Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
6 | g.6224773T>A | CA362740042 | F13A1 | c.886A>T (p.Ser296Cys) c.36A>T c.1048A>T (p.Ser350Cys) | |
6 | g.6224773T>C | CA362740040 | F13A1 | c.886A>G (p.Ser296Gly) c.36A>G c.1048A>G (p.Ser350Gly) | |
6 | g.6224773T>G | CA362740041 | F13A1 | c.886A>C (p.Ser296Arg) c.36A>C c.1048A>C (p.Ser350Arg) | |
6 | g.6224774T>A | CA448645842 | F13A1 | c.885A>T (p.Gly295=) c.35A>T c.1047A>T (p.Gly349=) | |
6 | g.6224774T>C | CA448645843 | F13A1 | c.885A>G (p.Gly295=) c.35A>G c.1047A>G (p.Gly349=) | |
6 | g.6224774T>G | CA448645844 | F13A1 | c.885A>C (p.Gly295=) c.35A>C c.1047A>C (p.Gly349=) | |
6 | g.6224775C>A | CA362740043 | F13A1 | c.884G>T (p.Gly295Val) c.34G>T c.1046G>T (p.Gly349Val) | |
6 | g.6224775C>G | CA362740045 | F13A1 | c.884G>C (p.Gly295Ala) c.34G>C c.1046G>C (p.Gly349Ala) | |
6 | g.6224775C>T | CA362740044 | F13A1 | c.884G>A (p.Gly295Glu) c.34G>A c.1046G>A (p.Gly349Glu) | |
6 | g.6224776C>A | CA362740046 | F13A1 | c.883G>T (p.Gly295Ter) c.33G>T c.1045G>T (p.Gly349Ter) | |
6 | g.6224776C>G | CA362740047 | F13A1 | c.883G>C (p.Gly295Arg) c.33G>C c.1045G>C (p.Gly349Arg) | |
6 | g.6224776C>T | CA362740048 | F13A1 | c.883G>A (p.Gly295Arg) c.33G>A c.1045G>A (p.Gly349Arg) | |
6 | g.6224777A= | CA1607987864 | F13A1 | c.882T= (p.Thr294=) c.32T= c.1044T= (p.Thr348=) | |
6 | g.6224777A>C | CA448645846 | F13A1 | c.882T>G (p.Thr294=) c.32T>G c.1044T>G (p.Thr348=) | COSMIC |
6 | g.6224777A>G | CA3624521 | F13A1 | c.882T>C (p.Thr294=) c.32T>C c.1044T>C (p.Thr348=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.6224777A>T | CA448645845 | F13A1 | c.882T>A (p.Thr294=) c.32T>A c.1044T>A (p.Thr348=) | |
6 | g.6224778G>A | CA362740049 | F13A1 | c.881C>T (p.Thr294Ile) c.31C>T c.1043C>T (p.Thr348Ile) | |
6 | g.6224778G>C | CA362740050 | F13A1 | c.881C>G (p.Thr294Ser) c.31C>G c.1043C>G (p.Thr348Ser) | |
6 | g.6224778G>T | CA362740051 | F13A1 | c.881C>A (p.Thr294Asn) c.31C>A c.1043C>A (p.Thr348Asn) | COSMIC |
6 | g.6224779T>A | CA362740052 | F13A1 | c.880A>T (p.Thr294Ser) c.30A>T c.1042A>T (p.Thr348Ser) | |
6 | g.6224779T>C | CA362740053 | F13A1 | c.880A>G (p.Thr294Ala) c.30A>G c.1042A>G (p.Thr348Ala) | |
6 | g.6224779T>G | CA362740054 | F13A1 | c.880A>C (p.Thr294Pro) c.30A>C c.1042A>C (p.Thr348Pro) | |
6 | g.6224780C>A | CA362740055 | F13A1 | c.879G>T (p.Trp293Cys) c.29G>T c.1041G>T (p.Trp347Cys) | |
6 | g.6224780C>G | CA362740056 | F13A1 | c.879G>C (p.Trp293Cys) c.29G>C c.1041G>C (p.Trp347Cys) | |
6 | g.6224780C>T | CA362740057 | F13A1 | c.879G>A (p.Trp293Ter) c.29G>A c.1041G>A (p.Trp347Ter) | gnomAD v4 |
6 | g.6224781C>A | CA362740058 | F13A1 | c.878G>T (p.Trp293Leu) c.28G>T c.1040G>T (p.Trp347Leu) | |
6 | g.6224781C>G | CA362740060 | F13A1 | c.878G>C (p.Trp293Ser) c.28G>C c.1040G>C (p.Trp347Ser) | |
6 | g.6224781C>T | CA362740059 | F13A1 | c.878G>A (p.Trp293Ter) c.28G>A c.1040G>A (p.Trp347Ter) | gnomAD v4 |
6 | g.6224782A>C | CA362740061 | F13A1 | c.877T>G (p.Trp293Gly) c.27T>G c.1039T>G (p.Trp347Gly) | |
6 | g.6224782A>G | CA362740062 | F13A1 | c.877T>C (p.Trp293Arg) c.27T>C c.1039T>C (p.Trp347Arg) | |
6 | g.6224782A>T | CA362740063 | F13A1 | c.877T>A (p.Trp293Arg) c.27T>A c.1039T>A (p.Trp347Arg) | |
6 | g.6224783G>A | CA448645847 | F13A1 | c.876C>T (p.Ala292=) c.26C>T c.1038C>T (p.Ala346=) | COSMIC |
6 | g.6224783G>C | CA448645849 | F13A1 | c.876C>G (p.Ala292=) c.26C>G c.1038C>G (p.Ala346=) | |
6 | g.6224783G>T | CA448645848 | F13A1 | c.876C>A (p.Ala292=) c.26C>A c.1038C>A (p.Ala346=) | |
6 | g.6224784G>A | CA362740064 | F13A1 | c.875C>T (p.Ala292Val) c.25C>T c.1037C>T (p.Ala346Val) | gnomAD v4 |
6 | g.6224784G>C | CA362740065 | F13A1 | c.875C>G (p.Ala292Gly) c.25C>G c.1037C>G (p.Ala346Gly) | |
6 | g.6224784G>T | CA362740066 | F13A1 | c.875C>A (p.Ala292Asp) c.25C>A c.1037C>A (p.Ala346Asp) | |
6 | g.6224785C>A | CA362740067 | F13A1 | c.874G>T (p.Ala292Ser) c.24G>T c.1036G>T (p.Ala346Ser) | |
6 | g.6224785C>G | CA362740068 | F13A1 | c.874G>C (p.Ala292Pro) c.24G>C c.1036G>C (p.Ala346Pro) | |
6 | g.6224785C>T | CA362740069 | F13A1 | c.874G>A (p.Ala292Thr) c.24G>A c.1036G>A (p.Ala346Thr) | gnomAD v4 |
6 | g.6224786dup | CA2695205939 | F13A1 | c.874dup (p.Ala292GlyfsTer7) c.24dup c.1036dup (p.Ala346GlyfsTer7) | |
6 | g.6224786C>A | CA448645850 | F13A1 | c.873G>T (p.Ser291=) c.23G>T c.1035G>T (p.Ser345=) | |
6 | g.6224786C= | CA1607987865 | F13A1 | c.873G= (p.Ser291=) c.23G= c.1035G= (p.Ser345=) | |
6 | g.6224786C>G | CA448645851 | F13A1 | c.873G>C (p.Ser291=) c.23G>C c.1035G>C (p.Ser345=) | gnomAD v4 |
6 | g.6224786C>T | CA3624522 | F13A1 | c.873G>A (p.Ser291=) c.23G>A c.1035G>A (p.Ser345=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.6224787G>A | CA362740072 | F13A1 | c.872C>T (p.Ser291Leu) c.22C>T c.1034C>T (p.Ser345Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
6 | g.6224787G>C | CA362740071 | F13A1 | c.872C>G (p.Ser291Trp) c.22C>G c.1034C>G (p.Ser345Trp) | ClinVar |
6 | g.6224787G= | CA1607987866 | F13A1 | c.872C= (p.Ser291=) c.22C= c.1034C= (p.Ser345=) | |
6 | g.6224787G>T | CA362740070 | F13A1 | c.872C>A (p.Ser291Ter) c.22C>A c.1034C>A (p.Ser345Ter) | |
6 | g.6224788A>C | CA362740075 | F13A1 | c.871T>G (p.Ser291Ala) c.21T>G c.1033T>G (p.Ser345Ala) |