Chr Mutation (hg38) CAid Gene Transcript Linkouts
4g.6302331_6302334dupCA549708053WFS1c.2572_2575dup (p.Cys859Ter)
c.2513_2516dup
c.2536_2539dup (p.Cys847Ter)
c.2287_2290dup (p.Cys764Ter)
n.2721_2724dup
c.2545_2548dup (p.Cys850Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6302332G>ACA356179164WFS1c.2573G>A (p.Ser858Asn)
c.2514G>A
c.2537G>A (p.Ser846Asn)
c.2288G>A (p.Ser763Asn)
n.2722G>A
c.2546G>A (p.Ser849Asn)
 gnomAD v4
4g.6302332G>CCA356179162WFS1c.2573G>C (p.Ser858Thr)
c.2514G>C
c.2537G>C (p.Ser846Thr)
c.2288G>C (p.Ser763Thr)
n.2722G>C
c.2546G>C (p.Ser849Thr)
 dbSNP gnomAD v2 gnomAD v4
4g.6302332G=CA1435772626WFS1c.2573G= (p.Ser858=)
c.2514G=
c.2537G= (p.Ser846=)
c.2288G= (p.Ser763=)
n.2722G=
c.2546G= (p.Ser849=)
4g.6302332G>TCA356179163WFS1c.2573G>T (p.Ser858Ile)
c.2514G>T
c.2537G>T (p.Ser846Ile)
c.2288G>T (p.Ser763Ile)
n.2722G>T
c.2546G>T (p.Ser849Ile)
 gnomAD v4 COSMIC
4g.6302333C>ACA356179165WFS1c.2574C>A (p.Ser858Arg)
c.2515C>A
c.2538C>A (p.Ser846Arg)
c.2289C>A (p.Ser763Arg)
n.2723C>A
c.2547C>A (p.Ser849Arg)
 dbSNP gnomAD v3 gnomAD v4
4g.6302333C=CA1435772628WFS1c.2574C= (p.Ser858=)
c.2515C=
c.2538C= (p.Ser846=)
c.2289C= (p.Ser763=)
n.2723C=
c.2547C= (p.Ser849=)
4g.6302333C>GCA356179166WFS1c.2574C>G (p.Ser858Arg)
c.2515C>G
c.2538C>G (p.Ser846Arg)
c.2289C>G (p.Ser763Arg)
n.2723C>G
c.2547C>G (p.Ser849Arg)
4g.6302333C>TCA2839770WFS1c.2574C>T (p.Ser858=)
c.2515C>T
c.2538C>T (p.Ser846=)
c.2289C>T (p.Ser763=)
n.2723C>T
c.2547C>T (p.Ser849=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
4g.6302334T>ACA356179167WFS1c.2575T>A (p.Cys859Ser)
c.2516T>A
c.2539T>A (p.Cys847Ser)
c.2290T>A (p.Cys764Ser)
n.2724T>A
c.2548T>A (p.Cys850Ser)
4g.6302334T>CCA356179168WFS1c.2575T>C (p.Cys859Arg)
c.2516T>C
c.2539T>C (p.Cys847Arg)
c.2290T>C (p.Cys764Arg)
n.2724T>C
c.2548T>C (p.Cys850Arg)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6302334T>GCA356179169WFS1c.2575T>G (p.Cys859Gly)
c.2516T>G
c.2539T>G (p.Cys847Gly)
c.2290T>G (p.Cys764Gly)
n.2724T>G
c.2548T>G (p.Cys850Gly)
 gnomAD v4
4g.6302334T=CA1435772632WFS1c.2575T= (p.Cys859=)
c.2516T=
c.2539T= (p.Cys847=)
c.2290T= (p.Cys764=)
n.2724T=
c.2548T= (p.Cys850=)
4g.6302335G>ACA356179170WFS1c.2576G>A (p.Cys859Tyr)
c.2517G>A
c.2540G>A (p.Cys847Tyr)
c.2291G>A (p.Cys764Tyr)
n.2725G>A
c.2549G>A (p.Cys850Tyr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302335G>CCA356179171WFS1c.2576G>C (p.Cys859Ser)
c.2517G>C
c.2540G>C (p.Cys847Ser)
c.2291G>C (p.Cys764Ser)
n.2725G>C
c.2549G>C (p.Cys850Ser)
4g.6302335G=CA1435772635WFS1c.2576G= (p.Cys859=)
c.2517G=
c.2540G= (p.Cys847=)
c.2291G= (p.Cys764=)
n.2725G=
c.2549G= (p.Cys850=)
4g.6302335G>TCA356179172WFS1c.2576G>T (p.Cys859Phe)
c.2517G>T
c.2540G>T (p.Cys847Phe)
c.2291G>T (p.Cys764Phe)
n.2725G>T
c.2549G>T (p.Cys850Phe)
4g.6302336C>ACA356179173WFS1c.2577C>A (p.Cys859Ter)
c.2518C>A
c.2541C>A (p.Cys847Ter)
c.2292C>A (p.Cys764Ter)
n.2726C>A
c.2550C>A (p.Cys850Ter)
4g.6302336C>GCA356179174WFS1c.2577C>G (p.Cys859Trp)
c.2518C>G
c.2541C>G (p.Cys847Trp)
c.2292C>G (p.Cys764Trp)
n.2726C>G
c.2550C>G (p.Cys850Trp)
4g.6302336C>TCA438211505WFS1c.2577C>T (p.Cys859=)
c.2518C>T
c.2541C>T (p.Cys847=)
c.2292C>T (p.Cys764=)
n.2726C>T
c.2550C>T (p.Cys850=)
 gnomAD v4
4g.6302337C>ACA356179176WFS1c.2578C>A (p.Leu860Ile)
c.2519C>A
c.2542C>A (p.Leu848Ile)
c.2293C>A (p.Leu765Ile)
n.2727C>A
c.2551C>A (p.Leu851Ile)
4g.6302337C>GCA356179177WFS1c.2578C>G (p.Leu860Val)
c.2519C>G
c.2542C>G (p.Leu848Val)
c.2293C>G (p.Leu765Val)
n.2727C>G
c.2551C>G (p.Leu851Val)
 ClinVar dbSNP gnomAD v4
4g.6302337C>TCA356179175WFS1c.2578C>T (p.Leu860Phe)
c.2519C>T
c.2542C>T (p.Leu848Phe)
c.2293C>T (p.Leu765Phe)
n.2727C>T
c.2551C>T (p.Leu851Phe)
 ClinVar gnomAD v4
4g.6302338T>ACA356179178WFS1c.2579T>A (p.Leu860His)
c.2520T>A
c.2543T>A (p.Leu848His)
c.2294T>A (p.Leu765His)
n.2728T>A
c.2552T>A (p.Leu851His)
4g.6302338T>CCA356179179WFS1c.2579T>C (p.Leu860Pro)
c.2520T>C
c.2543T>C (p.Leu848Pro)
c.2294T>C (p.Leu765Pro)
n.2728T>C
c.2552T>C (p.Leu851Pro)
4g.6302338T>GCA356179180WFS1c.2579T>G (p.Leu860Arg)
c.2520T>G
c.2543T>G (p.Leu848Arg)
c.2294T>G (p.Leu765Arg)
n.2728T>G
c.2552T>G (p.Leu851Arg)
4g.6302339C>ACA438211506WFS1c.2580C>A (p.Leu860=)
c.2521C>A
c.2544C>A (p.Leu848=)
c.2295C>A (p.Leu765=)
n.2729C>A
c.2553C>A (p.Leu851=)
4g.6302339C=CA1435772637WFS1c.2580C= (p.Leu860=)
c.2521C=
c.2544C= (p.Leu848=)
c.2295C= (p.Leu765=)
n.2729C=
c.2553C= (p.Leu851=)
4g.6302339C>GCA438211507WFS1c.2580C>G (p.Leu860=)
c.2521C>G
c.2544C>G (p.Leu848=)
c.2295C>G (p.Leu765=)
n.2729C>G
c.2553C>G (p.Leu851=)
4g.6302339C>TCA91797802WFS1c.2580C>T (p.Leu860=)
c.2521C>T
c.2544C>T (p.Leu848=)
c.2295C>T (p.Leu765=)
n.2729C>T
c.2553C>T (p.Leu851=)
 dbSNP gnomAD v4
4g.6302340A=CA1435772639WFS1c.2581A= (p.Asn861=)
c.2522A=
c.2545A= (p.Asn849=)
c.2296A= (p.Asn766=)
n.2730A=
c.2554A= (p.Asn852=)
4g.6302340A>CCA2839771WFS1c.2581A>C (p.Asn861His)
c.2522A>C
c.2545A>C (p.Asn849His)
c.2296A>C (p.Asn766His)
n.2730A>C
c.2554A>C (p.Asn852His)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302340A>GCA356179181WFS1c.2581A>G (p.Asn861Asp)
c.2522A>G
c.2545A>G (p.Asn849Asp)
c.2296A>G (p.Asn766Asp)
n.2730A>G
c.2554A>G (p.Asn852Asp)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6302340A>TCA356179182WFS1c.2581A>T (p.Asn861Tyr)
c.2522A>T
c.2545A>T (p.Asn849Tyr)
c.2296A>T (p.Asn766Tyr)
n.2730A>T
c.2554A>T (p.Asn852Tyr)
 gnomAD v4
4g.6302341A=CA1435772641WFS1c.2582A= (p.Asn861=)
c.2523A=
c.2546A= (p.Asn849=)
c.2297A= (p.Asn766=)
n.2731A=
c.2555A= (p.Asn852=)
4g.6302341A>CCA356179183WFS1c.2582A>C (p.Asn861Thr)
c.2523A>C
c.2546A>C (p.Asn849Thr)
c.2297A>C (p.Asn766Thr)
n.2731A>C
c.2555A>C (p.Asn852Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302341A>GCA2839772WFS1c.2582A>G (p.Asn861Ser)
c.2523A>G
c.2546A>G (p.Asn849Ser)
c.2297A>G (p.Asn766Ser)
n.2731A>G
c.2555A>G (p.Asn852Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302341A>TCA356179184WFS1c.2582A>T (p.Asn861Ile)
c.2523A>T
c.2546A>T (p.Asn849Ile)
c.2297A>T (p.Asn766Ile)
n.2731A>T
c.2555A>T (p.Asn852Ile)
4g.6302342C>ACA91797807WFS1c.2583C>A (p.Asn861Lys)
c.2524C>A
c.2547C>A (p.Asn849Lys)
c.2298C>A (p.Asn766Lys)
n.2732C>A
c.2556C>A (p.Asn852Lys)
 dbSNP gnomAD v2 gnomAD v4
4g.6302342C=CA1435772643WFS1c.2583C= (p.Asn861=)
c.2524C=
c.2547C= (p.Asn849=)
c.2298C= (p.Asn766=)
n.2732C=
c.2556C= (p.Asn852=)
4g.6302342C>GCA356179185WFS1c.2583C>G (p.Asn861Lys)
c.2524C>G
c.2547C>G (p.Asn849Lys)
c.2298C>G (p.Asn766Lys)
n.2732C>G
c.2556C>G (p.Asn852Lys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302342C>TCA438211508WFS1c.2583C>T (p.Asn861=)
c.2524C>T
c.2547C>T (p.Asn849=)
c.2298C>T (p.Asn766=)
n.2732C>T
c.2556C>T (p.Asn852=)
 gnomAD v4
4g.6302343T>ACA356179186WFS1c.2584T>A (p.Cys862Ser)
c.2525T>A
c.2548T>A (p.Cys850Ser)
c.2299T>A (p.Cys767Ser)
n.2733T>A
c.2557T>A (p.Cys853Ser)
4g.6302343T>CCA356179187WFS1c.2584T>C (p.Cys862Arg)
c.2525T>C
c.2548T>C (p.Cys850Arg)
c.2299T>C (p.Cys767Arg)
n.2733T>C
c.2557T>C (p.Cys853Arg)
 dbSNP gnomAD v3 gnomAD v4
4g.6302343T>GCA91797809WFS1c.2584T>G (p.Cys862Gly)
c.2525T>G
c.2548T>G (p.Cys850Gly)
c.2299T>G (p.Cys767Gly)
n.2733T>G
c.2557T>G (p.Cys853Gly)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6302343T=CA1435772645WFS1c.2584T= (p.Cys862=)
c.2525T=
c.2548T= (p.Cys850=)
c.2299T= (p.Cys767=)
n.2733T=
c.2557T= (p.Cys853=)
4g.6302344G>ACA2839773WFS1c.2585G>A (p.Cys862Tyr)
c.2526G>A
c.2549G>A (p.Cys850Tyr)
c.2300G>A (p.Cys767Tyr)
n.2734G>A
c.2558G>A (p.Cys853Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302344G>CCA356179189WFS1c.2585G>C (p.Cys862Ser)
c.2526G>C
c.2549G>C (p.Cys850Ser)
c.2300G>C (p.Cys767Ser)
n.2734G>C
c.2558G>C (p.Cys853Ser)
4g.6302344G=CA1435772647WFS1c.2585G= (p.Cys862=)
c.2526G=
c.2549G= (p.Cys850=)
c.2300G= (p.Cys767=)
n.2734G=
c.2558G= (p.Cys853=)
4g.6302344G>TCA356179188WFS1c.2585G>T (p.Cys862Phe)
c.2526G>T
c.2549G>T (p.Cys850Phe)
c.2300G>T (p.Cys767Phe)
n.2734G>T
c.2558G>T (p.Cys853Phe)
4g.6302345C>ACA356179190WFS1c.2586C>A (p.Cys862Ter)
c.2527C>A
c.2550C>A (p.Cys850Ter)
c.2301C>A (p.Cys767Ter)
n.2735C>A
c.2559C>A (p.Cys853Ter)
 dbSNP gnomAD v3 gnomAD v4
4g.6302345C=CA1435772650WFS1c.2586C= (p.Cys862=)
c.2527C=
c.2550C= (p.Cys850=)
c.2301C= (p.Cys767=)
n.2735C=
c.2559C= (p.Cys853=)
4g.6302345C>GCA356179191WFS1c.2586C>G (p.Cys862Trp)
c.2527C>G
c.2550C>G (p.Cys850Trp)
c.2301C>G (p.Cys767Trp)
n.2735C>G
c.2559C>G (p.Cys853Trp)
4g.6302345C>TCA438211509WFS1c.2586C>T (p.Cys862=)
c.2527C>T
c.2550C>T (p.Cys850=)
c.2301C>T (p.Cys767=)
n.2735C>T
c.2559C>T (p.Cys853=)
 ClinVar gnomAD v4
4g.6302346A=CA1435772652WFS1c.2587A= (p.Met863=)
c.2528A=
c.2551A= (p.Met851=)
c.2302A= (p.Met768=)
n.2736A=
c.2560A= (p.Met854=)
4g.6302346A>CCA356179193WFS1c.2587A>C (p.Met863Leu)
c.2528A>C
c.2551A>C (p.Met851Leu)
c.2302A>C (p.Met768Leu)
n.2736A>C
c.2560A>C (p.Met854Leu)
4g.6302346A>GCA356179195WFS1c.2587A>G (p.Met863Val)
c.2528A>G
c.2551A>G (p.Met851Val)
c.2302A>G (p.Met768Val)
n.2736A>G
c.2560A>G (p.Met854Val)
 dbSNP gnomAD v4
4g.6302346A>TCA356179197WFS1c.2587A>T (p.Met863Leu)
c.2528A>T
c.2551A>T (p.Met851Leu)
c.2302A>T (p.Met768Leu)
n.2736A>T
c.2560A>T (p.Met854Leu)
4g.6302347T>ACA356179199WFS1c.2588T>A (p.Met863Lys)
c.2529T>A
c.2552T>A (p.Met851Lys)
c.2303T>A (p.Met768Lys)
n.2737T>A
c.2561T>A (p.Met854Lys)
4g.6302347T>CCA356179201WFS1c.2588T>C (p.Met863Thr)
c.2529T>C
c.2552T>C (p.Met851Thr)
c.2303T>C (p.Met768Thr)
n.2737T>C
c.2561T>C (p.Met854Thr)
 ClinVar
4g.6302347T>GCA2839775WFS1c.2588T>G (p.Met863Arg)
c.2529T>G
c.2552T>G (p.Met851Arg)
c.2303T>G (p.Met768Arg)
n.2737T>G
c.2561T>G (p.Met854Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302347T=CA1435772655WFS1c.2588T= (p.Met863=)
c.2529T=
c.2552T= (p.Met851=)
c.2303T= (p.Met768=)
n.2737T=
c.2561T= (p.Met854=)
4g.6302347_6302348dupCA2839774WFS1c.2588_2589dup (p.Ala864TrpfsTer11)
c.2529_2530dup
c.2552_2553dup (p.Ala852TrpfsTer11)
c.2303_2304dup (p.Ala769TrpfsTer11)
n.2737_2738dup
c.2561_2562dup (p.Ala855TrpfsTer11)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302348G>ACA356179204WFS1c.2589G>A (p.Met863Ile)
c.2530G>A
c.2553G>A (p.Met851Ile)
c.2304G>A (p.Met768Ile)
n.2738G>A
c.2562G>A (p.Met854Ile)
4g.6302348G>CCA356179205WFS1c.2589G>C (p.Met863Ile)
c.2530G>C
c.2553G>C (p.Met851Ile)
c.2304G>C (p.Met768Ile)
n.2738G>C
c.2562G>C (p.Met854Ile)
4g.6302348G>TCA356179207WFS1c.2589G>T (p.Met863Ile)
c.2530G>T
c.2553G>T (p.Met851Ile)
c.2304G>T (p.Met768Ile)
n.2738G>T
c.2562G>T (p.Met854Ile)
4g.6302349G>ACA356179208WFS1c.2590G>A (p.Ala864Thr)
c.2531G>A
c.2554G>A (p.Ala852Thr)
c.2305G>A (p.Ala769Thr)
n.2739G>A
c.2563G>A (p.Ala855Thr)
4g.6302349G>CCA356179212WFS1c.2590G>C (p.Ala864Pro)
c.2531G>C
c.2554G>C (p.Ala852Pro)
c.2305G>C (p.Ala769Pro)
n.2739G>C
c.2563G>C (p.Ala855Pro)
4g.6302349G=CA1435772657WFS1c.2590G= (p.Ala864=)
c.2531G=
c.2554G= (p.Ala852=)
c.2305G= (p.Ala769=)
n.2739G=
c.2563G= (p.Ala855=)
4g.6302349G>TCA356179210WFS1c.2590G>T (p.Ala864Ser)
c.2531G>T
c.2554G>T (p.Ala852Ser)
c.2305G>T (p.Ala769Ser)
n.2739G>T
c.2563G>T (p.Ala855Ser)
 gnomAD v4
4g.6302350C>ACA356179216WFS1c.2591C>A (p.Ala864Asp)
c.2532C>A
c.2555C>A (p.Ala852Asp)
c.2306C>A (p.Ala769Asp)
n.2740C>A
c.2564C>A (p.Ala855Asp)
4g.6302350C=CA1435772660WFS1c.2591C= (p.Ala864=)
c.2532C=
c.2555C= (p.Ala852=)
c.2306C= (p.Ala769=)
n.2740C=
c.2564C= (p.Ala855=)
4g.6302350C>GCA356179218WFS1c.2591C>G (p.Ala864Gly)
c.2532C>G
c.2555C>G (p.Ala852Gly)
c.2306C>G (p.Ala769Gly)
n.2740C>G
c.2564C>G (p.Ala855Gly)
4g.6302350C>TCA2839776WFS1c.2591C>T (p.Ala864Val)
c.2532C>T
c.2555C>T (p.Ala852Val)
c.2306C>T (p.Ala769Val)
n.2740C>T
c.2564C>T (p.Ala855Val)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302350_6302355dupCA185112WFS1c.2591_2596dup (p.Gln865_Leu866insProGln)
c.2532_2537dup
c.2555_2560dup (p.Gln853_Leu854insProGln)
c.2306_2311dup (p.Gln770_Leu771insProGln)
n.2740_2745dup
c.2564_2569dup (p.Gln856_Leu857insProGln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302351C>ACA438211510WFS1c.2592C>A (p.Ala864=)
c.2533C>A
c.2556C>A (p.Ala852=)
c.2307C>A (p.Ala769=)
n.2741C>A
c.2565C>A (p.Ala855=)
 gnomAD v4
4g.6302351C=CA1435772661WFS1c.2592C= (p.Ala864=)
c.2533C=
c.2556C= (p.Ala852=)
c.2307C= (p.Ala769=)
n.2741C=
c.2565C= (p.Ala855=)
4g.6302351C>GCA2839777WFS1c.2592C>G (p.Ala864=)
c.2533C>G
c.2556C>G (p.Ala852=)
c.2307C>G (p.Ala769=)
n.2741C>G
c.2565C>G (p.Ala855=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302351C>TCA438211511WFS1c.2592C>T (p.Ala864=)
c.2533C>T
c.2556C>T (p.Ala852=)
c.2307C>T (p.Ala769=)
n.2741C>T
c.2565C>T (p.Ala855=)
 gnomAD v4
4g.6302352C>ACA356179224WFS1c.2593C>A (p.Gln865Lys)
c.2534C>A
c.2557C>A (p.Gln853Lys)
c.2308C>A (p.Gln770Lys)
n.2742C>A
c.2566C>A (p.Gln856Lys)
4g.6302352C>GCA356179221WFS1c.2593C>G (p.Gln865Glu)
c.2534C>G
c.2557C>G (p.Gln853Glu)
c.2308C>G (p.Gln770Glu)
n.2742C>G
c.2566C>G (p.Gln856Glu)
4g.6302352C>TCA356179223WFS1c.2593C>T (p.Gln865Ter)
c.2534C>T
c.2557C>T (p.Gln853Ter)
c.2308C>T (p.Gln770Ter)
n.2742C>T
c.2566C>T (p.Gln856Ter)
 gnomAD v4
4g.6302353A>CCA356179226WFS1c.2594A>C (p.Gln865Pro)
c.2535A>C
c.2558A>C (p.Gln853Pro)
c.2309A>C (p.Gln770Pro)
n.2743A>C
c.2567A>C (p.Gln856Pro)
 ClinVar
4g.6302353A>GCA356179227WFS1c.2594A>G (p.Gln865Arg)
c.2535A>G
c.2558A>G (p.Gln853Arg)
c.2309A>G (p.Gln770Arg)
n.2743A>G
c.2567A>G (p.Gln856Arg)
 gnomAD v4
4g.6302353A>TCA356179229WFS1c.2594A>T (p.Gln865Leu)
c.2535A>T
c.2558A>T (p.Gln853Leu)
c.2309A>T (p.Gln770Leu)
n.2743A>T
c.2567A>T (p.Gln856Leu)
 gnomAD v4
4g.6302354G>ACA438211512WFS1c.2595G>A (p.Gln865=)
c.2536G>A
c.2559G>A (p.Gln853=)
c.2310G>A (p.Gln770=)
n.2744G>A
c.2568G>A (p.Gln856=)
 gnomAD v4
4g.6302354G>CCA356179230WFS1c.2595G>C (p.Gln865His)
c.2536G>C
c.2559G>C (p.Gln853His)
c.2310G>C (p.Gln770His)
n.2744G>C
c.2568G>C (p.Gln856His)
4g.6302354G>TCA356179232WFS1c.2595G>T (p.Gln865His)
c.2536G>T
c.2559G>T (p.Gln853His)
c.2310G>T (p.Gln770His)
n.2744G>T
c.2568G>T (p.Gln856His)
 gnomAD v4
4g.6302355C>ACA356179235WFS1c.2596C>A (p.Leu866Ile)
c.2537C>A
c.2560C>A (p.Leu854Ile)
c.2311C>A (p.Leu771Ile)
n.2745C>A
c.2569C>A (p.Leu857Ile)
4g.6302355C=CA1435772663WFS1c.2596C= (p.Leu866=)
c.2537C=
c.2560C= (p.Leu854=)
c.2311C= (p.Leu771=)
n.2745C=
c.2569C= (p.Leu857=)
4g.6302355C>GCA356179236WFS1c.2596C>G (p.Leu866Val)
c.2537C>G
c.2560C>G (p.Leu854Val)
c.2311C>G (p.Leu771Val)
n.2745C>G
c.2569C>G (p.Leu857Val)
4g.6302355C>TCA2839778WFS1c.2596C>T (p.Leu866Phe)
c.2537C>T
c.2560C>T (p.Leu854Phe)
c.2311C>T (p.Leu771Phe)
n.2745C>T
c.2569C>T (p.Leu857Phe)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302356T>ACA356179237WFS1c.2597T>A (p.Leu866His)
c.2538T>A
c.2561T>A (p.Leu854His)
c.2312T>A (p.Leu771His)
n.2746T>A
c.2570T>A (p.Leu857His)
4g.6302356T>CCA2839779WFS1c.2597T>C (p.Leu866Pro)
c.2538T>C
c.2561T>C (p.Leu854Pro)
c.2312T>C (p.Leu771Pro)
n.2746T>C
c.2570T>C (p.Leu857Pro)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302356T>GCA356179239WFS1c.2597T>G (p.Leu866Arg)
c.2538T>G
c.2561T>G (p.Leu854Arg)
c.2312T>G (p.Leu771Arg)
n.2746T>G
c.2570T>G (p.Leu857Arg)
4g.6302356T=CA1435772665WFS1c.2597T= (p.Leu866=)
c.2538T=
c.2561T= (p.Leu854=)
c.2312T= (p.Leu771=)
n.2746T=
c.2570T= (p.Leu857=)
4g.6302357C>ACA438211513WFS1c.2598C>A (p.Leu866=)
c.2539C>A
c.2562C>A (p.Leu854=)
c.2313C>A (p.Leu771=)
n.2747C>A
c.2571C>A (p.Leu857=)
 gnomAD v4
4g.6302357C=CA1435772667WFS1c.2598C= (p.Leu866=)
c.2539C=
c.2562C= (p.Leu854=)
c.2313C= (p.Leu771=)
n.2747C=
c.2571C= (p.Leu857=)
4g.6302357C>GCA438211514WFS1c.2598C>G (p.Leu866=)
c.2539C>G
c.2562C>G (p.Leu854=)
c.2313C>G (p.Leu771=)
n.2747C>G
c.2571C>G (p.Leu857=)
 dbSNP gnomAD v3 gnomAD v4
4g.6302357C>TCA438211515WFS1c.2598C>T (p.Leu866=)
c.2539C>T
c.2562C>T (p.Leu854=)
c.2313C>T (p.Leu771=)
n.2747C>T
c.2571C>T (p.Leu857=)
 gnomAD v4
4g.6302357_6302359delCA2760271242WFS1c.2598_2600del (p.Ser867del)
c.2539_2541del
c.2562_2564del (p.Ser855del)
c.2313_2315del (p.Ser772del)
n.2747_2749del
c.2571_2573del (p.Ser858del)
4g.6302358T>ACA356179241WFS1c.2599T>A (p.Ser867Thr)
c.2540T>A
c.2563T>A (p.Ser855Thr)
c.2314T>A (p.Ser772Thr)
n.2748T>A
c.2572T>A (p.Ser858Thr)
4g.6302358T>CCA2839780WFS1c.2599T>C (p.Ser867Pro)
c.2540T>C
c.2563T>C (p.Ser855Pro)
c.2314T>C (p.Ser772Pro)
n.2748T>C
c.2572T>C (p.Ser858Pro)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302358T>GCA356179243WFS1c.2599T>G (p.Ser867Ala)
c.2540T>G
c.2563T>G (p.Ser855Ala)
c.2314T>G (p.Ser772Ala)
n.2748T>G
c.2572T>G (p.Ser858Ala)
4g.6302358T=CA1435772670WFS1c.2599T= (p.Ser867=)
c.2540T=
c.2563T= (p.Ser855=)
c.2314T= (p.Ser772=)
n.2748T=
c.2572T= (p.Ser858=)
4g.6302358_6302360delinsCCGCA891862708WFS1c.2599_2601delinsCCG (p.Ser867Pro)
c.2540_2542delinsCCG
c.2563_2565delinsCCG (p.Ser855Pro)
c.2314_2316delinsCCG (p.Ser772Pro)
n.2748_2750delinsCCG
c.2572_2574delinsCCG (p.Ser858Pro)
 ClinVar dbSNP
4g.6302358_6302360delinsTCACA1435772672WFS1c.2599_2601delinsTCA (p.Ser867=)
c.2540_2542delinsTCA
c.2563_2565delinsTCA (p.Ser855=)
c.2314_2316delinsTCA (p.Ser772=)
n.2748_2750delinsTCA
c.2572_2574delinsTCA (p.Ser858=)
4g.6302359C>ACA356179245WFS1c.2600C>A (p.Ser867Ter)
c.2541C>A
c.2564C>A (p.Ser855Ter)
c.2315C>A (p.Ser772Ter)
n.2749C>A
c.2573C>A (p.Ser858Ter)
4g.6302359C=CA1435772674WFS1c.2600C= (p.Ser867=)
c.2541C=
c.2564C= (p.Ser855=)
c.2315C= (p.Ser772=)
n.2749C=
c.2573C= (p.Ser858=)
4g.6302359C>GCA356179247WFS1c.2600C>G (p.Ser867Ter)
c.2541C>G
c.2564C>G (p.Ser855Ter)
c.2315C>G (p.Ser772Ter)
n.2749C>G
c.2573C>G (p.Ser858Ter)
4g.6302359C>TCA2839781WFS1c.2600C>T (p.Ser867Leu)
c.2541C>T
c.2564C>T (p.Ser855Leu)
c.2315C>T (p.Ser772Leu)
n.2749C>T
c.2573C>T (p.Ser858Leu)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302359_6302360delinsTGCA2573138345WFS1c.2600_2601delinsTG (p.Ser867Leu)
c.2541_2542delinsTG
c.2564_2565delinsTG (p.Ser855Leu)
c.2315_2316delinsTG (p.Ser772Leu)
n.2749_2750delinsTG
c.2573_2574delinsTG (p.Ser858Leu)
 ClinVar
4g.6302360A=CA1435772676WFS1c.2601A= (p.Ser867=)
c.2542A=
c.2565A= (p.Ser855=)
c.2316A= (p.Ser772=)
n.2750A=
c.2574A= (p.Ser858=)
4g.6302360A>CCA438211516WFS1c.2601A>C (p.Ser867=)
c.2542A>C
c.2565A>C (p.Ser855=)
c.2316A>C (p.Ser772=)
n.2750A>C
c.2574A>C (p.Ser858=)
 dbSNP
4g.6302360A>GCA136356WFS1c.2601A>G (p.Ser867=)
c.2542A>G
c.2565A>G (p.Ser855=)
c.2316A>G (p.Ser772=)
n.2750A>G
c.2574A>G (p.Ser858=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302360A>TCA2839782WFS1c.2601A>T (p.Ser867=)
c.2542A>T
c.2565A>T (p.Ser855=)
c.2316A>T (p.Ser772=)
n.2750A>T
c.2574A>T (p.Ser858=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302360dupCA2669843473WFS1c.2601dup (p.Pro868ThrfsTer?)
c.2542dup
c.2565dup (p.Pro856ThrfsTer?)
c.2316dup (p.Pro773ThrfsTer?)
n.2750dup
c.2574dup (p.Pro859ThrfsTer?)
 gnomAD v4
4g.6302361C>ACA356179250WFS1c.2602C>A (p.Pro868Thr)
c.2543C>A
c.2566C>A (p.Pro856Thr)
c.2317C>A (p.Pro773Thr)
n.2751C>A
c.2575C>A (p.Pro859Thr)
4g.6302361C>GCA356179254WFS1c.2602C>G (p.Pro868Ala)
c.2543C>G
c.2566C>G (p.Pro856Ala)
c.2317C>G (p.Pro773Ala)
n.2751C>G
c.2575C>G (p.Pro859Ala)
4g.6302361C>TCA356179251WFS1c.2602C>T (p.Pro868Ser)
c.2543C>T
c.2566C>T (p.Pro856Ser)
c.2317C>T (p.Pro773Ser)
n.2751C>T
c.2575C>T (p.Pro859Ser)
4g.6302362C>ACA356179256WFS1c.2603C>A (p.Pro868His)
c.2544C>A
c.2567C>A (p.Pro856His)
c.2318C>A (p.Pro773His)
n.2752C>A
c.2576C>A (p.Pro859His)
4g.6302362C=CA1435772679WFS1c.2603C= (p.Pro868=)
c.2544C=
c.2567C= (p.Pro856=)
c.2318C= (p.Pro773=)
n.2752C=
c.2576C= (p.Pro859=)
4g.6302362C>GCA356179259WFS1c.2603C>G (p.Pro868Arg)
c.2544C>G
c.2567C>G (p.Pro856Arg)
c.2318C>G (p.Pro773Arg)
n.2752C>G
c.2576C>G (p.Pro859Arg)
 ClinVar
4g.6302362C>TCA2839783WFS1c.2603C>T (p.Pro868Leu)
c.2544C>T
c.2567C>T (p.Pro856Leu)
c.2318C>T (p.Pro773Leu)
n.2752C>T
c.2576C>T (p.Pro859Leu)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302363C>ACA438211517WFS1c.2604C>A (p.Pro868=)
c.2545C>A
c.2568C>A (p.Pro856=)
c.2319C>A (p.Pro773=)
n.2753C>A
c.2577C>A (p.Pro859=)
4g.6302363C>GCA438211518WFS1c.2604C>G (p.Pro868=)
c.2545C>G
c.2568C>G (p.Pro856=)
c.2319C>G (p.Pro773=)
n.2753C>G
c.2577C>G (p.Pro859=)
4g.6302363C>TCA438211519WFS1c.2604C>T (p.Pro868=)
c.2545C>T
c.2568C>T (p.Pro856=)
c.2319C>T (p.Pro773=)
n.2753C>T
c.2577C>T (p.Pro859=)
 gnomAD v4
4g.6302364A=CA1435772680WFS1c.2605A= (p.Thr869=)
c.2546A=
c.2569A= (p.Thr857=)
c.2320A= (p.Thr774=)
n.2754A=
c.2578A= (p.Thr860=)
4g.6302364A>CCA356179261WFS1c.2605A>C (p.Thr869Pro)
c.2546A>C
c.2569A>C (p.Thr857Pro)
c.2320A>C (p.Thr774Pro)
n.2754A>C
c.2578A>C (p.Thr860Pro)
 dbSNP gnomAD v2 gnomAD v4
4g.6302364A>GCA356179262WFS1c.2605A>G (p.Thr869Ala)
c.2546A>G
c.2569A>G (p.Thr857Ala)
c.2320A>G (p.Thr774Ala)
n.2754A>G
c.2578A>G (p.Thr860Ala)
4g.6302364A>TCA356179264WFS1c.2605A>T (p.Thr869Ser)
c.2546A>T
c.2569A>T (p.Thr857Ser)
c.2320A>T (p.Thr774Ser)
n.2754A>T
c.2578A>T (p.Thr860Ser)
4g.6302365C>ACA356179266WFS1c.2606C>A (p.Thr869Asn)
c.2547C>A
c.2570C>A (p.Thr857Asn)
c.2321C>A (p.Thr774Asn)
n.2755C>A
c.2579C>A (p.Thr860Asn)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6302365C=CA1435772682WFS1c.2606C= (p.Thr869=)
c.2547C=
c.2570C= (p.Thr857=)
c.2321C= (p.Thr774=)
n.2755C=
c.2579C= (p.Thr860=)
4g.6302365C>GCA356179267WFS1c.2606C>G (p.Thr869Ser)
c.2547C>G
c.2570C>G (p.Thr857Ser)
c.2321C>G (p.Thr774Ser)
n.2755C>G
c.2579C>G (p.Thr860Ser)
 gnomAD v4
4g.6302365C>TCA2839784WFS1c.2606C>T (p.Thr869Ile)
c.2547C>T
c.2570C>T (p.Thr857Ile)
c.2321C>T (p.Thr774Ile)
n.2755C>T
c.2579C>T (p.Thr860Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302366C>ACA438211521WFS1c.2607C>A (p.Thr869=)
c.2548C>A
c.2571C>A (p.Thr857=)
c.2322C>A (p.Thr774=)
n.2756C>A
c.2580C>A (p.Thr860=)
 dbSNP gnomAD v2
4g.6302366C=CA1435772683WFS1c.2607C= (p.Thr869=)
c.2548C=
c.2571C= (p.Thr857=)
c.2322C= (p.Thr774=)
n.2756C=
c.2580C= (p.Thr860=)
4g.6302366C>GCA438211522WFS1c.2607C>G (p.Thr869=)
c.2548C>G
c.2571C>G (p.Thr857=)
c.2322C>G (p.Thr774=)
n.2756C>G
c.2580C>G (p.Thr860=)
4g.6302366C>TCA91797834WFS1c.2607C>T (p.Thr869=)
c.2548C>T
c.2571C>T (p.Thr857=)
c.2322C>T (p.Thr774=)
n.2756C>T
c.2580C>T (p.Thr860=)
 ClinVar dbSNP gnomAD v4
4g.6302367A>CCA438211524WFS1c.2608A>C (p.Arg870=)
c.2549A>C
c.2572A>C (p.Arg858=)
c.2323A>C (p.Arg775=)
n.2757A>C
c.2581A>C (p.Arg861=)
4g.6302367A>GCA356179270WFS1c.2608A>G (p.Arg870Gly)
c.2549A>G
c.2572A>G (p.Arg858Gly)
c.2323A>G (p.Arg775Gly)
n.2757A>G
c.2581A>G (p.Arg861Gly)
 gnomAD v4
4g.6302367A>TCA356179271WFS1c.2608A>T (p.Arg870Trp)
c.2549A>T
c.2572A>T (p.Arg858Trp)
c.2323A>T (p.Arg775Trp)
n.2757A>T
c.2581A>T (p.Arg861Trp)
4g.6302368G>ACA2839785WFS1c.2609G>A (p.Arg870Lys)
c.2550G>A
c.2573G>A (p.Arg858Lys)
c.2324G>A (p.Arg775Lys)
n.2758G>A
c.2582G>A (p.Arg861Lys)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302368G>CCA356179273WFS1c.2609G>C (p.Arg870Thr)
c.2550G>C
c.2573G>C (p.Arg858Thr)
c.2324G>C (p.Arg775Thr)
n.2758G>C
c.2582G>C (p.Arg861Thr)
 gnomAD v4
4g.6302368G=CA1435772685WFS1c.2609G= (p.Arg870=)
c.2550G=
c.2573G= (p.Arg858=)
c.2324G= (p.Arg775=)
n.2758G=
c.2582G= (p.Arg861=)
4g.6302368G>TCA356179275WFS1c.2609G>T (p.Arg870Met)
c.2550G>T
c.2573G>T (p.Arg858Met)
c.2324G>T (p.Arg775Met)
n.2758G>T
c.2582G>T (p.Arg861Met)
 gnomAD v4
4g.6302369G>ACA438211525WFS1c.2610G>A (p.Arg870=)
c.2551G>A
c.2574G>A (p.Arg858=)
c.2325G>A (p.Arg775=)
n.2759G>A
c.2583G>A (p.Arg861=)
 dbSNP
4g.6302369G>CCA356179277WFS1c.2610G>C (p.Arg870Ser)
c.2551G>C
c.2574G>C (p.Arg858Ser)
c.2325G>C (p.Arg775Ser)
n.2759G>C
c.2583G>C (p.Arg861Ser)
4g.6302369G=CA1435772686WFS1c.2610G= (p.Arg870=)
c.2551G=
c.2574G= (p.Arg858=)
c.2325G= (p.Arg775=)
n.2759G=
c.2583G= (p.Arg861=)
4g.6302369G>TCA356179278WFS1c.2610G>T (p.Arg870Ser)
c.2551G>T
c.2574G>T (p.Arg858Ser)
c.2325G>T (p.Arg775Ser)
n.2759G>T
c.2583G>T (p.Arg861Ser)
 dbSNP gnomAD v2
4g.6302370C>ACA10576642WFS1c.2611C>A (p.Arg871=)
c.2552C>A
c.2575C>A (p.Arg859=)
c.2326C>A (p.Arg776=)
n.2760C>A
c.2584C>A (p.Arg862=)
 ClinVar dbSNP
4g.6302370C=CA1435772688WFS1c.2611C= (p.Arg871=)
c.2552C=
c.2575C= (p.Arg859=)
c.2326C= (p.Arg776=)
n.2760C=
c.2584C= (p.Arg862=)
4g.6302370C>GCA356179281WFS1c.2611C>G (p.Arg871Gly)
c.2552C>G
c.2575C>G (p.Arg859Gly)
c.2326C>G (p.Arg776Gly)
n.2760C>G
c.2584C>G (p.Arg862Gly)
4g.6302370C>TCA2839786WFS1c.2611C>T (p.Arg871Trp)
c.2552C>T
c.2575C>T (p.Arg859Trp)
c.2326C>T (p.Arg776Trp)
n.2760C>T
c.2584C>T (p.Arg862Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302371G>ACA253207WFS1c.2612G>A (p.Arg871Gln)
c.2553G>A
c.2576G>A (p.Arg859Gln)
c.2327G>A (p.Arg776Gln)
n.2761G>A
c.2585G>A (p.Arg862Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302371G>CCA356179282WFS1c.2612G>C (p.Arg871Pro)
c.2553G>C
c.2576G>C (p.Arg859Pro)
c.2327G>C (p.Arg776Pro)
n.2761G>C
c.2585G>C (p.Arg862Pro)
4g.6302371G=CA1435772691WFS1c.2612G= (p.Arg871=)
c.2553G=
c.2576G= (p.Arg859=)
c.2327G= (p.Arg776=)
n.2761G=
c.2585G= (p.Arg862=)
4g.6302371G>TCA356179283WFS1c.2612G>T (p.Arg871Leu)
c.2553G>T
c.2576G>T (p.Arg859Leu)
c.2327G>T (p.Arg776Leu)
n.2761G>T
c.2585G>T (p.Arg862Leu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6302372G>ACA438211527WFS1c.2613G>A (p.Arg871=)
c.2554G>A
c.2577G>A (p.Arg859=)
c.2328G>A (p.Arg776=)
n.2762G>A
c.2586G>A (p.Arg862=)
 dbSNP gnomAD v2
4g.6302372G>CCA438211528WFS1c.2613G>C (p.Arg871=)
c.2554G>C
c.2577G>C (p.Arg859=)
c.2328G>C (p.Arg776=)
n.2762G>C
c.2586G>C (p.Arg862=)
4g.6302372G=CA1435772693WFS1c.2613G= (p.Arg871=)
c.2554G=
c.2577G= (p.Arg859=)
c.2328G= (p.Arg776=)
n.2762G=
c.2586G= (p.Arg862=)
4g.6302372G>TCA438211530WFS1c.2613G>T (p.Arg871=)
c.2554G>T
c.2577G>T (p.Arg859=)
c.2328G>T (p.Arg776=)
n.2762G>T
c.2586G>T (p.Arg862=)
4g.6302373C>ACA356179285WFS1c.2614C>A (p.His872Asn)
c.2555C>A
c.2578C>A (p.His860Asn)
c.2329C>A (p.His777Asn)
n.2763C>A
c.2587C>A (p.His863Asn)
4g.6302373C=CA1435772694WFS1c.2614C= (p.His872=)
c.2555C=
c.2578C= (p.His860=)
c.2329C= (p.His777=)
n.2763C=
c.2587C= (p.His863=)
4g.6302373C>GCA356179286WFS1c.2614C>G (p.His872Asp)
c.2555C>G
c.2578C>G (p.His860Asp)
c.2329C>G (p.His777Asp)
n.2763C>G
c.2587C>G (p.His863Asp)
4g.6302373C>TCA356179287WFS1c.2614C>T (p.His872Tyr)
c.2555C>T
c.2578C>T (p.His860Tyr)
c.2329C>T (p.His777Tyr)
n.2763C>T
c.2587C>T (p.His863Tyr)
 dbSNP COSMIC
4g.6302373_6302384delCA2580617581WFS1c.2614_2625del (p.His872_Ile875del)
c.2555_2566del
c.2578_2589del (p.His860_Ile863del)
c.2329_2340del (p.His777_Ile780del)
n.2763_2774del
c.2587_2598del (p.His863_Ile866del)
4g.6302374A>CCA356179289WFS1c.2615A>C (p.His872Pro)
c.2556A>C
c.2579A>C (p.His860Pro)
c.2330A>C (p.His777Pro)
n.2764A>C
c.2588A>C (p.His863Pro)
4g.6302374A>GCA356179291WFS1c.2615A>G (p.His872Arg)
c.2556A>G
c.2579A>G (p.His860Arg)
c.2330A>G (p.His777Arg)
n.2764A>G
c.2588A>G (p.His863Arg)
4g.6302374A>TCA356179294WFS1c.2615A>T (p.His872Leu)
c.2556A>T
c.2579A>T (p.His860Leu)
c.2330A>T (p.His777Leu)
n.2764A>T
c.2588A>T (p.His863Leu)
4g.6302375C>ACA2839787WFS1c.2616C>A (p.His872Gln)
c.2557C>A
c.2580C>A (p.His860Gln)
c.2331C>A (p.His777Gln)
n.2765C>A
c.2589C>A (p.His863Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302375C=CA1435772696WFS1c.2616C= (p.His872=)
c.2557C=
c.2580C= (p.His860=)
c.2331C= (p.His777=)
n.2765C=
c.2589C= (p.His863=)
4g.6302375C>GCA16621817WFS1c.2616C>G (p.His872Gln)
c.2557C>G
c.2580C>G (p.His860Gln)
c.2331C>G (p.His777Gln)
n.2765C>G
c.2589C>G (p.His863Gln)
 ClinVar dbSNP gnomAD v4
4g.6302375C>TCA2839788WFS1c.2616C>T (p.His872=)
c.2557C>T
c.2580C>T (p.His860=)
c.2331C>T (p.His777=)
n.2765C>T
c.2589C>T (p.His863=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302376G>ACA2839789WFS1c.2617G>A (p.Val873Met)
c.2558G>A
c.2581G>A (p.Val861Met)
c.2332G>A (p.Val778Met)
n.2766G>A
c.2590G>A (p.Val864Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302376G>CCA356179296WFS1c.2617G>C (p.Val873Leu)
c.2558G>C
c.2581G>C (p.Val861Leu)
c.2332G>C (p.Val778Leu)
n.2766G>C
c.2590G>C (p.Val864Leu)
 gnomAD v4
4g.6302376G=CA1435772699WFS1c.2617G= (p.Val873=)
c.2558G=
c.2581G= (p.Val861=)
c.2332G= (p.Val778=)
n.2766G=
c.2590G= (p.Val864=)
4g.6302376G>TCA356179298WFS1c.2617G>T (p.Val873Leu)
c.2558G>T
c.2581G>T (p.Val861Leu)
c.2332G>T (p.Val778Leu)
n.2766G>T
c.2590G>T (p.Val864Leu)
 gnomAD v4
4g.6302377T>ACA356179299WFS1c.2618T>A (p.Val873Glu)
c.2559T>A
c.2582T>A (p.Val861Glu)
c.2333T>A (p.Val778Glu)
n.2767T>A
c.2591T>A (p.Val864Glu)
 dbSNP
4g.6302377T>CCA356179301WFS1c.2618T>C (p.Val873Ala)
c.2559T>C
c.2582T>C (p.Val861Ala)
c.2333T>C (p.Val778Ala)
n.2767T>C
c.2591T>C (p.Val864Ala)
4g.6302377T>GCA321956WFS1c.2618T>G (p.Val873Gly)
c.2559T>G
c.2582T>G (p.Val861Gly)
c.2333T>G (p.Val778Gly)
n.2767T>G
c.2591T>G (p.Val864Gly)
 dbSNP COSMIC
4g.6302377T=CA1435772701WFS1c.2618T= (p.Val873=)
c.2559T=
c.2582T= (p.Val861=)
c.2333T= (p.Val778=)
n.2767T=
c.2591T= (p.Val864=)
4g.6302378G>ACA2839790WFS1c.2619G>A (p.Val873=)
c.2560G>A
c.2583G>A (p.Val861=)
c.2334G>A (p.Val778=)
n.2768G>A
c.2592G>A (p.Val864=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302378G>CCA438211534WFS1c.2619G>C (p.Val873=)
c.2560G>C
c.2583G>C (p.Val861=)
c.2334G>C (p.Val778=)
n.2768G>C
c.2592G>C (p.Val864=)
4g.6302378G=CA1435772702WFS1c.2619G= (p.Val873=)
c.2560G=
c.2583G= (p.Val861=)
c.2334G= (p.Val778=)
n.2768G=
c.2592G= (p.Val864=)
4g.6302378G>TCA438211535WFS1c.2619G>T (p.Val873=)
c.2560G>T
c.2583G>T (p.Val861=)
c.2334G>T (p.Val778=)
n.2768G>T
c.2592G>T (p.Val864=)
4g.6302380_6302382delCA2739270018WFS1c.2621_2623del (p.Lys874del)
c.2562_2564del
c.2585_2587del (p.Lys862del)
c.2336_2338del (p.Lys779del)
n.2770_2772del
c.2594_2596del (p.Lys865del)
 ClinVar
4g.6302379A=CA1435772704WFS1c.2620A= (p.Lys874=)
c.2561A=
c.2584A= (p.Lys862=)
c.2335A= (p.Lys779=)
n.2769A=
c.2593A= (p.Lys865=)
4g.6302379A>CCA356179307WFS1c.2620A>C (p.Lys874Gln)
c.2561A>C
c.2584A>C (p.Lys862Gln)
c.2335A>C (p.Lys779Gln)
n.2769A>C
c.2593A>C (p.Lys865Gln)
4g.6302379A>GCA356179313WFS1c.2620A>G (p.Lys874Glu)
c.2561A>G
c.2584A>G (p.Lys862Glu)
c.2335A>G (p.Lys779Glu)
n.2769A>G
c.2593A>G (p.Lys865Glu)
 gnomAD v4
4g.6302379A>TCA2839791WFS1c.2620A>T (p.Lys874Ter)
c.2561A>T
c.2584A>T (p.Lys862Ter)
c.2335A>T (p.Lys779Ter)
n.2769A>T
c.2593A>T (p.Lys865Ter)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302380A=CA1435772705WFS1c.2621A= (p.Lys874=)
c.2562A=
c.2585A= (p.Lys862=)
c.2336A= (p.Lys779=)
n.2770A=
c.2594A= (p.Lys865=)
4g.6302380A>CCA356179319WFS1c.2621A>C (p.Lys874Thr)
c.2562A>C
c.2585A>C (p.Lys862Thr)
c.2336A>C (p.Lys779Thr)
n.2770A>C
c.2594A>C (p.Lys865Thr)
 dbSNP
4g.6302380A>GCA356179320WFS1c.2621A>G (p.Lys874Arg)
c.2562A>G
c.2585A>G (p.Lys862Arg)
c.2336A>G (p.Lys779Arg)
n.2770A>G
c.2594A>G (p.Lys865Arg)
 dbSNP gnomAD v2 gnomAD v4
4g.6302380A>TCA356179321WFS1c.2621A>T (p.Lys874Met)
c.2562A>T
c.2585A>T (p.Lys862Met)
c.2336A>T (p.Lys779Met)
n.2770A>T
c.2594A>T (p.Lys865Met)
4g.6302381G>ACA2839792WFS1c.2622G>A (p.Lys874=)
c.2563G>A
c.2586G>A (p.Lys862=)
c.2337G>A (p.Lys779=)
n.2771G>A
c.2595G>A (p.Lys865=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302381G>CCA356179323WFS1c.2622G>C (p.Lys874Asn)
c.2563G>C
c.2586G>C (p.Lys862Asn)
c.2337G>C (p.Lys779Asn)
n.2771G>C
c.2595G>C (p.Lys865Asn)
4g.6302381G=CA1435772706WFS1c.2622G= (p.Lys874=)
c.2563G=
c.2586G= (p.Lys862=)
c.2337G= (p.Lys779=)
n.2771G=
c.2595G= (p.Lys865=)
4g.6302381G>TCA356179325WFS1c.2622G>T (p.Lys874Asn)
c.2563G>T
c.2586G>T (p.Lys862Asn)
c.2337G>T (p.Lys779Asn)
n.2771G>T
c.2595G>T (p.Lys865Asn)
 ClinVar dbSNP gnomAD v4
4g.6302382A=CA1435772707WFS1c.2623A= (p.Ile875=)
c.2564A=
c.2587A= (p.Ile863=)
c.2338A= (p.Ile780=)
n.2772A=
c.2596A= (p.Ile866=)
4g.6302382A>CCA356179328WFS1c.2623A>C (p.Ile875Leu)
c.2564A>C
c.2587A>C (p.Ile863Leu)
c.2338A>C (p.Ile780Leu)
n.2772A>C
c.2596A>C (p.Ile866Leu)
 dbSNP gnomAD v3 gnomAD v4
4g.6302382A>GCA356179330WFS1c.2623A>G (p.Ile875Val)
c.2564A>G
c.2587A>G (p.Ile863Val)
c.2338A>G (p.Ile780Val)
n.2772A>G
c.2596A>G (p.Ile866Val)
 dbSNP
4g.6302382A>TCA356179333WFS1c.2623A>T (p.Ile875Phe)
c.2564A>T
c.2587A>T (p.Ile863Phe)
c.2338A>T (p.Ile780Phe)
n.2772A>T
c.2596A>T (p.Ile866Phe)
4g.6302383T>ACA356179341WFS1c.2624T>A (p.Ile875Asn)
c.2565T>A
c.2588T>A (p.Ile863Asn)
c.2339T>A (p.Ile780Asn)
n.2773T>A
c.2597T>A (p.Ile866Asn)
 gnomAD v4
4g.6302383T>CCA91797851WFS1c.2624T>C (p.Ile875Thr)
c.2565T>C
c.2588T>C (p.Ile863Thr)
c.2339T>C (p.Ile780Thr)
n.2773T>C
c.2597T>C (p.Ile866Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6302383T>GCA356179345WFS1c.2624T>G (p.Ile875Ser)
c.2565T>G
c.2588T>G (p.Ile863Ser)
c.2339T>G (p.Ile780Ser)
n.2773T>G
c.2597T>G (p.Ile866Ser)
4g.6302383T=CA1435772709WFS1c.2624T= (p.Ile875=)
c.2565T=
c.2588T= (p.Ile863=)
c.2339T= (p.Ile780=)
n.2773T=
c.2597T= (p.Ile866=)
4g.6302384C>ACA2839795WFS1c.2625C>A (p.Ile875=)
c.2566C>A
c.2589C>A (p.Ile863=)
c.2340C>A (p.Ile780=)
n.2774C>A
c.2598C>A (p.Ile866=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302384C=CA1435772710WFS1c.2625C= (p.Ile875=)
c.2566C=
c.2589C= (p.Ile863=)
c.2340C= (p.Ile780=)
n.2774C=
c.2598C= (p.Ile866=)
4g.6302384C>GCA2839794WFS1c.2625C>G (p.Ile875Met)
c.2566C>G
c.2589C>G (p.Ile863Met)
c.2340C>G (p.Ile780Met)
n.2774C>G
c.2598C>G (p.Ile866Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302384C>TCA2839793WFS1c.2625C>T (p.Ile875=)
c.2566C>T
c.2589C>T (p.Ile863=)
c.2340C>T (p.Ile780=)
n.2774C>T
c.2598C>T (p.Ile866=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302384_6302385insTCGCA1058892867WFS1c.2625_2626insTCG (p.Ile875_Glu876insSer)
c.2566_2567insTCG
c.2589_2590insTCG (p.Ile863_Glu864insSer)
c.2340_2341insTCG (p.Ile780_Glu781insSer)
n.2774_2775insTCG
c.2598_2599insTCG (p.Ile866_Glu867insSer)
 gnomAD v3 gnomAD v4
4g.6302385G>ACA116903WFS1c.2626G>A (p.Glu876Lys)
c.2567G>A
c.2590G>A (p.Glu864Lys)
c.2341G>A (p.Glu781Lys)
n.2775G>A
c.2599G>A (p.Glu867Lys)
 ClinVar dbSNP
4g.6302385G>CCA356179356WFS1c.2626G>C (p.Glu876Gln)
c.2567G>C
c.2590G>C (p.Glu864Gln)
c.2341G>C (p.Glu781Gln)
n.2775G>C
c.2599G>C (p.Glu867Gln)
4g.6302385G=CA1435772712WFS1c.2626G= (p.Glu876=)
c.2567G=
c.2590G= (p.Glu864=)
c.2341G= (p.Glu781=)
n.2775G=
c.2599G= (p.Glu867=)
4g.6302385G>TCA356179358WFS1c.2626G>T (p.Glu876Ter)
c.2567G>T
c.2590G>T (p.Glu864Ter)
c.2341G>T (p.Glu781Ter)
n.2775G>T
c.2599G>T (p.Glu867Ter)
 gnomAD v4
4g.6302386A>CCA356179364WFS1c.2627A>C (p.Glu876Ala)
c.2568A>C
c.2591A>C (p.Glu864Ala)
c.2342A>C (p.Glu781Ala)
n.2776A>C
c.2600A>C (p.Glu867Ala)
4g.6302386A>GCA356179366WFS1c.2627A>G (p.Glu876Gly)
c.2568A>G
c.2591A>G (p.Glu864Gly)
c.2342A>G (p.Glu781Gly)
n.2776A>G
c.2600A>G (p.Glu867Gly)
 gnomAD v4
4g.6302386A>TCA356179362WFS1c.2627A>T (p.Glu876Val)
c.2568A>T
c.2591A>T (p.Glu864Val)
c.2342A>T (p.Glu781Val)
n.2776A>T
c.2600A>T (p.Glu867Val)
4g.6302386_6302393delCA1058892874WFS1c.2627_2634del (p.Glu876ValfsTer?)
c.2568_2575del
c.2591_2598del (p.Glu864ValfsTer?)
c.2342_2349del (p.Glu781ValfsTer?)
n.2776_2783del
c.2600_2607del (p.Glu867ValfsTer?)
 gnomAD v3 gnomAD v4
4g.6302387G>ACA438211543WFS1c.2628G>A (p.Glu876=)
c.2569G>A
c.2592G>A (p.Glu864=)
c.2343G>A (p.Glu781=)
n.2777G>A
c.2601G>A (p.Glu867=)
 gnomAD v4
4g.6302387G>CCA356179370WFS1c.2628G>C (p.Glu876Asp)
c.2569G>C
c.2592G>C (p.Glu864Asp)
c.2343G>C (p.Glu781Asp)
n.2777G>C
c.2601G>C (p.Glu867Asp)
4g.6302387G>TCA356179369WFS1c.2628G>T (p.Glu876Asp)
c.2569G>T
c.2592G>T (p.Glu864Asp)
c.2343G>T (p.Glu781Asp)
n.2777G>T
c.2601G>T (p.Glu867Asp)
 gnomAD v4
4g.6302388C>ACA356179372WFS1c.2629C>A (p.His877Asn)
c.2570C>A
c.2593C>A (p.His865Asn)
c.2344C>A (p.His782Asn)
n.2778C>A
c.2602C>A (p.His868Asn)
4g.6302388C>GCA356179374WFS1c.2629C>G (p.His877Asp)
c.2570C>G
c.2593C>G (p.His865Asp)
c.2344C>G (p.His782Asp)
n.2778C>G
c.2602C>G (p.His868Asp)
 gnomAD v4
4g.6302388C>TCA356179377WFS1c.2629C>T (p.His877Tyr)
c.2570C>T
c.2593C>T (p.His865Tyr)
c.2344C>T (p.His782Tyr)
n.2778C>T
c.2602C>T (p.His868Tyr)
 ClinVar gnomAD v4
4g.6302389A>CCA356179379WFS1c.2630A>C (p.His877Pro)
c.2571A>C
c.2594A>C (p.His865Pro)
c.2345A>C (p.His782Pro)
n.2779A>C
c.2603A>C (p.His868Pro)
4g.6302389A>GCA356179383WFS1c.2630A>G (p.His877Arg)
c.2571A>G
c.2594A>G (p.His865Arg)
c.2345A>G (p.His782Arg)
n.2779A>G
c.2603A>G (p.His868Arg)
 gnomAD v4
4g.6302389A>TCA356179385WFS1c.2630A>T (p.His877Leu)
c.2571A>T
c.2594A>T (p.His865Leu)
c.2345A>T (p.His782Leu)
n.2779A>T
c.2603A>T (p.His868Leu)
4g.6302390C>ACA2839797WFS1c.2631C>A (p.His877Gln)
c.2572C>A
c.2595C>A (p.His865Gln)
c.2346C>A (p.His782Gln)
n.2780C>A
c.2604C>A (p.His868Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302390C=CA1435772714WFS1c.2631C= (p.His877=)
c.2572C=
c.2595C= (p.His865=)
c.2346C= (p.His782=)
n.2780C=
c.2604C= (p.His868=)
4g.6302390C>GCA356179388WFS1c.2631C>G (p.His877Gln)
c.2572C>G
c.2595C>G (p.His865Gln)
c.2346C>G (p.His782Gln)
n.2780C>G
c.2604C>G (p.His868Gln)
4g.6302390C>TCA2839796WFS1c.2631C>T (p.His877=)
c.2572C>T
c.2595C>T (p.His865=)
c.2346C>T (p.His782=)
n.2780C>T
c.2604C>T (p.His868=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302391G>ACA182744WFS1c.2632G>A (p.Asp878Asn)
c.2573G>A
c.2596G>A (p.Asp866Asn)
c.2347G>A (p.Asp783Asn)
n.2781G>A
c.2605G>A (p.Asp869Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302391G>CCA356179394WFS1c.2632G>C (p.Asp878His)
c.2573G>C
c.2596G>C (p.Asp866His)
c.2347G>C (p.Asp783His)
n.2781G>C
c.2605G>C (p.Asp869His)
4g.6302391G=CA1435772716WFS1c.2632G= (p.Asp878=)
c.2573G=
c.2596G= (p.Asp866=)
c.2347G= (p.Asp783=)
n.2781G=
c.2605G= (p.Asp869=)
4g.6302391G>TCA2839798WFS1c.2632G>T (p.Asp878Tyr)
c.2573G>T
c.2596G>T (p.Asp866Tyr)
c.2347G>T (p.Asp783Tyr)
n.2781G>T
c.2605G>T (p.Asp869Tyr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302392A>CCA356179402WFS1c.2633A>C (p.Asp878Ala)
c.2574A>C
c.2597A>C (p.Asp866Ala)
c.2348A>C (p.Asp783Ala)
n.2782A>C
c.2606A>C (p.Asp869Ala)
4g.6302392A>GCA356179399WFS1c.2633A>G (p.Asp878Gly)
c.2574A>G
c.2597A>G (p.Asp866Gly)
c.2348A>G (p.Asp783Gly)
n.2782A>G
c.2606A>G (p.Asp869Gly)
 ClinVar dbSNP gnomAD v4
4g.6302392A>TCA356179397WFS1c.2633A>T (p.Asp878Val)
c.2574A>T
c.2597A>T (p.Asp866Val)
c.2348A>T (p.Asp783Val)
n.2782A>T
c.2606A>T (p.Asp869Val)
4g.6302393C>ACA356179404WFS1c.2634C>A (p.Asp878Glu)
c.2575C>A
c.2598C>A (p.Asp866Glu)
c.2349C>A (p.Asp783Glu)
n.2783C>A
c.2607C>A (p.Asp869Glu)
4g.6302393C=CA1435772718WFS1c.2634C= (p.Asp878=)
c.2575C=
c.2598C= (p.Asp866=)
c.2349C= (p.Asp783=)
n.2783C=
c.2607C= (p.Asp869=)
4g.6302393C>GCA2839799WFS1c.2634C>G (p.Asp878Glu)
c.2575C>G
c.2598C>G (p.Asp866Glu)
c.2349C>G (p.Asp783Glu)
n.2783C>G
c.2607C>G (p.Asp869Glu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302393C>TCA438211546WFS1c.2634C>T (p.Asp878=)
c.2575C>T
c.2598C>T (p.Asp866=)
c.2349C>T (p.Asp783=)
n.2783C>T
c.2607C>T (p.Asp869=)
 dbSNP gnomAD v2 gnomAD v4
4g.6302394T>ACA356179409WFS1c.2635T>A (p.Trp879Arg)
c.2576T>A
c.2599T>A (p.Trp867Arg)
c.2350T>A (p.Trp784Arg)
n.2784T>A
c.2608T>A (p.Trp870Arg)
4g.6302394T>CCA356179410WFS1c.2635T>C (p.Trp879Arg)
c.2576T>C
c.2599T>C (p.Trp867Arg)
c.2350T>C (p.Trp784Arg)
n.2784T>C
c.2608T>C (p.Trp870Arg)
 dbSNP
4g.6302394T>GCA356179414WFS1c.2635T>G (p.Trp879Gly)
c.2576T>G
c.2599T>G (p.Trp867Gly)
c.2350T>G (p.Trp784Gly)
n.2784T>G
c.2608T>G (p.Trp870Gly)
 gnomAD v4
4g.6302394T=CA1435772720WFS1c.2635T= (p.Trp879=)
c.2576T=
c.2599T= (p.Trp867=)
c.2350T= (p.Trp784=)
n.2784T=
c.2608T= (p.Trp870=)
4g.6302400_6302416dupCA2669843475WFS1c.2641_2657dup (p.Val887AlafsTer7)
c.2582_2598dup
c.2605_2621dup (p.Val875AlafsTer7)
c.2356_2372dup (p.Val792AlafsTer7)
n.2790_2806dup
c.2614_2630dup (p.Val878AlafsTer7)
 gnomAD v4
4g.6302400_6302416delCA2669843476WFS1c.2641_2657del (p.Ser881ArgfsTer?)
c.2582_2598del
c.2605_2621del (p.Ser869ArgfsTer?)
c.2356_2372del (p.Ser786ArgfsTer?)
n.2790_2806del
c.2614_2630del (p.Ser872ArgfsTer?)
 gnomAD v4
4g.6302395G>ACA356179417WFS1c.2636G>A (p.Trp879Ter)
c.2577G>A
c.2600G>A (p.Trp867Ter)
c.2351G>A (p.Trp784Ter)
n.2785G>A
c.2609G>A (p.Trp870Ter)
 ClinVar dbSNP gnomAD v4
4g.6302395G>CCA356179420WFS1c.2636G>C (p.Trp879Ser)
c.2577G>C
c.2600G>C (p.Trp867Ser)
c.2351G>C (p.Trp784Ser)
n.2785G>C
c.2609G>C (p.Trp870Ser)
4g.6302395G=CA1435772721WFS1c.2636G= (p.Trp879=)
c.2577G=
c.2600G= (p.Trp867=)
c.2351G= (p.Trp784=)
n.2785G=
c.2609G= (p.Trp870=)
4g.6302395G>TCA356179422WFS1c.2636G>T (p.Trp879Leu)
c.2577G>T
c.2600G>T (p.Trp867Leu)
c.2351G>T (p.Trp784Leu)
n.2785G>T
c.2609G>T (p.Trp870Leu)
4g.6302396G>ACA356179424WFS1c.2637G>A (p.Trp879Ter)
c.2578G>A
c.2601G>A (p.Trp867Ter)
c.2352G>A (p.Trp784Ter)
n.2786G>A
c.2610G>A (p.Trp870Ter)
4g.6302396G>CCA356179426WFS1c.2637G>C (p.Trp879Cys)
c.2578G>C
c.2601G>C (p.Trp867Cys)
c.2352G>C (p.Trp784Cys)
n.2786G>C
c.2610G>C (p.Trp870Cys)
 ClinVar dbSNP gnomAD v4
4g.6302396G>TCA356179429WFS1c.2637G>T (p.Trp879Cys)
c.2578G>T
c.2601G>T (p.Trp867Cys)
c.2352G>T (p.Trp784Cys)
n.2786G>T
c.2610G>T (p.Trp870Cys)
4g.6302396_6302397insTCA1058892891WFS1c.2637_2638insT (p.Arg880SerfsTer?)
c.2578_2579insT
c.2601_2602insT (p.Arg868SerfsTer?)
c.2352_2353insT (p.Arg785SerfsTer?)
n.2786_2787insT
c.2610_2611insT (p.Arg871SerfsTer?)
 gnomAD v3 gnomAD v4
4g.6302397C>ACA356179434WFS1c.2638C>A (p.Arg880Ser)
c.2579C>A
c.2602C>A (p.Arg868Ser)
c.2353C>A (p.Arg785Ser)
n.2787C>A
c.2611C>A (p.Arg871Ser)
4g.6302397C=CA1435772723WFS1c.2638C= (p.Arg880=)
c.2579C=
c.2602C= (p.Arg868=)
c.2353C= (p.Arg785=)
n.2787C=
c.2611C= (p.Arg871=)
4g.6302397C>GCA356179436WFS1c.2638C>G (p.Arg880Gly)
c.2579C>G
c.2602C>G (p.Arg868Gly)
c.2353C>G (p.Arg785Gly)
n.2787C>G
c.2611C>G (p.Arg871Gly)
 dbSNP gnomAD v2 gnomAD v4
4g.6302397C>TCA2839800WFS1c.2638C>T (p.Arg880Cys)
c.2579C>T
c.2602C>T (p.Arg868Cys)
c.2353C>T (p.Arg785Cys)
n.2787C>T
c.2611C>T (p.Arg871Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302398G>ACA324220WFS1c.2639G>A (p.Arg880His)
c.2580G>A
c.2603G>A (p.Arg868His)
c.2354G>A (p.Arg785His)
n.2788G>A
c.2612G>A (p.Arg871His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302398G>CCA91797871WFS1c.2639G>C (p.Arg880Pro)
c.2580G>C
c.2603G>C (p.Arg868Pro)
c.2354G>C (p.Arg785Pro)
n.2788G>C
c.2612G>C (p.Arg871Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302398G=CA1435772725WFS1c.2639G= (p.Arg880=)
c.2580G=
c.2603G= (p.Arg868=)
c.2354G= (p.Arg785=)
n.2788G=
c.2612G= (p.Arg871=)
4g.6302398G>TCA356179437WFS1c.2639G>T (p.Arg880Leu)
c.2580G>T
c.2603G>T (p.Arg868Leu)
c.2354G>T (p.Arg785Leu)
n.2788G>T
c.2612G>T (p.Arg871Leu)
4g.6302399C>ACA438211551WFS1c.2640C>A (p.Arg880=)
c.2581C>A
c.2604C>A (p.Arg868=)
c.2355C>A (p.Arg785=)
n.2789C>A
c.2613C>A (p.Arg871=)
 gnomAD v4
4g.6302399C=CA1435772727WFS1c.2640C= (p.Arg880=)
c.2581C=
c.2604C= (p.Arg868=)
c.2355C= (p.Arg785=)
n.2789C=
c.2613C= (p.Arg871=)
4g.6302399C>GCA438211552WFS1c.2640C>G (p.Arg880=)
c.2581C>G
c.2604C>G (p.Arg868=)
c.2355C>G (p.Arg785=)
n.2789C>G
c.2613C>G (p.Arg871=)
4g.6302399C>TCA2839801WFS1c.2640C>T (p.Arg880=)
c.2581C>T
c.2604C>T (p.Arg868=)
c.2355C>T (p.Arg785=)
n.2789C>T
c.2613C>T (p.Arg871=)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302400A=CA1435772729WFS1c.2641A= (p.Ser881=)
c.2582A=
c.2605A= (p.Ser869=)
c.2356A= (p.Ser786=)
n.2790A=
c.2614A= (p.Ser872=)
4g.6302400A>CCA356179439WFS1c.2641A>C (p.Ser881Arg)
c.2582A>C
c.2605A>C (p.Ser869Arg)
c.2356A>C (p.Ser786Arg)
n.2790A>C
c.2614A>C (p.Ser872Arg)
4g.6302400A>GCA91797876WFS1c.2641A>G (p.Ser881Gly)
c.2582A>G
c.2605A>G (p.Ser869Gly)
c.2356A>G (p.Ser786Gly)
n.2790A>G
c.2614A>G (p.Ser872Gly)
 dbSNP gnomAD v3 gnomAD v4
4g.6302400A>TCA356179442WFS1c.2641A>T (p.Ser881Cys)
c.2582A>T
c.2605A>T (p.Ser869Cys)
c.2356A>T (p.Ser786Cys)
n.2790A>T
c.2614A>T (p.Ser872Cys)
4g.6302400_6302411delCA2586973657WFS1c.2641_2652del (p.Ser881_His884del)
c.2582_2593del
c.2605_2616del (p.Ser869_His872del)
c.2356_2367del (p.Ser786_His789del)
n.2790_2801del
c.2614_2625del (p.Ser872_His875del)
4g.6302400_6302401insAGCACCGTGCATCA2586973659WFS1c.2641_2642insAGCACCGTGCAT (p.Ser881delinsLysHisArgAlaCys)
c.2582_2583insAGCACCGTGCAT
c.2605_2606insAGCACCGTGCAT (p.Ser869delinsLysHisArgAlaCys)
c.2356_2357insAGCACCGTGCAT (p.Ser786delinsLysHisArgAlaCys)
n.2790_2791insAGCACCGTGCAT
c.2614_2615insAGCACCGTGCAT (p.Ser872delinsLysHisArgAlaCys)
4g.6302401G>ACA2839802WFS1c.2642G>A (p.Ser881Asn)
c.2583G>A
c.2606G>A (p.Ser869Asn)
c.2357G>A (p.Ser786Asn)
n.2791G>A
c.2615G>A (p.Ser872Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302401G>CCA356179448WFS1c.2642G>C (p.Ser881Thr)
c.2583G>C
c.2606G>C (p.Ser869Thr)
c.2357G>C (p.Ser786Thr)
n.2791G>C
c.2615G>C (p.Ser872Thr)
4g.6302401G=CA1435772730WFS1c.2642G= (p.Ser881=)
c.2583G=
c.2606G= (p.Ser869=)
c.2357G= (p.Ser786=)
n.2791G=
c.2615G= (p.Ser872=)
4g.6302401G>TCA356179450WFS1c.2642G>T (p.Ser881Ile)
c.2583G>T
c.2606G>T (p.Ser869Ile)
c.2357G>T (p.Ser786Ile)
n.2791G>T
c.2615G>T (p.Ser872Ile)
4g.6302403_6302414dupCA2586973658WFS1c.2644_2655dup (p.Gly885_Ala886insThrValHisGly)
c.2585_2596dup
c.2608_2619dup (p.Gly873_Ala874insThrValHisGly)
c.2359_2370dup (p.Gly790_Ala791insThrValHisGly)
n.2793_2804dup
c.2617_2628dup (p.Gly876_Ala877insThrValHisGly)
4g.6302403_6302414delCA2669843477WFS1c.2644_2655del (p.Thr882_Gly885del)
c.2585_2596del
c.2608_2619del (p.Thr870_Gly873del)
c.2359_2370del (p.Thr787_Gly790del)
n.2793_2804del
c.2617_2628del (p.Thr873_Gly876del)
 gnomAD v4
4g.6302402_6302418dupCA2669843478WFS1c.2643_2659dup (p.Val887AlafsTer7)
c.2584_2600dup
c.2607_2623dup (p.Val875AlafsTer7)
c.2358_2374dup (p.Val792AlafsTer7)
n.2792_2808dup
c.2616_2632dup (p.Val878AlafsTer7)
 gnomAD v4
4g.6302402C>ACA356179453WFS1c.2643C>A (p.Ser881Arg)
c.2584C>A
c.2607C>A (p.Ser869Arg)
c.2358C>A (p.Ser786Arg)
n.2792C>A
c.2616C>A (p.Ser872Arg)
4g.6302402C=CA1435772732WFS1c.2643C= (p.Ser881=)
c.2584C=
c.2607C= (p.Ser869=)
c.2358C= (p.Ser786=)
n.2792C=
c.2616C= (p.Ser872=)
4g.6302402C>GCA356179454WFS1c.2643C>G (p.Ser881Arg)
c.2584C>G
c.2607C>G (p.Ser869Arg)
c.2358C>G (p.Ser786Arg)
n.2792C>G
c.2616C>G (p.Ser872Arg)
 gnomAD v4
4g.6302402C>TCA438211556WFS1c.2643C>T (p.Ser881=)
c.2584C>T
c.2607C>T (p.Ser869=)
c.2358C>T (p.Ser786=)
n.2792C>T
c.2616C>T (p.Ser872=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302403A=CA1435772734WFS1c.2644A= (p.Thr882=)
c.2585A=
c.2608A= (p.Thr870=)
c.2359A= (p.Thr787=)
n.2793A=
c.2617A= (p.Thr873=)
4g.6302403A>CCA2839803WFS1c.2644A>C (p.Thr882Pro)
c.2585A>C
c.2608A>C (p.Thr870Pro)
c.2359A>C (p.Thr787Pro)
n.2793A>C
c.2617A>C (p.Thr873Pro)
 dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302403A>GCA356179458WFS1c.2644A>G (p.Thr882Ala)
c.2585A>G
c.2608A>G (p.Thr870Ala)
c.2359A>G (p.Thr787Ala)
n.2793A>G
c.2617A>G (p.Thr873Ala)
4g.6302403A>TCA356179461WFS1c.2644A>T (p.Thr882Ser)
c.2585A>T
c.2608A>T (p.Thr870Ser)
c.2359A>T (p.Thr787Ser)
n.2793A>T
c.2617A>T (p.Thr873Ser)
4g.6302404C>ACA356179468WFS1c.2645C>A (p.Thr882Asn)
c.2586C>A
c.2609C>A (p.Thr870Asn)
c.2360C>A (p.Thr787Asn)
n.2794C>A
c.2618C>A (p.Thr873Asn)
4g.6302404C=CA1435772736WFS1c.2645C= (p.Thr882=)
c.2586C=
c.2609C= (p.Thr870=)
c.2360C= (p.Thr787=)
n.2794C=
c.2618C= (p.Thr873=)
4g.6302404C>GCA356179466WFS1c.2645C>G (p.Thr882Ser)
c.2586C>G
c.2609C>G (p.Thr870Ser)
c.2360C>G (p.Thr787Ser)
n.2794C>G
c.2618C>G (p.Thr873Ser)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302404C>TCA356179463WFS1c.2645C>T (p.Thr882Ile)
c.2586C>T
c.2609C>T (p.Thr870Ile)
c.2360C>T (p.Thr787Ile)
n.2794C>T
c.2618C>T (p.Thr873Ile)
 gnomAD v4
4g.6302409_6302420delCA2586973660WFS1c.2650_2661del (p.His884_Val887del)
c.2591_2602del
c.2614_2625del (p.His872_Val875del)
c.2365_2376del (p.His789_Val792del)
n.2799_2810del
c.2623_2634del (p.His875_Val878del)
 ClinVar gnomAD v4
4g.6302405C>ACA438211559WFS1c.2646C>A (p.Thr882=)
c.2587C>A
c.2610C>A (p.Thr870=)
c.2361C>A (p.Thr787=)
n.2795C>A
c.2619C>A (p.Thr873=)
4g.6302405C=CA1435772738WFS1c.2646C= (p.Thr882=)
c.2587C=
c.2610C= (p.Thr870=)
c.2361C= (p.Thr787=)
n.2795C=
c.2619C= (p.Thr873=)
4g.6302405C>GCA438211561WFS1c.2646C>G (p.Thr882=)
c.2587C>G
c.2610C>G (p.Thr870=)
c.2361C>G (p.Thr787=)
n.2795C>G
c.2619C>G (p.Thr873=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302405C>TCA179685WFS1c.2646C>T (p.Thr882=)
c.2587C>T
c.2610C>T (p.Thr870=)
c.2361C>T (p.Thr787=)
n.2795C>T
c.2619C>T (p.Thr873=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302406G>ACA285655WFS1c.2647G>A (p.Val883Met)
c.2588G>A
c.2611G>A (p.Val871Met)
c.2362G>A (p.Val788Met)
n.2796G>A
c.2620G>A (p.Val874Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302406G>CCA356179472WFS1c.2647G>C (p.Val883Leu)
c.2588G>C
c.2611G>C (p.Val871Leu)
c.2362G>C (p.Val788Leu)
n.2796G>C
c.2620G>C (p.Val874Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302406G=CA1435772740WFS1c.2647G= (p.Val883=)
c.2588G=
c.2611G= (p.Val871=)
c.2362G= (p.Val788=)
n.2796G=
c.2620G= (p.Val874=)
4g.6302406G>TCA356179475WFS1c.2647G>T (p.Val883Leu)
c.2588G>T
c.2611G>T (p.Val871Leu)
c.2362G>T (p.Val788Leu)
n.2796G>T
c.2620G>T (p.Val874Leu)
4g.6302407T>ACA356179477WFS1c.2648T>A (p.Val883Glu)
c.2589T>A
c.2612T>A (p.Val871Glu)
c.2363T>A (p.Val788Glu)
n.2797T>A
c.2621T>A (p.Val874Glu)
4g.6302407T>CCA356179480WFS1c.2648T>C (p.Val883Ala)
c.2589T>C
c.2612T>C (p.Val871Ala)
c.2363T>C (p.Val788Ala)
n.2797T>C
c.2621T>C (p.Val874Ala)
4g.6302407T>GCA2839804WFS1c.2648T>G (p.Val883Gly)
c.2589T>G
c.2612T>G (p.Val871Gly)
c.2363T>G (p.Val788Gly)
n.2797T>G
c.2621T>G (p.Val874Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302407T=CA1435772741WFS1c.2648T= (p.Val883=)
c.2589T=
c.2612T= (p.Val871=)
c.2363T= (p.Val788=)
n.2797T=
c.2621T= (p.Val874=)
4g.6302408G>ACA438211566WFS1c.2649G>A (p.Val883=)
c.2590G>A
c.2613G>A (p.Val871=)
c.2364G>A (p.Val788=)
n.2798G>A
c.2622G>A (p.Val874=)
4g.6302408G>CCA438211568WFS1c.2649G>C (p.Val883=)
c.2590G>C
c.2613G>C (p.Val871=)
c.2364G>C (p.Val788=)
n.2798G>C
c.2622G>C (p.Val874=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302408G=CA1435772743WFS1c.2649G= (p.Val883=)
c.2590G=
c.2613G= (p.Val871=)
c.2364G= (p.Val788=)
n.2798G=
c.2622G= (p.Val874=)
4g.6302408G>TCA438211567WFS1c.2649G>T (p.Val883=)
c.2590G>T
c.2613G>T (p.Val871=)
c.2364G>T (p.Val788=)
n.2798G>T
c.2622G>T (p.Val874=)
 gnomAD v3 gnomAD v4
4g.6302409C>ACA356179483WFS1c.2650C>A (p.His884Asn)
c.2591C>A
c.2614C>A (p.His872Asn)
c.2365C>A (p.His789Asn)
n.2799C>A
c.2623C>A (p.His875Asn)
4g.6302409C=CA1435772744WFS1c.2650C= (p.His884=)
c.2591C=
c.2614C= (p.His872=)
c.2365C= (p.His789=)
n.2799C=
c.2623C= (p.His875=)
4g.6302409C>GCA356179485WFS1c.2650C>G (p.His884Asp)
c.2591C>G
c.2614C>G (p.His872Asp)
c.2365C>G (p.His789Asp)
n.2799C>G
c.2623C>G (p.His875Asp)
4g.6302409C>TCA356179486WFS1c.2650C>T (p.His884Tyr)
c.2591C>T
c.2614C>T (p.His872Tyr)
c.2365C>T (p.His789Tyr)
n.2799C>T
c.2623C>T (p.His875Tyr)
 dbSNP
4g.6302410A=CA1435772746WFS1c.2651A= (p.His884=)
c.2592A=
c.2615A= (p.His872=)
c.2366A= (p.His789=)
n.2800A=
c.2624A= (p.His875=)
4g.6302410A>CCA356179488WFS1c.2651A>C (p.His884Pro)
c.2592A>C
c.2615A>C (p.His872Pro)
c.2366A>C (p.His789Pro)
n.2800A>C
c.2624A>C (p.His875Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302410A>GCA2839805WFS1c.2651A>G (p.His884Arg)
c.2592A>G
c.2615A>G (p.His872Arg)
c.2366A>G (p.His789Arg)
n.2800A>G
c.2624A>G (p.His875Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302410A>TCA356179491WFS1c.2651A>T (p.His884Leu)
c.2592A>T
c.2615A>T (p.His872Leu)
c.2366A>T (p.His789Leu)
n.2800A>T
c.2624A>T (p.His875Leu)
 gnomAD v4
4g.6302411T>ACA356179498WFS1c.2652T>A (p.His884Gln)
c.2593T>A
c.2616T>A (p.His872Gln)
c.2367T>A (p.His789Gln)
n.2801T>A
c.2625T>A (p.His875Gln)
4g.6302411T>CCA438211569WFS1c.2652T>C (p.His884=)
c.2593T>C
c.2616T>C (p.His872=)
c.2367T>C (p.His789=)
n.2801T>C
c.2625T>C (p.His875=)
4g.6302411T>GCA356179496WFS1c.2652T>G (p.His884Gln)
c.2593T>G
c.2616T>G (p.His872Gln)
c.2367T>G (p.His789Gln)
n.2801T>G
c.2625T>G (p.His875Gln)
4g.6302412G>ACA356179500WFS1c.2653G>A (p.Gly885Ser)
c.2594G>A
c.2617G>A (p.Gly873Ser)
c.2368G>A (p.Gly790Ser)
n.2802G>A
c.2626G>A (p.Gly876Ser)
4g.6302412G>CCA356179501WFS1c.2653G>C (p.Gly885Arg)
c.2594G>C
c.2617G>C (p.Gly873Arg)
c.2368G>C (p.Gly790Arg)
n.2802G>C
c.2626G>C (p.Gly876Arg)
4g.6302412G>TCA356179504WFS1c.2653G>T (p.Gly885Cys)
c.2594G>T
c.2617G>T (p.Gly873Cys)
c.2368G>T (p.Gly790Cys)
n.2802G>T
c.2626G>T (p.Gly876Cys)
4g.6302413G>ACA356179505WFS1c.2654G>A (p.Gly885Asp)
c.2595G>A
c.2618G>A (p.Gly873Asp)
c.2369G>A (p.Gly790Asp)
n.2803G>A
c.2627G>A (p.Gly876Asp)
 dbSNP
4g.6302413G>CCA356179508WFS1c.2654G>C (p.Gly885Ala)
c.2595G>C
c.2618G>C (p.Gly873Ala)
c.2369G>C (p.Gly790Ala)
n.2803G>C
c.2627G>C (p.Gly876Ala)
4g.6302413G=CA1435772747WFS1c.2654G= (p.Gly885=)
c.2595G=
c.2618G= (p.Gly873=)
c.2369G= (p.Gly790=)
n.2803G=
c.2627G= (p.Gly876=)
4g.6302413G>TCA356179510WFS1c.2654G>T (p.Gly885Val)
c.2595G>T
c.2618G>T (p.Gly873Val)
c.2369G>T (p.Gly790Val)
n.2803G>T
c.2627G>T (p.Gly876Val)
 gnomAD v4
4g.6302414C>ACA438211571WFS1c.2655C>A (p.Gly885=)
c.2596C>A
c.2619C>A (p.Gly873=)
c.2370C>A (p.Gly790=)
n.2804C>A
c.2628C>A (p.Gly876=)
4g.6302414C=CA1435772749WFS1c.2655C= (p.Gly885=)
c.2596C=
c.2619C= (p.Gly873=)
c.2370C= (p.Gly790=)
n.2804C=
c.2628C= (p.Gly876=)
4g.6302414C>GCA438211573WFS1c.2655C>G (p.Gly885=)
c.2596C>G
c.2619C>G (p.Gly873=)
c.2370C>G (p.Gly790=)
n.2804C>G
c.2628C>G (p.Gly876=)
4g.6302414C>TCA2839806WFS1c.2655C>T (p.Gly885=)
c.2596C>T
c.2619C>T (p.Gly873=)
c.2370C>T (p.Gly790=)
n.2804C>T
c.2628C>T (p.Gly876=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302415G>ACA2839807WFS1c.2656G>A (p.Ala886Thr)
c.2597G>A
c.2620G>A (p.Ala874Thr)
c.2371G>A (p.Ala791Thr)
n.2805G>A
c.2629G>A (p.Ala877Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302415G>CCA356179517WFS1c.2656G>C (p.Ala886Pro)
c.2597G>C
c.2620G>C (p.Ala874Pro)
c.2371G>C (p.Ala791Pro)
n.2805G>C
c.2629G>C (p.Ala877Pro)
 ClinVar dbSNP gnomAD v4
4g.6302415G=CA1435772751WFS1c.2656G= (p.Ala886=)
c.2597G=
c.2620G= (p.Ala874=)
c.2371G= (p.Ala791=)
n.2805G=
c.2629G= (p.Ala877=)
4g.6302415G>TCA356179519WFS1c.2656G>T (p.Ala886Ser)
c.2597G>T
c.2620G>T (p.Ala874Ser)
c.2371G>T (p.Ala791Ser)
n.2805G>T
c.2629G>T (p.Ala877Ser)
4g.6302416C>ACA356179521WFS1c.2657C>A (p.Ala886Asp)
c.2598C>A
c.2621C>A (p.Ala874Asp)
c.2372C>A (p.Ala791Asp)
n.2806C>A
c.2630C>A (p.Ala877Asp)
 ClinVar dbSNP
4g.6302416C=CA1435772753WFS1c.2657C= (p.Ala886=)
c.2598C=
c.2621C= (p.Ala874=)
c.2372C= (p.Ala791=)
n.2806C=
c.2630C= (p.Ala877=)
4g.6302416C>GCA2839808WFS1c.2657C>G (p.Ala886Gly)
c.2598C>G
c.2621C>G (p.Ala874Gly)
c.2372C>G (p.Ala791Gly)
n.2806C>G
c.2630C>G (p.Ala877Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302416C>TCA356179524WFS1c.2657C>T (p.Ala886Val)
c.2598C>T
c.2621C>T (p.Ala874Val)
c.2372C>T (p.Ala791Val)
n.2806C>T
c.2630C>T (p.Ala877Val)
 dbSNP gnomAD v2 gnomAD v4
4g.6302417C>ACA438211574WFS1c.2658C>A (p.Ala886=)
c.2599C>A
c.2622C>A (p.Ala874=)
c.2373C>A (p.Ala791=)
n.2807C>A
c.2631C>A (p.Ala877=)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302417C=CA1435772755WFS1c.2658C= (p.Ala886=)
c.2599C=
c.2622C= (p.Ala874=)
c.2373C= (p.Ala791=)
n.2807C=
c.2631C= (p.Ala877=)
4g.6302417C>GCA438211576WFS1c.2658C>G (p.Ala886=)
c.2599C>G
c.2622C>G (p.Ala874=)
c.2373C>G (p.Ala791=)
n.2807C>G
c.2631C>G (p.Ala877=)
 dbSNP gnomAD v3 gnomAD v4
4g.6302417C>TCA2839809WFS1c.2658C>T (p.Ala886=)
c.2599C>T
c.2622C>T (p.Ala874=)
c.2373C>T (p.Ala791=)
n.2807C>T
c.2631C>T (p.Ala877=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302418G>ACA2839810WFS1c.2659G>A (p.Val887Met)
c.2600G>A
c.2623G>A (p.Val875Met)
c.2374G>A (p.Val792Met)
n.2808G>A
c.2632G>A (p.Val878Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6302418G>CCA356179529WFS1c.2659G>C (p.Val887Leu)
c.2600G>C
c.2623G>C (p.Val875Leu)
c.2374G>C (p.Val792Leu)
n.2808G>C
c.2632G>C (p.Val878Leu)
 dbSNP
4g.6302418G=CA1435772758WFS1c.2659G= (p.Val887=)
c.2600G=
c.2623G= (p.Val875=)
c.2374G= (p.Val792=)
n.2808G=
c.2632G= (p.Val878=)
4g.6302418G>TCA356179527WFS1c.2659G>T (p.Val887Leu)
c.2600G>T
c.2623G>T (p.Val875Leu)
c.2374G>T (p.Val792Leu)
n.2808G>T
c.2632G>T (p.Val878Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6302419T>ACA356179532WFS1c.2660T>A (p.Val887Glu)
c.2601T>A
c.2624T>A (p.Val875Glu)
c.2375T>A (p.Val792Glu)
n.2809T>A
c.2633T>A (p.Val878Glu)
4g.6302419T>CCA356179534WFS1c.2660T>C (p.Val887Ala)
c.2601T>C
c.2624T>C (p.Val875Ala)
c.2375T>C (p.Val792Ala)
n.2809T>C
c.2633T>C (p.Val878Ala)
 ClinVar dbSNP gnomAD v4
4g.6302419T>GCA356179536WFS1c.2660T>G (p.Val887Gly)
c.2601T>G
c.2624T>G (p.Val875Gly)
c.2375T>G (p.Val792Gly)
n.2809T>G
c.2633T>G (p.Val878Gly)
4g.6302419T=CA1435772760WFS1c.2660T= (p.Val887=)
c.2601T=
c.2624T= (p.Val875=)
c.2375T= (p.Val792=)
n.2809T=
c.2633T= (p.Val878=)
4g.6302420G>ACA438211578WFS1c.2661G>A (p.Val887=)
c.2602G>A
c.2625G>A (p.Val875=)
c.2376G>A (p.Val792=)
n.2810G>A
c.2634G>A (p.Val878=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302420G>CCA438211579WFS1c.2661G>C (p.Val887=)
c.2602G>C
c.2625G>C (p.Val875=)
c.2376G>C (p.Val792=)
n.2810G>C
c.2634G>C (p.Val878=)
 gnomAD v4
4g.6302420G=CA1435772762WFS1c.2661G= (p.Val887=)
c.2602G=
c.2625G= (p.Val875=)
c.2376G= (p.Val792=)
n.2810G=
c.2634G= (p.Val878=)
4g.6302420G>TCA438211580WFS1c.2661G>T (p.Val887=)
c.2602G>T
c.2625G>T (p.Val875=)
c.2376G>T (p.Val792=)
n.2810G>T
c.2634G>T (p.Val878=)
4g.6302421A=CA1435772764WFS1c.2662A= (p.Lys888=)
c.2603A=
c.2626A= (p.Lys876=)
c.2377A= (p.Lys793=)
n.2811A=
c.2635A= (p.Lys879=)
4g.6302421A>CCA356179539WFS1c.2662A>C (p.Lys888Gln)
c.2603A>C
c.2626A>C (p.Lys876Gln)
c.2377A>C (p.Lys793Gln)
n.2811A>C
c.2635A>C (p.Lys879Gln)
 dbSNP gnomAD v4
4g.6302421A>GCA356179542WFS1c.2662A>G (p.Lys888Glu)
c.2603A>G
c.2626A>G (p.Lys876Glu)
c.2377A>G (p.Lys793Glu)
n.2811A>G
c.2635A>G (p.Lys879Glu)
4g.6302421A>TCA356179544WFS1c.2662A>T (p.Lys888Ter)
c.2603A>T
c.2626A>T (p.Lys876Ter)
c.2377A>T (p.Lys793Ter)
n.2811A>T
c.2635A>T (p.Lys879Ter)
4g.6302422A=CA1435772766WFS1c.2663A= (p.Lys888=)
c.2604A=
c.2627A= (p.Lys876=)
c.2378A= (p.Lys793=)
n.2812A=
c.2636A= (p.Lys879=)
4g.6302422A>CCA2839811WFS1c.2663A>C (p.Lys888Thr)
c.2604A>C
c.2627A>C (p.Lys876Thr)
c.2378A>C (p.Lys793Thr)
n.2812A>C
c.2636A>C (p.Lys879Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302422A>GCA2839812WFS1c.2663A>G (p.Lys888Arg)
c.2604A>G
c.2627A>G (p.Lys876Arg)
c.2378A>G (p.Lys793Arg)
n.2812A>G
c.2636A>G (p.Lys879Arg)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302422A>TCA356179549WFS1c.2663A>T (p.Lys888Met)
c.2604A>T
c.2627A>T (p.Lys876Met)
c.2378A>T (p.Lys793Met)
n.2812A>T
c.2636A>T (p.Lys879Met)
4g.6302423G>ACA438211581WFS1c.2664G>A (p.Lys888=)
c.2605G>A
c.2628G>A (p.Lys876=)
c.2379G>A (p.Lys793=)
n.2813G>A
c.2637G>A (p.Lys879=)
 dbSNP
4g.6302423G>CCA356179552WFS1c.2664G>C (p.Lys888Asn)
c.2605G>C
c.2628G>C (p.Lys876Asn)
c.2379G>C (p.Lys793Asn)
n.2813G>C
c.2637G>C (p.Lys879Asn)
4g.6302423G=CA1435772768WFS1c.2664G= (p.Lys888=)
c.2605G=
c.2628G= (p.Lys876=)
c.2379G= (p.Lys793=)
n.2813G=
c.2637G= (p.Lys879=)
4g.6302423G>TCA356179554WFS1c.2664G>T (p.Lys888Asn)
c.2605G>T
c.2628G>T (p.Lys876Asn)
c.2379G>T (p.Lys793Asn)
n.2813G>T
c.2637G>T (p.Lys879Asn)
4g.6302424T>ACA356179557WFS1c.2665T>A (p.Phe889Ile)
c.2606T>A
c.2629T>A (p.Phe877Ile)
c.2380T>A (p.Phe794Ile)
n.2814T>A
c.2638T>A (p.Phe880Ile)
4g.6302424T>CCA356179559WFS1c.2665T>C (p.Phe889Leu)
c.2606T>C
c.2629T>C (p.Phe877Leu)
c.2380T>C (p.Phe794Leu)
n.2814T>C
c.2638T>C (p.Phe880Leu)
4g.6302424T>GCA356179561WFS1c.2665T>G (p.Phe889Val)
c.2606T>G
c.2629T>G (p.Phe877Val)
c.2380T>G (p.Phe794Val)
n.2814T>G
c.2638T>G (p.Phe880Val)
 gnomAD v4
4g.6302425T>ACA356179566WFS1c.2666T>A (p.Phe889Tyr)
c.2607T>A
c.2630T>A (p.Phe877Tyr)
c.2381T>A (p.Phe794Tyr)
n.2815T>A
c.2639T>A (p.Phe880Tyr)
4g.6302425T>CCA356179567WFS1c.2666T>C (p.Phe889Ser)
c.2607T>C
c.2630T>C (p.Phe877Ser)
c.2381T>C (p.Phe794Ser)
n.2815T>C
c.2639T>C (p.Phe880Ser)
4g.6302425T>GCA356179564WFS1c.2666T>G (p.Phe889Cys)
c.2607T>G
c.2630T>G (p.Phe877Cys)
c.2381T>G (p.Phe794Cys)
n.2815T>G
c.2639T>G (p.Phe880Cys)
4g.6302426C>ACA356179570WFS1c.2667C>A (p.Phe889Leu)
c.2608C>A
c.2631C>A (p.Phe877Leu)
c.2382C>A (p.Phe794Leu)
n.2816C>A
c.2640C>A (p.Phe880Leu)
4g.6302426C=CA1435772770WFS1c.2667C= (p.Phe889=)
c.2608C=
c.2631C= (p.Phe877=)
c.2382C= (p.Phe794=)
n.2816C=
c.2640C= (p.Phe880=)
4g.6302426C>GCA356179572WFS1c.2667C>G (p.Phe889Leu)
c.2608C>G
c.2631C>G (p.Phe877Leu)
c.2382C>G (p.Phe794Leu)
n.2816C>G
c.2640C>G (p.Phe880Leu)
4g.6302426C>TCA2839813WFS1c.2667C>T (p.Phe889=)
c.2608C>T
c.2631C>T (p.Phe877=)
c.2382C>T (p.Phe794=)
n.2816C>T
c.2640C>T (p.Phe880=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6302427G>ACA2839814WFS1c.2668G>A (p.Ala890Thr)
c.2609G>A
c.2632G>A (p.Ala878Thr)
c.2383G>A (p.Ala795Thr)
n.2817G>A
c.2641G>A (p.Ala881Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302427G>CCA356179579WFS1c.2668G>C (p.Ala890Pro)
c.2609G>C
c.2632G>C (p.Ala878Pro)
c.2383G>C (p.Ala795Pro)
n.2817G>C
c.2641G>C (p.Ala881Pro)
 gnomAD v4
4g.6302427G=CA1435772772WFS1c.2668G= (p.Ala890=)
c.2609G=
c.2632G= (p.Ala878=)
c.2383G= (p.Ala795=)
n.2817G=
c.2641G= (p.Ala881=)
4g.6302427G>TCA356179581WFS1c.2668G>T (p.Ala890Ser)
c.2609G>T
c.2632G>T (p.Ala878Ser)
c.2383G>T (p.Ala795Ser)
n.2817G>T
c.2641G>T (p.Ala881Ser)
 gnomAD v4
4g.6302428C>ACA356179584WFS1c.2669C>A (p.Ala890Asp)
c.2610C>A
c.2633C>A (p.Ala878Asp)
c.2384C>A (p.Ala795Asp)
n.2818C>A
c.2642C>A (p.Ala881Asp)
4g.6302428C>GCA356179586WFS1c.2669C>G (p.Ala890Gly)
c.2610C>G
c.2633C>G (p.Ala878Gly)
c.2384C>G (p.Ala795Gly)
n.2818C>G
c.2642C>G (p.Ala881Gly)
4g.6302428C>TCA356179588WFS1c.2669C>T (p.Ala890Val)
c.2610C>T
c.2633C>T (p.Ala878Val)
c.2384C>T (p.Ala795Val)
n.2818C>T
c.2642C>T (p.Ala881Val)
4g.6302428_6302434delinsCCTTCGACA1435772775WFS1c.2669_2675delinsCCTTCGA (p.Ala890=)
c.2610_2616delinsCCTTCGA
c.2633_2639delinsCCTTCGA (p.Ala878=)
c.2384_2390delinsCCTTCGA (p.Ala795=)
n.2818_2824delinsCCTTCGA
c.2642_2648delinsCCTTCGA (p.Ala881=)
4g.6302429C>ACA438211586WFS1c.2670C>A (p.Ala890=)
c.2611C>A
c.2634C>A (p.Ala878=)
c.2385C>A (p.Ala795=)
n.2819C>A
c.2643C>A (p.Ala881=)
4g.6302429C=CA1435772778WFS1c.2670C= (p.Ala890=)
c.2611C=
c.2634C= (p.Ala878=)
c.2385C= (p.Ala795=)
n.2819C=
c.2643C= (p.Ala881=)
4g.6302429C>GCA438211588WFS1c.2670C>G (p.Ala890=)
c.2611C>G
c.2634C>G (p.Ala878=)
c.2385C>G (p.Ala795=)
n.2819C>G
c.2643C>G (p.Ala881=)
4g.6302429C>TCA438211587WFS1c.2670C>T (p.Ala890=)
c.2611C>T
c.2634C>T (p.Ala878=)
c.2385C>T (p.Ala795=)
n.2819C>T
c.2643C>T (p.Ala881=)
 dbSNP gnomAD v4
4g.6302433_6302438delCA797211390WFS1c.2674_2679del (p.Asp892_Phe893del)
c.2615_2620del
c.2638_2643del (p.Asp880_Phe881del)
c.2389_2394del (p.Asp797_Phe798del)
n.2823_2828del
c.2647_2652del (p.Asp883_Phe884del)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6302430T>ACA356179591WFS1c.2671T>A (p.Phe891Ile)
c.2612T>A
c.2635T>A (p.Phe879Ile)
c.2386T>A (p.Phe796Ile)
n.2820T>A
c.2644T>A (p.Phe882Ile)
4g.6302430T>CCA356179593WFS1c.2671T>C (p.Phe891Leu)
c.2612T>C
c.2635T>C (p.Phe879Leu)
c.2386T>C (p.Phe796Leu)
n.2820T>C
c.2644T>C (p.Phe882Leu)
4g.6302430T>GCA356179596WFS1c.2671T>G (p.Phe891Val)
c.2612T>G
c.2635T>G (p.Phe879Val)
c.2386T>G (p.Phe796Val)
n.2820T>G
c.2644T>G (p.Phe882Val)
4g.6302431T>ACA356179603WFS1c.2672T>A (p.Phe891Tyr)
c.2613T>A
c.2636T>A (p.Phe879Tyr)
c.2387T>A (p.Phe796Tyr)
n.2821T>A
c.2645T>A (p.Phe882Tyr)
4g.6302431T>CCA356179609WFS1c.2672T>C (p.Phe891Ser)
c.2613T>C
c.2636T>C (p.Phe879Ser)
c.2387T>C (p.Phe796Ser)
n.2821T>C
c.2645T>C (p.Phe882Ser)
4g.6302431T>GCA356179600WFS1c.2672T>G (p.Phe891Cys)
c.2613T>G
c.2636T>G (p.Phe879Cys)
c.2387T>G (p.Phe796Cys)
n.2821T>G
c.2645T>G (p.Phe882Cys)
4g.6302432C>ACA356179612WFS1c.2673C>A (p.Phe891Leu)
c.2614C>A
c.2637C>A (p.Phe879Leu)
c.2388C>A (p.Phe796Leu)
n.2822C>A
c.2646C>A (p.Phe882Leu)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6302432C=CA1435772783WFS1c.2673C= (p.Phe891=)
c.2614C=
c.2637C= (p.Phe879=)
c.2388C= (p.Phe796=)
n.2822C=
c.2646C= (p.Phe882=)
4g.6302432C>GCA356179613WFS1c.2673C>G (p.Phe891Leu)
c.2614C>G
c.2637C>G (p.Phe879Leu)
c.2388C>G (p.Phe796Leu)
n.2822C>G
c.2646C>G (p.Phe882Leu)
4g.6302432C>TCA2839815WFS1c.2673C>T (p.Phe891=)
c.2614C>T
c.2637C>T (p.Phe879=)
c.2388C>T (p.Phe796=)
n.2822C>T
c.2646C>T (p.Phe882=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6302432_6302436delinsCGACTCA1435772782WFS1c.2673_2677delinsCGACT (p.Phe891=)
c.2614_2618delinsCGACT
c.2637_2641delinsCGACT (p.Phe879=)
c.2388_2392delinsCGACT (p.Phe796=)
n.2822_2826delinsCGACT
c.2646_2650delinsCGACT (p.Phe882=)

Number of alleles fetched