ser)
c.2216A>T
c.2239A>T (p.Thr747Ser)
c.1990A>T (p.Thr664Ser)
c.1898A>T (n.1898A>T)
n.2424A>T
c.2248A>T (p.Thr750Ser)
4g.6302035C>ACA356178203WFS1c.2276C>A (p.Thr759Asn)
c.2217C>A
c.2240C>A (p.Thr747Asn)
c.1991C>A (p.Thr664Asn)
c.1899C>A (n.1899C>A)
n.2425C>A
c.2249C>A (p.Thr750Asn)
4g.6302035C>GCA356178204WFS1c.2276C>G (p.Thr759Ser)
c.2217C>G
c.2240C>G (p.Thr747Ser)
c.1991C>G (p.Thr664Ser)
c.1899C>G (n.1899C>G)
n.2425C>G
c.2249C>G (p.Thr750Ser)
4g.6302035C>TCA356178205WFS1c.2276C>T (p.Thr759Ile)
c.2217C>T
c.2240C>T (p.Thr747Ile)
c.1991C>T (p.Thr664Ile)
c.1899C>T (n.1899C>T)
n.2425C>T
c.2249C>T (p.Thr750Ile)
 gnomAD v4
4g.6302036C>ACA438368772WFS1c.2277C>A (p.Thr759=)
c.2218C>A
c.2241C>A (p.Thr747=)
c.1992C>A (p.Thr664=)
c.1900C>A (n.1900C>A)
n.2426C>A
c.2250C>A (p.Thr750=)
4g.6302036C=CA1435772245WFS1c.2277C= (p.Thr759=)
c.2218C=
c.2241C= (p.Thr747=)
c.1992C= (p.Thr664=)
c.1900C= (n.1900C=)
n.2426C=
c.2250C= (p.Thr750=)
4g.6302036C>GCA438368774WFS1c.2277C>G (p.Thr759=)
c.2218C>G
c.2241C>G (p.Thr747=)
c.1992C>G (p.Thr664=)
c.1900C>G (n.1900C>G)
n.2426C>G
c.2250C>G (p.Thr750=)
4g.6302036C>TCA438368773WFS1c.2277C>T (p.Thr759=)
c.2218C>T
c.2241C>T (p.Thr747=)
c.1992C>T (p.Thr664=)
c.1900C>T (n.1900C>T)
n.2426C>T
c.2250C>T (p.Thr750=)
 dbSNP gnomAD v3 gnomAD v4
4g.6302037T>ACA356178208WFS1c.2278T>A (p.Ser760Thr)
c.2219T>A
c.2242T>A (p.Ser748Thr)
c.1993T>A (p.Ser665Thr)
c.1901T>A (n.1901T>A)
n.2427T>A
c.2251T>A (p.Ser751Thr)
4g.6302037T>CCA356178207WFS1c.2278T>C (p.Ser760Pro)
c.2219T>C
c.2242T>C (p.Ser748Pro)
c.1993T>C (p.Ser665Pro)
c.1901T>C (n.1901T>C)
n.2427T>C
c.2251T>C (p.Ser751Pro)
4g.6302037T>GCA356178206WFS1c.2278T>G (p.Ser760Ala)
c.2219T>G
c.2242T>G (p.Ser748Ala)
c.1993T>G (p.Ser665Ala)
c.1901T>G (n.1901T>G)
n.2427T>G
c.2251T>G (p.Ser751Ala)
4g.6302038C>ACA356178209WFS1c.2279C>A (p.Ser760Tyr)
c.2220C>A
c.2243C>A (p.Ser748Tyr)
c.1994C>A (p.Ser665Tyr)
c.1902C>A (n.1902C>A)
n.2428C>A
c.2252C>A (p.Ser751Tyr)
4g.6302038C=CA1435772247WFS1c.2279C= (p.Ser760=)
c.2220C=
c.2243C= (p.Ser748=)
c.1994C= (p.Ser665=)
c.1902C= (n.1902C=)
n.2428C=
c.2252C= (p.Ser751=)
4g.6302038C>GCA356178210WFS1c.2279C>G (p.Ser760Cys)
c.2220C>G
c.2243C>G (p.Ser748Cys)
c.1994C>G (p.Ser665Cys)
c.1902C>G (n.1902C>G)
n.2428C>G
c.2252C>G (p.Ser751Cys)
4g.6302038C>TCA356178211WFS1c.2279C>T (p.Ser760Phe)
c.2220C>T
c.2243C>T (p.Ser748Phe)
c.1994C>T (p.Ser665Phe)
c.1902C>T (n.1902C>T)
n.2428C>T
c.2252C>T (p.Ser751Phe)
 dbSNP
4g.6302039dupCA2586973648WFS1c.2280dup (p.Thr761HisfsTer10)
c.2221dup
c.2244dup (p.Thr749HisfsTer10)
c.1995dup (p.Thr666HisfsTer10)
c.1903dup (n.1903dup)
n.2429dup
c.2253dup (p.Thr752HisfsTer10)
4g.6302039C>ACA438368780WFS1c.2280C>A (p.Ser760=)
c.2221C>A
c.2244C>A (p.Ser748=)
c.1995C>A (p.Ser665=)
c.1903C>A (n.1903C>A)
n.2429C>A
c.2253C>A (p.Ser751=)
4g.6302039C=CA1435772248WFS1c.2280C= (p.Ser760=)
c.2221C=
c.2244C= (p.Ser748=)
c.1995C= (p.Ser665=)
c.1903C= (n.1903C=)
n.2429C=
c.2253C= (p.Ser751=)
4g.6302039C>GCA438368781WFS1c.2280C>G (p.Ser760=)
c.2221C>G
c.2244C>G (p.Ser748=)
c.1995C>G (p.Ser665=)
c.1903C>G (n.1903C>G)
n.2429C>G
c.2253C>G (p.Ser751=)
4g.6302039C>TCA438368782WFS1c.2280C>T (p.Ser760=)
c.2221C>T
c.2244C>T (p.Ser748=)
c.1995C>T (p.Ser665=)
c.1903C>T (n.1903C>T)
n.2429C>T
c.2253C>T (p.Ser751=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302040A=CA1435772249WFS1c.2281A= (p.Thr761=)
c.2222A=
c.2245A= (p.Thr749=)
c.1996A= (p.Thr666=)
c.1904A= (n.1904A=)
n.2430A=
c.2254A= (p.Thr752=)
4g.6302040A>CCA356178212WFS1c.2281A>C (p.Thr761Pro)
c.2222A>C
c.2245A>C (p.Thr749Pro)
c.1996A>C (p.Thr666Pro)
c.1904A>C (n.1904A>C)
n.2430A>C
c.2254A>C (p.Thr752Pro)
 dbSNP gnomAD v4
4g.6302040A>GCA356178213WFS1c.2281A>G (p.Thr761Ala)
c.2222A>G
c.2245A>G (p.Thr749Ala)
c.1996A>G (p.Thr666Ala)
c.1904A>G (n.1904A>G)
n.2430A>G
c.2254A>G (p.Thr752Ala)
 dbSNP gnomAD v3 gnomAD v4
4g.6302040A>TCA356178214WFS1c.2281A>T (p.Thr761Ser)
c.2222A>T
c.2245A>T (p.Thr749Ser)
c.1996A>T (p.Thr666Ser)
c.1904A>T (n.1904A>T)
n.2430A>T
c.2254A>T (p.Thr752Ser)
4g.6302041C>ACA356178215WFS1c.2282C>A (p.Thr761Lys)
c.2223C>A
c.2246C>A (p.Thr749Lys)
c.1997C>A (p.Thr666Lys)
c.1905C>A (n.1905C>A)
n.2431C>A
c.2255C>A (p.Thr752Lys)
 gnomAD v4
4g.6302041C=CA1435772251WFS1c.2282C= (p.Thr761=)
c.2223C=
c.2246C= (p.Thr749=)
c.1997C= (p.Thr666=)
c.1905C= (n.1905C=)
n.2431C=
c.2255C= (p.Thr752=)
4g.6302041C>GCA2839659WFS1c.2282C>G (p.Thr761Arg)
c.2223C>G
c.2246C>G (p.Thr749Arg)
c.1997C>G (p.Thr666Arg)
c.1905C>G (n.1905C>G)
n.2431C>G
c.2255C>G (p.Thr752Arg)
 dbSNP ExAC gnomAD v3 gnomAD v4
4g.6302041C>TCA2839658WFS1c.2282C>T (p.Thr761Met)
c.2223C>T
c.2246C>T (p.Thr749Met)
c.1997C>T (p.Thr666Met)
c.1905C>T (n.1905C>T)
n.2431C>T
c.2255C>T (p.Thr752Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302042G>ACA282580WFS1c.2283G>A (p.Thr761=)
c.2224G>A
c.2247G>A (p.Thr749=)
c.1998G>A (p.Thr666=)
c.1906G>A (n.1906G>A)
n.2432G>A
c.2256G>A (p.Thr752=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302042G>CCA438368789WFS1c.2283G>C (p.Thr761=)
c.2224G>C
c.2247G>C (p.Thr749=)
c.1998G>C (p.Thr666=)
c.1906G>C (n.1906G>C)
n.2432G>C
c.2256G>C (p.Thr752=)
4g.6302042G=CA1435772253WFS1c.2283G= (p.Thr761=)
c.2224G=
c.2247G= (p.Thr749=)
c.1998G= (p.Thr666=)
c.1906G= (n.1906G=)
n.2432G=
c.2256G= (p.Thr752=)
4g.6302042G>TCA438368790WFS1c.2283G>T (p.Thr761=)
c.2224G>T
c.2247G>T (p.Thr749=)
c.1998G>T (p.Thr666=)
c.1906G>T (n.1906G>T)
n.2432G>T
c.2256G>T (p.Thr752=)
 gnomAD v4
4g.6302043dupCA2669843452WFS1c.2284dup (p.Ala762GlyfsTer9)
c.2225dup
c.2248dup (p.Ala750GlyfsTer9)
c.1999dup (p.Ala667GlyfsTer9)
c.1907dup (n.1907dup)
n.2433dup
c.2257dup (p.Ala753GlyfsTer9)
 gnomAD v4
4g.6302043G>ACA2839660WFS1c.2284G>A (p.Ala762Thr)
c.2225G>A
c.2248G>A (p.Ala750Thr)
c.1999G>A (p.Ala667Thr)
c.1907G>A (n.1907G>A)
n.2433G>A
c.2257G>A (p.Ala753Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302043G>CCA356178216WFS1c.2284G>C (p.Ala762Pro)
c.2225G>C
c.2248G>C (p.Ala750Pro)
c.1999G>C (p.Ala667Pro)
c.1907G>C (n.1907G>C)
n.2433G>C
c.2257G>C (p.Ala753Pro)
4g.6302043G=CA1435772254WFS1c.2284G= (p.Ala762=)
c.2225G=
c.2248G= (p.Ala750=)
c.1999G= (p.Ala667=)
c.1907G= (n.1907G=)
n.2433G=
c.2257G= (p.Ala753=)
4g.6302043G>TCA356178217WFS1c.2284G>T (p.Ala762Ser)
c.2225G>T
c.2248G>T (p.Ala750Ser)
c.1999G>T (p.Ala667Ser)
c.1907G>T (n.1907G>T)
n.2433G>T
c.2257G>T (p.Ala753Ser)
 dbSNP gnomAD v4
4g.6302044C>ACA356178219WFS1c.2285C>A (p.Ala762Asp)
c.2226C>A
c.2249C>A (p.Ala750Asp)
c.2000C>A (p.Ala667Asp)
c.1908C>A (n.1908C>A)
n.2434C>A
c.2258C>A (p.Ala753Asp)
 dbSNP gnomAD v3 gnomAD v4
4g.6302044C=CA1435772255WFS1c.2285C= (p.Ala762=)
c.2226C=
c.2249C= (p.Ala750=)
c.2000C= (p.Ala667=)
c.1908C= (n.1908C=)
n.2434C=
c.2258C= (p.Ala753=)
4g.6302044C>GCA356178220WFS1c.2285C>G (p.Ala762Gly)
c.2226C>G
c.2249C>G (p.Ala750Gly)
c.2000C>G (p.Ala667Gly)
c.1908C>G (n.1908C>G)
n.2434C>G
c.2258C>G (p.Ala753Gly)
4g.6302044C>TCA356178218WFS1c.2285C>T (p.Ala762Val)
c.2226C>T
c.2249C>T (p.Ala750Val)
c.2000C>T (p.Ala667Val)
c.1908C>T (n.1908C>T)
n.2434C>T
c.2258C>T (p.Ala753Val)
 ClinVar
4g.6302045C>ACA438368793WFS1c.2286C>A (p.Ala762=)
c.2227C>A
c.2250C>A (p.Ala750=)
c.2001C>A (p.Ala667=)
c.1909C>A (n.1909C>A)
n.2435C>A
c.2259C>A (p.Ala753=)
 ClinVar dbSNP
4g.6302045C=CA1435772258WFS1c.2286C= (p.Ala762=)
c.2227C=
c.2250C= (p.Ala750=)
c.2001C= (p.Ala667=)
c.1909C= (n.1909C=)
n.2435C=
c.2259C= (p.Ala753=)
4g.6302045C>GCA2839662WFS1c.2286C>G (p.Ala762=)
c.2227C>G
c.2250C>G (p.Ala750=)
c.2001C>G (p.Ala667=)
c.1909C>G (n.1909C>G)
n.2435C>G
c.2259C>G (p.Ala753=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302045C>TCA2839661WFS1c.2286C>T (p.Ala762=)
c.2227C>T
c.2250C>T (p.Ala750=)
c.2001C>T (p.Ala667=)
c.1909C>T (n.1909C>T)
n.2435C>T
c.2259C>T (p.Ala753=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302045_6302048delinsCGAGCA1435772260WFS1c.2286_2289delinsCGAG (p.Ala762=)
c.2227_2230delinsCGAG
c.2250_2253delinsCGAG (p.Ala750=)
c.2001_2004delinsCGAG (p.Ala667=)
c.1909_1912delinsCGAG (n.1909_1912delinsCGAG)
n.2435_2438delinsCGAG
c.2259_2262delinsCGAG (p.Ala753=)
4g.6302046G>ACA2839664WFS1c.2287G>A (p.Glu763Lys)
c.2228G>A
c.2251G>A (p.Glu751Lys)
c.2002G>A (p.Glu668Lys)
c.1910G>A (n.1910G>A)
n.2436G>A
c.2260G>A (p.Glu754Lys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302046G>CCA2839663WFS1c.2287G>C (p.Glu763Gln)
c.2228G>C
c.2251G>C (p.Glu751Gln)
c.2002G>C (p.Glu668Gln)
c.1910G>C (n.1910G>C)
n.2436G>C
c.2260G>C (p.Glu754Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302046G=CA1435772262WFS1c.2287G= (p.Glu763=)
c.2228G=
c.2251G= (p.Glu751=)
c.2002G= (p.Glu668=)
c.1910G= (n.1910G=)
n.2436G=
c.2260G= (p.Glu754=)
4g.6302046G>TCA356178221WFS1c.2287G>T (p.Glu763Ter)
c.2228G>T
c.2251G>T (p.Glu751Ter)
c.2002G>T (p.Glu668Ter)
c.1910G>T (n.1910G>T)
n.2436G>T
c.2260G>T (p.Glu754Ter)
 gnomAD v4
4g.6302052_6302054delCA549707941WFS1c.2293_2295del (p.Glu765del)
c.2234_2236del
c.2257_2259del (p.Glu753del)
c.2008_2010del (p.Glu670del)
c.1916_1918del (n.1916_1918del)
n.2442_2444del
c.2266_2268del (p.Glu756del)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302047A=CA1435772265WFS1c.2288A= (p.Glu763=)
c.2229A=
c.2252A= (p.Glu751=)
c.2003A= (p.Glu668=)
c.1911A= (n.1911A=)
n.2437A=
c.2261A= (p.Glu754=)
4g.6302047A>CCA356178222WFS1c.2288A>C (p.Glu763Ala)
c.2229A>C
c.2252A>C (p.Glu751Ala)
c.2003A>C (p.Glu668Ala)
c.1911A>C (n.1911A>C)
n.2437A>C
c.2261A>C (p.Glu754Ala)
4g.6302047A>GCA356178223WFS1c.2288A>G (p.Glu763Gly)
c.2229A>G
c.2252A>G (p.Glu751Gly)
c.2003A>G (p.Glu668Gly)
c.1911A>G (n.1911A>G)
n.2437A>G
c.2261A>G (p.Glu754Gly)
 dbSNP gnomAD v2 gnomAD v4
4g.6302047A>TCA356178224WFS1c.2288A>T (p.Glu763Val)
c.2229A>T
c.2252A>T (p.Glu751Val)
c.2003A>T (p.Glu668Val)
c.1911A>T (n.1911A>T)
n.2437A>T
c.2261A>T (p.Glu754Val)
 dbSNP gnomAD v3 gnomAD v4
4g.6302048G>ACA438368798WFS1c.2289G>A (p.Glu763=)
c.2230G>A
c.2253G>A (p.Glu751=)
c.2004G>A (p.Glu668=)
c.1912G>A (n.1912G>A)
n.2438G>A
c.2262G>A (p.Glu754=)
4g.6302048G>CCA356178225WFS1c.2289G>C (p.Glu763Asp)
c.2230G>C
c.2253G>C (p.Glu751Asp)
c.2004G>C (p.Glu668Asp)
c.1912G>C (n.1912G>C)
n.2438G>C
c.2262G>C (p.Glu754Asp)
4g.6302048G>TCA356178226WFS1c.2289G>T (p.Glu763Asp)
c.2230G>T
c.2253G>T (p.Glu751Asp)
c.2004G>T (p.Glu668Asp)
c.1912G>T (n.1912G>T)
n.2438G>T
c.2262G>T (p.Glu754Asp)
4g.6302049G>ACA356178227WFS1c.2290G>A (p.Glu764Lys)
c.2231G>A
c.2254G>A (p.Glu752Lys)
c.2005G>A (p.Glu669Lys)
c.1913G>A (n.1913G>A)
n.2439G>A
c.2263G>A (p.Glu755Lys)
4g.6302049G>CCA356178228WFS1c.2290G>C (p.Glu764Gln)
c.2231G>C
c.2254G>C (p.Glu752Gln)
c.2005G>C (p.Glu669Gln)
c.1913G>C (n.1913G>C)
n.2439G>C
c.2263G>C (p.Glu755Gln)
4g.6302049G=CA1435772266WFS1c.2290G= (p.Glu764=)
c.2231G=
c.2254G= (p.Glu752=)
c.2005G= (p.Glu669=)
c.1913G= (n.1913G=)
n.2439G=
c.2263G= (p.Glu755=)
4g.6302049G>TCA319834WFS1c.2290G>T (p.Glu764Ter)
c.2231G>T
c.2254G>T (p.Glu752Ter)
c.2005G>T (p.Glu669Ter)
c.1913G>T (n.1913G>T)
n.2439G>T
c.2263G>T (p.Glu755Ter)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302050A>CCA356178229WFS1c.2291A>C (p.Glu764Ala)
c.2232A>C
c.2255A>C (p.Glu752Ala)
c.2006A>C (p.Glu669Ala)
c.1914A>C (n.1914A>C)
n.2440A>C
c.2264A>C (p.Glu755Ala)
4g.6302050A>GCA356178231WFS1c.2291A>G (p.Glu764Gly)
c.2232A>G
c.2255A>G (p.Glu752Gly)
c.2006A>G (p.Glu669Gly)
c.1914A>G (n.1914A>G)
n.2440A>G
c.2264A>G (p.Glu755Gly)
4g.6302050A>TCA356178230WFS1c.2291A>T (p.Glu764Val)
c.2232A>T
c.2255A>T (p.Glu752Val)
c.2006A>T (p.Glu669Val)
c.1914A>T (n.1914A>T)
n.2440A>T
c.2264A>T (p.Glu755Val)
4g.6302051G>ACA438368804WFS1c.2292G>A (p.Glu764=)
c.2233G>A
c.2256G>A (p.Glu752=)
c.2007G>A (p.Glu669=)
c.1915G>A (n.1915G>A)
n.2441G>A
c.2265G>A (p.Glu755=)
4g.6302051G>CCA356178232WFS1c.2292G>C (p.Glu764Asp)
c.2233G>C
c.2256G>C (p.Glu752Asp)
c.2007G>C (p.Glu669Asp)
c.1915G>C (n.1915G>C)
n.2441G>C
c.2265G>C (p.Glu755Asp)
4g.6302051G=CA1435772267WFS1c.2292G= (p.Glu764=)
c.2233G=
c.2256G= (p.Glu752=)
c.2007G= (p.Glu669=)
c.1915G= (n.1915G=)
n.2441G=
c.2265G= (p.Glu755=)
4g.6302051G>TCA356178233WFS1c.2292G>T (p.Glu764Asp)
c.2233G>T
c.2256G>T (p.Glu752Asp)
c.2007G>T (p.Glu669Asp)
c.1915G>T (n.1915G>T)
n.2441G>T
c.2265G>T (p.Glu755Asp)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6302052G>ACA356178234WFS1c.2293G>A (p.Glu765Lys)
c.2234G>A
c.2257G>A (p.Glu753Lys)
c.2008G>A (p.Glu670Lys)
c.1916G>A (n.1916G>A)
n.2442G>A
c.2266G>A (p.Glu756Lys)
 dbSNP COSMIC
4g.6302052G>CCA356178235WFS1c.2293G>C (p.Glu765Gln)
c.2234G>C
c.2257G>C (p.Glu753Gln)
c.2008G>C (p.Glu670Gln)
c.1916G>C (n.1916G>C)
n.2442G>C
c.2266G>C (p.Glu756Gln)
 dbSNP gnomAD v2 gnomAD v4
4g.6302052G=CA1435772269WFS1c.2293G= (p.Glu765=)
c.2234G=
c.2257G= (p.Glu753=)
c.2008G= (p.Glu670=)
c.1916G= (n.1916G=)
n.2442G=
c.2266G= (p.Glu756=)
4g.6302052G>TCA356178236WFS1c.2293G>T (p.Glu765Ter)
c.2234G>T
c.2257G>T (p.Glu753Ter)
c.2008G>T (p.Glu670Ter)
c.1916G>T (n.1916G>T)
n.2442G>T
c.2266G>T (p.Glu756Ter)
 gnomAD v4
4g.6302053A>CCA356178237WFS1c.2294A>C (p.Glu765Ala)
c.2235A>C
c.2258A>C (p.Glu753Ala)
c.2009A>C (p.Glu670Ala)
c.1917A>C (n.1917A>C)
n.2443A>C
c.2267A>C (p.Glu756Ala)
 gnomAD v4
4g.6302053A>GCA356178238WFS1c.2294A>G (p.Glu765Gly)
c.2235A>G
c.2258A>G (p.Glu753Gly)
c.2009A>G (p.Glu670Gly)
c.1917A>G (n.1917A>G)
n.2443A>G
c.2267A>G (p.Glu756Gly)
4g.6302053A>TCA356178239WFS1c.2294A>T (p.Glu765Val)
c.2235A>T
c.2258A>T (p.Glu753Val)
c.2009A>T (p.Glu670Val)
c.1917A>T (n.1917A>T)
n.2443A>T
c.2267A>T (p.Glu756Val)
4g.6302054G>ACA438368808WFS1c.2295G>A (p.Glu765=)
c.2236G>A
c.2259G>A (p.Glu753=)
c.2010G>A (p.Glu670=)
c.1918G>A (n.1918G>A)
n.2444G>A
c.2268G>A (p.Glu756=)
4g.6302054G>CCA91796991WFS1c.2295G>C (p.Glu765Asp)
c.2236G>C
c.2259G>C (p.Glu753Asp)
c.2010G>C (p.Glu670Asp)
c.1918G>C (n.1918G>C)
n.2444G>C
c.2268G>C (p.Glu756Asp)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302054G=CA1435772271WFS1c.2295G= (p.Glu765=)
c.2236G=
c.2259G= (p.Glu753=)
c.2010G= (p.Glu670=)
c.1918G= (n.1918G=)
n.2444G=
c.2268G= (p.Glu756=)
4g.6302054G>TCA356178240WFS1c.2295G>T (p.Glu765Asp)
c.2236G>T
c.2259G>T (p.Glu753Asp)
c.2010G>T (p.Glu670Asp)
c.1918G>T (n.1918G>T)
n.2444G>T
c.2268G>T (p.Glu756Asp)
4g.6302055C>ACA356178243WFS1c.2296C>A (p.Leu766Ile)
c.2237C>A
c.2260C>A (p.Leu754Ile)
c.2011C>A (p.Leu671Ile)
c.1919C>A (n.1919C>A)
n.2445C>A
c.2269C>A (p.Leu757Ile)
4g.6302055C=CA1435772273WFS1c.2296C= (p.Leu766=)
c.2237C=
c.2260C= (p.Leu754=)
c.2011C= (p.Leu671=)
c.1919C= (n.1919C=)
n.2445C=
c.2269C= (p.Leu757=)
4g.6302055C>GCA356178242WFS1c.2296C>G (p.Leu766Val)
c.2237C>G
c.2260C>G (p.Leu754Val)
c.2011C>G (p.Leu671Val)
c.1919C>G (n.1919C>G)
n.2445C>G
c.2269C>G (p.Leu757Val)
4g.6302055C>TCA356178241WFS1c.2296C>T (p.Leu766Phe)
c.2237C>T
c.2260C>T (p.Leu754Phe)
c.2011C>T (p.Leu671Phe)
c.1919C>T (n.1919C>T)
n.2445C>T
c.2269C>T (p.Leu757Phe)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302057_6302058delCA2586973649WFS1c.2298_2299del (p.Cys767SerfsTer3)
c.2239_2240del
c.2262_2263del (p.Cys755SerfsTer3)
c.2013_2014del (p.Cys672SerfsTer3)
c.1921_1922del (n.1921_1922del)
n.2447_2448del
c.2271_2272del (p.Cys758SerfsTer3)
 gnomAD v4
4g.6302056T>ACA356178245WFS1c.2297T>A (p.Leu766His)
c.2238T>A
c.2261T>A (p.Leu754His)
c.2012T>A (p.Leu671His)
c.1920T>A (n.1920T>A)
n.2446T>A
c.2270T>A (p.Leu757His)
4g.6302056T>CCA356178244WFS1c.2297T>C (p.Leu766Pro)
c.2238T>C
c.2261T>C (p.Leu754Pro)
c.2012T>C (p.Leu671Pro)
c.1920T>C (n.1920T>C)
n.2446T>C
c.2270T>C (p.Leu757Pro)
4g.6302056T>GCA356178246WFS1c.2297T>G (p.Leu766Arg)
c.2238T>G
c.2261T>G (p.Leu754Arg)
c.2012T>G (p.Leu671Arg)
c.1920T>G (n.1920T>G)
n.2446T>G
c.2270T>G (p.Leu757Arg)
4g.6302057C>ACA438368818WFS1c.2298C>A (p.Leu766=)
c.2239C>A
c.2262C>A (p.Leu754=)
c.2013C>A (p.Leu671=)
c.1921C>A (n.1921C>A)
n.2447C>A
c.2271C>A (p.Leu757=)
4g.6302057C=CA1435772274WFS1c.2298C= (p.Leu766=)
c.2239C=
c.2262C= (p.Leu754=)
c.2013C= (p.Leu671=)
c.1921C= (n.1921C=)
n.2447C=
c.2271C= (p.Leu757=)
4g.6302057C>GCA438368813WFS1c.2298C>G (p.Leu766=)
c.2239C>G
c.2262C>G (p.Leu754=)
c.2013C>G (p.Leu671=)
c.1921C>G (n.1921C>G)
n.2447C>G
c.2271C>G (p.Leu757=)
 dbSNP gnomAD v3 gnomAD v4
4g.6302057C>TCA438368814WFS1c.2298C>T (p.Leu766=)
c.2239C>T
c.2262C>T (p.Leu754=)
c.2013C>T (p.Leu671=)
c.1921C>T (n.1921C>T)
n.2447C>T
c.2271C>T (p.Leu757=)
 ClinVar dbSNP
4g.6302058T>ACA356178247WFS1c.2299T>A (p.Cys767Ser)
c.2240T>A
c.2263T>A (p.Cys755Ser)
c.2014T>A (p.Cys672Ser)
c.1922T>A (n.1922T>A)
n.2448T>A
c.2272T>A (p.Cys758Ser)
 gnomAD v4
4g.6302058T>CCA276183WFS1c.2299T>C (p.Cys767Arg)
c.2240T>C
c.2263T>C (p.Cys755Arg)
c.2014T>C (p.Cys672Arg)
c.1922T>C (n.1922T>C)
n.2448T>C
c.2272T>C (p.Cys758Arg)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6302058T>GCA356178248WFS1c.2299T>G (p.Cys767Gly)
c.2240T>G
c.2263T>G (p.Cys755Gly)
c.2014T>G (p.Cys672Gly)
c.1922T>G (n.1922T>G)
n.2448T>G
c.2272T>G (p.Cys758Gly)
4g.6302058T=CA1435772277WFS1c.2299T= (p.Cys767=)
c.2240T=
c.2263T= (p.Cys755=)
c.2014T= (p.Cys672=)
c.1922T= (n.1922T=)
n.2448T=
c.2272T= (p.Cys758=)
4g.6302059G>ACA356178249WFS1c.2300G>A (p.Cys767Tyr)
c.2241G>A
c.2264G>A (p.Cys755Tyr)
c.2015G>A (p.Cys672Tyr)
c.1923G>A (n.1923G>A)
n.2449G>A
c.2273G>A (p.Cys758Tyr)
4g.6302059G>CCA356178250WFS1c.2300G>C (p.Cys767Ser)
c.2241G>C
c.2264G>C (p.Cys755Ser)
c.2015G>C (p.Cys672Ser)
c.1923G>C (n.1923G>C)
n.2449G>C
c.2273G>C (p.Cys758Ser)
4g.6302059G>TCA356178251WFS1c.2300G>T (p.Cys767Phe)
c.2241G>T
c.2264G>T (p.Cys755Phe)
c.2015G>T (p.Cys672Phe)
c.1923G>T (n.1923G>T)
n.2449G>T
c.2273G>T (p.Cys758Phe)
4g.6302060T>ACA356178253WFS1c.2301T>A (p.Cys767Ter)
c.2242T>A
c.2265T>A (p.Cys755Ter)
c.2016T>A (p.Cys672Ter)
c.1924T>A (n.1924T>A)
n.2450T>A
c.2274T>A (p.Cys758Ter)
4g.6302060T>CCA438368824WFS1c.2301T>C (p.Cys767=)
c.2242T>C
c.2265T>C (p.Cys755=)
c.2016T>C (p.Cys672=)
c.1924T>C (n.1924T>C)
n.2450T>C
c.2274T>C (p.Cys758=)
4g.6302060T>GCA356178252WFS1c.2301T>G (p.Cys767Trp)
c.2242T>G
c.2265T>G (p.Cys755Trp)
c.2016T>G (p.Cys672Trp)
c.1924T>G (n.1924T>G)
n.2450T>G
c.2274T>G (p.Cys758Trp)
4g.6302061C>ACA356178254WFS1c.2302C>A (p.Arg768Ser)
c.2243C>A
c.2266C>A (p.Arg756Ser)
c.2017C>A (p.Arg673Ser)
c.1925C>A (n.1925C>A)
n.2451C>A
c.2275C>A (p.Arg759Ser)
 dbSNP gnomAD v2
4g.6302061C=CA1435772279WFS1c.2302C= (p.Arg768=)
c.2243C=
c.2266C= (p.Arg756=)
c.2017C= (p.Arg673=)
c.1925C= (n.1925C=)
n.2451C=
c.2275C= (p.Arg759=)
4g.6302061C>GCA356178255WFS1c.2302C>G (p.Arg768Gly)
c.2243C>G
c.2266C>G (p.Arg756Gly)
c.2017C>G (p.Arg673Gly)
c.1925C>G (n.1925C>G)
n.2451C>G
c.2275C>G (p.Arg759Gly)
4g.6302061C>TCA2839665WFS1c.2302C>T (p.Arg768Cys)
c.2243C>T
c.2266C>T (p.Arg756Cys)
c.2017C>T (p.Arg673Cys)
c.1925C>T (n.1925C>T)
n.2451C>T
c.2275C>T (p.Arg759Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302062G>ACA91796996WFS1c.2303G>A (p.Arg768His)
c.2244G>A
c.2267G>A (p.Arg756His)
c.2018G>A (p.Arg673His)
c.1926G>A (n.1926G>A)
n.2452G>A
c.2276G>A (p.Arg759His)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302062G>CCA356178256WFS1c.2303G>C (p.Arg768Pro)
c.2244G>C
c.2267G>C (p.Arg756Pro)
c.2018G>C (p.Arg673Pro)
c.1926G>C (n.1926G>C)
n.2452G>C
c.2276G>C (p.Arg759Pro)
 dbSNP
4g.6302062G=CA1435772280WFS1c.2303G= (p.Arg768=)
c.2244G=
c.2267G= (p.Arg756=)
c.2018G= (p.Arg673=)
c.1926G= (n.1926G=)
n.2452G=
c.2276G= (p.Arg759=)
4g.6302062G>TCA356178257WFS1c.2303G>T (p.Arg768Leu)
c.2244G>T
c.2267G>T (p.Arg756Leu)
c.2018G>T (p.Arg673Leu)
c.1926G>T (n.1926G>T)
n.2452G>T
c.2276G>T (p.Arg759Leu)
4g.6302063C>ACA438368841WFS1c.2304C>A (p.Arg768=)
c.2245C>A
c.2268C>A (p.Arg756=)
c.2019C>A (p.Arg673=)
c.1927C>A (n.1927C>A)
n.2453C>A
c.2277C>A (p.Arg759=)
4g.6302063C>GCA438368838WFS1c.2304C>G (p.Arg768=)
c.2245C>G
c.2268C>G (p.Arg756=)
c.2019C>G (p.Arg673=)
c.1927C>G (n.1927C>G)
n.2453C>G
c.2277C>G (p.Arg759=)
 gnomAD v4
4g.6302063C>TCA438368840WFS1c.2304C>T (p.Arg768=)
c.2245C>T
c.2268C>T (p.Arg756=)
c.2019C>T (p.Arg673=)
c.1927C>T (n.1927C>T)
n.2453C>T
c.2277C>T (p.Arg759=)
 ClinVar gnomAD v4
4g.6302064C>ACA2839666WFS1c.2305C>A (p.Leu769Ile)
c.2246C>A
c.2269C>A (p.Leu757Ile)
c.2020C>A (p.Leu674Ile)
c.1928C>A (n.1928C>A)
n.2454C>A
c.2278C>A (p.Leu760Ile)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302064C=CA1435772282WFS1c.2305C= (p.Leu769=)
c.2246C=
c.2269C= (p.Leu757=)
c.2020C= (p.Leu674=)
c.1928C= (n.1928C=)
n.2454C=
c.2278C= (p.Leu760=)
4g.6302064C>GCA356178259WFS1c.2305C>G (p.Leu769Val)
c.2246C>G
c.2269C>G (p.Leu757Val)
c.2020C>G (p.Leu674Val)
c.1928C>G (n.1928C>G)
n.2454C>G
c.2278C>G (p.Leu760Val)
 dbSNP gnomAD v2 gnomAD v4
4g.6302064C>TCA356178258WFS1c.2305C>T (p.Leu769Phe)
c.2246C>T
c.2269C>T (p.Leu757Phe)
c.2020C>T (p.Leu674Phe)
c.1928C>T (n.1928C>T)
n.2454C>T
c.2278C>T (p.Leu760Phe)
 dbSNP gnomAD v4
4g.6302066_6302112dupCA2669843454WFS1c.2307_2353dup (p.Tyr785LeufsTer?)
c.2248_2294dup
c.2271_2317dup (p.Tyr773LeufsTer?)
c.2022_2068dup (p.Tyr690LeufsTer?)
c.1930_1976dup (n.1930_1976dup)
n.2456_2502dup
c.2280_2326dup (p.Tyr776LeufsTer?)
 gnomAD v4
4g.6302065T>ACA356178260WFS1c.2306T>A (p.Leu769His)
c.2247T>A
c.2270T>A (p.Leu757His)
c.2021T>A (p.Leu674His)
c.1929T>A (n.1929T>A)
n.2455T>A
c.2279T>A (p.Leu760His)
4g.6302065T>CCA356178261WFS1c.2306T>C (p.Leu769Pro)
c.2247T>C
c.2270T>C (p.Leu757Pro)
c.2021T>C (p.Leu674Pro)
c.1929T>C (n.1929T>C)
n.2455T>C
c.2279T>C (p.Leu760Pro)
4g.6302065T>GCA356178262WFS1c.2306T>G (p.Leu769Arg)
c.2247T>G
c.2270T>G (p.Leu757Arg)
c.2021T>G (p.Leu674Arg)
c.1929T>G (n.1929T>G)
n.2455T>G
c.2279T>G (p.Leu760Arg)
 gnomAD v4
4g.6302066T>ACA438368845WFS1c.2307T>A (p.Leu769=)
c.2248T>A
c.2271T>A (p.Leu757=)
c.2022T>A (p.Leu674=)
c.1930T>A (n.1930T>A)
n.2456T>A
c.2280T>A (p.Leu760=)
4g.6302066T>CCA438368846WFS1c.2307T>C (p.Leu769=)
c.2248T>C
c.2271T>C (p.Leu757=)
c.2022T>C (p.Leu674=)
c.1930T>C (n.1930T>C)
n.2456T>C
c.2280T>C (p.Leu760=)
4g.6302066T>GCA438368848WFS1c.2307T>G (p.Leu769=)
c.2248T>G
c.2271T>G (p.Leu757=)
c.2022T>G (p.Leu674=)
c.1930T>G (n.1930T>G)
n.2456T>G
c.2280T>G (p.Leu760=)
 gnomAD v4
4g.6302067A>CCA356178263WFS1c.2308A>C (p.Lys770Gln)
c.2249A>C
c.2272A>C (p.Lys758Gln)
c.2023A>C (p.Lys675Gln)
c.1931A>C (n.1931A>C)
n.2457A>C
c.2281A>C (p.Lys761Gln)
 gnomAD v4
4g.6302067A>GCA356178264WFS1c.2308A>G (p.Lys770Glu)
c.2249A>G
c.2272A>G (p.Lys758Glu)
c.2023A>G (p.Lys675Glu)
c.1931A>G (n.1931A>G)
n.2457A>G
c.2281A>G (p.Lys761Glu)
 dbSNP gnomAD v4
4g.6302067A>TCA356178265WFS1c.2308A>T (p.Lys770Ter)
c.2249A>T
c.2272A>T (p.Lys758Ter)
c.2023A>T (p.Lys675Ter)
c.1931A>T (n.1931A>T)
n.2457A>T
c.2281A>T (p.Lys761Ter)
4g.6302068A=CA1435772284WFS1c.2309A= (p.Lys770=)
c.2250A=
c.2273A= (p.Lys758=)
c.2024A= (p.Lys675=)
c.1932A= (n.1932A=)
n.2458A=
c.2282A= (p.Lys761=)
4g.6302068A>CCA356178266WFS1c.2309A>C (p.Lys770Thr)
c.2250A>C
c.2273A>C (p.Lys758Thr)
c.2024A>C (p.Lys675Thr)
c.1932A>C (n.1932A>C)
n.2458A>C
c.2282A>C (p.Lys761Thr)
4g.6302068A>GCA356178267WFS1c.2309A>G (p.Lys770Arg)
c.2250A>G
c.2273A>G (p.Lys758Arg)
c.2024A>G (p.Lys675Arg)
c.1932A>G (n.1932A>G)
n.2458A>G
c.2282A>G (p.Lys761Arg)
 ClinVar
4g.6302068A>TCA356178268WFS1c.2309A>T (p.Lys770Met)
c.2250A>T
c.2273A>T (p.Lys758Met)
c.2024A>T (p.Lys675Met)
c.1932A>T (n.1932A>T)
n.2458A>T
c.2282A>T (p.Lys761Met)
 ClinVar dbSNP gnomAD v4
4g.6302069G>ACA438368852WFS1c.2310G>A (p.Lys770=)
c.2251G>A
c.2274G>A (p.Lys758=)
c.2025G>A (p.Lys675=)
c.1933G>A (n.1933G>A)
n.2459G>A
c.2283G>A (p.Lys761=)
4g.6302069G>CCA356178269WFS1c.2310G>C (p.Lys770Asn)
c.2251G>C
c.2274G>C (p.Lys758Asn)
c.2025G>C (p.Lys675Asn)
c.1933G>C (n.1933G>C)
n.2459G>C
c.2283G>C (p.Lys761Asn)
4g.6302069G>TCA356178270WFS1c.2310G>T (p.Lys770Asn)
c.2251G>T
c.2274G>T (p.Lys758Asn)
c.2025G>T (p.Lys675Asn)
c.1933G>T (n.1933G>T)
n.2459G>T
c.2283G>T (p.Lys761Asn)
4g.6302070C>ACA356178271WFS1c.2311C>A (p.Leu771Met)
c.2252C>A
c.2275C>A (p.Leu759Met)
c.2026C>A (p.Leu676Met)
c.1934C>A (n.1934C>A)
n.2460C>A
c.2284C>A (p.Leu762Met)
4g.6302070C=CA1435772285WFS1c.2311C= (p.Leu771=)
c.2252C=
c.2275C= (p.Leu759=)
c.2026C= (p.Leu676=)
c.1934C= (n.1934C=)
n.2460C=
c.2284C= (p.Leu762=)
4g.6302070C>GCA2839667WFS1c.2311C>G (p.Leu771Val)
c.2252C>G
c.2275C>G (p.Leu759Val)
c.2026C>G (p.Leu676Val)
c.1934C>G (n.1934C>G)
n.2460C>G
c.2284C>G (p.Leu762Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302070C>TCA438368856WFS1c.2311C>T (p.Leu771=)
c.2252C>T
c.2275C>T (p.Leu759=)
c.2026C>T (p.Leu676=)
c.1934C>T (n.1934C>T)
n.2460C>T
c.2284C>T (p.Leu762=)
 ClinVar
4g.6302071T>ACA2839668WFS1c.2312T>A (p.Leu771Gln)
c.2253T>A
c.2276T>A (p.Leu759Gln)
c.2027T>A (p.Leu676Gln)
c.1935T>A (n.1935T>A)
n.2461T>A
c.2285T>A (p.Leu762Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302071T>CCA356178272WFS1c.2312T>C (p.Leu771Pro)
c.2253T>C
c.2276T>C (p.Leu759Pro)
c.2027T>C (p.Leu676Pro)
c.1935T>C (n.1935T>C)
n.2461T>C
c.2285T>C (p.Leu762Pro)
4g.6302071T>GCA356178273WFS1c.2312T>G (p.Leu771Arg)
c.2253T>G
c.2276T>G (p.Leu759Arg)
c.2027T>G (p.Leu676Arg)
c.1935T>G (n.1935T>G)
n.2461T>G
c.2285T>G (p.Leu762Arg)
4g.6302071T=CA1435772287WFS1c.2312T= (p.Leu771=)
c.2253T=
c.2276T= (p.Leu759=)
c.2027T= (p.Leu676=)
c.1935T= (n.1935T=)
n.2461T=
c.2285T= (p.Leu762=)
4g.6302072G>ACA438368236WFS1c.2313G>A (p.Leu771=)
c.2254G>A
c.2277G>A (p.Leu759=)
c.2028G>A (p.Leu676=)
c.1936G>A (n.1936G>A)
n.2462G>A
c.2286G>A (p.Leu762=)
 dbSNP gnomAD v2
4g.6302072G>CCA438368237WFS1c.2313G>C (p.Leu771=)
c.2254G>C
c.2277G>C (p.Leu759=)
c.2028G>C (p.Leu676=)
c.1936G>C (n.1936G>C)
n.2462G>C
c.2286G>C (p.Leu762=)
 gnomAD v4
4g.6302072G=CA1435772289WFS1c.2313G= (p.Leu771=)
c.2254G=
c.2277G= (p.Leu759=)
c.2028G= (p.Leu676=)
c.1936G= (n.1936G=)
n.2462G=
c.2286G= (p.Leu762=)
4g.6302072G>TCA438368238WFS1c.2313G>T (p.Leu771=)
c.2254G>T
c.2277G>T (p.Leu759=)
c.2028G>T (p.Leu676=)
c.1936G>T (n.1936G>T)
n.2462G>T
c.2286G>T (p.Leu762=)
4g.6302073C>ACA356178274WFS1c.2314C>A (p.Leu772Met)
c.2255C>A
c.2278C>A (p.Leu760Met)
c.2029C>A (p.Leu677Met)
c.1937C>A (n.1937C>A)
n.2463C>A
c.2287C>A (p.Leu763Met)
 ClinVar dbSNP gnomAD v4
4g.6302073C=CA1435772291WFS1c.2314C= (p.Leu772=)
c.2255C=
c.2278C= (p.Leu760=)
c.2029C= (p.Leu677=)
c.1937C= (n.1937C=)
n.2463C=
c.2287C= (p.Leu763=)
4g.6302073C>GCA356178275WFS1c.2314C>G (p.Leu772Val)
c.2255C>G
c.2278C>G (p.Leu760Val)
c.2029C>G (p.Leu677Val)
c.1937C>G (n.1937C>G)
n.2463C>G
c.2287C>G (p.Leu763Val)
4g.6302073C>TCA438368239WFS1c.2314C>T (p.Leu772=)
c.2255C>T
c.2278C>T (p.Leu760=)
c.2029C>T (p.Leu677=)
c.1937C>T (n.1937C>T)
n.2463C>T
c.2287C>T (p.Leu763=)
 gnomAD v4
4g.6302074T>ACA356178276WFS1c.2315T>A (p.Leu772Gln)
c.2256T>A
c.2279T>A (p.Leu760Gln)
c.2030T>A (p.Leu677Gln)
c.1938T>A (n.1938T>A)
n.2464T>A
c.2288T>A (p.Leu763Gln)
4g.6302074T>CCA356178277WFS1c.2315T>C (p.Leu772Pro)
c.2256T>C
c.2279T>C (p.Leu760Pro)
c.2030T>C (p.Leu677Pro)
c.1938T>C (n.1938T>C)
n.2464T>C
c.2288T>C (p.Leu763Pro)
 gnomAD v4
4g.6302074T>GCA356178278WFS1c.2315T>G (p.Leu772Arg)
c.2256T>G
c.2279T>G (p.Leu760Arg)
c.2030T>G (p.Leu677Arg)
c.1938T>G (n.1938T>G)
n.2464T>G
c.2288T>G (p.Leu763Arg)
 dbSNP gnomAD v2 gnomAD v4
4g.6302074T=CA1435772293WFS1c.2315T= (p.Leu772=)
c.2256T=
c.2279T= (p.Leu760=)
c.2030T= (p.Leu677=)
c.1938T= (n.1938T=)
n.2464T=
c.2288T= (p.Leu763=)
4g.6302075G>ACA2839669WFS1c.2316G>A (p.Leu772=)
c.2257G>A
c.2280G>A (p.Leu760=)
c.2031G>A (p.Leu677=)
c.1939G>A (n.1939G>A)
n.2465G>A
c.2289G>A (p.Leu763=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302075G>CCA438368240WFS1c.2316G>C (p.Leu772=)
c.2257G>C
c.2280G>C (p.Leu760=)
c.2031G>C (p.Leu677=)
c.1939G>C (n.1939G>C)
n.2465G>C
c.2289G>C (p.Leu763=)
 dbSNP
4g.6302075G=CA1435772294WFS1c.2316G= (p.Leu772=)
c.2257G=
c.2280G= (p.Leu760=)
c.2031G= (p.Leu677=)
c.1939G= (n.1939G=)
n.2465G=
c.2289G= (p.Leu763=)
4g.6302075G>TCA438368241WFS1c.2316G>T (p.Leu772=)
c.2257G>T
c.2280G>T (p.Leu760=)
c.2031G>T (p.Leu677=)
c.1939G>T (n.1939G>T)
n.2465G>T
c.2289G>T (p.Leu763=)
 gnomAD v4
4g.6302076G>ACA356178279WFS1c.2317G>A (p.Ala773Thr)
c.2258G>A
c.2281G>A (p.Ala761Thr)
c.2032G>A (p.Ala678Thr)
c.1940G>A (n.1940G>A)
n.2466G>A
c.2290G>A (p.Ala764Thr)
 gnomAD v4
4g.6302076G>CCA356178280WFS1c.2317G>C (p.Ala773Pro)
c.2258G>C
c.2281G>C (p.Ala761Pro)
c.2032G>C (p.Ala678Pro)
c.1940G>C (n.1940G>C)
n.2466G>C
c.2290G>C (p.Ala764Pro)
4g.6302076G>TCA356178281WFS1c.2317G>T (p.Ala773Ser)
c.2258G>T
c.2281G>T (p.Ala761Ser)
c.2032G>T (p.Ala678Ser)
c.1940G>T (n.1940G>T)
n.2466G>T
c.2290G>T (p.Ala764Ser)
4g.6302077C>ACA356178283WFS1c.2318C>A (p.Ala773Asp)
c.2259C>A
c.2282C>A (p.Ala761Asp)
c.2033C>A (p.Ala678Asp)
c.1941C>A (n.1941C>A)
n.2467C>A
c.2291C>A (p.Ala764Asp)
4g.6302077C=CA1435772295WFS1c.2318C= (p.Ala773=)
c.2259C=
c.2282C= (p.Ala761=)
c.2033C= (p.Ala678=)
c.1941C= (n.1941C=)
n.2467C=
c.2291C= (p.Ala764=)
4g.6302077C>GCA356178282WFS1c.2318C>G (p.Ala773Gly)
c.2259C>G
c.2282C>G (p.Ala761Gly)
c.2033C>G (p.Ala678Gly)
c.1941C>G (n.1941C>G)
n.2467C>G
c.2291C>G (p.Ala764Gly)
4g.6302077C>TCA91797005WFS1c.2318C>T (p.Ala773Val)
c.2259C>T
c.2282C>T (p.Ala761Val)
c.2033C>T (p.Ala678Val)
c.1941C>T (n.1941C>T)
n.2467C>T
c.2291C>T (p.Ala764Val)
 ClinVar dbSNP gnomAD v4
4g.6302078C>ACA438368242WFS1c.2319C>A (p.Ala773=)
c.2260C>A
c.2283C>A (p.Ala761=)
c.2034C>A (p.Ala678=)
c.1942C>A (n.1942C>A)
n.2468C>A
c.2292C>A (p.Ala764=)
4g.6302078C=CA1435772296WFS1c.2319C= (p.Ala773=)
c.2260C=
c.2283C= (p.Ala761=)
c.2034C= (p.Ala678=)
c.1942C= (n.1942C=)
n.2468C=
c.2292C= (p.Ala764=)
4g.6302078C>GCA438368243WFS1c.2319C>G (p.Ala773=)
c.2260C>G
c.2283C>G (p.Ala761=)
c.2034C>G (p.Ala678=)
c.1942C>G (n.1942C>G)
n.2468C>G
c.2292C>G (p.Ala764=)
 gnomAD v4
4g.6302078C>TCA2839670WFS1c.2319C>T (p.Ala773=)
c.2260C>T
c.2283C>T (p.Ala761=)
c.2034C>T (p.Ala678=)
c.1942C>T (n.1942C>T)
n.2468C>T
c.2292C>T (p.Ala764=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302079A=CA1435772298WFS1c.2320A= (p.Lys774=)
c.2261A=
c.2284A= (p.Lys762=)
c.2035A= (p.Lys679=)
c.1943A= (n.1943A=)
n.2469A=
c.2293A= (p.Lys765=)
4g.6302079A>CCA356178284WFS1c.2320A>C (p.Lys774Gln)
c.2261A>C
c.2284A>C (p.Lys762Gln)
c.2035A>C (p.Lys679Gln)
c.1943A>C (n.1943A>C)
n.2469A>C
c.2293A>C (p.Lys765Gln)
4g.6302079A>GCA2839671WFS1c.2320A>G (p.Lys774Glu)
c.2261A>G
c.2284A>G (p.Lys762Glu)
c.2035A>G (p.Lys679Glu)
c.1943A>G (n.1943A>G)
n.2469A>G
c.2293A>G (p.Lys765Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302079A>TCA356178285WFS1c.2320A>T (p.Lys774Ter)
c.2261A>T
c.2284A>T (p.Lys762Ter)
c.2035A>T (p.Lys679Ter)
c.1943A>T (n.1943A>T)
n.2469A>T
c.2293A>T (p.Lys765Ter)
4g.6302080A=CA1435772301WFS1c.2321A= (p.Lys774=)
c.2262A=
c.2285A= (p.Lys762=)
c.2036A= (p.Lys679=)
c.1944A= (n.1944A=)
n.2470A=
c.2294A= (p.Lys765=)
4g.6302080A>CCA356178286WFS1c.2321A>C (p.Lys774Thr)
c.2262A>C
c.2285A>C (p.Lys762Thr)
c.2036A>C (p.Lys679Thr)
c.1944A>C (n.1944A>C)
n.2470A>C
c.2294A>C (p.Lys765Thr)
4g.6302080A>GCA10576640WFS1c.2321A>G (p.Lys774Arg)
c.2262A>G
c.2285A>G (p.Lys762Arg)
c.2036A>G (p.Lys679Arg)
c.1944A>G (n.1944A>G)
n.2470A>G
c.2294A>G (p.Lys765Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6302080A>TCA356178287WFS1c.2321A>T (p.Lys774Met)
c.2262A>T
c.2285A>T (p.Lys762Met)
c.2036A>T (p.Lys679Met)
c.1944A>T (n.1944A>T)
n.2470A>T
c.2294A>T (p.Lys765Met)
4g.6302081G>ACA2839672WFS1c.2322G>A (p.Lys774=)
c.2263G>A
c.2286G>A (p.Lys762=)
c.2037G>A (p.Lys679=)
c.1945G>A (n.1945G>A)
n.2471G>A
c.2295G>A (p.Lys765=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302081G>CCA356178288WFS1c.2322G>C (p.Lys774Asn)
c.2263G>C
c.2286G>C (p.Lys762Asn)
c.2037G>C (p.Lys679Asn)
c.1945G>C (n.1945G>C)
n.2471G>C
c.2295G>C (p.Lys765Asn)
4g.6302081G=CA1435772303WFS1c.2322G= (p.Lys774=)
c.2263G=
c.2286G= (p.Lys762=)
c.2037G= (p.Lys679=)
c.1945G= (n.1945G=)
n.2471G=
c.2295G= (p.Lys765=)
4g.6302081G>TCA356178289WFS1c.2322G>T (p.Lys774Asn)
c.2263G>T
c.2286G>T (p.Lys762Asn)
c.2037G>T (p.Lys679Asn)
c.1945G>T (n.1945G>T)
n.2471G>T
c.2295G>T (p.Lys765Asn)
 dbSNP
4g.6302082C>ACA356178290WFS1c.2323C>A (p.His775Asn)
c.2264C>A
c.2287C>A (p.His763Asn)
c.2038C>A (p.His680Asn)
c.1946C>A (n.1946C>A)
n.2472C>A
c.2296C>A (p.His766Asn)
4g.6302082C=CA1435772305WFS1c.2323C= (p.His775=)
c.2264C=
c.2287C= (p.His763=)
c.2038C= (p.His680=)
c.1946C= (n.1946C=)
n.2472C=
c.2296C= (p.His766=)
4g.6302082C>GCA356178291WFS1c.2323C>G (p.His775Asp)
c.2264C>G
c.2287C>G (p.His763Asp)
c.2038C>G (p.His680Asp)
c.1946C>G (n.1946C>G)
n.2472C>G
c.2296C>G (p.His766Asp)
4g.6302082C>TCA2839673WFS1c.2323C>T (p.His775Tyr)
c.2264C>T
c.2287C>T (p.His763Tyr)
c.2038C>T (p.His680Tyr)
c.1946C>T (n.1946C>T)
n.2472C>T
c.2296C>T (p.His766Tyr)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302083A=CA1435772306WFS1c.2324A= (p.His775=)
c.2265A=
c.2288A= (p.His763=)
c.2039A= (p.His680=)
c.1947A= (n.1947A=)
n.2473A=
c.2297A= (p.His766=)
4g.6302083A>CCA2839674WFS1c.2324A>C (p.His775Pro)
c.2265A>C
c.2288A>C (p.His763Pro)
c.2039A>C (p.His680Pro)
c.1947A>C (n.1947A>C)
n.2473A>C
c.2297A>C (p.His766Pro)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6302083A>GCA356178293WFS1c.2324A>G (p.His775Arg)
c.2265A>G
c.2288A>G (p.His763Arg)
c.2039A>G (p.His680Arg)
c.1947A>G (n.1947A>G)
n.2473A>G
c.2297A>G (p.His766Arg)
 ClinVar gnomAD v4
4g.6302083A>TCA356178292WFS1c.2324A>T (p.His775Leu)
c.2265A>T
c.2288A>T (p.His763Leu)
c.2039A>T (p.His680Leu)
c.1947A>T (n.1947A>T)
n.2473A>T
c.2297A>T (p.His766Leu)
4g.6302084C>ACA2839675WFS1c.2325C>A (p.His775Gln)
c.2266C>A
c.2289C>A (p.His763Gln)
c.2040C>A (p.His680Gln)
c.1948C>A (n.1948C>A)
n.2474C>A
c.2298C>A (p.His766Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302084C=CA1435772308WFS1c.2325C= (p.His775=)
c.2266C=
c.2289C= (p.His763=)
c.2040C= (p.His680=)
c.1948C= (n.1948C=)
n.2474C=
c.2298C= (p.His766=)
4g.6302084C>GCA356178294WFS1c.2325C>G (p.His775Gln)
c.2266C>G
c.2289C>G (p.His763Gln)
c.2040C>G (p.His680Gln)
c.1948C>G (n.1948C>G)
n.2474C>G
c.2298C>G (p.His766Gln)
4g.6302084C>TCA438368244WFS1c.2325C>T (p.His775=)
c.2266C>T
c.2289C>T (p.His763=)
c.2040C>T (p.His680=)
c.1948C>T (n.1948C>T)
n.2474C>T
c.2298C>T (p.His766=)
 gnomAD v4
4g.6302085C>ACA356178295WFS1c.2326C>A (p.Pro776Thr)
c.2267C>A
c.2290C>A (p.Pro764Thr)
c.2041C>A (p.Pro681Thr)
c.1949C>A (n.1949C>A)
n.2475C>A
c.2299C>A (p.Pro767Thr)
4g.6302085C=CA1435772310WFS1c.2326C= (p.Pro776=)
c.2267C=
c.2290C= (p.Pro764=)
c.2041C= (p.Pro681=)
c.1949C= (n.1949C=)
n.2475C=
c.2299C= (p.Pro767=)
4g.6302085C>GCA2839676WFS1c.2326C>G (p.Pro776Ala)
c.2267C>G
c.2290C>G (p.Pro764Ala)
c.2041C>G (p.Pro681Ala)
c.1949C>G (n.1949C>G)
n.2475C>G
c.2299C>G (p.Pro767Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302085C>TCA91797019WFS1c.2326C>T (p.Pro776Ser)
c.2267C>T
c.2290C>T (p.Pro764Ser)
c.2041C>T (p.Pro681Ser)
c.1949C>T (n.1949C>T)
n.2475C>T
c.2299C>T (p.Pro767Ser)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6302086C>ACA356178296WFS1c.2327C>A (p.Pro776His)
c.2268C>A
c.2291C>A (p.Pro764His)
c.2042C>A (p.Pro681His)
c.1950C>A (n.1950C>A)
n.2476C>A
c.2300C>A (p.Pro767His)
4g.6302086C>GCA356178297WFS1c.2327C>G (p.Pro776Arg)
c.2268C>G
c.2291C>G (p.Pro764Arg)
c.2042C>G (p.Pro681Arg)
c.1950C>G (n.1950C>G)
n.2476C>G
c.2300C>G (p.Pro767Arg)
4g.6302086C>TCA356178298WFS1c.2327C>T (p.Pro776Leu)
c.2268C>T
c.2291C>T (p.Pro764Leu)
c.2042C>T (p.Pro681Leu)
c.1950C>T (n.1950C>T)
n.2476C>T
c.2300C>T (p.Pro767Leu)
4g.6302087C>ACA438368245WFS1c.2328C>A (p.Pro776=)
c.2269C>A
c.2292C>A (p.Pro764=)
c.2043C>A (p.Pro681=)
c.1951C>A (n.1951C>A)
n.2477C>A
c.2301C>A (p.Pro767=)
 gnomAD v4
4g.6302087C=CA1435772313WFS1c.2328C= (p.Pro776=)
c.2269C=
c.2292C= (p.Pro764=)
c.2043C= (p.Pro681=)
c.1951C= (n.1951C=)
n.2477C=
c.2301C= (p.Pro767=)
4g.6302087C>GCA438368246WFS1c.2328C>G (p.Pro776=)
c.2269C>G
c.2292C>G (p.Pro764=)
c.2043C>G (p.Pro681=)
c.1951C>G (n.1951C>G)
n.2477C>G
c.2301C>G (p.Pro767=)
 dbSNP gnomAD v2 gnomAD v4
4g.6302087C>TCA438368247WFS1c.2328C>T (p.Pro776=)
c.2269C>T
c.2292C>T (p.Pro764=)
c.2043C>T (p.Pro681=)
c.1951C>T (n.1951C>T)
n.2477C>T
c.2301C>T (p.Pro767=)
4g.6302087_6302088delinsCTCA1435772314WFS1c.2328_2329delinsCT (p.Pro776=)
c.2269_2270delinsCT
c.2292_2293delinsCT (p.Pro764=)
c.2043_2044delinsCT (p.Pro681=)
c.1951_1952delinsCT (n.1951_1952delinsCT)
n.2477_2478delinsCT
c.2301_2302delinsCT (p.Pro767=)
4g.6302088delCA549707919WFS1c.2329del (p.Cys777AlafsTer?)
c.2270del
c.2293del (p.Cys765AlafsTer?)
c.2044del (p.Cys682AlafsTer?)
c.1952del (n.1952del)
n.2478del
c.2302del (p.Cys768AlafsTer?)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302088T>ACA356178299WFS1c.2329T>A (p.Cys777Ser)
c.2270T>A
c.2293T>A (p.Cys765Ser)
c.2044T>A (p.Cys682Ser)
c.1952T>A (n.1952T>A)
n.2478T>A
c.2302T>A (p.Cys768Ser)
4g.6302088T>CCA179671WFS1c.2329T>C (p.Cys777Arg)
c.2270T>C
c.2293T>C (p.Cys765Arg)
c.2044T>C (p.Cys682Arg)
c.1952T>C (n.1952T>C)
n.2478T>C
c.2302T>C (p.Cys768Arg)
 ClinVar dbSNP gnomAD v4
4g.6302088T>GCA356178300WFS1c.2329T>G (p.Cys777Gly)
c.2270T>G
c.2293T>G (p.Cys765Gly)
c.2044T>G (p.Cys682Gly)
c.1952T>G (n.1952T>G)
n.2478T>G
c.2302T>G (p.Cys768Gly)
4g.6302088T=CA1435772317WFS1c.2329T= (p.Cys777=)
c.2270T=
c.2293T= (p.Cys765=)
c.2044T= (p.Cys682=)
c.1952T= (n.1952T=)
n.2478T=
c.2302T= (p.Cys768=)
4g.6302089G>ACA2839677WFS1c.2330G>A (p.Cys777Tyr)
c.2271G>A
c.2294G>A (p.Cys765Tyr)
c.2045G>A (p.Cys682Tyr)
c.1953G>A (n.1953G>A)
n.2479G>A
c.2303G>A (p.Cys768Tyr)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302089G>CCA356178301WFS1c.2330G>C (p.Cys777Ser)
c.2271G>C
c.2294G>C (p.Cys765Ser)
c.2045G>C (p.Cys682Ser)
c.1953G>C (n.1953G>C)
n.2479G>C
c.2303G>C (p.Cys768Ser)
4g.6302089G=CA1435772318WFS1c.2330G= (p.Cys777=)
c.2271G=
c.2294G= (p.Cys765=)
c.2045G= (p.Cys682=)
c.1953G= (n.1953G=)
n.2479G=
c.2303G= (p.Cys768=)
4g.6302089G>TCA356178302WFS1c.2330G>T (p.Cys777Phe)
c.2271G>T
c.2294G>T (p.Cys765Phe)
c.2045G>T (p.Cys682Phe)
c.1953G>T (n.1953G>T)
n.2479G>T
c.2303G>T (p.Cys768Phe)
4g.6302090C>ACA356178303WFS1c.2331C>A (p.Cys777Ter)
c.2272C>A
c.2295C>A (p.Cys765Ter)
c.2046C>A (p.Cys682Ter)
c.1954C>A (n.1954C>A)
n.2480C>A
c.2304C>A (p.Cys768Ter)
4g.6302090C>GCA356178304WFS1c.2331C>G (p.Cys777Trp)
c.2272C>G
c.2295C>G (p.Cys765Trp)
c.2046C>G (p.Cys682Trp)
c.1954C>G (n.1954C>G)
n.2480C>G
c.2304C>G (p.Cys768Trp)
4g.6302090C>TCA438368248WFS1c.2331C>T (p.Cys777=)
c.2272C>T
c.2295C>T (p.Cys765=)
c.2046C>T (p.Cys682=)
c.1954C>T (n.1954C>T)
n.2480C>T
c.2304C>T (p.Cys768=)
 gnomAD v4
4g.6302091C>ACA356178307WFS1c.2332C>A (p.His778Asn)
c.2273C>A
c.2296C>A (p.His766Asn)
c.2047C>A (p.His683Asn)
c.1955C>A (n.1955C>A)
n.2481C>A
c.2305C>A (p.His769Asn)
4g.6302091C=CA1435772320WFS1c.2332C= (p.His778=)
c.2273C=
c.2296C= (p.His766=)
c.2047C= (p.His683=)
c.1955C= (n.1955C=)
n.2481C=
c.2305C= (p.His769=)
4g.6302091C>GCA356178306WFS1c.2332C>G (p.His778Asp)
c.2273C>G
c.2296C>G (p.His766Asp)
c.2047C>G (p.His683Asp)
c.1955C>G (n.1955C>G)
n.2481C>G
c.2305C>G (p.His769Asp)
 ClinVar dbSNP
4g.6302091C>TCA356178305WFS1c.2332C>T (p.His778Tyr)
c.2273C>T
c.2296C>T (p.His766Tyr)
c.2047C>T (p.His683Tyr)
c.1955C>T (n.1955C>T)
n.2481C>T
c.2305C>T (p.His769Tyr)
 ClinVar dbSNP gnomAD v4
4g.6302092A>CCA356178308WFS1c.2333A>C (p.His778Pro)
c.2274A>C
c.2297A>C (p.His766Pro)
c.2048A>C (p.His683Pro)
c.1956A>C (n.1956A>C)
n.2482A>C
c.2306A>C (p.His769Pro)
4g.6302092A>GCA356178309WFS1c.2333A>G (p.His778Arg)
c.2274A>G
c.2297A>G (p.His766Arg)
c.2048A>G (p.His683Arg)
c.1956A>G (n.1956A>G)
n.2482A>G
c.2306A>G (p.His769Arg)
 gnomAD v4
4g.6302092A>TCA356178310WFS1c.2333A>T (p.His778Leu)
c.2274A>T
c.2297A>T (p.His766Leu)
c.2048A>T (p.His683Leu)
c.1956A>T (n.1956A>T)
n.2482A>T
c.2306A>T (p.His769Leu)
4g.6302093C>ACA10619009WFS1c.2334C>A (p.His778Gln)
c.2275C>A
c.2298C>A (p.His766Gln)
c.2049C>A (p.His683Gln)
c.1957C>A (n.1957C>A)
n.2483C>A
c.2307C>A (p.His769Gln)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6302093C=CA1435772322WFS1c.2334C= (p.His778=)
c.2275C=
c.2298C= (p.His766=)
c.2049C= (p.His683=)
c.1957C= (n.1957C=)
n.2483C=
c.2307C= (p.His769=)
4g.6302093C>GCA356178311WFS1c.2334C>G (p.His778Gln)
c.2275C>G
c.2298C>G (p.His766Gln)
c.2049C>G (p.His683Gln)
c.1957C>G (n.1957C>G)
n.2483C>G
c.2307C>G (p.His769Gln)
4g.6302093C>TCA2839678WFS1c.2334C>T (p.His778=)
c.2275C>T
c.2298C>T (p.His766=)
c.2049C>T (p.His683=)
c.1957C>T (n.1957C>T)
n.2483C>T
c.2307C>T (p.His769=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302095_6302097delCA2580617579WFS1c.2336_2338del (p.Ile779del)
c.2277_2279del
c.2300_2302del (p.Ile767del)
c.2051_2053del (p.Ile684del)
c.1959_1961del (n.1959_1961del)
n.2485_2487del
c.2309_2311del (p.Ile770del)
4g.6302094A=CA1435772325WFS1c.2335A= (p.Ile779=)
c.2276A=
c.2299A= (p.Ile767=)
c.2050A= (p.Ile684=)
c.1958A= (n.1958A=)
n.2484A=
c.2308A= (p.Ile770=)
4g.6302094A>CCA2839679WFS1c.2335A>C (p.Ile779Leu)
c.2276A>C
c.2299A>C (p.Ile767Leu)
c.2050A>C (p.Ile684Leu)
c.1958A>C (n.1958A>C)
n.2484A>C
c.2308A>C (p.Ile770Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302094A>GCA356178312WFS1c.2335A>G (p.Ile779Val)
c.2276A>G
c.2299A>G (p.Ile767Val)
c.2050A>G (p.Ile684Val)
c.1958A>G (n.1958A>G)
n.2484A>G
c.2308A>G (p.Ile770Val)
 dbSNP gnomAD v2 gnomAD v4
4g.6302094A>TCA356178313WFS1c.2335A>T (p.Ile779Phe)
c.2276A>T
c.2299A>T (p.Ile767Phe)
c.2050A>T (p.Ile684Phe)
c.1958A>T (n.1958A>T)
n.2484A>T
c.2308A>T (p.Ile770Phe)
 gnomAD v4
4g.6302095T>ACA356178314WFS1c.2336T>A (p.Ile779Asn)
c.2277T>A
c.2300T>A (p.Ile767Asn)
c.2051T>A (p.Ile684Asn)
c.1959T>A (n.1959T>A)
n.2485T>A
c.2309T>A (p.Ile770Asn)
4g.6302095T>CCA356178315WFS1c.2336T>C (p.Ile779Thr)
c.2277T>C
c.2300T>C (p.Ile767Thr)
c.2051T>C (p.Ile684Thr)
c.1959T>C (n.1959T>C)
n.2485T>C
c.2309T>C (p.Ile770Thr)
 gnomAD v4
4g.6302095T>GCA356178316WFS1c.2336T>G (p.Ile779Ser)
c.2277T>G
c.2300T>G (p.Ile767Ser)
c.2051T>G (p.Ile684Ser)
c.1959T>G (n.1959T>G)
n.2485T>G
c.2309T>G (p.Ile770Ser)
4g.6302096C>ACA91797029WFS1c.2337C>A (p.Ile779=)
c.2278C>A
c.2301C>A (p.Ile767=)
c.2052C>A (p.Ile684=)
c.1960C>A (n.1960C>A)
n.2486C>A
c.2310C>A (p.Ile770=)
 dbSNP
4g.6302096C=CA1435772328WFS1c.2337C= (p.Ile779=)
c.2278C=
c.2301C= (p.Ile767=)
c.2052C= (p.Ile684=)
c.1960C= (n.1960C=)
n.2486C=
c.2310C= (p.Ile770=)
4g.6302096C>GCA356178317WFS1c.2337C>G (p.Ile779Met)
c.2278C>G
c.2301C>G (p.Ile767Met)
c.2052C>G (p.Ile684Met)
c.1960C>G (n.1960C>G)
n.2486C>G
c.2310C>G (p.Ile770Met)
 gnomAD v4
4g.6302096C>TCA438368249WFS1c.2337C>T (p.Ile779=)
c.2278C>T
c.2301C>T (p.Ile767=)
c.2052C>T (p.Ile684=)
c.1960C>T (n.1960C>T)
n.2486C>T
c.2310C>T (p.Ile770=)
 dbSNP
4g.6302097A>CCA356178318WFS1c.2338A>C (p.Lys780Gln)
c.2279A>C
c.2302A>C (p.Lys768Gln)
c.2053A>C (p.Lys685Gln)
c.1961A>C (n.1961A>C)
n.2487A>C
c.2311A>C (p.Lys771Gln)
 gnomAD v4
4g.6302097A>GCA356178319WFS1c.2338A>G (p.Lys780Glu)
c.2279A>G
c.2302A>G (p.Lys768Glu)
c.2053A>G (p.Lys685Glu)
c.1961A>G (n.1961A>G)
n.2487A>G
c.2311A>G (p.Lys771Glu)
4g.6302097A>TCA356178320WFS1c.2338A>T (p.Lys780Ter)
c.2279A>T
c.2302A>T (p.Lys768Ter)
c.2053A>T (p.Lys685Ter)
c.1961A>T (n.1961A>T)
n.2487A>T
c.2311A>T (p.Lys771Ter)
4g.6302100_6302102delCA2669843458WFS1c.2341_2343del (p.Lys781del)
c.2282_2284del
c.2305_2307del (p.Lys769del)
c.2056_2058del (p.Lys686del)
c.1964_1966del (n.1964_1966del)
n.2490_2492del
c.2314_2316del (p.Lys772del)
 gnomAD v4
4g.6302098A=CA1435772329WFS1c.2339A= (p.Lys780=)
c.2280A=
c.2303A= (p.Lys768=)
c.2054A= (p.Lys685=)
c.1962A= (n.1962A=)
n.2488A=
c.2312A= (p.Lys771=)
4g.6302098A>CCA356178321WFS1c.2339A>C (p.Lys780Thr)
c.2280A>C
c.2303A>C (p.Lys768Thr)
c.2054A>C (p.Lys685Thr)
c.1962A>C (n.1962A>C)
n.2488A>C
c.2312A>C (p.Lys771Thr)
4g.6302098A>GCA356178322WFS1c.2339A>G (p.Lys780Arg)
c.2280A>G
c.2303A>G (p.Lys768Arg)
c.2054A>G (p.Lys685Arg)
c.1962A>G (n.1962A>G)
n.2488A>G
c.2312A>G (p.Lys771Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6302098A>TCA356178323WFS1c.2339A>T (p.Lys780Met)
c.2280A>T
c.2303A>T (p.Lys768Met)
c.2054A>T (p.Lys685Met)
c.1962A>T (n.1962A>T)
n.2488A>T
c.2312A>T (p.Lys771Met)
4g.6302099G>ACA438368250WFS1c.2340G>A (p.Lys780=)
c.2281G>A
c.2304G>A (p.Lys768=)
c.2055G>A (p.Lys685=)
c.1963G>A (n.1963G>A)
n.2489G>A
c.2313G>A (p.Lys771=)
4g.6302099G>CCA356178324WFS1c.2340G>C (p.Lys780Asn)
c.2281G>C
c.2304G>C (p.Lys768Asn)
c.2055G>C (p.Lys685Asn)
c.1963G>C (n.1963G>C)
n.2489G>C
c.2313G>C (p.Lys771Asn)
4g.6302099G>TCA356178325WFS1c.2340G>T (p.Lys780Asn)
c.2281G>T
c.2304G>T (p.Lys768Asn)
c.2055G>T (p.Lys685Asn)
c.1963G>T (n.1963G>T)
n.2489G>T
c.2313G>T (p.Lys771Asn)
4g.6302100A>CCA356178326WFS1c.2341A>C (p.Lys781Gln)
c.2282A>C
c.2305A>C (p.Lys769Gln)
c.2056A>C (p.Lys686Gln)
c.1964A>C (n.1964A>C)
n.2490A>C
c.2314A>C (p.Lys772Gln)
4g.6302100A>GCA356178327WFS1c.2341A>G (p.Lys781Glu)
c.2282A>G
c.2305A>G (p.Lys769Glu)
c.2056A>G (p.Lys686Glu)
c.1964A>G (n.1964A>G)
n.2490A>G
c.2314A>G (p.Lys772Glu)
4g.6302100A>TCA356178328WFS1c.2341A>T (p.Lys781Ter)
c.2282A>T
c.2305A>T (p.Lys769Ter)
c.2056A>T (p.Lys686Ter)
c.1964A>T (n.1964A>T)
n.2490A>T
c.2314A>T (p.Lys772Ter)
4g.6302101A=CA1435772331WFS1c.2342A= (p.Lys781=)
c.2283A=
c.2306A= (p.Lys769=)
c.2057A= (p.Lys686=)
c.1965A= (n.1965A=)
n.2491A=
c.2315A= (p.Lys772=)
4g.6302101A>CCA356178329WFS1c.2342A>C (p.Lys781Thr)
c.2283A>C
c.2306A>C (p.Lys769Thr)
c.2057A>C (p.Lys686Thr)
c.1965A>C (n.1965A>C)
n.2491A>C
c.2315A>C (p.Lys772Thr)
4g.6302101A>GCA356178330WFS1c.2342A>G (p.Lys781Arg)
c.2283A>G
c.2306A>G (p.Lys769Arg)
c.2057A>G (p.Lys686Arg)
c.1965A>G (n.1965A>G)
n.2491A>G
c.2315A>G (p.Lys772Arg)
 dbSNP gnomAD v4
4g.6302101A>TCA356178331WFS1c.2342A>T (p.Lys781Met)
c.2283A>T
c.2306A>T (p.Lys769Met)
c.2057A>T (p.Lys686Met)
c.1965A>T (n.1965A>T)
n.2491A>T
c.2315A>T (p.Lys772Met)
4g.6302102G>ACA438368251WFS1c.2343G>A (p.Lys781=)
c.2284G>A
c.2307G>A (p.Lys769=)
c.2058G>A (p.Lys686=)
c.1966G>A (n.1966G>A)
n.2492G>A
c.2316G>A (p.Lys772=)
 gnomAD v4
4g.6302102G>CCA356178332WFS1c.2343G>C (p.Lys781Asn)
c.2284G>C
c.2307G>C (p.Lys769Asn)
c.2058G>C (p.Lys686Asn)
c.1966G>C (n.1966G>C)
n.2492G>C
c.2316G>C (p.Lys772Asn)
 gnomAD v4
4g.6302102G>TCA356178333WFS1c.2343G>T (p.Lys781Asn)
c.2284G>T
c.2307G>T (p.Lys769Asn)
c.2058G>T (p.Lys686Asn)
c.1966G>T (n.1966G>T)
n.2492G>T
c.2316G>T (p.Lys772Asn)
4g.6302103T>ACA356178334WFS1c.2344T>A (p.Phe782Ile)
c.2285T>A
c.2308T>A (p.Phe770Ile)
c.2059T>A (p.Phe687Ile)
c.1967T>A (n.1967T>A)
n.2493T>A
c.2317T>A (p.Phe773Ile)
4g.6302103T>CCA356178335WFS1c.2344T>C (p.Phe782Leu)
c.2285T>C
c.2308T>C (p.Phe770Leu)
c.2059T>C (p.Phe687Leu)
c.1967T>C (n.1967T>C)
n.2493T>C
c.2317T>C (p.Phe773Leu)
4g.6302103T>GCA356178336WFS1c.2344T>G (p.Phe782Val)
c.2285T>G
c.2308T>G (p.Phe770Val)
c.2059T>G (p.Phe687Val)
c.1967T>G (n.1967T>G)
n.2493T>G
c.2317T>G (p.Phe773Val)
4g.6302104T>ACA356178337WFS1c.2345T>A (p.Phe782Tyr)
c.2286T>A
c.2309T>A (p.Phe770Tyr)
c.2060T>A (p.Phe687Tyr)
c.1968T>A (n.1968T>A)
n.2494T>A
c.2318T>A (p.Phe773Tyr)
4g.6302104T>CCA356178338WFS1c.2345T>C (p.Phe782Ser)
c.2286T>C
c.2309T>C (p.Phe770Ser)
c.2060T>C (p.Phe687Ser)
c.1968T>C (n.1968T>C)
n.2494T>C
c.2318T>C (p.Phe773Ser)
4g.6302104T>GCA356178339WFS1c.2345T>G (p.Phe782Cys)
c.2286T>G
c.2309T>G (p.Phe770Cys)
c.2060T>G (p.Phe687Cys)
c.1968T>G (n.1968T>G)
n.2494T>G
c.2318T>G (p.Phe773Cys)
 dbSNP gnomAD v2 gnomAD v4
4g.6302104T=CA1435772332WFS1c.2345T= (p.Phe782=)
c.2286T=
c.2309T= (p.Phe770=)
c.2060T= (p.Phe687=)
c.1968T= (n.1968T=)
n.2494T=
c.2318T= (p.Phe773=)
4g.6302105C>ACA356178340WFS1c.2346C>A (p.Phe782Leu)
c.2287C>A
c.2310C>A (p.Phe770Leu)
c.2061C>A (p.Phe687Leu)
c.1969C>A (n.1969C>A)
n.2495C>A
c.2319C>A (p.Phe773Leu)
 gnomAD v4
4g.6302105C=CA1435772334WFS1c.2346C= (p.Phe782=)
c.2287C=
c.2310C= (p.Phe770=)
c.2061C= (p.Phe687=)
c.1969C= (n.1969C=)
n.2495C=
c.2319C= (p.Phe773=)
4g.6302105C>GCA356178341WFS1c.2346C>G (p.Phe782Leu)
c.2287C>G
c.2310C>G (p.Phe770Leu)
c.2061C>G (p.Phe687Leu)
c.1969C>G (n.1969C>G)
n.2495C>G
c.2319C>G (p.Phe773Leu)
 dbSNP gnomAD v3 gnomAD v4
4g.6302105C>TCA2839680WFS1c.2346C>T (p.Phe782=)
c.2287C>T
c.2310C>T (p.Phe770=)
c.2061C>T (p.Phe687=)
c.1969C>T (n.1969C>T)
n.2495C>T
c.2319C>T (p.Phe773=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6302106G>ACA2839681WFS1c.2347G>A (p.Asp783Asn)
c.2288G>A
c.2311G>A (p.Asp771Asn)
c.2062G>A (p.Asp688Asn)
c.1970G>A (n.1970G>A)
n.2496G>A
c.2320G>A (p.Asp774Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302106G>CCA356178342WFS1c.2347G>C (p.Asp783His)
c.2288G>C
c.2311G>C (p.Asp771His)
c.2062G>C (p.Asp688His)
c.1970G>C (n.1970G>C)
n.2496G>C
c.2320G>C (p.Asp774His)
 ClinVar dbSNP
4g.6302106G=CA1435772336WFS1c.2347G= (p.Asp783=)
c.2288G=
c.2311G= (p.Asp771=)
c.2062G= (p.Asp688=)
c.1970G= (n.1970G=)
n.2496G=
c.2320G= (p.Asp774=)
4g.6302106G>TCA356178343WFS1c.2347G>T (p.Asp783Tyr)
c.2288G>T
c.2311G>T (p.Asp771Tyr)
c.2062G>T (p.Asp688Tyr)
c.1970G>T (n.1970G>T)
n.2496G>T
c.2320G>T (p.Asp774Tyr)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6302107A>CCA356178346WFS1c.2348A>C (p.Asp783Ala)
c.2289A>C
c.2312A>C (p.Asp771Ala)
c.2063A>C (p.Asp688Ala)
c.1971A>C (n.1971A>C)
n.2497A>C
c.2321A>C (p.Asp774Ala)
4g.6302107A>GCA356178345WFS1c.2348A>G (p.Asp783Gly)
c.2289A>G
c.2312A>G (p.Asp771Gly)
c.2063A>G (p.Asp688Gly)
c.1971A>G (n.1971A>G)
n.2497A>G
c.2321A>G (p.Asp774Gly)
 gnomAD v4
4g.6302107A>TCA356178344WFS1c.2348A>T (p.Asp783Val)
c.2289A>T
c.2312A>T (p.Asp771Val)
c.2063A>T (p.Asp688Val)
c.1971A>T (n.1971A>T)
n.2497A>T
c.2321A>T (p.Asp774Val)

Number of alleles fetched