Chr Mutation (hg38) CAid Gene Transcript Linkouts
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=)
4g.6302433G>ACA2839816WFS1c.2674G>A (p.Asp892Asn)
c.2615G>A
c.2638G>A (p.Asp880Asn)
c.2389G>A (p.Asp797Asn)
n.2823G>A
c.2647G>A (p.Asp883Asn)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302433G>CCA2839817WFS1c.2674G>C (p.Asp892His)
c.2615G>C
c.2638G>C (p.Asp880His)
c.2389G>C (p.Asp797His)
n.2823G>C
c.2647G>C (p.Asp883His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302433G=CA1435772784WFS1c.2674G= (p.Asp892=)
c.2615G=
c.2638G= (p.Asp880=)
c.2389G= (p.Asp797=)
n.2823G=
c.2647G= (p.Asp883=)
4g.6302433G>TCA356179620WFS1c.2674G>T (p.Asp892Tyr)
c.2615G>T
c.2638G>T (p.Asp880Tyr)
c.2389G>T (p.Asp797Tyr)
n.2823G>T
c.2647G>T (p.Asp883Tyr)
 dbSNP gnomAD v2 gnomAD v4
4g.6302433_6302436delCA1058892966WFS1c.2674_2677del (p.Asp892SerfsTer?)
c.2615_2618del
c.2638_2641del (p.Asp880SerfsTer?)
c.2389_2392del (p.Asp797SerfsTer?)
n.2823_2826del
c.2647_2650del (p.Asp883SerfsTer?)
 dbSNP gnomAD v3 gnomAD v4
4g.6302434A=CA1435772787WFS1c.2675A= (p.Asp892=)
c.2616A=
c.2639A= (p.Asp880=)
c.2390A= (p.Asp797=)
n.2824A=
c.2648A= (p.Asp883=)
4g.6302434A>CCA356179623WFS1c.2675A>C (p.Asp892Ala)
c.2616A>C
c.2639A>C (p.Asp880Ala)
c.2390A>C (p.Asp797Ala)
n.2824A>C
c.2648A>C (p.Asp883Ala)
 dbSNP gnomAD v3 gnomAD v4
4g.6302434A>GCA356179631WFS1c.2675A>G (p.Asp892Gly)
c.2616A>G
c.2639A>G (p.Asp880Gly)
c.2390A>G (p.Asp797Gly)
n.2824A>G
c.2648A>G (p.Asp883Gly)
4g.6302434A>TCA356179628WFS1c.2675A>T (p.Asp892Val)
c.2616A>T
c.2639A>T (p.Asp880Val)
c.2390A>T (p.Asp797Val)
n.2824A>T
c.2648A>T (p.Asp883Val)
4g.6302434_6302437delinsACTTCA1435772786WFS1c.2675_2678delinsACTT (p.Asp892=)
c.2616_2619delinsACTT
c.2639_2642delinsACTT (p.Asp880=)
c.2390_2393delinsACTT (p.Asp797=)
n.2824_2827delinsACTT
c.2648_2651delinsACTT (p.Asp883=)
4g.6302435C>ACA356179633WFS1c.2676C>A (p.Asp892Glu)
c.2617C>A
c.2640C>A (p.Asp880Glu)
c.2391C>A (p.Asp797Glu)
n.2825C>A
c.2649C>A (p.Asp883Glu)
4g.6302435C=CA1435772791WFS1c.2676C= (p.Asp892=)
c.2617C=
c.2640C= (p.Asp880=)
c.2391C= (p.Asp797=)
n.2825C=
c.2649C= (p.Asp883=)
4g.6302435C>GCA356179635WFS1c.2676C>G (p.Asp892Glu)
c.2617C>G
c.2640C>G (p.Asp880Glu)
c.2391C>G (p.Asp797Glu)
n.2825C>G
c.2649C>G (p.Asp883Glu)
 gnomAD v4
4g.6302435C>TCA2839819WFS1c.2676C>T (p.Asp892=)
c.2617C>T
c.2640C>T (p.Asp880=)
c.2391C>T (p.Asp797=)
n.2825C>T
c.2649C>T (p.Asp883=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302435_6302439delinsCTTCTCA1435772792WFS1c.2676_2680delinsCTTCT (p.Asp892=)
c.2617_2621delinsCTTCT
c.2640_2644delinsCTTCT (p.Asp880=)
c.2391_2395delinsCTTCT (p.Asp797=)
n.2825_2829delinsCTTCT
c.2649_2653delinsCTTCT (p.Asp883=)
4g.6302438_6302440dupCA1435772790WFS1c.2679_2681dup (p.Phe894_Phe895insPhe)
c.2620_2622dup
c.2643_2645dup (p.Phe882_Phe883insPhe)
c.2394_2396dup (p.Phe799_Phe800insPhe)
n.2828_2830dup
c.2652_2654dup (p.Phe885_Phe886insPhe)
 ClinVar dbSNP gnomAD v4
4g.6302438_6302440delCA2839818WFS1c.2679_2681del (p.Phe894del)
c.2620_2622del
c.2643_2645del (p.Phe882del)
c.2394_2396del (p.Phe799del)
n.2828_2830del
c.2652_2654del (p.Phe885del)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302436T>ACA356179642WFS1c.2677T>A (p.Phe893Ile)
c.2618T>A
c.2641T>A (p.Phe881Ile)
c.2392T>A (p.Phe798Ile)
n.2826T>A
c.2650T>A (p.Phe884Ile)
4g.6302436T>CCA356179647WFS1c.2677T>C (p.Phe893Leu)
c.2618T>C
c.2641T>C (p.Phe881Leu)
c.2392T>C (p.Phe798Leu)
n.2826T>C
c.2650T>C (p.Phe884Leu)
4g.6302436T>GCA356179645WFS1c.2677T>G (p.Phe893Val)
c.2618T>G
c.2641T>G (p.Phe881Val)
c.2392T>G (p.Phe798Val)
n.2826T>G
c.2650T>G (p.Phe884Val)
4g.6302436_6302438delinsTTCCA1435772794WFS1c.2677_2679delinsTTC (p.Phe893=)
c.2618_2620delinsTTC
c.2641_2643delinsTTC (p.Phe881=)
c.2392_2394delinsTTC (p.Phe798=)
n.2826_2828delinsTTC
c.2650_2652delinsTTC (p.Phe884=)
4g.6302438_6302441delCA549708054WFS1c.2679_2682del (p.Phe894SerfsTer?)
c.2620_2623del
c.2643_2646del (p.Phe882SerfsTer?)
c.2394_2397del (p.Phe799SerfsTer?)
n.2828_2831del
c.2652_2655del (p.Phe885SerfsTer?)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302437T>ACA356179650WFS1c.2678T>A (p.Phe893Tyr)
c.2619T>A
c.2642T>A (p.Phe881Tyr)
c.2393T>A (p.Phe798Tyr)
n.2827T>A
c.2651T>A (p.Phe884Tyr)
4g.6302437T>CCA356179657WFS1c.2678T>C (p.Phe893Ser)
c.2619T>C
c.2642T>C (p.Phe881Ser)
c.2393T>C (p.Phe798Ser)
n.2827T>C
c.2651T>C (p.Phe884Ser)
4g.6302437T>GCA356179656WFS1c.2678T>G (p.Phe893Cys)
c.2619T>G
c.2642T>G (p.Phe881Cys)
c.2393T>G (p.Phe798Cys)
n.2827T>G
c.2651T>G (p.Phe884Cys)
4g.6302438_6302439delCA324155WFS1c.2679_2680del (p.Phe895LeufsTer?)
c.2620_2621del
c.2643_2644del (p.Phe883LeufsTer?)
c.2394_2395del (p.Phe800LeufsTer?)
n.2828_2829del
c.2652_2653del (p.Phe886LeufsTer?)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302438C>ACA356179660WFS1c.2679C>A (p.Phe893Leu)
c.2620C>A
c.2643C>A (p.Phe881Leu)
c.2394C>A (p.Phe798Leu)
n.2828C>A
c.2652C>A (p.Phe884Leu)
4g.6302438C>GCA356179661WFS1c.2679C>G (p.Phe893Leu)
c.2620C>G
c.2643C>G (p.Phe881Leu)
c.2394C>G (p.Phe798Leu)
n.2828C>G
c.2652C>G (p.Phe884Leu)
4g.6302438C>TCA438211591WFS1c.2679C>T (p.Phe893=)
c.2620C>T
c.2643C>T (p.Phe881=)
c.2394C>T (p.Phe798=)
n.2828C>T
c.2652C>T (p.Phe884=)
 gnomAD v4
4g.6302438_6302441delinsCTTTCA1435772797WFS1c.2679_2682delinsCTTT (p.Phe893=)
c.2620_2623delinsCTTT
c.2643_2646delinsCTTT (p.Phe881=)
c.2394_2397delinsCTTT (p.Phe798=)
n.2828_2831delinsCTTT
c.2652_2655delinsCTTT (p.Phe884=)
4g.6302439T>ACA356179662WFS1c.2680T>A (p.Phe894Ile)
c.2621T>A
c.2644T>A (p.Phe882Ile)
c.2395T>A (p.Phe799Ile)
n.2829T>A
c.2653T>A (p.Phe885Ile)
4g.6302439T>CCA356179663WFS1c.2680T>C (p.Phe894Leu)
c.2621T>C
c.2644T>C (p.Phe882Leu)
c.2395T>C (p.Phe799Leu)
n.2829T>C
c.2653T>C (p.Phe885Leu)
4g.6302439T>GCA356179664WFS1c.2680T>G (p.Phe894Val)
c.2621T>G
c.2644T>G (p.Phe882Val)
c.2395T>G (p.Phe799Val)
n.2829T>G
c.2653T>G (p.Phe885Val)
4g.6302442_6302443delCA2839820WFS1c.2683_2684del (p.Phe895LeufsTer?)
c.2624_2625del
c.2647_2648del (p.Phe883LeufsTer?)
c.2398_2399del (p.Phe800LeufsTer?)
n.2832_2833del
c.2656_2657del (p.Phe886LeufsTer?)
 dbSNP ExAC gnomAD v3 gnomAD v4
4g.6302441_6302443delCA549708055WFS1c.2682_2684del (p.Phe895del)
c.2623_2625del
c.2646_2648del (p.Phe883del)
c.2397_2399del (p.Phe800del)
n.2831_2833del
c.2655_2657del (p.Phe886del)
 dbSNP gnomAD v2 gnomAD v4
4g.6302440T>ACA356179666WFS1c.2681T>A (p.Phe894Tyr)
c.2622T>A
c.2645T>A (p.Phe882Tyr)
c.2396T>A (p.Phe799Tyr)
n.2830T>A
c.2654T>A (p.Phe885Tyr)
4g.6302440T>CCA356179668WFS1c.2681T>C (p.Phe894Ser)
c.2622T>C
c.2645T>C (p.Phe882Ser)
c.2396T>C (p.Phe799Ser)
n.2830T>C
c.2654T>C (p.Phe885Ser)
 dbSNP
4g.6302440T>GCA2839821WFS1c.2681T>G (p.Phe894Cys)
c.2622T>G
c.2645T>G (p.Phe882Cys)
c.2396T>G (p.Phe799Cys)
n.2830T>G
c.2654T>G (p.Phe885Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302440T=CA1435772800WFS1c.2681T= (p.Phe894=)
c.2622T=
c.2645T= (p.Phe882=)
c.2396T= (p.Phe799=)
n.2830T=
c.2654T= (p.Phe885=)
4g.6302440_6302444delinsTTTTCCA1435772801WFS1c.2681_2685delinsTTTTC (p.Phe894=)
c.2622_2626delinsTTTTC
c.2645_2649delinsTTTTC (p.Phe882=)
c.2396_2400delinsTTTTC (p.Phe799=)
n.2830_2834delinsTTTTC
c.2654_2658delinsTTTTC (p.Phe885=)
4g.6302441T>ACA91797914WFS1c.2682T>A (p.Phe894Leu)
c.2623T>A
c.2646T>A (p.Phe882Leu)
c.2397T>A (p.Phe799Leu)
n.2831T>A
c.2655T>A (p.Phe885Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302441T>CCA438211593WFS1c.2682T>C (p.Phe894=)
c.2623T>C
c.2646T>C (p.Phe882=)
c.2397T>C (p.Phe799=)
n.2831T>C
c.2655T>C (p.Phe885=)
 gnomAD v4
4g.6302441T>GCA356179678WFS1c.2682T>G (p.Phe894Leu)
c.2623T>G
c.2646T>G (p.Phe882Leu)
c.2397T>G (p.Phe799Leu)
n.2831T>G
c.2655T>G (p.Phe885Leu)
 dbSNP
4g.6302441T=CA1435772804WFS1c.2682T= (p.Phe894=)
c.2623T=
c.2646T= (p.Phe882=)
c.2397T= (p.Phe799=)
n.2831T=
c.2655T= (p.Phe885=)
4g.6302443_6302446delCA276185WFS1c.2684_2687del (p.Phe895SerfsTer?)
c.2625_2628del
c.2648_2651del (p.Phe883SerfsTer?)
c.2399_2402del (p.Phe800SerfsTer?)
n.2833_2836del
c.2657_2660del (p.Phe886SerfsTer?)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302442T>ACA356179690WFS1c.2683T>A (p.Phe895Ile)
c.2624T>A
c.2647T>A (p.Phe883Ile)
c.2398T>A (p.Phe800Ile)
n.2832T>A
c.2656T>A (p.Phe886Ile)
4g.6302442T>CCA356179688WFS1c.2683T>C (p.Phe895Leu)
c.2624T>C
c.2647T>C (p.Phe883Leu)
c.2398T>C (p.Phe800Leu)
n.2832T>C
c.2656T>C (p.Phe886Leu)
4g.6302442T>GCA356179686WFS1c.2683T>G (p.Phe895Val)
c.2624T>G
c.2647T>G (p.Phe883Val)
c.2398T>G (p.Phe800Val)
n.2832T>G
c.2656T>G (p.Phe886Val)
 dbSNP gnomAD v2 gnomAD v4
4g.6302442T=CA1435772805WFS1c.2683T= (p.Phe895=)
c.2624T=
c.2647T= (p.Phe883=)
c.2398T= (p.Phe800=)
n.2832T=
c.2656T= (p.Phe886=)
4g.6302443T>ACA356179692WFS1c.2684T>A (p.Phe895Tyr)
c.2625T>A
c.2648T>A (p.Phe883Tyr)
c.2399T>A (p.Phe800Tyr)
n.2833T>A
c.2657T>A (p.Phe886Tyr)
4g.6302443T>CCA356179695WFS1c.2684T>C (p.Phe895Ser)
c.2625T>C
c.2648T>C (p.Phe883Ser)
c.2399T>C (p.Phe800Ser)
n.2833T>C
c.2657T>C (p.Phe886Ser)
4g.6302443T>GCA356179697WFS1c.2684T>G (p.Phe895Cys)
c.2625T>G
c.2648T>G (p.Phe883Cys)
c.2399T>G (p.Phe800Cys)
n.2833T>G
c.2657T>G (p.Phe886Cys)
4g.6302443_6302444delinsTCCA1435772807WFS1c.2684_2685delinsTC (p.Phe895=)
c.2625_2626delinsTC
c.2648_2649delinsTC (p.Phe883=)
c.2399_2400delinsTC (p.Phe800=)
n.2833_2834delinsTC
c.2657_2658delinsTC (p.Phe886=)
4g.6302444delCA91797917WFS1c.2685del (p.Phe896SerfsTer?)
c.2626del
c.2649del (p.Phe884SerfsTer?)
c.2400del (p.Phe801SerfsTer?)
n.2834del
c.2658del (p.Phe887SerfsTer?)
 ClinVar dbSNP gnomAD v3 gnomAD v4
4g.6302444C>ACA356179700WFS1c.2685C>A (p.Phe895Leu)
c.2626C>A
c.2649C>A (p.Phe883Leu)
c.2400C>A (p.Phe800Leu)
n.2834C>A
c.2658C>A (p.Phe886Leu)
4g.6302444C>GCA356179702WFS1c.2685C>G (p.Phe895Leu)
c.2626C>G
c.2649C>G (p.Phe883Leu)
c.2400C>G (p.Phe800Leu)
n.2834C>G
c.2658C>G (p.Phe886Leu)
 ClinVar
4g.6302444C>TCA438211599WFS1c.2685C>T (p.Phe895=)
c.2626C>T
c.2649C>T (p.Phe883=)
c.2400C>T (p.Phe800=)
n.2834C>T
c.2658C>T (p.Phe886=)
4g.6302445T>ACA356179705WFS1c.2686T>A (p.Phe896Ile)
c.2627T>A
c.2650T>A (p.Phe884Ile)
c.2401T>A (p.Phe801Ile)
n.2835T>A
c.2659T>A (p.Phe887Ile)
4g.6302445T>CCA356179708WFS1c.2686T>C (p.Phe896Leu)
c.2627T>C
c.2650T>C (p.Phe884Leu)
c.2401T>C (p.Phe801Leu)
n.2835T>C
c.2659T>C (p.Phe887Leu)
4g.6302445T>GCA2839822WFS1c.2686T>G (p.Phe896Val)
c.2627T>G
c.2650T>G (p.Phe884Val)
c.2401T>G (p.Phe801Val)
n.2835T>G
c.2659T>G (p.Phe887Val)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302445T=CA1435772809WFS1c.2686T= (p.Phe896=)
c.2627T=
c.2650T= (p.Phe884=)
c.2401T= (p.Phe801=)
n.2835T=
c.2659T= (p.Phe887=)
4g.6302446T>ACA320140WFS1c.2687T>A (p.Phe896Tyr)
c.2628T>A
c.2651T>A (p.Phe884Tyr)
c.2402T>A (p.Phe801Tyr)
n.2836T>A
c.2660T>A (p.Phe887Tyr)
 ClinVar dbSNP gnomAD v2
4g.6302446T>CCA356179723WFS1c.2687T>C (p.Phe896Ser)
c.2628T>C
c.2651T>C (p.Phe884Ser)
c.2402T>C (p.Phe801Ser)
n.2836T>C
c.2660T>C (p.Phe887Ser)
 gnomAD v4
4g.6302446T>GCA356179713WFS1c.2687T>G (p.Phe896Cys)
c.2628T>G
c.2651T>G (p.Phe884Cys)
c.2402T>G (p.Phe801Cys)
n.2836T>G
c.2660T>G (p.Phe887Cys)
4g.6302446T=CA1435772812WFS1c.2687T= (p.Phe896=)
c.2628T=
c.2651T= (p.Phe884=)
c.2402T= (p.Phe801=)
n.2836T=
c.2660T= (p.Phe887=)
4g.6302447C>ACA356179725WFS1c.2688C>A (p.Phe896Leu)
c.2629C>A
c.2652C>A (p.Phe884Leu)
c.2403C>A (p.Phe801Leu)
n.2837C>A
c.2661C>A (p.Phe887Leu)
4g.6302447C=CA1435772814WFS1c.2688C= (p.Phe896=)
c.2629C=
c.2652C= (p.Phe884=)
c.2403C= (p.Phe801=)
n.2837C=
c.2661C= (p.Phe887=)
4g.6302447C>GCA356179728WFS1c.2688C>G (p.Phe896Leu)
c.2629C>G
c.2652C>G (p.Phe884Leu)
c.2403C>G (p.Phe801Leu)
n.2837C>G
c.2661C>G (p.Phe887Leu)
 ClinVar dbSNP gnomAD v4
4g.6302447C>TCA438211602WFS1c.2688C>T (p.Phe896=)
c.2629C>T
c.2652C>T (p.Phe884=)
c.2403C>T (p.Phe801=)
n.2837C>T
c.2661C>T (p.Phe887=)
 gnomAD v4 COSMIC
4g.6302448C>ACA356179731WFS1c.2689C>A (p.Pro897Thr)
c.2630C>A
c.2653C>A (p.Pro885Thr)
c.2404C>A (p.Pro802Thr)
n.2838C>A
c.2662C>A (p.Pro888Thr)
4g.6302448C=CA1435772816WFS1c.2689C= (p.Pro897=)
c.2630C=
c.2653C= (p.Pro885=)
c.2404C= (p.Pro802=)
n.2838C=
c.2662C= (p.Pro888=)
4g.6302448C>GCA356179734WFS1c.2689C>G (p.Pro897Ala)
c.2630C>G
c.2653C>G (p.Pro885Ala)
c.2404C>G (p.Pro802Ala)
n.2838C>G
c.2662C>G (p.Pro888Ala)
4g.6302448C>TCA356179739WFS1c.2689C>T (p.Pro897Ser)
c.2630C>T
c.2653C>T (p.Pro885Ser)
c.2404C>T (p.Pro802Ser)
n.2838C>T
c.2662C>T (p.Pro888Ser)
 dbSNP COSMIC
4g.6302449C>ACA356179742WFS1c.2690C>A (p.Pro897Gln)
c.2631C>A
c.2654C>A (p.Pro885Gln)
c.2405C>A (p.Pro802Gln)
n.2839C>A
c.2663C>A (p.Pro888Gln)
4g.6302449C=CA1435772818WFS1c.2690C= (p.Pro897=)
c.2631C=
c.2654C= (p.Pro885=)
c.2405C= (p.Pro802=)
n.2839C=
c.2663C= (p.Pro888=)
4g.6302449C>GCA356179743WFS1c.2690C>G (p.Pro897Arg)
c.2631C>G
c.2654C>G (p.Pro885Arg)
c.2405C>G (p.Pro802Arg)
n.2839C>G
c.2663C>G (p.Pro888Arg)
 dbSNP gnomAD v4
4g.6302449C>TCA2839823WFS1c.2690C>T (p.Pro897Leu)
c.2631C>T
c.2654C>T (p.Pro885Leu)
c.2405C>T (p.Pro802Leu)
n.2839C>T
c.2663C>T (p.Pro888Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302450A=CA1435772819WFS1c.2691A= (p.Pro897=)
c.2632A=
c.2655A= (p.Pro885=)
c.2406A= (p.Pro802=)
n.2840A=
c.2664A= (p.Pro888=)
4g.6302450A>CCA438211608WFS1c.2691A>C (p.Pro897=)
c.2632A>C
c.2655A>C (p.Pro885=)
c.2406A>C (p.Pro802=)
n.2840A>C
c.2664A>C (p.Pro888=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6302450A>GCA438211606WFS1c.2691A>G (p.Pro897=)
c.2632A>G
c.2655A>G (p.Pro885=)
c.2406A>G (p.Pro802=)
n.2840A>G
c.2664A>G (p.Pro888=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302450A>TCA438211604WFS1c.2691A>T (p.Pro897=)
c.2632A>T
c.2655A>T (p.Pro885=)
c.2406A>T (p.Pro802=)
n.2840A>T
c.2664A>T (p.Pro888=)
4g.6302451T>ACA356179749WFS1c.2692T>A (p.Phe898Ile)
c.2633T>A
c.2656T>A (p.Phe886Ile)
c.2407T>A (p.Phe803Ile)
n.2841T>A
c.2665T>A (p.Phe889Ile)
4g.6302451T>CCA356179759WFS1c.2692T>C (p.Phe898Leu)
c.2633T>C
c.2656T>C (p.Phe886Leu)
c.2407T>C (p.Phe803Leu)
n.2841T>C
c.2665T>C (p.Phe889Leu)
4g.6302451T>GCA356179762WFS1c.2692T>G (p.Phe898Val)
c.2633T>G
c.2656T>G (p.Phe886Val)
c.2407T>G (p.Phe803Val)
n.2841T>G
c.2665T>G (p.Phe889Val)
4g.6302451_6302452insACA2586973661WFS1c.2692_2693insA (p.Phe898TyrfsTer?)
c.2633_2634insA
c.2656_2657insA (p.Phe886TyrfsTer?)
c.2407_2408insA (p.Phe803TyrfsTer?)
n.2841_2842insA
c.2665_2666insA (p.Phe889TyrfsTer?)
 gnomAD v4
4g.6302452T>ACA356179772WFS1c.2693T>A (p.Phe898Tyr)
c.2634T>A
c.2657T>A (p.Phe886Tyr)
c.2408T>A (p.Phe803Tyr)
n.2842T>A
c.2666T>A (p.Phe889Tyr)
4g.6302452T>CCA356179774WFS1c.2693T>C (p.Phe898Ser)
c.2634T>C
c.2657T>C (p.Phe886Ser)
c.2408T>C (p.Phe803Ser)
n.2842T>C
c.2666T>C (p.Phe889Ser)
4g.6302452T>GCA356179766WFS1c.2693T>G (p.Phe898Cys)
c.2634T>G
c.2657T>G (p.Phe886Cys)
c.2408T>G (p.Phe803Cys)
n.2842T>G
c.2666T>G (p.Phe889Cys)
 gnomAD v4
4g.6302453C>ACA356179776WFS1c.2694C>A (p.Phe898Leu)
c.2635C>A
c.2658C>A (p.Phe886Leu)
c.2409C>A (p.Phe803Leu)
n.2843C>A
c.2667C>A (p.Phe889Leu)
 dbSNP
4g.6302453C=CA1435772821WFS1c.2694C= (p.Phe898=)
c.2635C=
c.2658C= (p.Phe886=)
c.2409C= (p.Phe803=)
n.2843C=
c.2667C= (p.Phe889=)
4g.6302453C>GCA356179780WFS1c.2694C>G (p.Phe898Leu)
c.2635C>G
c.2658C>G (p.Phe886Leu)
c.2409C>G (p.Phe803Leu)
n.2843C>G
c.2667C>G (p.Phe889Leu)
 dbSNP gnomAD v4
4g.6302453C>TCA2839824WFS1c.2694C>T (p.Phe898=)
c.2635C>T
c.2658C>T (p.Phe886=)
c.2409C>T (p.Phe803=)
n.2843C>T
c.2667C>T (p.Phe889=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302454C>ACA356179786WFS1c.2695C>A (p.Leu899Met)
c.2636C>A
c.2659C>A (p.Leu887Met)
c.2410C>A (p.Leu804Met)
n.2844C>A
c.2668C>A (p.Leu890Met)
4g.6302454C=CA1435772822WFS1c.2695C= (p.Leu899=)
c.2636C=
c.2659C= (p.Leu887=)
c.2410C= (p.Leu804=)
n.2844C=
c.2668C= (p.Leu890=)
4g.6302454C>GCA356179791WFS1c.2695C>G (p.Leu899Val)
c.2636C>G
c.2659C>G (p.Leu887Val)
c.2410C>G (p.Leu804Val)
n.2844C>G
c.2668C>G (p.Leu890Val)
 gnomAD v4
4g.6302454C>TCA438211609WFS1c.2695C>T (p.Leu899=)
c.2636C>T
c.2659C>T (p.Leu887=)
c.2410C>T (p.Leu804=)
n.2844C>T
c.2668C>T (p.Leu890=)
 ClinVar dbSNP gnomAD v4
4g.6302455T>ACA356179796WFS1c.2696T>A (p.Leu899Gln)
c.2637T>A
c.2660T>A (p.Leu887Gln)
c.2411T>A (p.Leu804Gln)
n.2845T>A
c.2669T>A (p.Leu890Gln)
4g.6302455T>CCA356179794WFS1c.2696T>C (p.Leu899Pro)
c.2637T>C
c.2660T>C (p.Leu887Pro)
c.2411T>C (p.Leu804Pro)
n.2845T>C
c.2669T>C (p.Leu890Pro)
4g.6302455T>GCA356179795WFS1c.2696T>G (p.Leu899Arg)
c.2637T>G
c.2660T>G (p.Leu887Arg)
c.2411T>G (p.Leu804Arg)
n.2845T>G
c.2669T>G (p.Leu890Arg)
4g.6302456G>ACA438211610WFS1c.2697G>A (p.Leu899=)
c.2638G>A
c.2661G>A (p.Leu887=)
c.2412G>A (p.Leu804=)
n.2846G>A
c.2670G>A (p.Leu890=)
 dbSNP gnomAD v4
4g.6302456G>CCA438211611WFS1c.2697G>C (p.Leu899=)
c.2638G>C
c.2661G>C (p.Leu887=)
c.2412G>C (p.Leu804=)
n.2846G>C
c.2670G>C (p.Leu890=)
4g.6302456G=CA1435772823WFS1c.2697G= (p.Leu899=)
c.2638G=
c.2661G= (p.Leu887=)
c.2412G= (p.Leu804=)
n.2846G=
c.2670G= (p.Leu890=)
4g.6302456G>TCA438211612WFS1c.2697G>T (p.Leu899=)
c.2638G>T
c.2661G>T (p.Leu887=)
c.2412G>T (p.Leu804=)
n.2846G>T
c.2670G>T (p.Leu890=)
4g.6302457T>ACA356179797WFS1c.2698T>A (p.Ser900Thr)
c.2639T>A
c.2662T>A (p.Ser888Thr)
c.2413T>A (p.Ser805Thr)
n.2847T>A
c.2671T>A (p.Ser891Thr)
4g.6302457T>CCA356179798WFS1c.2698T>C (p.Ser900Pro)
c.2639T>C
c.2662T>C (p.Ser888Pro)
c.2413T>C (p.Ser805Pro)
n.2847T>C
c.2671T>C (p.Ser891Pro)
4g.6302457T>GCA356179806WFS1c.2698T>G (p.Ser900Ala)
c.2639T>G
c.2662T>G (p.Ser888Ala)
c.2413T>G (p.Ser805Ala)
n.2847T>G
c.2671T>G (p.Ser891Ala)
 ClinVar dbSNP
4g.6302457T=CA1435772825WFS1c.2698T= (p.Ser900=)
c.2639T=
c.2662T= (p.Ser888=)
c.2413T= (p.Ser805=)
n.2847T=
c.2671T= (p.Ser891=)
4g.6302457_6302460delinsTCGGCA1435772824WFS1c.2698_2701delinsTCGG (p.Ser900=)
c.2639_2642delinsTCGG
c.2662_2665delinsTCGG (p.Ser888=)
c.2413_2416delinsTCGG (p.Ser805=)
n.2847_2850delinsTCGG
c.2671_2674delinsTCGG (p.Ser891=)
4g.6302458C>ACA356179808WFS1c.2699C>A (p.Ser900Ter)
c.2640C>A
c.2663C>A (p.Ser888Ter)
c.2414C>A (p.Ser805Ter)
n.2848C>A
c.2672C>A (p.Ser891Ter)
 ClinVar dbSNP gnomAD v2 gnomAD v4
4g.6302458C=CA1435772828WFS1c.2699C= (p.Ser900=)
c.2640C=
c.2663C= (p.Ser888=)
c.2414C= (p.Ser805=)
n.2848C=
c.2672C= (p.Ser891=)
4g.6302458C>GCA356179811WFS1c.2699C>G (p.Ser900Trp)
c.2640C>G
c.2663C>G (p.Ser888Trp)
c.2414C>G (p.Ser805Trp)
n.2848C>G
c.2672C>G (p.Ser891Trp)
4g.6302458C>TCA323386WFS1c.2699C>T (p.Ser900Leu)
c.2640C>T
c.2663C>T (p.Ser888Leu)
c.2414C>T (p.Ser805Leu)
n.2848C>T
c.2672C>T (p.Ser891Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6302462_6302464delCA549708056WFS1c.2703_2705del (p.Ala902del)
c.2644_2646del
c.2667_2669del (p.Ala890del)
c.2418_2420del (p.Ala807del)
n.2852_2854del
c.2676_2678del (p.Ala893del)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
4g.6302459G>ACA2839825WFS1c.2700G>A (p.Ser900=)
c.2641G>A
c.2664G>A (p.Ser888=)
c.2415G>A (p.Ser805=)
n.2849G>A
c.2673G>A (p.Ser891=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302459G>CCA2839826WFS1c.2700G>C (p.Ser900=)
c.2641G>C
c.2664G>C (p.Ser888=)
c.2415G>C (p.Ser805=)
n.2849G>C
c.2673G>C (p.Ser891=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
4g.6302459G=CA1435772830WFS1c.2700G= (p.Ser900=)
c.2641G=
c.2664G= (p.Ser888=)
c.2415G= (p.Ser805=)
n.2849G=
c.2673G= (p.Ser891=)
4g.6302459G>TCA438211615WFS1c.2700G>T (p.Ser900=)
c.2641G>T
c.2664G>T (p.Ser888=)
c.2415G>T (p.Ser805=)
n.2849G>T
c.2673G>T (p.Ser891=)
 dbSNP gnomAD v4
4g.6302460G>ACA356179822WFS1c.2701G>A (p.Ala901Thr)
c.2642G>A
c.2665G>A (p.Ala889Thr)
c.2416G>A (p.Ala806Thr)
n.2850G>A
c.2674G>A (p.Ala892Thr)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
4g.6302460G>CCA356179828WFS1c.2701G>C (p.Ala901Pro)
c.2642G>C
c.2665G>C (p.Ala889Pro)
c.2416G>C (p.Ala806Pro)
n.2850G>C
c.2674G>C (p.Ala892Pro)
4g.6302460G=CA1435772831WFS1c.2701G= (p.Ala901=)
c.2642G=
c.2665G= (p.Ala889=)
c.2416G= (p.Ala806=)
n.2850G=
c.2674G= (p.Ala892=)
4g.6302460G>TCA356179825WFS1c.2701G>T (p.Ala901Ser)
c.2642G>T
c.2665G>T (p.Ala889Ser)
c.2416G>T (p.Ala806Ser)
n.2850G>T
c.2674G>T (p.Ala892Ser)
4g.6302461C>ACA356179831WFS1c.2702C>A (p.Ala901Glu)
c.2643C>A
c.2666C>A (p.Ala889Glu)
c.2417C>A (p.Ala806Glu)
n.2851C>A
c.2675C>A (p.Ala892Glu)
4g.6302461C=CA1435772832WFS1c.2702C= (p.Ala901=)
c.2643C=
c.2666C= (p.Ala889=)
c.2417C= (p.Ala806=)
n.2851C=
c.2675C= (p.Ala892=)
4g.6302461C>GCA356179833WFS1c.2702C>G (p.Ala901Gly)
c.2643C>G
c.2666C>G (p.Ala889Gly)
c.2417C>G (p.Ala806Gly)
n.2851C>G
c.2675C>G (p.Ala892Gly)
4g.6302461C>TCA323493WFS1c.2702C>T (p.Ala901Val)
c.2643C>T
c.2666C>T (p.Ala889Val)
c.2417C>T (p.Ala806Val)
n.2851C>T
c.2675C>T (p.Ala892Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
4g.6302462G>ACA179687WFS1c.2703G>A (p.Ala901=)
c.2644G>A
c.2667G>A (p.Ala889=)
c.2418G>A (p.Ala806=)
n.2852G>A
c.2676G>A (p.Ala892=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
4g.6302462G>CCA438211617WFS1c.2703G>C (p.Ala901=)
c.2644G>C
c.2667G>C (p.Ala889=)
c.2418G>C (p.Ala806=)
n.2852G>C
c.2676G>C (p.Ala892=)
4g.6302462G=CA1435772834WFS1c.2703G= (p.Ala901=)
c.2644G=
c.2667G= (p.Ala889=)
c.2418G= (p.Ala806=)
n.2852G=
c.2676G= (p.Ala892=)
4g.6302462G>TCA438211618WFS1c.2703G>T (p.Ala901=)
c.2644G>T
c.2667G>T (p.Ala889=)
c.2418G>T (p.Ala806=)
n.2852G>T
c.2676G>T (p.Ala892=)

Number of alleles fetched