Chr Mutation (hg38) CAid Gene Transcript Linkouts
10g.65966617A=CA1916183190CTNNA3n.571T=
c.2395T= (p.Ser799=)
c.2194T= (p.Ser732=)
c.*1934T= (n.*1934T=)
c.*1919T= (n.*1919T=)
c.2431T= (p.Ser811=)
c.2464T= (p.Ser822=)
c.2620T= (p.Ser874=)
c.1612T= (p.Ser538=)
c.1300T= (p.Ser434=)
10g.65966617A>CCA377089882CTNNA3n.571T>G
c.2395T>G (p.Ser799Ala)
c.2194T>G (p.Ser732Ala)
c.*1934T>G (n.*1934T>G)
c.*1919T>G (n.*1919T>G)
c.2431T>G (p.Ser811Ala)
c.2464T>G (p.Ser822Ala)
c.2620T>G (p.Ser874Ala)
c.1612T>G (p.Ser538Ala)
c.1300T>G (p.Ser434Ala)
10g.65966617A>GCA377089883CTNNA3n.571T>C
c.2395T>C (p.Ser799Pro)
c.2194T>C (p.Ser732Pro)
c.*1934T>C (n.*1934T>C)
c.*1919T>C (n.*1919T>C)
c.2431T>C (p.Ser811Pro)
c.2464T>C (p.Ser822Pro)
c.2620T>C (p.Ser874Pro)
c.1612T>C (p.Ser538Pro)
c.1300T>C (p.Ser434Pro)
ClinVar dbSNP gnomAD v4
10g.65966617A>TCA377089884CTNNA3n.571T>A
c.2395T>A (p.Ser799Thr)
c.2194T>A (p.Ser732Thr)
c.*1934T>A (n.*1934T>A)
c.*1919T>A (n.*1919T>A)
c.2431T>A (p.Ser811Thr)
c.2464T>A (p.Ser822Thr)
c.2620T>A (p.Ser874Thr)
c.1612T>A (p.Ser538Thr)
c.1300T>A (p.Ser434Thr)
10g.65966618C>ACA377089885CTNNA3n.570G>T
c.2394G>T (p.Met798Ile)
c.2193G>T (p.Met731Ile)
c.*1933G>T (n.*1933G>T)
c.*1918G>T (n.*1918G>T)
c.2430G>T (p.Met810Ile)
c.2463G>T (p.Met821Ile)
c.2619G>T (p.Met873Ile)
c.1611G>T (p.Met537Ile)
c.1299G>T (p.Met433Ile)
10g.65966618C>GCA377089886CTNNA3n.570G>C
c.2394G>C (p.Met798Ile)
c.2193G>C (p.Met731Ile)
c.*1933G>C (n.*1933G>C)
c.*1918G>C (n.*1918G>C)
c.2430G>C (p.Met810Ile)
c.2463G>C (p.Met821Ile)
c.2619G>C (p.Met873Ile)
c.1611G>C (p.Met537Ile)
c.1299G>C (p.Met433Ile)
10g.65966618C>TCA377089887CTNNA3n.570G>A
c.2394G>A (p.Met798Ile)
c.2193G>A (p.Met731Ile)
c.*1933G>A (n.*1933G>A)
c.*1918G>A (n.*1918G>A)
c.2430G>A (p.Met810Ile)
c.2463G>A (p.Met821Ile)
c.2619G>A (p.Met873Ile)
c.1611G>A (p.Met537Ile)
c.1299G>A (p.Met433Ile)
10g.65966619A=CA1916183191CTNNA3n.569T=
c.2393T= (p.Met798=)
c.2192T= (p.Met731=)
c.*1932T= (n.*1932T=)
c.*1917T= (n.*1917T=)
c.2429T= (p.Met810=)
c.2462T= (p.Met821=)
c.2618T= (p.Met873=)
c.1610T= (p.Met537=)
c.1298T= (p.Met433=)
10g.65966619A>CCA377089888CTNNA3n.569T>G
c.2393T>G (p.Met798Arg)
c.2192T>G (p.Met731Arg)
c.*1932T>G (n.*1932T>G)
c.*1917T>G (n.*1917T>G)
c.2429T>G (p.Met810Arg)
c.2462T>G (p.Met821Arg)
c.2618T>G (p.Met873Arg)
c.1610T>G (p.Met537Arg)
c.1298T>G (p.Met433Arg)
10g.65966619A>GCA377089889CTNNA3n.569T>C
c.2393T>C (p.Met798Thr)
c.2192T>C (p.Met731Thr)
c.*1932T>C (n.*1932T>C)
c.*1917T>C (n.*1917T>C)
c.2429T>C (p.Met810Thr)
c.2462T>C (p.Met821Thr)
c.2618T>C (p.Met873Thr)
c.1610T>C (p.Met537Thr)
c.1298T>C (p.Met433Thr)
dbSNP gnomAD v3 gnomAD v4
10g.65966619A>TCA377089890CTNNA3n.569T>A
c.2393T>A (p.Met798Lys)
c.2192T>A (p.Met731Lys)
c.*1932T>A (n.*1932T>A)
c.*1917T>A (n.*1917T>A)
c.2429T>A (p.Met810Lys)
c.2462T>A (p.Met821Lys)
c.2618T>A (p.Met873Lys)
c.1610T>A (p.Met537Lys)
c.1298T>A (p.Met433Lys)
10g.65966620T>ACA377089891CTNNA3n.568A>T
c.2392A>T (p.Met798Leu)
c.2191A>T (p.Met731Leu)
c.*1931A>T (n.*1931A>T)
c.*1916A>T (n.*1916A>T)
c.2428A>T (p.Met810Leu)
c.2461A>T (p.Met821Leu)
c.2617A>T (p.Met873Leu)
c.1609A>T (p.Met537Leu)
c.1297A>T (p.Met433Leu)
10g.65966620T>CCA377089892CTNNA3n.568A>G
c.2392A>G (p.Met798Val)
c.2191A>G (p.Met731Val)
c.*1931A>G (n.*1931A>G)
c.*1916A>G (n.*1916A>G)
c.2428A>G (p.Met810Val)
c.2461A>G (p.Met821Val)
c.2617A>G (p.Met873Val)
c.1609A>G (p.Met537Val)
c.1297A>G (p.Met433Val)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.65966620T>GCA377089893CTNNA3n.568A>C
c.2392A>C (p.Met798Leu)
c.2191A>C (p.Met731Leu)
c.*1931A>C (n.*1931A>C)
c.*1916A>C (n.*1916A>C)
c.2428A>C (p.Met810Leu)
c.2461A>C (p.Met821Leu)
c.2617A>C (p.Met873Leu)
c.1609A>C (p.Met537Leu)
c.1297A>C (p.Met433Leu)
10g.65966620T=CA1916183192CTNNA3n.568A=
c.2392A= (p.Met798=)
c.2191A= (p.Met731=)
c.*1931A= (n.*1931A=)
c.*1916A= (n.*1916A=)
c.2428A= (p.Met810=)
c.2461A= (p.Met821=)
c.2617A= (p.Met873=)
c.1609A= (p.Met537=)
c.1297A= (p.Met433=)
10g.65966621G>ACA5519614CTNNA3n.567C>T
c.2391C>T (p.Ile797=)
c.2190C>T (p.Ile730=)
c.*1930C>T (n.*1930C>T)
c.*1915C>T (n.*1915C>T)
c.2427C>T (p.Ile809=)
c.2460C>T (p.Ile820=)
c.2616C>T (p.Ile872=)
c.1608C>T (p.Ile536=)
c.1296C>T (p.Ile432=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
10g.65966621G>CCA377089894CTNNA3n.567C>G
c.2391C>G (p.Ile797Met)
c.2190C>G (p.Ile730Met)
c.*1930C>G (n.*1930C>G)
c.*1915C>G (n.*1915C>G)
c.2427C>G (p.Ile809Met)
c.2460C>G (p.Ile820Met)
c.2616C>G (p.Ile872Met)
c.1608C>G (p.Ile536Met)
c.1296C>G (p.Ile432Met)
10g.65966621G=CA1916183193CTNNA3n.567C=
c.2391C= (p.Ile797=)
c.2190C= (p.Ile730=)
c.*1930C= (n.*1930C=)
c.*1915C= (n.*1915C=)
c.2427C= (p.Ile809=)
c.2460C= (p.Ile820=)
c.2616C= (p.Ile872=)
c.1608C= (p.Ile536=)
c.1296C= (p.Ile432=)
10g.65966621G>TCA469961158CTNNA3n.567C>A
c.2391C>A (p.Ile797=)
c.2190C>A (p.Ile730=)
c.*1930C>A (n.*1930C>A)
c.*1915C>A (n.*1915C>A)
c.2427C>A (p.Ile809=)
c.2460C>A (p.Ile820=)
c.2616C>A (p.Ile872=)
c.1608C>A (p.Ile536=)
c.1296C>A (p.Ile432=)
10g.65966622A>CCA377089896CTNNA3n.566T>G
c.2390T>G (p.Ile797Ser)
c.2189T>G (p.Ile730Ser)
c.*1929T>G (n.*1929T>G)
c.*1914T>G (n.*1914T>G)
c.2426T>G (p.Ile809Ser)
c.2459T>G (p.Ile820Ser)
c.2615T>G (p.Ile872Ser)
c.1607T>G (p.Ile536Ser)
c.1295T>G (p.Ile432Ser)
10g.65966622A>GCA377089897CTNNA3n.566T>C
c.2390T>C (p.Ile797Thr)
c.2189T>C (p.Ile730Thr)
c.*1929T>C (n.*1929T>C)
c.*1914T>C (n.*1914T>C)
c.2426T>C (p.Ile809Thr)
c.2459T>C (p.Ile820Thr)
c.2615T>C (p.Ile872Thr)
c.1607T>C (p.Ile536Thr)
c.1295T>C (p.Ile432Thr)
10g.65966622A>TCA377089895CTNNA3n.566T>A
c.2390T>A (p.Ile797Asn)
c.2189T>A (p.Ile730Asn)
c.*1929T>A (n.*1929T>A)
c.*1914T>A (n.*1914T>A)
c.2426T>A (p.Ile809Asn)
c.2459T>A (p.Ile820Asn)
c.2615T>A (p.Ile872Asn)
c.1607T>A (p.Ile536Asn)
c.1295T>A (p.Ile432Asn)
10g.65966623T>ACA377089898CTNNA3n.565A>T
c.2389A>T (p.Ile797Phe)
c.2188A>T (p.Ile730Phe)
c.*1928A>T (n.*1928A>T)
c.*1913A>T (n.*1913A>T)
c.2425A>T (p.Ile809Phe)
c.2458A>T (p.Ile820Phe)
c.2614A>T (p.Ile872Phe)
c.1606A>T (p.Ile536Phe)
c.1294A>T (p.Ile432Phe)
10g.65966623T>CCA377089899CTNNA3n.565A>G
c.2389A>G (p.Ile797Val)
c.2188A>G (p.Ile730Val)
c.*1928A>G (n.*1928A>G)
c.*1913A>G (n.*1913A>G)
c.2425A>G (p.Ile809Val)
c.2458A>G (p.Ile820Val)
c.2614A>G (p.Ile872Val)
c.1606A>G (p.Ile536Val)
c.1294A>G (p.Ile432Val)
gnomAD v4
10g.65966623T>GCA377089900CTNNA3n.565A>C
c.2389A>C (p.Ile797Leu)
c.2188A>C (p.Ile730Leu)
c.*1928A>C (n.*1928A>C)
c.*1913A>C (n.*1913A>C)
c.2425A>C (p.Ile809Leu)
c.2458A>C (p.Ile820Leu)
c.2614A>C (p.Ile872Leu)
c.1606A>C (p.Ile536Leu)
c.1294A>C (p.Ile432Leu)
dbSNP
10g.65966623T=CA1916183194CTNNA3n.565A=
c.2389A= (p.Ile797=)
c.2188A= (p.Ile730=)
c.*1928A= (n.*1928A=)
c.*1913A= (n.*1913A=)
c.2425A= (p.Ile809=)
c.2458A= (p.Ile820=)
c.2614A= (p.Ile872=)
c.1606A= (p.Ile536=)
c.1294A= (p.Ile432=)
10g.65966624G>ACA469961160CTNNA3n.564C>T
c.2388C>T (p.Leu796=)
c.2187C>T (p.Leu729=)
c.*1927C>T (n.*1927C>T)
c.*1912C>T (n.*1912C>T)
c.2424C>T (p.Leu808=)
c.2457C>T (p.Leu819=)
c.2613C>T (p.Leu871=)
c.1605C>T (p.Leu535=)
c.1293C>T (p.Leu431=)
gnomAD v4
10g.65966624G>CCA469961161CTNNA3n.564C>G
c.2388C>G (p.Leu796=)
c.2187C>G (p.Leu729=)
c.*1927C>G (n.*1927C>G)
c.*1912C>G (n.*1912C>G)
c.2424C>G (p.Leu808=)
c.2457C>G (p.Leu819=)
c.2613C>G (p.Leu871=)
c.1605C>G (p.Leu535=)
c.1293C>G (p.Leu431=)
10g.65966624G>TCA469961164CTNNA3n.564C>A
c.2388C>A (p.Leu796=)
c.2187C>A (p.Leu729=)
c.*1927C>A (n.*1927C>A)
c.*1912C>A (n.*1912C>A)
c.2424C>A (p.Leu808=)
c.2457C>A (p.Leu819=)
c.2613C>A (p.Leu871=)
c.1605C>A (p.Leu535=)
c.1293C>A (p.Leu431=)
10g.65966625A>CCA377089901CTNNA3n.563T>G
c.2387T>G (p.Leu796Arg)
c.2186T>G (p.Leu729Arg)
c.*1926T>G (n.*1926T>G)
c.*1911T>G (n.*1911T>G)
c.2423T>G (p.Leu808Arg)
c.2456T>G (p.Leu819Arg)
c.2612T>G (p.Leu871Arg)
c.1604T>G (p.Leu535Arg)
c.1292T>G (p.Leu431Arg)
10g.65966625A>GCA377089902CTNNA3n.563T>C
c.2387T>C (p.Leu796Pro)
c.2186T>C (p.Leu729Pro)
c.*1926T>C (n.*1926T>C)
c.*1911T>C (n.*1911T>C)
c.2423T>C (p.Leu808Pro)
c.2456T>C (p.Leu819Pro)
c.2612T>C (p.Leu871Pro)
c.1604T>C (p.Leu535Pro)
c.1292T>C (p.Leu431Pro)
10g.65966625A>TCA377089903CTNNA3n.563T>A
c.2387T>A (p.Leu796His)
c.2186T>A (p.Leu729His)
c.*1926T>A (n.*1926T>A)
c.*1911T>A (n.*1911T>A)
c.2423T>A (p.Leu808His)
c.2456T>A (p.Leu819His)
c.2612T>A (p.Leu871His)
c.1604T>A (p.Leu535His)
c.1292T>A (p.Leu431His)
10g.65966626G>ACA377089904CTNNA3n.562C>T
c.2386C>T (p.Leu796Phe)
c.2185C>T (p.Leu729Phe)
c.*1925C>T (n.*1925C>T)
c.*1910C>T (n.*1910C>T)
c.2422C>T (p.Leu808Phe)
c.2455C>T (p.Leu819Phe)
c.2611C>T (p.Leu871Phe)
c.1603C>T (p.Leu535Phe)
c.1291C>T (p.Leu431Phe)
ClinVar dbSNP gnomAD v2 gnomAD v4
10g.65966626G>CCA377089905CTNNA3n.562C>G
c.2386C>G (p.Leu796Val)
c.2185C>G (p.Leu729Val)
c.*1925C>G (n.*1925C>G)
c.*1910C>G (n.*1910C>G)
c.2422C>G (p.Leu808Val)
c.2455C>G (p.Leu819Val)
c.2611C>G (p.Leu871Val)
c.1603C>G (p.Leu535Val)
c.1291C>G (p.Leu431Val)
10g.65966626G=CA1916183195CTNNA3n.562C=
c.2386C= (p.Leu796=)
c.2185C= (p.Leu729=)
c.*1925C= (n.*1925C=)
c.*1910C= (n.*1910C=)
c.2422C= (p.Leu808=)
c.2455C= (p.Leu819=)
c.2611C= (p.Leu871=)
c.1603C= (p.Leu535=)
c.1291C= (p.Leu431=)
10g.65966626G>TCA377089906CTNNA3n.562C>A
c.2386C>A (p.Leu796Ile)
c.2185C>A (p.Leu729Ile)
c.*1925C>A (n.*1925C>A)
c.*1910C>A (n.*1910C>A)
c.2422C>A (p.Leu808Ile)
c.2455C>A (p.Leu819Ile)
c.2611C>A (p.Leu871Ile)
c.1603C>A (p.Leu535Ile)
c.1291C>A (p.Leu431Ile)
dbSNP COSMIC COSMIC
10g.65966627C>ACA377089907CTNNA3n.561G>T
c.2385G>T (p.Glu795Asp)
c.2184G>T (p.Glu728Asp)
c.*1924G>T (n.*1924G>T)
c.*1909G>T (n.*1909G>T)
c.2421G>T (p.Glu807Asp)
c.2454G>T (p.Glu818Asp)
c.2610G>T (p.Glu870Asp)
c.1602G>T (p.Glu534Asp)
c.1290G>T (p.Glu430Asp)
gnomAD v4
10g.65966627C=CA1916183196CTNNA3n.561G=
c.2385G= (p.Glu795=)
c.2184G= (p.Glu728=)
c.*1924G= (n.*1924G=)
c.*1909G= (n.*1909G=)
c.2421G= (p.Glu807=)
c.2454G= (p.Glu818=)
c.2610G= (p.Glu870=)
c.1602G= (p.Glu534=)
c.1290G= (p.Glu430=)
10g.65966627C>GCA377089908CTNNA3n.561G>C
c.2385G>C (p.Glu795Asp)
c.2184G>C (p.Glu728Asp)
c.*1924G>C (n.*1924G>C)
c.*1909G>C (n.*1909G>C)
c.2421G>C (p.Glu807Asp)
c.2454G>C (p.Glu818Asp)
c.2610G>C (p.Glu870Asp)
c.1602G>C (p.Glu534Asp)
c.1290G>C (p.Glu430Asp)
10g.65966627C>TCA469961167CTNNA3n.561G>A
c.2385G>A (p.Glu795=)
c.2184G>A (p.Glu728=)
c.*1924G>A (n.*1924G>A)
c.*1909G>A (n.*1909G>A)
c.2421G>A (p.Glu807=)
c.2454G>A (p.Glu818=)
c.2610G>A (p.Glu870=)
c.1602G>A (p.Glu534=)
c.1290G>A (p.Glu430=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
10g.65966628T>ACA377089911CTNNA3n.560A>T
c.2384A>T (p.Glu795Val)
c.2183A>T (p.Glu728Val)
c.*1923A>T (n.*1923A>T)
c.*1908A>T (n.*1908A>T)
c.2420A>T (p.Glu807Val)
c.2453A>T (p.Glu818Val)
c.2609A>T (p.Glu870Val)
c.1601A>T (p.Glu534Val)
c.1289A>T (p.Glu430Val)
10g.65966628T>CCA377089910CTNNA3n.560A>G
c.2384A>G (p.Glu795Gly)
c.2183A>G (p.Glu728Gly)
c.*1923A>G (n.*1923A>G)
c.*1908A>G (n.*1908A>G)
c.2420A>G (p.Glu807Gly)
c.2453A>G (p.Glu818Gly)
c.2609A>G (p.Glu870Gly)
c.1601A>G (p.Glu534Gly)
c.1289A>G (p.Glu430Gly)
10g.65966628T>GCA377089909CTNNA3n.560A>C
c.2384A>C (p.Glu795Ala)
c.2183A>C (p.Glu728Ala)
c.*1923A>C (n.*1923A>C)
c.*1908A>C (n.*1908A>C)
c.2420A>C (p.Glu807Ala)
c.2453A>C (p.Glu818Ala)
c.2609A>C (p.Glu870Ala)
c.1601A>C (p.Glu534Ala)
c.1289A>C (p.Glu430Ala)
gnomAD v4
10g.65966629C>ACA377089912CTNNA3n.559G>T
c.2383G>T (p.Glu795Ter)
c.2182G>T (p.Glu728Ter)
c.*1922G>T (n.*1922G>T)
c.*1907G>T (n.*1907G>T)
c.2419G>T (p.Glu807Ter)
c.2452G>T (p.Glu818Ter)
c.2608G>T (p.Glu870Ter)
c.1600G>T (p.Glu534Ter)
c.1288G>T (p.Glu430Ter)
10g.65966629C=CA1916183197CTNNA3n.559G=
c.2383G= (p.Glu795=)
c.2182G= (p.Glu728=)
c.*1922G= (n.*1922G=)
c.*1907G= (n.*1907G=)
c.2419G= (p.Glu807=)
c.2452G= (p.Glu818=)
c.2608G= (p.Glu870=)
c.1600G= (p.Glu534=)
c.1288G= (p.Glu430=)
10g.65966629C>GCA377089913CTNNA3n.559G>C
c.2383G>C (p.Glu795Gln)
c.2182G>C (p.Glu728Gln)
c.*1922G>C (n.*1922G>C)
c.*1907G>C (n.*1907G>C)
c.2419G>C (p.Glu807Gln)
c.2452G>C (p.Glu818Gln)
c.2608G>C (p.Glu870Gln)
c.1600G>C (p.Glu534Gln)
c.1288G>C (p.Glu430Gln)
10g.65966629C>TCA377089914CTNNA3n.559G>A
c.2383G>A (p.Glu795Lys)
c.2182G>A (p.Glu728Lys)
c.*1922G>A (n.*1922G>A)
c.*1907G>A (n.*1907G>A)
c.2419G>A (p.Glu807Lys)
c.2452G>A (p.Glu818Lys)
c.2608G>A (p.Glu870Lys)
c.1600G>A (p.Glu534Lys)
c.1288G>A (p.Glu430Lys)
dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC
10g.65966633_65966635delCA2609350470CTNNA3n.557_559del
c.2381_2383del (p.Gly794del)
c.2180_2182del (p.Gly727del)
c.*1920_*1922del (n.*1920_*1922del)
c.*1905_*1907del (n.*1905_*1907del)
c.2417_2419del (p.Gly806del)
c.2450_2452del (p.Gly817del)
c.2606_2608del (p.Gly869del)
c.1598_1600del (p.Gly533del)
c.1286_1288del (p.Gly429del)
ClinVar gnomAD v4
10g.65966630T>ACA469961168CTNNA3n.558A>T
c.2382A>T (p.Gly794=)
c.2181A>T (p.Gly727=)
c.*1921A>T (n.*1921A>T)
c.*1906A>T (n.*1906A>T)
c.2418A>T (p.Gly806=)
c.2451A>T (p.Gly817=)
c.2607A>T (p.Gly869=)
c.1599A>T (p.Gly533=)
c.1287A>T (p.Gly429=)
10g.65966630T>CCA469961169CTNNA3n.558A>G
c.2382A>G (p.Gly794=)
c.2181A>G (p.Gly727=)
c.*1921A>G (n.*1921A>G)
c.*1906A>G (n.*1906A>G)
c.2418A>G (p.Gly806=)
c.2451A>G (p.Gly817=)
c.2607A>G (p.Gly869=)
c.1599A>G (p.Gly533=)
c.1287A>G (p.Gly429=)
ClinVar

Number of alleles fetched