Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.72218693C>A | CA381744252 | FOLR2 | c.109C>A (p.His37Asn) c.148C>A (p.His50Asn) c.160C>A (p.His54Asn) c.27+1768C>A (n.27+1768C>A) c.154C>A (p.His52Asn) c.142C>A (p.His48Asn) c.247C>A (p.His83Asn) c.136C>A (p.His46Asn) | |
11 | g.72218693C>G | CA381744261 | FOLR2 | c.109C>G (p.His37Asp) c.148C>G (p.His50Asp) c.160C>G (p.His54Asp) c.27+1768C>G (n.27+1768C>G) c.154C>G (p.His52Asp) c.142C>G (p.His48Asp) c.247C>G (p.His83Asp) c.136C>G (p.His46Asp) | |
11 | g.72218693C>T | CA381744256 | FOLR2 | c.109C>T (p.His37Tyr) c.148C>T (p.His50Tyr) c.160C>T (p.His54Tyr) c.27+1768C>T (n.27+1768C>T) c.154C>T (p.His52Tyr) c.142C>T (p.His48Tyr) c.247C>T (p.His83Tyr) c.136C>T (p.His46Tyr) | |
11 | g.72218694A>C | CA381744266 | FOLR2 | c.110A>C (p.His37Pro) c.149A>C (p.His50Pro) c.161A>C (p.His54Pro) c.27+1769A>C (n.27+1769A>C) c.155A>C (p.His52Pro) c.143A>C (p.His48Pro) c.248A>C (p.His83Pro) c.137A>C (p.His46Pro) | |
11 | g.72218694A>G | CA381744271 | FOLR2 | c.110A>G (p.His37Arg) c.149A>G (p.His50Arg) c.161A>G (p.His54Arg) c.27+1769A>G (n.27+1769A>G) c.155A>G (p.His52Arg) c.143A>G (p.His48Arg) c.248A>G (p.His83Arg) c.137A>G (p.His46Arg) | |
11 | g.72218694A>T | CA381744268 | FOLR2 | c.110A>T (p.His37Leu) c.149A>T (p.His50Leu) c.161A>T (p.His54Leu) c.27+1769A>T (n.27+1769A>T) c.155A>T (p.His52Leu) c.143A>T (p.His48Leu) c.248A>T (p.His83Leu) c.137A>T (p.His46Leu) | |
11 | g.72218695C>A | CA381744275 | FOLR2 | c.111C>A (p.His37Gln) c.150C>A (p.His50Gln) c.162C>A (p.His54Gln) c.27+1770C>A (n.27+1770C>A) c.156C>A (p.His52Gln) c.144C>A (p.His48Gln) c.249C>A (p.His83Gln) c.138C>A (p.His46Gln) | |
11 | g.72218695C>G | CA381744278 | FOLR2 | c.111C>G (p.His37Gln) c.150C>G (p.His50Gln) c.162C>G (p.His54Gln) c.27+1770C>G (n.27+1770C>G) c.156C>G (p.His52Gln) c.144C>G (p.His48Gln) c.249C>G (p.His83Gln) c.138C>G (p.His46Gln) | |
11 | g.72218695C>T | CA475606001 | FOLR2 | c.111C>T (p.His37=) c.150C>T (p.His50=) c.162C>T (p.His54=) c.27+1770C>T (n.27+1770C>T) c.156C>T (p.His52=) c.144C>T (p.His48=) c.249C>T (p.His83=) c.138C>T (p.His46=) | |
11 | g.72218696A>C | CA381744284 | FOLR2 | c.112A>C (p.Lys38Gln) c.151A>C (p.Lys51Gln) c.163A>C (p.Lys55Gln) c.27+1771A>C (n.27+1771A>C) c.157A>C (p.Lys53Gln) c.145A>C (p.Lys49Gln) c.250A>C (p.Lys84Gln) c.139A>C (p.Lys47Gln) | |
11 | g.72218696A>G | CA381744287 | FOLR2 | c.112A>G (p.Lys38Glu) c.151A>G (p.Lys51Glu) c.163A>G (p.Lys55Glu) c.27+1771A>G (n.27+1771A>G) c.157A>G (p.Lys53Glu) c.145A>G (p.Lys49Glu) c.250A>G (p.Lys84Glu) c.139A>G (p.Lys47Glu) | gnomAD v4 |
11 | g.72218696A>T | CA381744293 | FOLR2 | c.112A>T (p.Lys38Ter) c.151A>T (p.Lys51Ter) c.163A>T (p.Lys55Ter) c.27+1771A>T (n.27+1771A>T) c.157A>T (p.Lys53Ter) c.145A>T (p.Lys49Ter) c.250A>T (p.Lys84Ter) c.139A>T (p.Lys47Ter) | |
11 | g.72218697A>C | CA381744296 | FOLR2 | c.113A>C (p.Lys38Thr) c.152A>C (p.Lys51Thr) c.164A>C (p.Lys55Thr) c.27+1772A>C (n.27+1772A>C) c.158A>C (p.Lys53Thr) c.146A>C (p.Lys49Thr) c.251A>C (p.Lys84Thr) c.140A>C (p.Lys47Thr) | |
11 | g.72218697A>G | CA381744299 | FOLR2 | c.113A>G (p.Lys38Arg) c.152A>G (p.Lys51Arg) c.164A>G (p.Lys55Arg) c.27+1772A>G (n.27+1772A>G) c.158A>G (p.Lys53Arg) c.146A>G (p.Lys49Arg) c.251A>G (p.Lys84Arg) c.140A>G (p.Lys47Arg) | |
11 | g.72218697A>T | CA381744309 | FOLR2 | c.113A>T (p.Lys38Met) c.152A>T (p.Lys51Met) c.164A>T (p.Lys55Met) c.27+1772A>T (n.27+1772A>T) c.158A>T (p.Lys53Met) c.146A>T (p.Lys49Met) c.251A>T (p.Lys84Met) c.140A>T (p.Lys47Met) | |
11 | g.72218698G>A | CA475606003 | FOLR2 | c.114G>A (p.Lys38=) c.153G>A (p.Lys51=) c.165G>A (p.Lys55=) c.27+1773G>A (n.27+1773G>A) c.159G>A (p.Lys53=) c.147G>A (p.Lys49=) c.252G>A (p.Lys84=) c.141G>A (p.Lys47=) | gnomAD v4 |
11 | g.72218698G>C | CA381744323 | FOLR2 | c.114G>C (p.Lys38Asn) c.153G>C (p.Lys51Asn) c.165G>C (p.Lys55Asn) c.27+1773G>C (n.27+1773G>C) c.159G>C (p.Lys53Asn) c.147G>C (p.Lys49Asn) c.252G>C (p.Lys84Asn) c.141G>C (p.Lys47Asn) | dbSNP |
11 | g.72218698G>T | CA381744328 | FOLR2 | c.114G>T (p.Lys38Asn) c.153G>T (p.Lys51Asn) c.165G>T (p.Lys55Asn) c.27+1773G>T (n.27+1773G>T) c.159G>T (p.Lys53Asn) c.147G>T (p.Lys49Asn) c.252G>T (p.Lys84Asn) c.141G>T (p.Lys47Asn) | |
11 | g.72218699A>C | CA381744338 | FOLR2 | c.115A>C (p.Thr39Pro) c.154A>C (p.Thr52Pro) c.166A>C (p.Thr56Pro) c.27+1774A>C (n.27+1774A>C) c.160A>C (p.Thr54Pro) c.148A>C (p.Thr50Pro) c.253A>C (p.Thr85Pro) c.142A>C (p.Thr48Pro) | |
11 | g.72218699A>G | CA381744337 | FOLR2 | c.115A>G (p.Thr39Ala) c.154A>G (p.Thr52Ala) c.166A>G (p.Thr56Ala) c.27+1774A>G (n.27+1774A>G) c.160A>G (p.Thr54Ala) c.148A>G (p.Thr50Ala) c.253A>G (p.Thr85Ala) c.142A>G (p.Thr48Ala) | gnomAD v4 |
11 | g.72218699A>T | CA381744334 | FOLR2 | c.115A>T (p.Thr39Ser) c.154A>T (p.Thr52Ser) c.166A>T (p.Thr56Ser) c.27+1774A>T (n.27+1774A>T) c.160A>T (p.Thr54Ser) c.148A>T (p.Thr50Ser) c.253A>T (p.Thr85Ser) c.142A>T (p.Thr48Ser) | |
11 | g.72218700C>A | CA381744342 | FOLR2 | c.116C>A (p.Thr39Lys) c.155C>A (p.Thr52Lys) c.167C>A (p.Thr56Lys) c.27+1775C>A (n.27+1775C>A) c.161C>A (p.Thr54Lys) c.149C>A (p.Thr50Lys) c.254C>A (p.Thr85Lys) c.143C>A (p.Thr48Lys) | |
11 | g.72218700C>G | CA381744343 | FOLR2 | c.116C>G (p.Thr39Arg) c.155C>G (p.Thr52Arg) c.167C>G (p.Thr56Arg) c.27+1775C>G (n.27+1775C>G) c.161C>G (p.Thr54Arg) c.149C>G (p.Thr50Arg) c.254C>G (p.Thr85Arg) c.143C>G (p.Thr48Arg) | |
11 | g.72218700C>T | CA381744344 | FOLR2 | c.116C>T (p.Thr39Ile) c.155C>T (p.Thr52Ile) c.167C>T (p.Thr56Ile) c.27+1775C>T (n.27+1775C>T) c.161C>T (p.Thr54Ile) c.149C>T (p.Thr50Ile) c.254C>T (p.Thr85Ile) c.143C>T (p.Thr48Ile) | |
11 | g.72218701A>C | CA475606005 | FOLR2 | c.117A>C (p.Thr39=) c.156A>C (p.Thr52=) c.168A>C (p.Thr56=) c.27+1776A>C (n.27+1776A>C) c.162A>C (p.Thr54=) c.150A>C (p.Thr50=) c.255A>C (p.Thr85=) c.144A>C (p.Thr48=) | |
11 | g.72218701A>G | CA475606006 | FOLR2 | c.117A>G (p.Thr39=) c.156A>G (p.Thr52=) c.168A>G (p.Thr56=) c.27+1776A>G (n.27+1776A>G) c.162A>G (p.Thr54=) c.150A>G (p.Thr50=) c.255A>G (p.Thr85=) c.144A>G (p.Thr48=) | |
11 | g.72218701A>T | CA475606007 | FOLR2 | c.117A>T (p.Thr39=) c.156A>T (p.Thr52=) c.168A>T (p.Thr56=) c.27+1776A>T (n.27+1776A>T) c.162A>T (p.Thr54=) c.150A>T (p.Thr50=) c.255A>T (p.Thr85=) c.144A>T (p.Thr48=) | |
11 | g.72218702A>C | CA381744345 | FOLR2 | c.118A>C (p.Lys40Gln) c.157A>C (p.Lys53Gln) c.169A>C (p.Lys57Gln) c.27+1777A>C (n.27+1777A>C) c.163A>C (p.Lys55Gln) c.151A>C (p.Lys51Gln) c.256A>C (p.Lys86Gln) c.145A>C (p.Lys49Gln) | |
11 | g.72218702A>G | CA381744347 | FOLR2 | c.118A>G (p.Lys40Glu) c.157A>G (p.Lys53Glu) c.169A>G (p.Lys57Glu) c.27+1777A>G (n.27+1777A>G) c.163A>G (p.Lys55Glu) c.151A>G (p.Lys51Glu) c.256A>G (p.Lys86Glu) c.145A>G (p.Lys49Glu) | |
11 | g.72218702A>T | CA381744349 | FOLR2 | c.118A>T (p.Lys40Ter) c.157A>T (p.Lys53Ter) c.169A>T (p.Lys57Ter) c.27+1777A>T (n.27+1777A>T) c.163A>T (p.Lys55Ter) c.151A>T (p.Lys51Ter) c.256A>T (p.Lys86Ter) c.145A>T (p.Lys49Ter) | |
11 | g.72218703A>C | CA381744353 | FOLR2 | c.119A>C (p.Lys40Thr) c.158A>C (p.Lys53Thr) c.170A>C (p.Lys57Thr) c.27+1778A>C (n.27+1778A>C) c.164A>C (p.Lys55Thr) c.152A>C (p.Lys51Thr) c.257A>C (p.Lys86Thr) c.146A>C (p.Lys49Thr) | gnomAD v4 |
11 | g.72218703A>G | CA381744355 | FOLR2 | c.119A>G (p.Lys40Arg) c.158A>G (p.Lys53Arg) c.170A>G (p.Lys57Arg) c.27+1778A>G (n.27+1778A>G) c.164A>G (p.Lys55Arg) c.152A>G (p.Lys51Arg) c.257A>G (p.Lys86Arg) c.146A>G (p.Lys49Arg) | |
11 | g.72218703A>T | CA381744357 | FOLR2 | c.119A>T (p.Lys40Met) c.158A>T (p.Lys53Met) c.170A>T (p.Lys57Met) c.27+1778A>T (n.27+1778A>T) c.164A>T (p.Lys55Met) c.152A>T (p.Lys51Met) c.257A>T (p.Lys86Met) c.146A>T (p.Lys49Met) | |
11 | g.72218704G>A | CA475606009 | FOLR2 | c.120G>A (p.Lys40=) c.159G>A (p.Lys53=) c.171G>A (p.Lys57=) c.27+1779G>A (n.27+1779G>A) c.165G>A (p.Lys55=) c.153G>A (p.Lys51=) c.258G>A (p.Lys86=) c.147G>A (p.Lys49=) | gnomAD v4 |
11 | g.72218704G>C | CA381744358 | FOLR2 | c.120G>C (p.Lys40Asn) c.159G>C (p.Lys53Asn) c.171G>C (p.Lys57Asn) c.27+1779G>C (n.27+1779G>C) c.165G>C (p.Lys55Asn) c.153G>C (p.Lys51Asn) c.258G>C (p.Lys86Asn) c.147G>C (p.Lys49Asn) | |
11 | g.72218704G>T | CA381744360 | FOLR2 | c.120G>T (p.Lys40Asn) c.159G>T (p.Lys53Asn) c.171G>T (p.Lys57Asn) c.27+1779G>T (n.27+1779G>T) c.165G>T (p.Lys55Asn) c.153G>T (p.Lys51Asn) c.258G>T (p.Lys86Asn) c.147G>T (p.Lys49Asn) | |
11 | g.72218705C>A | CA381744362 | FOLR2 | c.121C>A (p.Pro41Thr) c.160C>A (p.Pro54Thr) c.172C>A (p.Pro58Thr) c.27+1780C>A (n.27+1780C>A) c.166C>A (p.Pro56Thr) c.154C>A (p.Pro52Thr) c.259C>A (p.Pro87Thr) c.148C>A (p.Pro50Thr) | |
11 | g.72218705C>G | CA381744363 | FOLR2 | c.121C>G (p.Pro41Ala) c.160C>G (p.Pro54Ala) c.172C>G (p.Pro58Ala) c.27+1780C>G (n.27+1780C>G) c.166C>G (p.Pro56Ala) c.154C>G (p.Pro52Ala) c.259C>G (p.Pro87Ala) c.148C>G (p.Pro50Ala) | |
11 | g.72218705C>T | CA381744361 | FOLR2 | c.121C>T (p.Pro41Ser) c.160C>T (p.Pro54Ser) c.172C>T (p.Pro58Ser) c.27+1780C>T (n.27+1780C>T) c.166C>T (p.Pro56Ser) c.154C>T (p.Pro52Ser) c.259C>T (p.Pro87Ser) c.148C>T (p.Pro50Ser) | |
11 | g.72218706C>A | CA381744367 | FOLR2 | c.122C>A (p.Pro41Gln) c.161C>A (p.Pro54Gln) c.173C>A (p.Pro58Gln) c.27+1781C>A (n.27+1781C>A) c.167C>A (p.Pro56Gln) c.155C>A (p.Pro52Gln) c.260C>A (p.Pro87Gln) c.149C>A (p.Pro50Gln) | |
11 | g.72218706C= | CA1981892179 | FOLR2 | c.122C= (p.Pro41=) c.161C= (p.Pro54=) c.173C= (p.Pro58=) c.27+1781C= (n.27+1781C=) c.167C= (p.Pro56=) c.155C= (p.Pro52=) c.260C= (p.Pro87=) c.149C= (p.Pro50=) | |
11 | g.72218706C>G | CA6169321 | FOLR2 | c.122C>G (p.Pro41Arg) c.161C>G (p.Pro54Arg) c.173C>G (p.Pro58Arg) c.27+1781C>G (n.27+1781C>G) c.167C>G (p.Pro56Arg) c.155C>G (p.Pro52Arg) c.260C>G (p.Pro87Arg) c.149C>G (p.Pro50Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.72218706C>T | CA381744382 | FOLR2 | c.122C>T (p.Pro41Leu) c.161C>T (p.Pro54Leu) c.173C>T (p.Pro58Leu) c.27+1781C>T (n.27+1781C>T) c.167C>T (p.Pro56Leu) c.155C>T (p.Pro52Leu) c.260C>T (p.Pro87Leu) c.149C>T (p.Pro50Leu) | |
11 | g.72218707A>C | CA475606012 | FOLR2 | c.123A>C (p.Pro41=) c.162A>C (p.Pro54=) c.174A>C (p.Pro58=) c.27+1782A>C (n.27+1782A>C) c.168A>C (p.Pro56=) c.156A>C (p.Pro52=) c.261A>C (p.Pro87=) c.150A>C (p.Pro50=) | |
11 | g.72218707A>G | CA475606013 | FOLR2 | c.123A>G (p.Pro41=) c.162A>G (p.Pro54=) c.174A>G (p.Pro58=) c.27+1782A>G (n.27+1782A>G) c.168A>G (p.Pro56=) c.156A>G (p.Pro52=) c.261A>G (p.Pro87=) c.150A>G (p.Pro50=) | |
11 | g.72218707A>T | CA475606014 | FOLR2 | c.123A>T (p.Pro41=) c.162A>T (p.Pro54=) c.174A>T (p.Pro58=) c.27+1782A>T (n.27+1782A>T) c.168A>T (p.Pro56=) c.156A>T (p.Pro52=) c.261A>T (p.Pro87=) c.150A>T (p.Pro50=) | |
11 | g.72218708G>A | CA381744388 | FOLR2 | c.124G>A (p.Gly42Ser) c.163G>A (p.Gly55Ser) c.175G>A (p.Gly59Ser) c.27+1783G>A (n.27+1783G>A) c.169G>A (p.Gly57Ser) c.157G>A (p.Gly53Ser) c.262G>A (p.Gly88Ser) c.151G>A (p.Gly51Ser) | gnomAD v4 |
11 | g.72218708G>C | CA6169322 | FOLR2 | c.124G>C (p.Gly42Arg) c.163G>C (p.Gly55Arg) c.175G>C (p.Gly59Arg) c.27+1783G>C (n.27+1783G>C) c.169G>C (p.Gly57Arg) c.157G>C (p.Gly53Arg) c.262G>C (p.Gly88Arg) c.151G>C (p.Gly51Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.72218708G= | CA1981892180 | FOLR2 | c.124G= (p.Gly42=) c.163G= (p.Gly55=) c.175G= (p.Gly59=) c.27+1783G= (n.27+1783G=) c.169G= (p.Gly57=) c.157G= (p.Gly53=) c.262G= (p.Gly88=) c.151G= (p.Gly51=) | |
11 | g.72218708G>T | CA381744389 | FOLR2 | c.124G>T (p.Gly42Cys) c.163G>T (p.Gly55Cys) c.175G>T (p.Gly59Cys) c.27+1783G>T (n.27+1783G>T) c.169G>T (p.Gly57Cys) c.157G>T (p.Gly53Cys) c.262G>T (p.Gly88Cys) c.151G>T (p.Gly51Cys) |