Chr Mutation (hg38) CAid Gene Transcript Linkouts
12g.9079679A=CA2015332127A2M,KLRG1c.2991T= (p.Thr997=)
n.346T=
n.451+10233T=
n.349-6958T=
c.2691T= (p.Thr897=)
c.2541T= (p.Thr847=)
c.*33+21513A= (n.*33+21513A=)
12g.9079679A>CCA478323110A2M,KLRG1c.2991T>G (p.Thr997=)
n.346T>G
n.451+10233T>G
n.349-6958T>G
c.2691T>G (p.Thr897=)
c.2541T>G (p.Thr847=)
c.*33+21513A>C (n.*33+21513A>C)
12g.9079679A>GCA478323111A2M,KLRG1c.2991T>C (p.Thr997=)
n.346T>C
n.451+10233T>C
n.349-6958T>C
c.2691T>C (p.Thr897=)
c.2541T>C (p.Thr847=)
c.*33+21513A>G (n.*33+21513A>G)
12g.9079679A>TCA6438241A2M,KLRG1c.2991T>A (p.Thr997=)
n.346T>A
n.451+10233T>A
n.349-6958T>A
c.2691T>A (p.Thr897=)
c.2541T>A (p.Thr847=)
c.*33+21513A>T (n.*33+21513A>T)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.9079680G>ACA6438242A2M,KLRG1c.2990C>T (p.Thr997Ile)
n.345C>T
n.451+10232C>T
n.349-6959C>T
c.2690C>T (p.Thr897Ile)
c.2540C>T (p.Thr847Ile)
c.*33+21514G>A (n.*33+21514G>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
12g.9079680G>CCA383839281A2M,KLRG1c.2990C>G (p.Thr997Ser)
n.345C>G
n.451+10232C>G
n.349-6959C>G
c.2690C>G (p.Thr897Ser)
c.2540C>G (p.Thr847Ser)
c.*33+21514G>C (n.*33+21514G>C)
12g.9079680G=CA2015332128A2M,KLRG1c.2990C= (p.Thr997=)
n.345C=
n.451+10232C=
n.349-6959C=
c.2690C= (p.Thr897=)
c.2540C= (p.Thr847=)
c.*33+21514G= (n.*33+21514G=)
12g.9079680G>TCA383839284A2M,KLRG1c.2990C>A (p.Thr997Asn)
n.345C>A
n.451+10232C>A
n.349-6959C>A
c.2690C>A (p.Thr897Asn)
c.2540C>A (p.Thr847Asn)
c.*33+21514G>T (n.*33+21514G>T)
12g.9079681T>ACA383839288A2M,KLRG1c.2989A>T (p.Thr997Ser)
n.344A>T
n.451+10231A>T
n.349-6960A>T
c.2689A>T (p.Thr897Ser)
c.2539A>T (p.Thr847Ser)
c.*33+21515T>A (n.*33+21515T>A)
12g.9079681T>CCA383839290A2M,KLRG1c.2989A>G (p.Thr997Ala)
n.344A>G
n.451+10231A>G
n.349-6960A>G
c.2689A>G (p.Thr897Ala)
c.2539A>G (p.Thr847Ala)
c.*33+21515T>C (n.*33+21515T>C)
12g.9079681T>GCA383839292A2M,KLRG1c.2989A>C (p.Thr997Pro)
n.344A>C
n.451+10231A>C
n.349-6960A>C
c.2689A>C (p.Thr897Pro)
c.2539A>C (p.Thr847Pro)
c.*33+21515T>G (n.*33+21515T>G)
12g.9079682A=CA2015332129A2M,KLRG1c.2988T= (p.Leu996=)
n.343T=
n.451+10230T=
n.349-6961T=
c.2688T= (p.Leu896=)
c.2538T= (p.Leu846=)
c.*33+21516A= (n.*33+21516A=)
12g.9079682A>CCA478323112A2M,KLRG1c.2988T>G (p.Leu996=)
n.343T>G
n.451+10230T>G
n.349-6961T>G
c.2688T>G (p.Leu896=)
c.2538T>G (p.Leu846=)
c.*33+21516A>C (n.*33+21516A>C)
12g.9079682A>GCA478323113A2M,KLRG1c.2988T>C (p.Leu996=)
n.343T>C
n.451+10230T>C
n.349-6961T>C
c.2688T>C (p.Leu896=)
c.2538T>C (p.Leu846=)
c.*33+21516A>G (n.*33+21516A>G)
 dbSNP gnomAD v3 gnomAD v4
12g.9079682A>TCA478323114A2M,KLRG1c.2988T>A (p.Leu996=)
n.343T>A
n.451+10230T>A
n.349-6961T>A
c.2688T>A (p.Leu896=)
c.2538T>A (p.Leu846=)
c.*33+21516A>T (n.*33+21516A>T)
12g.9079683A>CCA383839305A2M,KLRG1c.2987T>G (p.Leu996Arg)
n.342T>G
n.451+10229T>G
n.349-6962T>G
c.2687T>G (p.Leu896Arg)
c.2537T>G (p.Leu846Arg)
c.*33+21517A>C (n.*33+21517A>C)
12g.9079683A>GCA383839299A2M,KLRG1c.2987T>C (p.Leu996Pro)
n.342T>C
n.451+10229T>C
n.349-6962T>C
c.2687T>C (p.Leu896Pro)
c.2537T>C (p.Leu846Pro)
c.*33+21517A>G (n.*33+21517A>G)
 gnomAD v4
12g.9079683A>TCA383839302A2M,KLRG1c.2987T>A (p.Leu996His)
n.342T>A
n.451+10229T>A
n.349-6962T>A
c.2687T>A (p.Leu896His)
c.2537T>A (p.Leu846His)
c.*33+21517A>T (n.*33+21517A>T)
12g.9079684G>ACA383839309A2M,KLRG1c.2986C>T (p.Leu996Phe)
n.341C>T
n.451+10228C>T
n.349-6963C>T
c.2686C>T (p.Leu896Phe)
c.2536C>T (p.Leu846Phe)
c.*33+21518G>A (n.*33+21518G>A)
12g.9079684G>CCA383839312A2M,KLRG1c.2986C>G (p.Leu996Val)
n.341C>G
n.451+10228C>G
n.349-6963C>G
c.2686C>G (p.Leu896Val)
c.2536C>G (p.Leu846Val)
c.*33+21518G>C (n.*33+21518G>C)
12g.9079684G>TCA383839314A2M,KLRG1c.2986C>A (p.Leu996Ile)
n.341C>A
n.451+10228C>A
n.349-6963C>A
c.2686C>A (p.Leu896Ile)
c.2536C>A (p.Leu846Ile)
c.*33+21518G>T (n.*33+21518G>T)
12g.9079685C>ACA383839317A2M,KLRG1c.2985G>T (p.Gln995His)
n.340G>T
n.451+10227G>T
n.349-6964G>T
c.2685G>T (p.Gln895His)
c.2535G>T (p.Gln845His)
c.*33+21519C>A (n.*33+21519C>A)
12g.9079685C>GCA383839319A2M,KLRG1c.2985G>C (p.Gln995His)
n.340G>C
n.451+10227G>C
n.349-6964G>C
c.2685G>C (p.Gln895His)
c.2535G>C (p.Gln845His)
c.*33+21519C>G (n.*33+21519C>G)
12g.9079685C>TCA478323126A2M,KLRG1c.2985G>A (p.Gln995=)
n.340G>A
n.451+10227G>A
n.349-6964G>A
c.2685G>A (p.Gln895=)
c.2535G>A (p.Gln845=)
c.*33+21519C>T (n.*33+21519C>T)
 gnomAD v4
12g.9079686T>ACA383839324A2M,KLRG1c.2984A>T (p.Gln995Leu)
n.339A>T
n.451+10226A>T
n.349-6965A>T
c.2684A>T (p.Gln895Leu)
c.2534A>T (p.Gln845Leu)
c.*33+21520T>A (n.*33+21520T>A)
12g.9079686T>CCA383839330A2M,KLRG1c.2984A>G (p.Gln995Arg)
n.339A>G
n.451+10226A>G
n.349-6965A>G
c.2684A>G (p.Gln895Arg)
c.2534A>G (p.Gln845Arg)
c.*33+21520T>C (n.*33+21520T>C)
12g.9079686T>GCA383839327A2M,KLRG1c.2984A>C (p.Gln995Pro)
n.339A>C
n.451+10226A>C
n.349-6965A>C
c.2684A>C (p.Gln895Pro)
c.2534A>C (p.Gln845Pro)
c.*33+21520T>G (n.*33+21520T>G)
12g.9079687G>ACA383839335A2M,KLRG1c.2983C>T (p.Gln995Ter)
n.338C>T
n.451+10225C>T
n.349-6966C>T
c.2683C>T (p.Gln895Ter)
c.2533C>T (p.Gln845Ter)
c.*33+21521G>A (n.*33+21521G>A)
12g.9079687G>CCA383839344A2M,KLRG1c.2983C>G (p.Gln995Glu)
n.338C>G
n.451+10225C>G
n.349-6966C>G
c.2683C>G (p.Gln895Glu)
c.2533C>G (p.Gln845Glu)
c.*33+21521G>C (n.*33+21521G>C)
12g.9079687G>TCA383839346A2M,KLRG1c.2983C>A (p.Gln995Lys)
n.338C>A
n.451+10225C>A
n.349-6966C>A
c.2683C>A (p.Gln895Lys)
c.2533C>A (p.Gln845Lys)
c.*33+21521G>T (n.*33+21521G>T)
 gnomAD v4
12g.9079688C>ACA383839350A2M,KLRG1c.2982G>T (p.Gln994His)
n.337G>T
n.451+10224G>T
n.349-6967G>T
c.2682G>T (p.Gln894His)
c.2532G>T (p.Gln844His)
c.*33+21522C>A (n.*33+21522C>A)
12g.9079688C>GCA383839353A2M,KLRG1c.2982G>C (p.Gln994His)
n.337G>C
n.451+10224G>C
n.349-6967G>C
c.2682G>C (p.Gln894His)
c.2532G>C (p.Gln844His)
c.*33+21522C>G (n.*33+21522C>G)
12g.9079688C>TCA478323135A2M,KLRG1c.2982G>A (p.Gln994=)
n.337G>A
n.451+10224G>A
n.349-6967G>A
c.2682G>A (p.Gln894=)
c.2532G>A (p.Gln844=)
c.*33+21522C>T (n.*33+21522C>T)
12g.9079689T>ACA383839357A2M,KLRG1c.2981A>T (p.Gln994Leu)
n.336A>T
n.451+10223A>T
n.349-6968A>T
c.2681A>T (p.Gln894Leu)
c.2531A>T (p.Gln844Leu)
c.*33+21523T>A (n.*33+21523T>A)
 gnomAD v4
12g.9079689T>CCA383839359A2M,KLRG1c.2981A>G (p.Gln994Arg)
n.336A>G
n.451+10223A>G
n.349-6968A>G
c.2681A>G (p.Gln894Arg)
c.2531A>G (p.Gln844Arg)
c.*33+21523T>C (n.*33+21523T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
12g.9079689T>GCA383839362A2M,KLRG1c.2981A>C (p.Gln994Pro)
n.336A>C
n.451+10223A>C
n.349-6968A>C
c.2681A>C (p.Gln894Pro)
c.2531A>C (p.Gln844Pro)
c.*33+21523T>G (n.*33+21523T>G)
 gnomAD v4
12g.9079689T=CA2015332130A2M,KLRG1c.2981A= (p.Gln994=)
n.336A=
n.451+10223A=
n.349-6968A=
c.2681A= (p.Gln894=)
c.2531A= (p.Gln844=)
c.*33+21523T= (n.*33+21523T=)
12g.9079690G>ACA232667434A2M,KLRG1c.2980C>T (p.Gln994Ter)
n.335C>T
n.451+10222C>T
n.349-6969C>T
c.2680C>T (p.Gln894Ter)
c.2530C>T (p.Gln844Ter)
c.*33+21524G>A (n.*33+21524G>A)
 dbSNP gnomAD v2 gnomAD v4
12g.9079690G>CCA383839370A2M,KLRG1c.2980C>G (p.Gln994Glu)
n.335C>G
n.451+10222C>G
n.349-6969C>G
c.2680C>G (p.Gln894Glu)
c.2530C>G (p.Gln844Glu)
c.*33+21524G>C (n.*33+21524G>C)
12g.9079690G=CA2015332131A2M,KLRG1c.2980C= (p.Gln994=)
n.335C=
n.451+10222C=
n.349-6969C=
c.2680C= (p.Gln894=)
c.2530C= (p.Gln844=)
c.*33+21524G= (n.*33+21524G=)
12g.9079690G>TCA383839372A2M,KLRG1c.2980C>A (p.Gln994Lys)
n.335C>A
n.451+10222C>A
n.349-6969C>A
c.2680C>A (p.Gln894Lys)
c.2530C>A (p.Gln844Lys)
c.*33+21524G>T (n.*33+21524G>T)
12g.9079691T>ACA478323145A2M,KLRG1c.2979A>T (p.Thr993=)
n.334A>T
n.451+10221A>T
n.349-6970A>T
c.2679A>T (p.Thr893=)
c.2529A>T (p.Thr843=)
c.*33+21525T>A (n.*33+21525T>A)
12g.9079691T>CCA478323147A2M,KLRG1c.2979A>G (p.Thr993=)
n.334A>G
n.451+10221A>G
n.349-6970A>G
c.2679A>G (p.Thr893=)
c.2529A>G (p.Thr843=)
c.*33+21525T>C (n.*33+21525T>C)
12g.9079691T>GCA478323149A2M,KLRG1c.2979A>C (p.Thr993=)
n.334A>C
n.451+10221A>C
n.349-6970A>C
c.2679A>C (p.Thr893=)
c.2529A>C (p.Thr843=)
c.*33+21525T>G (n.*33+21525T>G)
12g.9079692G>ACA6438243A2M,KLRG1c.2978C>T (p.Thr993Ile)
n.333C>T
n.451+10220C>T
n.349-6971C>T
c.2678C>T (p.Thr893Ile)
c.2528C>T (p.Thr843Ile)
c.*33+21526G>A (n.*33+21526G>A)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
12g.9079692G>CCA383839379A2M,KLRG1c.2978C>G (p.Thr993Arg)
n.333C>G
n.451+10220C>G
n.349-6971C>G
c.2678C>G (p.Thr893Arg)
c.2528C>G (p.Thr843Arg)
c.*33+21526G>C (n.*33+21526G>C)
12g.9079692G=CA2015332132A2M,KLRG1c.2978C= (p.Thr993=)
n.333C=
n.451+10220C=
n.349-6971C=
c.2678C= (p.Thr893=)
c.2528C= (p.Thr843=)
c.*33+21526G= (n.*33+21526G=)
12g.9079692G>TCA383839376A2M,KLRG1c.2978C>A (p.Thr993Lys)
n.333C>A
n.451+10220C>A
n.349-6971C>A
c.2678C>A (p.Thr893Lys)
c.2528C>A (p.Thr843Lys)
c.*33+21526G>T (n.*33+21526G>T)
12g.9079693T>ACA383839384A2M,KLRG1c.2977A>T (p.Thr993Ser)
n.332A>T
n.451+10219A>T
n.349-6972A>T
c.2677A>T (p.Thr893Ser)
c.2527A>T (p.Thr843Ser)
c.*33+21527T>A (n.*33+21527T>A)
 gnomAD v4
12g.9079693T>CCA383839393A2M,KLRG1c.2977A>G (p.Thr993Ala)
n.332A>G
n.451+10219A>G
n.349-6972A>G
c.2677A>G (p.Thr893Ala)
c.2527A>G (p.Thr843Ala)
c.*33+21527T>C (n.*33+21527T>C)

Number of alleles fetched