Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.209623933G>A | CA423142420 | LAMB3 | c.2044C>T (p.Leu682=) c.1852C>T (p.Leu618=) | gnomAD v4 |
1 | g.209623933G>C | CA344588861 | LAMB3 | c.2044C>G (p.Leu682Val) c.1852C>G (p.Leu618Val) | |
1 | g.209623933G>T | CA344588862 | LAMB3 | c.2044C>A (p.Leu682Met) c.1852C>A (p.Leu618Met) | |
1 | g.209623934G>A | CA423142424 | LAMB3 | c.2043C>T (p.Asp681=) c.1851C>T (p.Asp617=) | ClinVar dbSNP gnomAD v4 |
1 | g.209623934G>C | CA344588863 | LAMB3 | c.2043C>G (p.Asp681Glu) c.1851C>G (p.Asp617Glu) | |
1 | g.209623934G= | CA2484298437 | LAMB3 | c.2043C= (p.Asp681=) c.1851C= (p.Asp617=) | |
1 | g.209623934G>T | CA344588864 | LAMB3 | c.2043C>A (p.Asp681Glu) c.1851C>A (p.Asp617Glu) | |
1 | g.209623935T>A | CA344588867 | LAMB3 | c.2042A>T (p.Asp681Val) c.1850A>T (p.Asp617Val) | |
1 | g.209623935T>C | CA344588866 | LAMB3 | c.2042A>G (p.Asp681Gly) c.1850A>G (p.Asp617Gly) | |
1 | g.209623935T>G | CA344588865 | LAMB3 | c.2042A>C (p.Asp681Ala) c.1850A>C (p.Asp617Ala) | |
1 | g.209623936C>A | CA344588868 | LAMB3 | c.2041G>T (p.Asp681Tyr) c.1849G>T (p.Asp617Tyr) | |
1 | g.209623936C= | CA2484298438 | LAMB3 | c.2041G= (p.Asp681=) c.1849G= (p.Asp617=) | |
1 | g.209623936C>G | CA344588870 | LAMB3 | c.2041G>C (p.Asp681His) c.1849G>C (p.Asp617His) | |
1 | g.209623936C>T | CA344588869 | LAMB3 | c.2041G>A (p.Asp681Asn) c.1849G>A (p.Asp617Asn) | dbSNP |
1 | g.209623937T>A | CA344588871 | LAMB3 | c.2040A>T (p.Arg680Ser) c.1848A>T (p.Arg616Ser) | |
1 | g.209623937T>C | CA423142439 | LAMB3 | c.2040A>G (p.Arg680=) c.1848A>G (p.Arg616=) | |
1 | g.209623937T>G | CA344588872 | LAMB3 | c.2040A>C (p.Arg680Ser) c.1848A>C (p.Arg616Ser) | |
1 | g.209623938C>A | CA344588873 | LAMB3 | c.2039G>T (p.Arg680Ile) c.1847G>T (p.Arg616Ile) | |
1 | g.209623938C>G | CA344588874 | LAMB3 | c.2039G>C (p.Arg680Thr) c.1847G>C (p.Arg616Thr) | gnomAD v4 |
1 | g.209623938C>T | CA344588875 | LAMB3 | c.2039G>A (p.Arg680Lys) c.1847G>A (p.Arg616Lys) | |
1 | g.209623939T>A | CA344588876 | LAMB3 | c.2038A>T (p.Arg680Ter) c.1846A>T (p.Arg616Ter) | COSMIC |
1 | g.209623939T>C | CA344588877 | LAMB3 | c.2038A>G (p.Arg680Gly) c.1846A>G (p.Arg616Gly) | |
1 | g.209623939T>G | CA423142443 | LAMB3 | c.2038A>C (p.Arg680=) c.1846A>C (p.Arg616=) | |
1 | g.209623940C>A | CA423142449 | LAMB3 | c.2037G>T (p.Pro679=) c.1845G>T (p.Pro615=) | ClinVar dbSNP |
1 | g.209623940C= | CA2484298439 | LAMB3 | c.2037G= (p.Pro679=) c.1845G= (p.Pro615=) | |
1 | g.209623940C>G | CA1375396 | LAMB3 | c.2037G>C (p.Pro679=) c.1845G>C (p.Pro615=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.209623940C>T | CA1375397 | LAMB3 | c.2037G>A (p.Pro679=) c.1845G>A (p.Pro615=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209623941G>A | CA1375398 | LAMB3 | c.2036C>T (p.Pro679Leu) c.1844C>T (p.Pro615Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209623941G>C | CA344588878 | LAMB3 | c.2036C>G (p.Pro679Arg) c.1844C>G (p.Pro615Arg) | |
1 | g.209623941G= | CA1143469367 | LAMB3 | c.2036C= (p.Pro679=) c.1844C= (p.Pro615=) | |
1 | g.209623941G>T | CA344588879 | LAMB3 | c.2036C>A (p.Pro679Gln) c.1844C>A (p.Pro615Gln) | gnomAD v4 |
1 | g.209623942G>A | CA344588881 | LAMB3 | c.2035C>T (p.Pro679Ser) c.1843C>T (p.Pro615Ser) | COSMIC |
1 | g.209623942G>C | CA1375399 | LAMB3 | c.2035C>G (p.Pro679Ala) c.1843C>G (p.Pro615Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.209623942G= | CA2484298440 | LAMB3 | c.2035C= (p.Pro679=) c.1843C= (p.Pro615=) | |
1 | g.209623942G>T | CA344588880 | LAMB3 | c.2035C>A (p.Pro679Thr) c.1843C>A (p.Pro615Thr) | |
1 | g.209623943A>C | CA423142458 | LAMB3 | c.2034T>G (p.Leu678=) c.1842T>G (p.Leu614=) | |
1 | g.209623943A>G | CA423142460 | LAMB3 | c.2034T>C (p.Leu678=) c.1842T>C (p.Leu614=) | |
1 | g.209623943A>T | CA423142461 | LAMB3 | c.2034T>A (p.Leu678=) c.1842T>A (p.Leu614=) | |
1 | g.209623944A>C | CA344588882 | LAMB3 | c.2033T>G (p.Leu678Arg) c.1841T>G (p.Leu614Arg) | |
1 | g.209623944A>G | CA344588883 | LAMB3 | c.2033T>C (p.Leu678Pro) c.1841T>C (p.Leu614Pro) | |
1 | g.209623944A>T | CA344588884 | LAMB3 | c.2033T>A (p.Leu678His) c.1841T>A (p.Leu614His) | |
1 | g.209623945G>A | CA344588885 | LAMB3 | c.2032C>T (p.Leu678Phe) c.1840C>T (p.Leu614Phe) | COSMIC |
1 | g.209623945G>C | CA344588886 | LAMB3 | c.2032C>G (p.Leu678Val) c.1840C>G (p.Leu614Val) | |
1 | g.209623945G>T | CA344588887 | LAMB3 | c.2032C>A (p.Leu678Ile) c.1840C>A (p.Leu614Ile) | |
1 | g.209623946G>A | CA423142466 | LAMB3 | c.2031C>T (p.Ser677=) c.1839C>T (p.Ser613=) | COSMIC |
1 | g.209623946G>C | CA423142467 | LAMB3 | c.2031C>G (p.Ser677=) c.1839C>G (p.Ser613=) | |
1 | g.209623946G= | CA2484298441 | LAMB3 | c.2031C= (p.Ser677=) c.1839C= (p.Ser613=) | |
1 | g.209623946G>T | CA36752898 | LAMB3 | c.2031C>A (p.Ser677=) c.1839C>A (p.Ser613=) | ClinVar dbSNP gnomAD v4 |
1 | g.209623947G>A | CA344588888 | LAMB3 | c.2030C>T (p.Ser677Phe) c.1838C>T (p.Ser613Phe) | |
1 | g.209623947G>C | CA344588889 | LAMB3 | c.2030C>G (p.Ser677Cys) c.1838C>G (p.Ser613Cys) |