Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
10 | g.65966617A= | CA1916183190 | CTNNA3 | n.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=) | |
10 | g.65966617A>C | CA377089882 | CTNNA3 | n.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) | |
10 | g.65966617A>G | CA377089883 | CTNNA3 | n.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 |
10 | g.65966617A>T | CA377089884 | CTNNA3 | n.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) | |
10 | g.65966618C>A | CA377089885 | CTNNA3 | n.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) | |
10 | g.65966618C>G | CA377089886 | CTNNA3 | n.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) | |
10 | g.65966618C>T | CA377089887 | CTNNA3 | n.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) | |
10 | g.65966619A= | CA1916183191 | CTNNA3 | n.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=) | |
10 | g.65966619A>C | CA377089888 | CTNNA3 | n.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) | |
10 | g.65966619A>G | CA377089889 | CTNNA3 | n.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 |
10 | g.65966619A>T | CA377089890 | CTNNA3 | n.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) | |
10 | g.65966620T>A | CA377089891 | CTNNA3 | n.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) | |
10 | g.65966620T>C | CA377089892 | CTNNA3 | n.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 |
10 | g.65966620T>G | CA377089893 | CTNNA3 | n.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) | |
10 | g.65966620T= | CA1916183192 | CTNNA3 | n.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=) | |
10 | g.65966621G>A | CA5519614 | CTNNA3 | n.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 |
10 | g.65966621G>C | CA377089894 | CTNNA3 | n.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) | |
10 | g.65966621G= | CA1916183193 | CTNNA3 | n.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=) | |
10 | g.65966621G>T | CA469961158 | CTNNA3 | n.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=) | |
10 | g.65966622A>C | CA377089896 | CTNNA3 | n.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) | |
10 | g.65966622A>G | CA377089897 | CTNNA3 | n.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) | |
10 | g.65966622A>T | CA377089895 | CTNNA3 | n.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) | |
10 | g.65966623T>A | CA377089898 | CTNNA3 | n.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) | |
10 | g.65966623T>C | CA377089899 | CTNNA3 | n.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 |
10 | g.65966623T>G | CA377089900 | CTNNA3 | n.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 |
10 | g.65966623T= | CA1916183194 | CTNNA3 | n.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=) | |
10 | g.65966624G>A | CA469961160 | CTNNA3 | n.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 |
10 | g.65966624G>C | CA469961161 | CTNNA3 | n.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=) | |
10 | g.65966624G>T | CA469961164 | CTNNA3 | n.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=) | |
10 | g.65966625A>C | CA377089901 | CTNNA3 | n.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) | |
10 | g.65966625A>G | CA377089902 | CTNNA3 | n.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) | |
10 | g.65966625A>T | CA377089903 | CTNNA3 | n.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) | |
10 | g.65966626G>A | CA377089904 | CTNNA3 | n.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 |
10 | g.65966626G>C | CA377089905 | CTNNA3 | n.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) | |
10 | g.65966626G= | CA1916183195 | CTNNA3 | n.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=) | |
10 | g.65966626G>T | CA377089906 | CTNNA3 | n.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 |
10 | g.65966627C>A | CA377089907 | CTNNA3 | n.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 |
10 | g.65966627C= | CA1916183196 | CTNNA3 | n.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=) | |
10 | g.65966627C>G | CA377089908 | CTNNA3 | n.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) | |
10 | g.65966627C>T | CA469961167 | CTNNA3 | n.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 |
10 | g.65966628T>A | CA377089911 | CTNNA3 | n.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) | |
10 | g.65966628T>C | CA377089910 | CTNNA3 | n.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) | |
10 | g.65966628T>G | CA377089909 | CTNNA3 | n.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 |
10 | g.65966629C>A | CA377089912 | CTNNA3 | n.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) | |
10 | g.65966629C= | CA1916183197 | CTNNA3 | n.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=) | |
10 | g.65966629C>G | CA377089913 | CTNNA3 | n.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) | |
10 | g.65966629C>T | CA377089914 | CTNNA3 | n.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 |
10 | g.65966633_65966635del | CA2609350470 | CTNNA3 | n.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 |
10 | g.65966630T>A | CA469961168 | CTNNA3 | n.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=) | |
10 | g.65966630T>C | CA469961169 | CTNNA3 | n.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 |