Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
18 | g.23876319A= | CA2290312332 | LAMA3 | c.197A= (p.Asp66=) c.5024A= (p.Asp1675=) c.1916A= (p.Asp639=) c.5051A= (p.Asp1684=) c.5042A= (p.Asp1681=) c.5033A= (p.Asp1678=) c.4919A= (p.Asp1640=) c.2903A= (p.Asp968=) c.593A= (p.Asp198=) n.5292A= | |
18 | g.23876319A>C | CA402044900 | LAMA3 | c.197A>C (p.Asp66Ala) c.5024A>C (p.Asp1675Ala) c.1916A>C (p.Asp639Ala) c.5051A>C (p.Asp1684Ala) c.5042A>C (p.Asp1681Ala) c.5033A>C (p.Asp1678Ala) c.4919A>C (p.Asp1640Ala) c.2903A>C (p.Asp968Ala) c.593A>C (p.Asp198Ala) n.5292A>C | |
18 | g.23876319A>G | CA402044901 | LAMA3 | c.197A>G (p.Asp66Gly) c.5024A>G (p.Asp1675Gly) c.1916A>G (p.Asp639Gly) c.5051A>G (p.Asp1684Gly) c.5042A>G (p.Asp1681Gly) c.5033A>G (p.Asp1678Gly) c.4919A>G (p.Asp1640Gly) c.2903A>G (p.Asp968Gly) c.593A>G (p.Asp198Gly) n.5292A>G | dbSNP gnomAD v3 gnomAD v4 |
18 | g.23876319A>T | CA402044902 | LAMA3 | c.197A>T (p.Asp66Val) c.5024A>T (p.Asp1675Val) c.1916A>T (p.Asp639Val) c.5051A>T (p.Asp1684Val) c.5042A>T (p.Asp1681Val) c.5033A>T (p.Asp1678Val) c.4919A>T (p.Asp1640Val) c.2903A>T (p.Asp968Val) c.593A>T (p.Asp198Val) n.5292A>T | gnomAD v4 |
18 | g.23876320T>A | CA402044903 | LAMA3 | c.198T>A (p.Asp66Glu) c.5025T>A (p.Asp1675Glu) c.1917T>A (p.Asp639Glu) c.5052T>A (p.Asp1684Glu) c.5043T>A (p.Asp1681Glu) c.5034T>A (p.Asp1678Glu) c.4920T>A (p.Asp1640Glu) c.2904T>A (p.Asp968Glu) c.594T>A (p.Asp198Glu) n.5293T>A | |
18 | g.23876320T>C | CA503327834 | LAMA3 | c.198T>C (p.Asp66=) c.5025T>C (p.Asp1675=) c.1917T>C (p.Asp639=) c.5052T>C (p.Asp1684=) c.5043T>C (p.Asp1681=) c.5034T>C (p.Asp1678=) c.4920T>C (p.Asp1640=) c.2904T>C (p.Asp968=) c.594T>C (p.Asp198=) n.5293T>C | |
18 | g.23876320T>G | CA402044904 | LAMA3 | c.198T>G (p.Asp66Glu) c.5025T>G (p.Asp1675Glu) c.1917T>G (p.Asp639Glu) c.5052T>G (p.Asp1684Glu) c.5043T>G (p.Asp1681Glu) c.5034T>G (p.Asp1678Glu) c.4920T>G (p.Asp1640Glu) c.2904T>G (p.Asp968Glu) c.594T>G (p.Asp198Glu) n.5293T>G | |
18 | g.23876321C>A | CA402044905 | LAMA3 | c.199C>A (p.His67Asn) c.5026C>A (p.His1676Asn) c.1918C>A (p.His640Asn) c.5053C>A (p.His1685Asn) c.5044C>A (p.His1682Asn) c.5035C>A (p.His1679Asn) c.4921C>A (p.His1641Asn) c.2905C>A (p.His969Asn) c.595C>A (p.His199Asn) n.5294C>A | |
18 | g.23876321C>G | CA402044906 | LAMA3 | c.199C>G (p.His67Asp) c.5026C>G (p.His1676Asp) c.1918C>G (p.His640Asp) c.5053C>G (p.His1685Asp) c.5044C>G (p.His1682Asp) c.5035C>G (p.His1679Asp) c.4921C>G (p.His1641Asp) c.2905C>G (p.His969Asp) c.595C>G (p.His199Asp) n.5294C>G | gnomAD v4 |
18 | g.23876321C>T | CA402044907 | LAMA3 | c.199C>T (p.His67Tyr) c.5026C>T (p.His1676Tyr) c.1918C>T (p.His640Tyr) c.5053C>T (p.His1685Tyr) c.5044C>T (p.His1682Tyr) c.5035C>T (p.His1679Tyr) c.4921C>T (p.His1641Tyr) c.2905C>T (p.His969Tyr) c.595C>T (p.His199Tyr) n.5294C>T | |
18 | g.23876322A= | CA2290312333 | LAMA3 | c.200A= (p.His67=) c.5027A= (p.His1676=) c.1919A= (p.His640=) c.5054A= (p.His1685=) c.5045A= (p.His1682=) c.5036A= (p.His1679=) c.4922A= (p.His1641=) c.2906A= (p.His969=) c.596A= (p.His199=) n.5295A= | |
18 | g.23876322A>C | CA8915867 | LAMA3 | c.200A>C (p.His67Pro) c.5027A>C (p.His1676Pro) c.1919A>C (p.His640Pro) c.5054A>C (p.His1685Pro) c.5045A>C (p.His1682Pro) c.5036A>C (p.His1679Pro) c.4922A>C (p.His1641Pro) c.2906A>C (p.His969Pro) c.596A>C (p.His199Pro) n.5295A>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
18 | g.23876322A>G | CA402044908 | LAMA3 | c.200A>G (p.His67Arg) c.5027A>G (p.His1676Arg) c.1919A>G (p.His640Arg) c.5054A>G (p.His1685Arg) c.5045A>G (p.His1682Arg) c.5036A>G (p.His1679Arg) c.4922A>G (p.His1641Arg) c.2906A>G (p.His969Arg) c.596A>G (p.His199Arg) n.5295A>G | dbSNP gnomAD v3 gnomAD v4 |
18 | g.23876322A>T | CA402044909 | LAMA3 | c.200A>T (p.His67Leu) c.5027A>T (p.His1676Leu) c.1919A>T (p.His640Leu) c.5054A>T (p.His1685Leu) c.5045A>T (p.His1682Leu) c.5036A>T (p.His1679Leu) c.4922A>T (p.His1641Leu) c.2906A>T (p.His969Leu) c.596A>T (p.His199Leu) n.5295A>T | |
18 | g.23876323T>A | CA402044911 | LAMA3 | c.201T>A (p.His67Gln) c.5028T>A (p.His1676Gln) c.1920T>A (p.His640Gln) c.5055T>A (p.His1685Gln) c.5046T>A (p.His1682Gln) c.5037T>A (p.His1679Gln) c.4923T>A (p.His1641Gln) c.2907T>A (p.His969Gln) c.597T>A (p.His199Gln) n.5296T>A | |
18 | g.23876323T>C | CA503327839 | LAMA3 | c.201T>C (p.His67=) c.5028T>C (p.His1676=) c.1920T>C (p.His640=) c.5055T>C (p.His1685=) c.5046T>C (p.His1682=) c.5037T>C (p.His1679=) c.4923T>C (p.His1641=) c.2907T>C (p.His969=) c.597T>C (p.His199=) n.5296T>C | |
18 | g.23876323T>G | CA402044910 | LAMA3 | c.201T>G (p.His67Gln) c.5028T>G (p.His1676Gln) c.1920T>G (p.His640Gln) c.5055T>G (p.His1685Gln) c.5046T>G (p.His1682Gln) c.5037T>G (p.His1679Gln) c.4923T>G (p.His1641Gln) c.2907T>G (p.His969Gln) c.597T>G (p.His199Gln) n.5296T>G | |
18 | g.23876324A>C | CA402044912 | LAMA3 | c.202A>C (p.Lys68Gln) c.5029A>C (p.Lys1677Gln) c.1921A>C (p.Lys641Gln) c.5056A>C (p.Lys1686Gln) c.5047A>C (p.Lys1683Gln) c.5038A>C (p.Lys1680Gln) c.4924A>C (p.Lys1642Gln) c.2908A>C (p.Lys970Gln) c.598A>C (p.Lys200Gln) n.5297A>C | |
18 | g.23876324A>G | CA402044913 | LAMA3 | c.202A>G (p.Lys68Glu) c.5029A>G (p.Lys1677Glu) c.1921A>G (p.Lys641Glu) c.5056A>G (p.Lys1686Glu) c.5047A>G (p.Lys1683Glu) c.5038A>G (p.Lys1680Glu) c.4924A>G (p.Lys1642Glu) c.2908A>G (p.Lys970Glu) c.598A>G (p.Lys200Glu) n.5297A>G | |
18 | g.23876324A>T | CA402044914 | LAMA3 | c.202A>T (p.Lys68Ter) c.5029A>T (p.Lys1677Ter) c.1921A>T (p.Lys641Ter) c.5056A>T (p.Lys1686Ter) c.5047A>T (p.Lys1683Ter) c.5038A>T (p.Lys1680Ter) c.4924A>T (p.Lys1642Ter) c.2908A>T (p.Lys970Ter) c.598A>T (p.Lys200Ter) n.5297A>T | |
18 | g.23876325A>C | CA402044915 | LAMA3 | c.203A>C (p.Lys68Thr) c.5030A>C (p.Lys1677Thr) c.1922A>C (p.Lys641Thr) c.5057A>C (p.Lys1686Thr) c.5048A>C (p.Lys1683Thr) c.5039A>C (p.Lys1680Thr) c.4925A>C (p.Lys1642Thr) c.2909A>C (p.Lys970Thr) c.599A>C (p.Lys200Thr) n.5298A>C | |
18 | g.23876325A>G | CA402044916 | LAMA3 | c.203A>G (p.Lys68Arg) c.5030A>G (p.Lys1677Arg) c.1922A>G (p.Lys641Arg) c.5057A>G (p.Lys1686Arg) c.5048A>G (p.Lys1683Arg) c.5039A>G (p.Lys1680Arg) c.4925A>G (p.Lys1642Arg) c.2909A>G (p.Lys970Arg) c.599A>G (p.Lys200Arg) n.5298A>G | |
18 | g.23876325A>T | CA402044917 | LAMA3 | c.203A>T (p.Lys68Ile) c.5030A>T (p.Lys1677Ile) c.1922A>T (p.Lys641Ile) c.5057A>T (p.Lys1686Ile) c.5048A>T (p.Lys1683Ile) c.5039A>T (p.Lys1680Ile) c.4925A>T (p.Lys1642Ile) c.2909A>T (p.Lys970Ile) c.599A>T (p.Lys200Ile) n.5298A>T | |
18 | g.23876326A>C | CA402044918 | LAMA3 | c.204A>C (p.Lys68Asn) c.5031A>C (p.Lys1677Asn) c.1923A>C (p.Lys641Asn) c.5058A>C (p.Lys1686Asn) c.5049A>C (p.Lys1683Asn) c.5040A>C (p.Lys1680Asn) c.4926A>C (p.Lys1642Asn) c.2910A>C (p.Lys970Asn) c.600A>C (p.Lys200Asn) n.5299A>C | COSMIC COSMIC |
18 | g.23876326A>G | CA503327842 | LAMA3 | c.204A>G (p.Lys68=) c.5031A>G (p.Lys1677=) c.1923A>G (p.Lys641=) c.5058A>G (p.Lys1686=) c.5049A>G (p.Lys1683=) c.5040A>G (p.Lys1680=) c.4926A>G (p.Lys1642=) c.2910A>G (p.Lys970=) c.600A>G (p.Lys200=) n.5299A>G | |
18 | g.23876326A>T | CA402044919 | LAMA3 | c.204A>T (p.Lys68Asn) c.5031A>T (p.Lys1677Asn) c.1923A>T (p.Lys641Asn) c.5058A>T (p.Lys1686Asn) c.5049A>T (p.Lys1683Asn) c.5040A>T (p.Lys1680Asn) c.4926A>T (p.Lys1642Asn) c.2910A>T (p.Lys970Asn) c.600A>T (p.Lys200Asn) n.5299A>T | |
18 | g.23876327G>A | CA402044920 | LAMA3 | c.205G>A (p.Gly69Ser) c.5032G>A (p.Gly1678Ser) c.1924G>A (p.Gly642Ser) c.5059G>A (p.Gly1687Ser) c.5050G>A (p.Gly1684Ser) c.5041G>A (p.Gly1681Ser) c.4927G>A (p.Gly1643Ser) c.2911G>A (p.Gly971Ser) c.601G>A (p.Gly201Ser) n.5300G>A | dbSNP |
18 | g.23876327G>C | CA402044921 | LAMA3 | c.205G>C (p.Gly69Arg) c.5032G>C (p.Gly1678Arg) c.1924G>C (p.Gly642Arg) c.5059G>C (p.Gly1687Arg) c.5050G>C (p.Gly1684Arg) c.5041G>C (p.Gly1681Arg) c.4927G>C (p.Gly1643Arg) c.2911G>C (p.Gly971Arg) c.601G>C (p.Gly201Arg) n.5300G>C | |
18 | g.23876327G= | CA2290312334 | LAMA3 | c.205G= (p.Gly69=) c.5032G= (p.Gly1678=) c.1924G= (p.Gly642=) c.5059G= (p.Gly1687=) c.5050G= (p.Gly1684=) c.5041G= (p.Gly1681=) c.4927G= (p.Gly1643=) c.2911G= (p.Gly971=) c.601G= (p.Gly201=) n.5300G= | |
18 | g.23876327G>T | CA402044922 | LAMA3 | c.205G>T (p.Gly69Cys) c.5032G>T (p.Gly1678Cys) c.1924G>T (p.Gly642Cys) c.5059G>T (p.Gly1687Cys) c.5050G>T (p.Gly1684Cys) c.5041G>T (p.Gly1681Cys) c.4927G>T (p.Gly1643Cys) c.2911G>T (p.Gly971Cys) c.601G>T (p.Gly201Cys) n.5300G>T | |
18 | g.23876328G>A | CA402044923 | LAMA3 | c.206G>A (p.Gly69Asp) c.5033G>A (p.Gly1678Asp) c.1925G>A (p.Gly642Asp) c.5060G>A (p.Gly1687Asp) c.5051G>A (p.Gly1684Asp) c.5042G>A (p.Gly1681Asp) c.4928G>A (p.Gly1643Asp) c.2912G>A (p.Gly971Asp) c.602G>A (p.Gly201Asp) n.5301G>A | |
18 | g.23876328G>C | CA402044924 | LAMA3 | c.206G>C (p.Gly69Ala) c.5033G>C (p.Gly1678Ala) c.1925G>C (p.Gly642Ala) c.5060G>C (p.Gly1687Ala) c.5051G>C (p.Gly1684Ala) c.5042G>C (p.Gly1681Ala) c.4928G>C (p.Gly1643Ala) c.2912G>C (p.Gly971Ala) c.602G>C (p.Gly201Ala) n.5301G>C | |
18 | g.23876328G= | CA2290312335 | LAMA3 | c.206G= (p.Gly69=) c.5033G= (p.Gly1678=) c.1925G= (p.Gly642=) c.5060G= (p.Gly1687=) c.5051G= (p.Gly1684=) c.5042G= (p.Gly1681=) c.4928G= (p.Gly1643=) c.2912G= (p.Gly971=) c.602G= (p.Gly201=) n.5301G= | |
18 | g.23876328G>T | CA402044925 | LAMA3 | c.206G>T (p.Gly69Val) c.5033G>T (p.Gly1678Val) c.1925G>T (p.Gly642Val) c.5060G>T (p.Gly1687Val) c.5051G>T (p.Gly1684Val) c.5042G>T (p.Gly1681Val) c.4928G>T (p.Gly1643Val) c.2912G>T (p.Gly971Val) c.602G>T (p.Gly201Val) n.5301G>T | dbSNP gnomAD v4 |
18 | g.23876329C>A | CA503327847 | LAMA3 | c.207C>A (p.Gly69=) c.5034C>A (p.Gly1678=) c.1926C>A (p.Gly642=) c.5061C>A (p.Gly1687=) c.5052C>A (p.Gly1684=) c.5043C>A (p.Gly1681=) c.4929C>A (p.Gly1643=) c.2913C>A (p.Gly971=) c.603C>A (p.Gly201=) n.5302C>A | |
18 | g.23876329C>G | CA503327848 | LAMA3 | c.207C>G (p.Gly69=) c.5034C>G (p.Gly1678=) c.1926C>G (p.Gly642=) c.5061C>G (p.Gly1687=) c.5052C>G (p.Gly1684=) c.5043C>G (p.Gly1681=) c.4929C>G (p.Gly1643=) c.2913C>G (p.Gly971=) c.603C>G (p.Gly201=) n.5302C>G | ClinVar gnomAD v4 |
18 | g.23876329C>T | CA503327850 | LAMA3 | c.207C>T (p.Gly69=) c.5034C>T (p.Gly1678=) c.1926C>T (p.Gly642=) c.5061C>T (p.Gly1687=) c.5052C>T (p.Gly1684=) c.5043C>T (p.Gly1681=) c.4929C>T (p.Gly1643=) c.2913C>T (p.Gly971=) c.603C>T (p.Gly201=) n.5302C>T | |
18 | g.23876330T>A | CA402044926 | LAMA3 | c.208T>A (p.Leu70Met) c.5035T>A (p.Leu1679Met) c.1927T>A (p.Leu643Met) c.5062T>A (p.Leu1688Met) c.5053T>A (p.Leu1685Met) c.5044T>A (p.Leu1682Met) c.4930T>A (p.Leu1644Met) c.2914T>A (p.Leu972Met) c.604T>A (p.Leu202Met) n.5303T>A | |
18 | g.23876330T>C | CA503327851 | LAMA3 | c.208T>C (p.Leu70=) c.5035T>C (p.Leu1679=) c.1927T>C (p.Leu643=) c.5062T>C (p.Leu1688=) c.5053T>C (p.Leu1685=) c.5044T>C (p.Leu1682=) c.4930T>C (p.Leu1644=) c.2914T>C (p.Leu972=) c.604T>C (p.Leu202=) n.5303T>C | |
18 | g.23876330T>G | CA402044927 | LAMA3 | c.208T>G (p.Leu70Val) c.5035T>G (p.Leu1679Val) c.1927T>G (p.Leu643Val) c.5062T>G (p.Leu1688Val) c.5053T>G (p.Leu1685Val) c.5044T>G (p.Leu1682Val) c.4930T>G (p.Leu1644Val) c.2914T>G (p.Leu972Val) c.604T>G (p.Leu202Val) n.5303T>G | |
18 | g.23876331T>A | CA402044928 | LAMA3 | c.209T>A (p.Leu70Ter) c.5036T>A (p.Leu1679Ter) c.1928T>A (p.Leu643Ter) c.5063T>A (p.Leu1688Ter) c.5054T>A (p.Leu1685Ter) c.5045T>A (p.Leu1682Ter) c.4931T>A (p.Leu1644Ter) c.2915T>A (p.Leu972Ter) c.605T>A (p.Leu202Ter) n.5304T>A | |
18 | g.23876331T>C | CA402044929 | LAMA3 | c.209T>C (p.Leu70Ser) c.5036T>C (p.Leu1679Ser) c.1928T>C (p.Leu643Ser) c.5063T>C (p.Leu1688Ser) c.5054T>C (p.Leu1685Ser) c.5045T>C (p.Leu1682Ser) c.4931T>C (p.Leu1644Ser) c.2915T>C (p.Leu972Ser) c.605T>C (p.Leu202Ser) n.5304T>C | |
18 | g.23876331T>G | CA402044930 | LAMA3 | c.209T>G (p.Leu70Trp) c.5036T>G (p.Leu1679Trp) c.1928T>G (p.Leu643Trp) c.5063T>G (p.Leu1688Trp) c.5054T>G (p.Leu1685Trp) c.5045T>G (p.Leu1682Trp) c.4931T>G (p.Leu1644Trp) c.2915T>G (p.Leu972Trp) c.605T>G (p.Leu202Trp) n.5304T>G | |
18 | g.23876332G>A | CA503327854 | LAMA3 | c.210G>A (p.Leu70=) c.5037G>A (p.Leu1679=) c.1929G>A (p.Leu643=) c.5064G>A (p.Leu1688=) c.5055G>A (p.Leu1685=) c.5046G>A (p.Leu1682=) c.4932G>A (p.Leu1644=) c.2916G>A (p.Leu972=) c.606G>A (p.Leu202=) n.5305G>A | ClinVar |
18 | g.23876332G>C | CA402044931 | LAMA3 | c.210G>C (p.Leu70Phe) c.5037G>C (p.Leu1679Phe) c.1929G>C (p.Leu643Phe) c.5064G>C (p.Leu1688Phe) c.5055G>C (p.Leu1685Phe) c.5046G>C (p.Leu1682Phe) c.4932G>C (p.Leu1644Phe) c.2916G>C (p.Leu972Phe) c.606G>C (p.Leu202Phe) n.5305G>C | |
18 | g.23876332G>T | CA402044932 | LAMA3 | c.210G>T (p.Leu70Phe) c.5037G>T (p.Leu1679Phe) c.1929G>T (p.Leu643Phe) c.5064G>T (p.Leu1688Phe) c.5055G>T (p.Leu1685Phe) c.5046G>T (p.Leu1682Phe) c.4932G>T (p.Leu1644Phe) c.2916G>T (p.Leu972Phe) c.606G>T (p.Leu202Phe) n.5305G>T | |
18 | g.23876333T>A | CA402044933 | LAMA3 | c.211T>A (p.Tyr71Asn) c.5038T>A (p.Tyr1680Asn) c.1930T>A (p.Tyr644Asn) c.5065T>A (p.Tyr1689Asn) c.5056T>A (p.Tyr1686Asn) c.5047T>A (p.Tyr1683Asn) c.4933T>A (p.Tyr1645Asn) c.2917T>A (p.Tyr973Asn) c.607T>A (p.Tyr203Asn) n.5306T>A | |
18 | g.23876333T>C | CA297091427 | LAMA3 | c.211T>C (p.Tyr71His) c.5038T>C (p.Tyr1680His) c.1930T>C (p.Tyr644His) c.5065T>C (p.Tyr1689His) c.5056T>C (p.Tyr1686His) c.5047T>C (p.Tyr1683His) c.4933T>C (p.Tyr1645His) c.2917T>C (p.Tyr973His) c.607T>C (p.Tyr203His) n.5306T>C | dbSNP gnomAD v3 gnomAD v4 |
18 | g.23876333T>G | CA402044934 | LAMA3 | c.211T>G (p.Tyr71Asp) c.5038T>G (p.Tyr1680Asp) c.1930T>G (p.Tyr644Asp) c.5065T>G (p.Tyr1689Asp) c.5056T>G (p.Tyr1686Asp) c.5047T>G (p.Tyr1683Asp) c.4933T>G (p.Tyr1645Asp) c.2917T>G (p.Tyr973Asp) c.607T>G (p.Tyr203Asp) n.5306T>G | |
18 | g.23876333T= | CA2290312336 | LAMA3 | c.211T= (p.Tyr71=) c.5038T= (p.Tyr1680=) c.1930T= (p.Tyr644=) c.5065T= (p.Tyr1689=) c.5056T= (p.Tyr1686=) c.5047T= (p.Tyr1683=) c.4933T= (p.Tyr1645=) c.2917T= (p.Tyr973=) c.607T= (p.Tyr203=) n.5306T= |