Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.169525949C>A | CA343124881 | F5 | c.5668G>T (p.Glu1890Ter) c.5683G>T (p.Glu1895Ter) c.5257G>T (p.Glu1753Ter) | |
1 | g.169525949C= | CA1144229039 | F5 | c.5668G= (p.Glu1890=) c.5683G= (p.Glu1895=) c.5257G= (p.Glu1753=) | |
1 | g.169525949C>G | CA343124880 | F5 | c.5668G>C (p.Glu1890Gln) c.5683G>C (p.Glu1895Gln) c.5257G>C (p.Glu1753Gln) | |
1 | g.169525949C>T | CA215974 | F5 | c.5668G>A (p.Glu1890Lys) c.5683G>A (p.Glu1895Lys) c.5257G>A (p.Glu1753Lys) | ClinVar dbSNP COSMIC |
1 | g.169525950T>A | CA421735116 | F5 | c.5667A>T (p.Gly1889=) c.5682A>T (p.Gly1894=) c.5256A>T (p.Gly1752=) | |
1 | g.169525950T>C | CA421735117 | F5 | c.5667A>G (p.Gly1889=) c.5682A>G (p.Gly1894=) c.5256A>G (p.Gly1752=) | |
1 | g.169525950T>G | CA421735118 | F5 | c.5667A>C (p.Gly1889=) c.5682A>C (p.Gly1894=) c.5256A>C (p.Gly1752=) | |
1 | g.169525951C>A | CA343124883 | F5 | c.5666G>T (p.Gly1889Val) c.5681G>T (p.Gly1894Val) c.5255G>T (p.Gly1752Val) | |
1 | g.169525951C>G | CA343124885 | F5 | c.5666G>C (p.Gly1889Ala) c.5681G>C (p.Gly1894Ala) c.5255G>C (p.Gly1752Ala) | |
1 | g.169525951C>T | CA343124884 | F5 | c.5666G>A (p.Gly1889Glu) c.5681G>A (p.Gly1894Glu) c.5255G>A (p.Gly1752Glu) | |
1 | g.169525952C>A | CA343124887 | F5 | c.5665G>T (p.Gly1889Ter) c.5680G>T (p.Gly1894Ter) c.5254G>T (p.Gly1752Ter) | |
1 | g.169525952C= | CA1206133688 | F5 | c.5665G= (p.Gly1889=) c.5680G= (p.Gly1894=) c.5254G= (p.Gly1752=) | |
1 | g.169525952C>G | CA343124890 | F5 | c.5665G>C (p.Gly1889Arg) c.5680G>C (p.Gly1894Arg) c.5254G>C (p.Gly1752Arg) | |
1 | g.169525952C>T | CA1233446 | F5 | c.5665G>A (p.Gly1889Arg) c.5680G>A (p.Gly1894Arg) c.5254G>A (p.Gly1752Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.169525953A>C | CA421735119 | F5 | c.5664T>G (p.Val1888=) c.5679T>G (p.Val1893=) c.5253T>G (p.Val1751=) | |
1 | g.169525953A>G | CA421735121 | F5 | c.5664T>C (p.Val1888=) c.5679T>C (p.Val1893=) c.5253T>C (p.Val1751=) | |
1 | g.169525953A>T | CA421735120 | F5 | c.5664T>A (p.Val1888=) c.5679T>A (p.Val1893=) c.5253T>A (p.Val1751=) | |
1 | g.169525954A= | CA1206133690 | F5 | c.5663T= (p.Val1888=) c.5678T= (p.Val1893=) c.5252T= (p.Val1751=) | |
1 | g.169525954A>C | CA343124893 | F5 | c.5663T>G (p.Val1888Gly) c.5678T>G (p.Val1893Gly) c.5252T>G (p.Val1751Gly) | dbSNP |
1 | g.169525954A>G | CA343124895 | F5 | c.5663T>C (p.Val1888Ala) c.5678T>C (p.Val1893Ala) c.5252T>C (p.Val1751Ala) | |
1 | g.169525954A>T | CA343124897 | F5 | c.5663T>A (p.Val1888Asp) c.5678T>A (p.Val1893Asp) c.5252T>A (p.Val1751Asp) | |
1 | g.169525955C>A | CA343124905 | F5 | c.5662G>T (p.Val1888Phe) c.5677G>T (p.Val1893Phe) c.5251G>T (p.Val1751Phe) | gnomAD v4 |
1 | g.169525955C= | CA1206133692 | F5 | c.5662G= (p.Val1888=) c.5677G= (p.Val1893=) c.5251G= (p.Val1751=) | |
1 | g.169525955C>G | CA343124908 | F5 | c.5662G>C (p.Val1888Leu) c.5677G>C (p.Val1893Leu) c.5251G>C (p.Val1751Leu) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.169525955C>T | CA343124911 | F5 | c.5662G>A (p.Val1888Ile) c.5677G>A (p.Val1893Ile) c.5251G>A (p.Val1751Ile) | gnomAD v4 |
1 | g.169525956C>A | CA343124914 | F5 | c.5661G>T (p.Glu1887Asp) c.5676G>T (p.Glu1892Asp) c.5250G>T (p.Glu1750Asp) | |
1 | g.169525956C>G | CA343124917 | F5 | c.5661G>C (p.Glu1887Asp) c.5676G>C (p.Glu1892Asp) c.5250G>C (p.Glu1750Asp) | |
1 | g.169525956C>T | CA421735123 | F5 | c.5661G>A (p.Glu1887=) c.5676G>A (p.Glu1892=) c.5250G>A (p.Glu1750=) | |
1 | g.169525957T>A | CA343124924 | F5 | c.5660A>T (p.Glu1887Val) c.5675A>T (p.Glu1892Val) c.5249A>T (p.Glu1750Val) | |
1 | g.169525957T>C | CA343124922 | F5 | c.5660A>G (p.Glu1887Gly) c.5675A>G (p.Glu1892Gly) c.5249A>G (p.Glu1750Gly) | dbSNP |
1 | g.169525957T>G | CA343124920 | F5 | c.5660A>C (p.Glu1887Ala) c.5675A>C (p.Glu1892Ala) c.5249A>C (p.Glu1750Ala) | dbSNP |
1 | g.169525957T= | CA1206133694 | F5 | c.5660A= (p.Glu1887=) c.5675A= (p.Glu1892=) c.5249A= (p.Glu1750=) | |
1 | g.169525958C>A | CA343124926 | F5 | c.5659G>T (p.Glu1887Ter) c.5674G>T (p.Glu1892Ter) c.5248G>T (p.Glu1750Ter) | |
1 | g.169525958C>G | CA343124928 | F5 | c.5659G>C (p.Glu1887Gln) c.5674G>C (p.Glu1892Gln) c.5248G>C (p.Glu1750Gln) | |
1 | g.169525958C>T | CA343124931 | F5 | c.5659G>A (p.Glu1887Lys) c.5674G>A (p.Glu1892Lys) c.5248G>A (p.Glu1750Lys) | |
1 | g.169525959T>A | CA421735124 | F5 | c.5658A>T (p.Thr1886=) c.5673A>T (p.Thr1891=) c.5247A>T (p.Thr1749=) | |
1 | g.169525959T>C | CA421735125 | F5 | c.5658A>G (p.Thr1886=) c.5673A>G (p.Thr1891=) c.5247A>G (p.Thr1749=) | |
1 | g.169525959T>G | CA1233447 | F5 | c.5658A>C (p.Thr1886=) c.5673A>C (p.Thr1891=) c.5247A>C (p.Thr1749=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
1 | g.169525959T= | CA1206133696 | F5 | c.5658A= (p.Thr1886=) c.5673A= (p.Thr1891=) c.5247A= (p.Thr1749=) | |
1 | g.169525960G>A | CA343124937 | F5 | c.5657C>T (p.Thr1886Ile) c.5672C>T (p.Thr1891Ile) c.5246C>T (p.Thr1749Ile) | gnomAD v4 |
1 | g.169525960G>C | CA343124939 | F5 | c.5657C>G (p.Thr1886Arg) c.5672C>G (p.Thr1891Arg) c.5246C>G (p.Thr1749Arg) | |
1 | g.169525960G>T | CA343124943 | F5 | c.5657C>A (p.Thr1886Lys) c.5672C>A (p.Thr1891Lys) c.5246C>A (p.Thr1749Lys) | |
1 | g.169525961T>A | CA343124948 | F5 | c.5656A>T (p.Thr1886Ser) c.5671A>T (p.Thr1891Ser) c.5245A>T (p.Thr1749Ser) | |
1 | g.169525961T>C | CA343124955 | F5 | c.5656A>G (p.Thr1886Ala) c.5671A>G (p.Thr1891Ala) c.5245A>G (p.Thr1749Ala) | gnomAD v4 |
1 | g.169525961T>G | CA343124959 | F5 | c.5656A>C (p.Thr1886Pro) c.5671A>C (p.Thr1891Pro) c.5245A>C (p.Thr1749Pro) | dbSNP gnomAD v3 gnomAD v4 |
1 | g.169525961T= | CA1206133698 | F5 | c.5656A= (p.Thr1886=) c.5671A= (p.Thr1891=) c.5245A= (p.Thr1749=) | |
1 | g.169525962G>A | CA421735126 | F5 | c.5655C>T (p.Asn1885=) c.5670C>T (p.Asn1890=) c.5244C>T (p.Asn1748=) | |
1 | g.169525962G>C | CA343124962 | F5 | c.5655C>G (p.Asn1885Lys) c.5670C>G (p.Asn1890Lys) c.5244C>G (p.Asn1748Lys) | |
1 | g.169525962G>T | CA343124965 | F5 | c.5655C>A (p.Asn1885Lys) c.5670C>A (p.Asn1890Lys) c.5244C>A (p.Asn1748Lys) | |
1 | g.169525963T>A | CA343124978 | F5 | c.5654A>T (p.Asn1885Ile) c.5669A>T (p.Asn1890Ile) c.5243A>T (p.Asn1748Ile) |