Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.44951956dup | CA299698615 | SETBP1 | c.2616dup (p.Thr873AspfsTer8) c.2694dup (p.Thr899AspfsTer8) c.2139dup (p.Thr714AspfsTer8) | dbSNP |
18 | g.44951956G>A | CA503982146 | SETBP1 | c.2616G>A (p.Gly872=) c.2694G>A (p.Gly898=) c.2139G>A (p.Gly713=) | ClinVar |
18 | g.44951956G>C | CA299698620 | SETBP1 | c.2616G>C (p.Gly872=) c.2694G>C (p.Gly898=) c.2139G>C (p.Gly713=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.44951956G= | CA2300140790 | SETBP1 | c.2616G= (p.Gly872=) c.2694G= (p.Gly898=) c.2139G= (p.Gly713=) | |
18 | g.44951956G>T | CA503982147 | SETBP1 | c.2616G>T (p.Gly872=) c.2694G>T (p.Gly898=) c.2139G>T (p.Gly713=) | |
18 | g.44951957A>C | CA402321831 | SETBP1 | c.2617A>C (p.Thr873Pro) c.2695A>C (p.Thr899Pro) c.2140A>C (p.Thr714Pro) | |
18 | g.44951957A>G | CA402321832 | SETBP1 | c.2617A>G (p.Thr873Ala) c.2695A>G (p.Thr899Ala) c.2140A>G (p.Thr714Ala) | |
18 | g.44951957A>T | CA402321833 | SETBP1 | c.2617A>T (p.Thr873Ser) c.2695A>T (p.Thr899Ser) c.2140A>T (p.Thr714Ser) | |
18 | g.44951958C>A | CA402321834 | SETBP1 | c.2618C>A (p.Thr873Lys) c.2696C>A (p.Thr899Lys) c.2141C>A (p.Thr714Lys) | |
18 | g.44951958C>G | CA402321835 | SETBP1 | c.2618C>G (p.Thr873Arg) c.2696C>G (p.Thr899Arg) c.2141C>G (p.Thr714Arg) | COSMIC |
18 | g.44951958C>T | CA402321836 | SETBP1 | c.2618C>T (p.Thr873Ile) c.2696C>T (p.Thr899Ile) c.2141C>T (p.Thr714Ile) | |
18 | g.44951959A>C | CA503982150 | SETBP1 | c.2619A>C (p.Thr873=) c.2697A>C (p.Thr899=) c.2142A>C (p.Thr714=) | |
18 | g.44951959A>G | CA503982152 | SETBP1 | c.2619A>G (p.Thr873=) c.2697A>G (p.Thr899=) c.2142A>G (p.Thr714=) | gnomAD v4 |
18 | g.44951959A>T | CA503982154 | SETBP1 | c.2619A>T (p.Thr873=) c.2697A>T (p.Thr899=) c.2142A>T (p.Thr714=) | |
18 | g.44951960G>A | CA402321837 | SETBP1 | c.2620G>A (p.Asp874Asn) c.2698G>A (p.Asp900Asn) c.2143G>A (p.Asp715Asn) | |
18 | g.44951960G>C | CA402321838 | SETBP1 | c.2620G>C (p.Asp874His) c.2698G>C (p.Asp900His) c.2143G>C (p.Asp715His) | |
18 | g.44951960G>T | CA402321839 | SETBP1 | c.2620G>T (p.Asp874Tyr) c.2698G>T (p.Asp900Tyr) c.2143G>T (p.Asp715Tyr) | COSMIC |
18 | g.44951960_44951963delinsGACA | CA2300140791 | SETBP1 | c.2620_2623delinsGACA (p.Asp874=) c.2698_2701delinsGACA (p.Asp900=) c.2143_2146delinsGACA (p.Asp715=) | |
18 | g.44951961A= | CA2300140792 | SETBP1 | c.2621A= (p.Asp874=) c.2699A= (p.Asp900=) c.2144A= (p.Asp715=) | |
18 | g.44951961A>C | CA402321840 | SETBP1 | c.2621A>C (p.Asp874Ala) c.2699A>C (p.Asp900Ala) c.2144A>C (p.Asp715Ala) | |
18 | g.44951961A>G | CA402321841 | SETBP1 | c.2621A>G (p.Asp874Gly) c.2699A>G (p.Asp900Gly) c.2144A>G (p.Asp715Gly) | ClinVar dbSNP |
18 | g.44951961A>T | CA402321842 | SETBP1 | c.2621A>T (p.Asp874Val) c.2699A>T (p.Asp900Val) c.2144A>T (p.Asp715Val) | |
18 | g.44951967_44951969del | CA299698629 | SETBP1 | c.2627_2629del (p.Asn876del) c.2705_2707del (p.Asn902del) c.2150_2152del (p.Asn717del) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
18 | g.44951962C>A | CA402321843 | SETBP1 | c.2622C>A (p.Asp874Glu) c.2700C>A (p.Asp900Glu) c.2145C>A (p.Asp715Glu) | |
18 | g.44951962C>G | CA402321844 | SETBP1 | c.2622C>G (p.Asp874Glu) c.2700C>G (p.Asp900Glu) c.2145C>G (p.Asp715Glu) | |
18 | g.44951962C>T | CA503982159 | SETBP1 | c.2622C>T (p.Asp874=) c.2700C>T (p.Asp900=) c.2145C>T (p.Asp715=) | ClinVar dbSNP gnomAD v4 |
18 | g.44951963A>C | CA402321845 | SETBP1 | c.2623A>C (p.Asn875His) c.2701A>C (p.Asn901His) c.2146A>C (p.Asn716His) | |
18 | g.44951963A>G | CA402321846 | SETBP1 | c.2623A>G (p.Asn875Asp) c.2701A>G (p.Asn901Asp) c.2146A>G (p.Asn716Asp) | |
18 | g.44951963A>T | CA402321847 | SETBP1 | c.2623A>T (p.Asn875Tyr) c.2701A>T (p.Asn901Tyr) c.2146A>T (p.Asn716Tyr) | |
18 | g.44951964A= | CA2300140793 | SETBP1 | c.2624A= (p.Asn875=) c.2702A= (p.Asn901=) c.2147A= (p.Asn716=) | |
18 | g.44951964A>C | CA402321848 | SETBP1 | c.2624A>C (p.Asn875Thr) c.2702A>C (p.Asn901Thr) c.2147A>C (p.Asn716Thr) | |
18 | g.44951964A>G | CA402321849 | SETBP1 | c.2624A>G (p.Asn875Ser) c.2702A>G (p.Asn901Ser) c.2147A>G (p.Asn716Ser) | dbSNP |
18 | g.44951964A>T | CA402321850 | SETBP1 | c.2624A>T (p.Asn875Ile) c.2702A>T (p.Asn901Ile) c.2147A>T (p.Asn716Ile) | |
18 | g.44951965C>A | CA402321851 | SETBP1 | c.2625C>A (p.Asn875Lys) c.2703C>A (p.Asn901Lys) c.2148C>A (p.Asn716Lys) | |
18 | g.44951965C>G | CA402321852 | SETBP1 | c.2625C>G (p.Asn875Lys) c.2703C>G (p.Asn901Lys) c.2148C>G (p.Asn716Lys) | |
18 | g.44951965C>T | CA503982161 | SETBP1 | c.2625C>T (p.Asn875=) c.2703C>T (p.Asn901=) c.2148C>T (p.Asn716=) | gnomAD v3 gnomAD v4 |
18 | g.44951966A>C | CA402321853 | SETBP1 | c.2626A>C (p.Asn876His) c.2704A>C (p.Asn902His) c.2149A>C (p.Asn717His) | |
18 | g.44951966A>G | CA402321854 | SETBP1 | c.2626A>G (p.Asn876Asp) c.2704A>G (p.Asn902Asp) c.2149A>G (p.Asn717Asp) | |
18 | g.44951966A>T | CA402321855 | SETBP1 | c.2626A>T (p.Asn876Tyr) c.2704A>T (p.Asn902Tyr) c.2149A>T (p.Asn717Tyr) | |
18 | g.44951967A= | CA2300140794 | SETBP1 | c.2627A= (p.Asn876=) c.2705A= (p.Asn902=) c.2150A= (p.Asn717=) | |
18 | g.44951967A>C | CA402321856 | SETBP1 | c.2627A>C (p.Asn876Thr) c.2705A>C (p.Asn902Thr) c.2150A>C (p.Asn717Thr) | |
18 | g.44951967A>G | CA402321857 | SETBP1 | c.2627A>G (p.Asn876Ser) c.2705A>G (p.Asn902Ser) c.2150A>G (p.Asn717Ser) | dbSNP gnomAD v4 |
18 | g.44951967A>T | CA402321858 | SETBP1 | c.2627A>T (p.Asn876Ile) c.2705A>T (p.Asn902Ile) c.2150A>T (p.Asn717Ile) | |
18 | g.44951968C>A | CA402321859 | SETBP1 | c.2628C>A (p.Asn876Lys) c.2706C>A (p.Asn902Lys) c.2151C>A (p.Asn717Lys) | |
18 | g.44951968C>G | CA402321860 | SETBP1 | c.2628C>G (p.Asn876Lys) c.2706C>G (p.Asn902Lys) c.2151C>G (p.Asn717Lys) | |
18 | g.44951968C>T | CA503982163 | SETBP1 | c.2628C>T (p.Asn876=) c.2706C>T (p.Asn902=) c.2151C>T (p.Asn717=) | gnomAD v4 |
18 | g.44951969A>C | CA402321861 | SETBP1 | c.2629A>C (p.Ser877Arg) c.2707A>C (p.Ser903Arg) c.2152A>C (p.Ser718Arg) | |
18 | g.44951969A>G | CA402321862 | SETBP1 | c.2629A>G (p.Ser877Gly) c.2707A>G (p.Ser903Gly) c.2152A>G (p.Ser718Gly) | |
18 | g.44951969A>T | CA402321863 | SETBP1 | c.2629A>T (p.Ser877Cys) c.2707A>T (p.Ser903Cys) c.2152A>T (p.Ser718Cys) | |
18 | g.44951970G>A | CA402321864 | SETBP1 | c.2630G>A (p.Ser877Asn) c.2708G>A (p.Ser903Asn) c.2153G>A (p.Ser718Asn) |