Chr Mutation (hg38) CAid Gene Transcript Linkouts
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.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=)

Number of alleles fetched