Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.149978103del | CA274352 | SLC26A2 | n.683del c.451del (p.Tyr151IlefsTer21) c.124del (p.Tyr42IlefsTer21) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.149978103T>A | CA361705020 | SLC26A2 | n.683T>A c.451T>A (p.Tyr151Asn) c.124T>A (p.Tyr42Asn) | |
5 | g.149978103T>C | CA361705021 | SLC26A2 | n.683T>C c.451T>C (p.Tyr151His) c.124T>C (p.Tyr42His) | |
5 | g.149978103T>G | CA361705022 | SLC26A2 | n.683T>G c.451T>G (p.Tyr151Asp) c.124T>G (p.Tyr42Asp) | |
5 | g.149978104A>C | CA361705023 | SLC26A2 | n.684A>C c.452A>C (p.Tyr151Ser) c.125A>C (p.Tyr42Ser) | |
5 | g.149978104A>G | CA361705024 | SLC26A2 | n.684A>G c.452A>G (p.Tyr151Cys) c.125A>G (p.Tyr42Cys) | gnomAD v4 |
5 | g.149978104A>T | CA361705025 | SLC26A2 | n.684A>T c.452A>T (p.Tyr151Phe) c.125A>T (p.Tyr42Phe) | |
5 | g.149978105T>A | CA361705026 | SLC26A2 | n.685T>A c.453T>A (p.Tyr151Ter) c.126T>A (p.Tyr42Ter) | |
5 | g.149978105T>C | CA447401999 | SLC26A2 | n.685T>C c.453T>C (p.Tyr151=) c.126T>C (p.Tyr42=) | |
5 | g.149978105T>G | CA361705027 | SLC26A2 | n.685T>G c.453T>G (p.Tyr151Ter) c.126T>G (p.Tyr42Ter) | |
5 | g.149978106T>A | CA361705028 | SLC26A2 | n.686T>A c.454T>A (p.Phe152Ile) c.127T>A (p.Phe43Ile) | gnomAD v4 |
5 | g.149978106T>C | CA361705029 | SLC26A2 | n.686T>C c.454T>C (p.Phe152Leu) c.127T>C (p.Phe43Leu) | |
5 | g.149978106T>G | CA361705030 | SLC26A2 | n.686T>G c.454T>G (p.Phe152Val) c.127T>G (p.Phe43Val) | |
5 | g.149978107T>A | CA361705032 | SLC26A2 | n.687T>A c.455T>A (p.Phe152Tyr) c.128T>A (p.Phe43Tyr) | |
5 | g.149978107T>C | CA361705033 | SLC26A2 | n.687T>C c.455T>C (p.Phe152Ser) c.128T>C (p.Phe43Ser) | |
5 | g.149978107T>G | CA361705031 | SLC26A2 | n.687T>G c.455T>G (p.Phe152Cys) c.128T>G (p.Phe43Cys) | |
5 | g.149978108T>A | CA361705035 | SLC26A2 | n.688T>A c.456T>A (p.Phe152Leu) c.129T>A (p.Phe43Leu) | |
5 | g.149978108T>C | CA447402000 | SLC26A2 | n.688T>C c.456T>C (p.Phe152=) c.129T>C (p.Phe43=) | |
5 | g.149978108T>G | CA361705034 | SLC26A2 | n.688T>G c.456T>G (p.Phe152Leu) c.129T>G (p.Phe43Leu) | |
5 | g.149978109C>A | CA361705036 | SLC26A2 | n.689C>A c.457C>A (p.Leu153Ile) c.130C>A (p.Leu44Ile) | gnomAD v4 |
5 | g.149978109C>G | CA361705037 | SLC26A2 | n.689C>G c.457C>G (p.Leu153Val) c.130C>G (p.Leu44Val) | |
5 | g.149978109C>T | CA361705038 | SLC26A2 | n.689C>T c.457C>T (p.Leu153Phe) c.130C>T (p.Leu44Phe) | |
5 | g.149978110T>A | CA361705039 | SLC26A2 | n.690T>A c.458T>A (p.Leu153His) c.131T>A (p.Leu44His) | |
5 | g.149978110T>C | CA361705040 | SLC26A2 | n.690T>C c.458T>C (p.Leu153Pro) c.131T>C (p.Leu44Pro) | gnomAD v4 |
5 | g.149978110T>G | CA361705041 | SLC26A2 | n.690T>G c.458T>G (p.Leu153Arg) c.131T>G (p.Leu44Arg) | |
5 | g.149978111C>A | CA447402003 | SLC26A2 | n.691C>A c.459C>A (p.Leu153=) c.132C>A (p.Leu44=) | |
5 | g.149978111C= | CA1590737408 | SLC26A2 | n.691C= c.459C= (p.Leu153=) c.132C= (p.Leu44=) | |
5 | g.149978111C>G | CA447402002 | SLC26A2 | n.691C>G c.459C>G (p.Leu153=) c.132C>G (p.Leu44=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
5 | g.149978111C>T | CA447402001 | SLC26A2 | n.691C>T c.459C>T (p.Leu153=) c.132C>T (p.Leu44=) | |
5 | g.149978112T>A | CA361705042 | SLC26A2 | n.692T>A c.460T>A (p.Leu154Met) c.133T>A (p.Leu45Met) | |
5 | g.149978112T>C | CA447402004 | SLC26A2 | n.692T>C c.460T>C (p.Leu154=) c.133T>C (p.Leu45=) | gnomAD v4 |
5 | g.149978112T>G | CA361705043 | SLC26A2 | n.692T>G c.460T>G (p.Leu154Val) c.133T>G (p.Leu45Val) | |
5 | g.149978113T>A | CA361705044 | SLC26A2 | n.693T>A c.461T>A (p.Leu154Ter) c.134T>A (p.Leu45Ter) | |
5 | g.149978113T>C | CA361705045 | SLC26A2 | n.693T>C c.461T>C (p.Leu154Ser) c.134T>C (p.Leu45Ser) | |
5 | g.149978113T>G | CA361705046 | SLC26A2 | n.693T>G c.461T>G (p.Leu154Trp) c.134T>G (p.Leu45Trp) | |
5 | g.149978114G>A | CA447402005 | SLC26A2 | n.694G>A c.462G>A (p.Leu154=) c.135G>A (p.Leu45=) | dbSNP |
5 | g.149978114G>C | CA3505250 | SLC26A2 | n.694G>C c.462G>C (p.Leu154Phe) c.135G>C (p.Leu45Phe) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.149978114G= | CA1590737409 | SLC26A2 | n.694G= c.462G= (p.Leu154=) c.135G= (p.Leu45=) | |
5 | g.149978114G>T | CA361705047 | SLC26A2 | n.694G>T c.462G>T (p.Leu154Phe) c.135G>T (p.Leu45Phe) | |
5 | g.149978115G>A | CA361705048 | SLC26A2 | n.695G>A c.463G>A (p.Gly155Ser) c.136G>A (p.Gly46Ser) | |
5 | g.149978115G>C | CA361705050 | SLC26A2 | n.695G>C c.463G>C (p.Gly155Arg) c.136G>C (p.Gly46Arg) | |
5 | g.149978115G>T | CA361705049 | SLC26A2 | n.695G>T c.463G>T (p.Gly155Cys) c.136G>T (p.Gly46Cys) | |
5 | g.149978116G>A | CA361705051 | SLC26A2 | n.696G>A c.464G>A (p.Gly155Asp) c.137G>A (p.Gly46Asp) | dbSNP gnomAD v4 |
5 | g.149978116G>C | CA361705052 | SLC26A2 | n.696G>C c.464G>C (p.Gly155Ala) c.137G>C (p.Gly46Ala) | |
5 | g.149978116G= | CA1590737410 | SLC26A2 | n.696G= c.464G= (p.Gly155=) c.137G= (p.Gly46=) | |
5 | g.149978116G>T | CA361705053 | SLC26A2 | n.696G>T c.464G>T (p.Gly155Val) c.137G>T (p.Gly46Val) | |
5 | g.149978117T>A | CA447402008 | SLC26A2 | n.697T>A c.465T>A (p.Gly155=) c.138T>A (p.Gly46=) | |
5 | g.149978117T>C | CA447402006 | SLC26A2 | n.697T>C c.465T>C (p.Gly155=) c.138T>C (p.Gly46=) | COSMIC |
5 | g.149978117T>G | CA447402007 | SLC26A2 | n.697T>G c.465T>G (p.Gly155=) c.138T>G (p.Gly46=) | |
5 | g.149978118A= | CA1590737411 | SLC26A2 | n.698A= c.466A= (p.Thr156=) c.139A= (p.Thr47=) | |
5 | g.149978118A>C | CA361705054 | SLC26A2 | n.698A>C c.466A>C (p.Thr156Pro) c.139A>C (p.Thr47Pro) | |
5 | g.149978118A>G | CA361705055 | SLC26A2 | n.698A>G c.466A>G (p.Thr156Ala) c.139A>G (p.Thr47Ala) | dbSNP |
5 | g.149978118A>T | CA361705056 | SLC26A2 | n.698A>T c.466A>T (p.Thr156Ser) c.139A>T (p.Thr47Ser) | |
5 | g.149978119C>A | CA3505251 | SLC26A2 | n.699C>A c.467C>A (p.Thr156Asn) c.140C>A (p.Thr47Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.149978119C= | CA1590737412 | SLC26A2 | n.699C= c.467C= (p.Thr156=) c.140C= (p.Thr47=) | |
5 | g.149978119C>G | CA361705057 | SLC26A2 | n.699C>G c.467C>G (p.Thr156Ser) c.140C>G (p.Thr47Ser) | |
5 | g.149978119C>T | CA129082524 | SLC26A2 | n.699C>T c.467C>T (p.Thr156Ile) c.140C>T (p.Thr47Ile) | dbSNP |
5 | g.149978120C>A | CA447402009 | SLC26A2 | n.700C>A c.468C>A (p.Thr156=) c.141C>A (p.Thr47=) | |
5 | g.149978120C= | CA1590737413 | SLC26A2 | n.700C= c.468C= (p.Thr156=) c.141C= (p.Thr47=) | |
5 | g.149978120C>G | CA447402010 | SLC26A2 | n.700C>G c.468C>G (p.Thr156=) c.141C>G (p.Thr47=) | |
5 | g.149978120C>T | CA3505252 | SLC26A2 | n.700C>T c.468C>T (p.Thr156=) c.141C>T (p.Thr47=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978121T>A | CA361705059 | SLC26A2 | n.701T>A c.469T>A (p.Ser157Thr) c.142T>A (p.Ser48Thr) | ClinVar gnomAD v4 |
5 | g.149978121T>C | CA3505253 | SLC26A2 | n.701T>C c.469T>C (p.Ser157Pro) c.142T>C (p.Ser48Pro) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.149978121T>G | CA361705058 | SLC26A2 | n.701T>G c.469T>G (p.Ser157Ala) c.142T>G (p.Ser48Ala) | |
5 | g.149978121T= | CA1590737414 | SLC26A2 | n.701T= c.469T= (p.Ser157=) c.142T= (p.Ser48=) | |
5 | g.149978122C>A | CA361705060 | SLC26A2 | n.702C>A c.470C>A (p.Ser157Tyr) c.143C>A (p.Ser48Tyr) | |
5 | g.149978122C= | CA1590737415 | SLC26A2 | n.702C= c.470C= (p.Ser157=) c.143C= (p.Ser48=) | |
5 | g.149978122C>G | CA361705061 | SLC26A2 | n.702C>G c.470C>G (p.Ser157Cys) c.143C>G (p.Ser48Cys) | |
5 | g.149978122C>T | CA361705062 | SLC26A2 | n.702C>T c.470C>T (p.Ser157Phe) c.143C>T (p.Ser48Phe) | dbSNP COSMIC |
5 | g.149978123C>A | CA447402013 | SLC26A2 | n.703C>A c.471C>A (p.Ser157=) c.144C>A (p.Ser48=) | |
5 | g.149978123C>G | CA447402011 | SLC26A2 | n.703C>G c.471C>G (p.Ser157=) c.144C>G (p.Ser48=) | |
5 | g.149978123C>T | CA447402012 | SLC26A2 | n.703C>T c.471C>T (p.Ser157=) c.144C>T (p.Ser48=) | |
5 | g.149978124C>A | CA361705063 | SLC26A2 | n.704C>A c.472C>A (p.Arg158Ser) c.145C>A (p.Arg49Ser) | |
5 | g.149978124C= | CA1590737416 | SLC26A2 | n.704C= c.472C= (p.Arg158=) c.145C= (p.Arg49=) | |
5 | g.149978124C>G | CA361705064 | SLC26A2 | n.704C>G c.472C>G (p.Arg158Gly) c.145C>G (p.Arg49Gly) | |
5 | g.149978124C>T | CA3505254 | SLC26A2 | n.704C>T c.472C>T (p.Arg158Cys) c.145C>T (p.Arg49Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978125G>A | CA3505255 | SLC26A2 | n.705G>A c.473G>A (p.Arg158His) c.146G>A (p.Arg49His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978125G>C | CA361705065 | SLC26A2 | n.705G>C c.473G>C (p.Arg158Pro) c.146G>C (p.Arg49Pro) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.149978125G= | CA1590737417 | SLC26A2 | n.705G= c.473G= (p.Arg158=) c.146G= (p.Arg49=) | |
5 | g.149978125G>T | CA361705066 | SLC26A2 | n.705G>T c.473G>T (p.Arg158Leu) c.146G>T (p.Arg49Leu) | ClinVar dbSNP |
5 | g.149978126T>A | CA447402014 | SLC26A2 | n.706T>A c.474T>A (p.Arg158=) c.147T>A (p.Arg49=) | |
5 | g.149978126T>C | CA3505256 | SLC26A2 | n.706T>C c.474T>C (p.Arg158=) c.147T>C (p.Arg49=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978126T>G | CA447402015 | SLC26A2 | n.706T>G c.474T>G (p.Arg158=) c.147T>G (p.Arg49=) | |
5 | g.149978126T= | CA1590737418 | SLC26A2 | n.706T= c.474T= (p.Arg158=) c.147T= (p.Arg49=) | |
5 | g.149978127C>A | CA361705067 | SLC26A2 | n.707C>A c.475C>A (p.His159Asn) c.148C>A (p.His50Asn) | |
5 | g.149978127C>G | CA361705068 | SLC26A2 | n.707C>G c.475C>G (p.His159Asp) c.148C>G (p.His50Asp) | |
5 | g.149978127C>T | CA361705069 | SLC26A2 | n.707C>T c.475C>T (p.His159Tyr) c.148C>T (p.His50Tyr) | |
5 | g.149978128A>C | CA361705072 | SLC26A2 | n.708A>C c.476A>C (p.His159Pro) c.149A>C (p.His50Pro) | |
5 | g.149978128A>G | CA361705070 | SLC26A2 | n.708A>G c.476A>G (p.His159Arg) c.149A>G (p.His50Arg) | |
5 | g.149978128A>T | CA361705071 | SLC26A2 | n.708A>T c.476A>T (p.His159Leu) c.149A>T (p.His50Leu) | |
5 | g.149978129C>A | CA361705073 | SLC26A2 | n.709C>A c.477C>A (p.His159Gln) c.150C>A (p.His50Gln) | gnomAD v4 |
5 | g.149978129C= | CA1590737419 | SLC26A2 | n.709C= c.477C= (p.His159=) c.150C= (p.His50=) | |
5 | g.149978129C>G | CA361705074 | SLC26A2 | n.709C>G c.477C>G (p.His159Gln) c.150C>G (p.His50Gln) | |
5 | g.149978129C>T | CA3505257 | SLC26A2 | n.709C>T c.477C>T (p.His159=) c.150C>T (p.His50=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978130A= | CA1590737420 | SLC26A2 | n.710A= c.478A= (p.Ile160=) c.151A= (p.Ile51=) | |
5 | g.149978130A>C | CA361705075 | SLC26A2 | n.710A>C c.478A>C (p.Ile160Leu) c.151A>C (p.Ile51Leu) | |
5 | g.149978130A>G | CA3505258 | SLC26A2 | n.710A>G c.478A>G (p.Ile160Val) c.151A>G (p.Ile51Val) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978130A>T | CA361705076 | SLC26A2 | n.710A>T c.478A>T (p.Ile160Phe) c.151A>T (p.Ile51Phe) | |
5 | g.149978131T>A | CA361705077 | SLC26A2 | n.711T>A c.479T>A (p.Ile160Asn) c.152T>A (p.Ile51Asn) | |
5 | g.149978131T>C | CA361705078 | SLC26A2 | n.711T>C c.479T>C (p.Ile160Thr) c.152T>C (p.Ile51Thr) | |
5 | g.149978131T>G | CA361705079 | SLC26A2 | n.711T>G c.479T>G (p.Ile160Ser) c.152T>G (p.Ile51Ser) | |
5 | g.149978132C>A | CA447402016 | SLC26A2 | n.712C>A c.480C>A (p.Ile160=) c.153C>A (p.Ile51=) | ClinVar |
5 | g.149978132C>G | CA361705080 | SLC26A2 | n.712C>G c.480C>G (p.Ile160Met) c.153C>G (p.Ile51Met) | |
5 | g.149978132C>T | CA447402017 | SLC26A2 | n.712C>T c.480C>T (p.Ile160=) c.153C>T (p.Ile51=) | |
5 | g.149978133T>A | CA361705081 | SLC26A2 | n.713T>A c.481T>A (p.Ser161Thr) c.154T>A (p.Ser52Thr) | |
5 | g.149978133T>C | CA361705082 | SLC26A2 | n.713T>C c.481T>C (p.Ser161Pro) c.154T>C (p.Ser52Pro) | dbSNP gnomAD v4 |
5 | g.149978133T>G | CA361705083 | SLC26A2 | n.713T>G c.481T>G (p.Ser161Ala) c.154T>G (p.Ser52Ala) | |
5 | g.149978134C>A | CA361705085 | SLC26A2 | n.714C>A c.482C>A (p.Ser161Tyr) c.155C>A (p.Ser52Tyr) | |
5 | g.149978134C>G | CA361705086 | SLC26A2 | n.714C>G c.482C>G (p.Ser161Cys) c.155C>G (p.Ser52Cys) | |
5 | g.149978134C>T | CA361705084 | SLC26A2 | n.714C>T c.482C>T (p.Ser161Phe) c.155C>T (p.Ser52Phe) | COSMIC |
5 | g.149978134_149978136delinsCTG | CA1590737421 | SLC26A2 | n.714_716delinsCTG c.482_484delinsCTG (p.Ser161=) c.155_157delinsCTG (p.Ser52=) | |
5 | g.149978135T>A | CA447402018 | SLC26A2 | n.715T>A c.483T>A (p.Ser161=) c.156T>A (p.Ser52=) | |
5 | g.149978135T>C | CA447402019 | SLC26A2 | n.715T>C c.483T>C (p.Ser161=) c.156T>C (p.Ser52=) | |
5 | g.149978135T>G | CA447402020 | SLC26A2 | n.715T>G c.483T>G (p.Ser161=) c.156T>G (p.Ser52=) | |
5 | g.149978137_149978138del | CA3505259 | SLC26A2 | n.717_718del c.485_486del (p.Val162GlyfsTer12) c.158_159del (p.Val53GlyfsTer12) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978136G>A | CA361705087 | SLC26A2 | n.716G>A c.484G>A (p.Val162Met) c.157G>A (p.Val53Met) | |
5 | g.149978136G>C | CA361705088 | SLC26A2 | n.716G>C c.484G>C (p.Val162Leu) c.157G>C (p.Val53Leu) | |
5 | g.149978136G= | CA1590737422 | SLC26A2 | n.716G= c.484G= (p.Val162=) c.157G= (p.Val53=) | |
5 | g.149978136G>T | CA3505260 | SLC26A2 | n.716G>T c.484G>T (p.Val162Leu) c.157G>T (p.Val53Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978137T>A | CA361705089 | SLC26A2 | n.717T>A c.485T>A (p.Val162Glu) c.158T>A (p.Val53Glu) | |
5 | g.149978137T>C | CA3505261 | SLC26A2 | n.717T>C c.485T>C (p.Val162Ala) c.158T>C (p.Val53Ala) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978137T>G | CA361705090 | SLC26A2 | n.717T>G c.485T>G (p.Val162Gly) c.158T>G (p.Val53Gly) | |
5 | g.149978137T= | CA1590737423 | SLC26A2 | n.717T= c.485T= (p.Val162=) c.158T= (p.Val53=) | |
5 | g.149978138G>A | CA447402023 | SLC26A2 | n.718G>A c.486G>A (p.Val162=) c.159G>A (p.Val53=) | |
5 | g.149978138G>C | CA447402021 | SLC26A2 | n.718G>C c.486G>C (p.Val162=) c.159G>C (p.Val53=) | |
5 | g.149978138G>T | CA447402022 | SLC26A2 | n.718G>T c.486G>T (p.Val162=) c.159G>T (p.Val53=) | |
5 | g.149978139G>A | CA361705091 | SLC26A2 | n.719G>A c.487G>A (p.Gly163Ser) c.160G>A (p.Gly54Ser) | |
5 | g.149978139G>C | CA361705092 | SLC26A2 | n.719G>C c.487G>C (p.Gly163Arg) c.160G>C (p.Gly54Arg) | |
5 | g.149978139G>T | CA361705093 | SLC26A2 | n.719G>T c.487G>T (p.Gly163Cys) c.160G>T (p.Gly54Cys) | |
5 | g.149978140G>A | CA3505262 | SLC26A2 | n.720G>A c.488G>A (p.Gly163Asp) c.161G>A (p.Gly54Asp) | dbSNP ExAC gnomAD v2 |
5 | g.149978140G>C | CA361705094 | SLC26A2 | n.720G>C c.488G>C (p.Gly163Ala) c.161G>C (p.Gly54Ala) | |
5 | g.149978140G= | CA1590737424 | SLC26A2 | n.720G= c.488G= (p.Gly163=) c.161G= (p.Gly54=) | |
5 | g.149978140G>T | CA361705095 | SLC26A2 | n.720G>T c.488G>T (p.Gly163Val) c.161G>T (p.Gly54Val) | |
5 | g.149978141C>A | CA447402024 | SLC26A2 | n.721C>A c.489C>A (p.Gly163=) c.162C>A (p.Gly54=) | |
5 | g.149978141C>G | CA447402025 | SLC26A2 | n.721C>G c.489C>G (p.Gly163=) c.162C>G (p.Gly54=) | |
5 | g.149978141C>T | CA447402026 | SLC26A2 | n.721C>T c.489C>T (p.Gly163=) c.162C>T (p.Gly54=) | |
5 | g.149978142A= | CA1590737425 | SLC26A2 | n.722A= c.490A= (p.Ile164=) c.163A= (p.Ile55=) | |
5 | g.149978142A>C | CA361705097 | SLC26A2 | n.722A>C c.490A>C (p.Ile164Leu) c.163A>C (p.Ile55Leu) | |
5 | g.149978142A>G | CA3505263 | SLC26A2 | n.722A>G c.490A>G (p.Ile164Val) c.163A>G (p.Ile55Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.149978142A>T | CA361705096 | SLC26A2 | n.722A>T c.490A>T (p.Ile164Phe) c.163A>T (p.Ile55Phe) | gnomAD v4 |
5 | g.149978143T>A | CA361705098 | SLC26A2 | n.723T>A c.491T>A (p.Ile164Asn) c.164T>A (p.Ile55Asn) | |
5 | g.149978143T>C | CA361705099 | SLC26A2 | n.723T>C c.491T>C (p.Ile164Thr) c.164T>C (p.Ile55Thr) | gnomAD v4 |
5 | g.149978143T>G | CA361705100 | SLC26A2 | n.723T>G c.491T>G (p.Ile164Ser) c.164T>G (p.Ile55Ser) | |
5 | g.149978144T>A | CA447402027 | SLC26A2 | n.724T>A c.492T>A (p.Ile164=) c.165T>A (p.Ile55=) | gnomAD v4 |
5 | g.149978144T>C | CA447402028 | SLC26A2 | n.724T>C c.492T>C (p.Ile164=) c.165T>C (p.Ile55=) | gnomAD v4 |
5 | g.149978144T>G | CA361705101 | SLC26A2 | n.724T>G c.492T>G (p.Ile164Met) c.165T>G (p.Ile55Met) | |
5 | g.149978145T>A | CA361705102 | SLC26A2 | n.725T>A c.493T>A (p.Phe165Ile) c.166T>A (p.Phe56Ile) | |
5 | g.149978145T>C | CA361705103 | SLC26A2 | n.725T>C c.493T>C (p.Phe165Leu) c.166T>C (p.Phe56Leu) | |
5 | g.149978145T>G | CA361705104 | SLC26A2 | n.725T>G c.493T>G (p.Phe165Val) c.166T>G (p.Phe56Val) | gnomAD v4 |
5 | g.149978146T>A | CA361705105 | SLC26A2 | n.726T>A c.494T>A (p.Phe165Tyr) c.167T>A (p.Phe56Tyr) | |
5 | g.149978146T>C | CA361705106 | SLC26A2 | n.726T>C c.494T>C (p.Phe165Ser) c.167T>C (p.Phe56Ser) | |
5 | g.149978146T>G | CA361705107 | SLC26A2 | n.726T>G c.494T>G (p.Phe165Cys) c.167T>G (p.Phe56Cys) | |
5 | g.149978147T>A | CA361705108 | SLC26A2 | n.727T>A c.495T>A (p.Phe165Leu) c.168T>A (p.Phe56Leu) | |
5 | g.149978147T>C | CA447402029 | SLC26A2 | n.727T>C c.495T>C (p.Phe165=) c.168T>C (p.Phe56=) | |
5 | g.149978147T>G | CA361705109 | SLC26A2 | n.727T>G c.495T>G (p.Phe165Leu) c.168T>G (p.Phe56Leu) | |
5 | g.149978148G>A | CA263269 | SLC26A2 | n.728G>A c.496G>A (p.Gly166Arg) c.169G>A (p.Gly57Arg) | ClinVar dbSNP gnomAD v4 |
5 | g.149978148G>C | CA361705111 | SLC26A2 | n.728G>C c.496G>C (p.Gly166Arg) c.169G>C (p.Gly57Arg) | |
5 | g.149978148G= | CA1590737426 | SLC26A2 | n.728G= c.496G= (p.Gly166=) c.169G= (p.Gly57=) | |
5 | g.149978148G>T | CA361705110 | SLC26A2 | n.728G>T c.496G>T (p.Gly166Ter) c.169G>T (p.Gly57Ter) | |
5 | g.149978149G>A | CA361705112 | SLC26A2 | n.729G>A c.497G>A (p.Gly166Glu) c.170G>A (p.Gly57Glu) | |
5 | g.149978149G>C | CA361705113 | SLC26A2 | n.729G>C c.497G>C (p.Gly166Ala) c.170G>C (p.Gly57Ala) | |
5 | g.149978149G>T | CA361705114 | SLC26A2 | n.729G>T c.497G>T (p.Gly166Val) c.170G>T (p.Gly57Val) | |
5 | g.149978150_149978151del | CA913108443 | SLC26A2 | n.730_731del c.498_499del (p.Val167ThrfsTer7) c.171_172del (p.Val58ThrfsTer7) | |
5 | g.149978150A>C | CA447402030 | SLC26A2 | n.730A>C c.498A>C (p.Gly166=) c.171A>C (p.Gly57=) | |
5 | g.149978150A>G | CA447402031 | SLC26A2 | n.730A>G c.498A>G (p.Gly166=) c.171A>G (p.Gly57=) | |
5 | g.149978150A>T | CA447402032 | SLC26A2 | n.730A>T c.498A>T (p.Gly166=) c.171A>T (p.Gly57=) | |
5 | g.149978150_149978151delinsAG | CA1590737427 | SLC26A2 | n.730_731delinsAG c.498_499delinsAG (p.Gly166=) c.171_172delinsAG (p.Gly57=) | |
5 | g.149978151del | CA658822213 | SLC26A2 | n.731del c.499del (p.Val167TyrfsTer5) c.172del (p.Val58TyrfsTer5) | ClinVar dbSNP |
5 | g.149978151G>A | CA361705115 | SLC26A2 | n.731G>A c.499G>A (p.Val167Ile) c.172G>A (p.Val58Ile) | dbSNP gnomAD v2 |
5 | g.149978151G>C | CA361705116 | SLC26A2 | n.731G>C c.499G>C (p.Val167Leu) c.172G>C (p.Val58Leu) | |
5 | g.149978151G= | CA1590737428 | SLC26A2 | n.731G= c.499G= (p.Val167=) c.172G= (p.Val58=) | |
5 | g.149978151G>T | CA361705117 | SLC26A2 | n.731G>T c.499G>T (p.Val167Leu) c.172G>T (p.Val58Leu) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.149978152T>A | CA361705118 | SLC26A2 | n.732T>A c.500T>A (p.Val167Glu) c.173T>A (p.Val58Glu) | |
5 | g.149978152T>C | CA361705119 | SLC26A2 | n.732T>C c.500T>C (p.Val167Ala) c.173T>C (p.Val58Ala) | |
5 | g.149978152T>G | CA361705120 | SLC26A2 | n.732T>G c.500T>G (p.Val167Gly) c.173T>G (p.Val58Gly) | |
5 | g.149978153A>C | CA447402034 | SLC26A2 | n.733A>C c.501A>C (p.Val167=) c.174A>C (p.Val58=) | |
5 | g.149978153A>G | CA447402035 | SLC26A2 | n.733A>G c.501A>G (p.Val167=) c.174A>G (p.Val58=) | |
5 | g.149978153A>T | CA447402033 | SLC26A2 | n.733A>T c.501A>T (p.Val167=) c.174A>T (p.Val58=) | |
5 | g.149978154C>A | CA361705121 | SLC26A2 | n.734C>A c.502C>A (p.Leu168Met) c.175C>A (p.Leu59Met) | |
5 | g.149978154C= | CA1590737429 | SLC26A2 | n.734C= c.502C= (p.Leu168=) c.175C= (p.Leu59=) | |
5 | g.149978154C>G | CA361705122 | SLC26A2 | n.734C>G c.502C>G (p.Leu168Val) c.175C>G (p.Leu59Val) | |
5 | g.149978154C>T | CA3505264 | SLC26A2 | n.734C>T c.502C>T (p.Leu168=) c.175C>T (p.Leu59=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978155T>A | CA361705124 | SLC26A2 | n.735T>A c.503T>A (p.Leu168Gln) c.176T>A (p.Leu59Gln) | |
5 | g.149978155T>C | CA361705125 | SLC26A2 | n.735T>C c.503T>C (p.Leu168Pro) c.176T>C (p.Leu59Pro) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.149978155T>G | CA361705123 | SLC26A2 | n.735T>G c.503T>G (p.Leu168Arg) c.176T>G (p.Leu59Arg) | |
5 | g.149978155T= | CA1590737430 | SLC26A2 | n.735T= c.503T= (p.Leu168=) c.176T= (p.Leu59=) | |
5 | g.149978156G>A | CA447402036 | SLC26A2 | n.736G>A c.504G>A (p.Leu168=) c.177G>A (p.Leu59=) | |
5 | g.149978156G>C | CA447402037 | SLC26A2 | n.736G>C c.504G>C (p.Leu168=) c.177G>C (p.Leu59=) | |
5 | g.149978156G>T | CA447402038 | SLC26A2 | n.736G>T c.504G>T (p.Leu168=) c.177G>T (p.Leu59=) | |
5 | g.149978157T>A | CA361705126 | SLC26A2 | n.737T>A c.505T>A (p.Cys169Ser) c.178T>A (p.Cys60Ser) | |
5 | g.149978157T>C | CA361705127 | SLC26A2 | n.737T>C c.505T>C (p.Cys169Arg) c.178T>C (p.Cys60Arg) | dbSNP |
5 | g.149978157T>G | CA361705128 | SLC26A2 | n.737T>G c.505T>G (p.Cys169Gly) c.178T>G (p.Cys60Gly) | |
5 | g.149978157T= | CA1590737431 | SLC26A2 | n.737T= c.505T= (p.Cys169=) c.178T= (p.Cys60=) | |
5 | g.149978158G>A | CA361705129 | SLC26A2 | n.738G>A c.506G>A (p.Cys169Tyr) c.179G>A (p.Cys60Tyr) | |
5 | g.149978158G>C | CA361705130 | SLC26A2 | n.738G>C c.506G>C (p.Cys169Ser) c.179G>C (p.Cys60Ser) | |
5 | g.149978158G>T | CA361705131 | SLC26A2 | n.738G>T c.506G>T (p.Cys169Phe) c.179G>T (p.Cys60Phe) | COSMIC |
5 | g.149978159C>A | CA361705133 | SLC26A2 | n.739C>A c.507C>A (p.Cys169Ter) c.180C>A (p.Cys60Ter) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.149978159C= | CA1590737432 | SLC26A2 | n.739C= c.507C= (p.Cys169=) c.180C= (p.Cys60=) | |
5 | g.149978159C>G | CA361705132 | SLC26A2 | n.739C>G c.507C>G (p.Cys169Trp) c.180C>G (p.Cys60Trp) | gnomAD v4 |
5 | g.149978159C>T | CA447402039 | SLC26A2 | n.739C>T c.507C>T (p.Cys169=) c.180C>T (p.Cys60=) | |
5 | g.149978160C>A | CA361705134 | SLC26A2 | n.740C>A c.508C>A (p.Leu170Ile) c.181C>A (p.Leu61Ile) | |
5 | g.149978160C= | CA1590737433 | SLC26A2 | n.740C= c.508C= (p.Leu170=) c.181C= (p.Leu61=) | |
5 | g.149978160C>G | CA361705135 | SLC26A2 | n.740C>G c.508C>G (p.Leu170Val) c.181C>G (p.Leu61Val) | |
5 | g.149978160C>T | CA361705136 | SLC26A2 | n.740C>T c.508C>T (p.Leu170Phe) c.181C>T (p.Leu61Phe) | dbSNP |
5 | g.149978161T>A | CA361705137 | SLC26A2 | n.741T>A c.509T>A (p.Leu170His) c.182T>A (p.Leu61His) | |
5 | g.149978161T>C | CA361705138 | SLC26A2 | n.741T>C c.509T>C (p.Leu170Pro) c.182T>C (p.Leu61Pro) | |
5 | g.149978161T>G | CA361705139 | SLC26A2 | n.741T>G c.509T>G (p.Leu170Arg) c.182T>G (p.Leu61Arg) | |
5 | g.149978162T>A | CA447402040 | SLC26A2 | n.742T>A c.510T>A (p.Leu170=) c.183T>A (p.Leu61=) | |
5 | g.149978162T>C | CA447402041 | SLC26A2 | n.742T>C c.510T>C (p.Leu170=) c.183T>C (p.Leu61=) | |
5 | g.149978162T>G | CA447402042 | SLC26A2 | n.742T>G c.510T>G (p.Leu170=) c.183T>G (p.Leu61=) | |
5 | g.149978163A>C | CA361705142 | SLC26A2 | n.743A>C c.511A>C (p.Met171Leu) c.184A>C (p.Met62Leu) | |
5 | g.149978163A>G | CA361705141 | SLC26A2 | n.743A>G c.511A>G (p.Met171Val) c.184A>G (p.Met62Val) | gnomAD v4 |
5 | g.149978163A>T | CA361705140 | SLC26A2 | n.743A>T c.511A>T (p.Met171Leu) c.184A>T (p.Met62Leu) | |
5 | g.149978164T>A | CA361705143 | SLC26A2 | n.744T>A c.512T>A (p.Met171Lys) c.185T>A (p.Met62Lys) | |
5 | g.149978164T>C | CA3505265 | SLC26A2 | n.744T>C c.512T>C (p.Met171Thr) c.185T>C (p.Met62Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978164T>G | CA361705144 | SLC26A2 | n.744T>G c.512T>G (p.Met171Arg) c.185T>G (p.Met62Arg) | |
5 | g.149978164T= | CA1590737434 | SLC26A2 | n.744T= c.512T= (p.Met171=) c.185T= (p.Met62=) | |
5 | g.149978165G>A | CA3505266 | SLC26A2 | n.745G>A c.513G>A (p.Met171Ile) c.186G>A (p.Met62Ile) | dbSNP ExAC gnomAD v2 gnomAD v4 |
5 | g.149978165G>C | CA361705145 | SLC26A2 | n.745G>C c.513G>C (p.Met171Ile) c.186G>C (p.Met62Ile) | gnomAD v4 |
5 | g.149978165G= | CA1590737435 | SLC26A2 | n.745G= c.513G= (p.Met171=) c.186G= (p.Met62=) | |
5 | g.149978165G>T | CA361705146 | SLC26A2 | n.745G>T c.513G>T (p.Met171Ile) c.186G>T (p.Met62Ile) | |
5 | g.149978166A>C | CA361705147 | SLC26A2 | n.746A>C c.514A>C (p.Ile172Leu) c.187A>C (p.Ile63Leu) | |
5 | g.149978166A>G | CA361705148 | SLC26A2 | n.746A>G c.514A>G (p.Ile172Val) c.187A>G (p.Ile63Val) | |
5 | g.149978166A>T | CA361705149 | SLC26A2 | n.746A>T c.514A>T (p.Ile172Phe) c.187A>T (p.Ile63Phe) | gnomAD v4 |
5 | g.149978167T>A | CA361705150 | SLC26A2 | n.747T>A c.515T>A (p.Ile172Asn) c.188T>A (p.Ile63Asn) | |
5 | g.149978167T>C | CA3505267 | SLC26A2 | n.747T>C c.515T>C (p.Ile172Thr) c.188T>C (p.Ile63Thr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978167T>G | CA361705151 | SLC26A2 | n.747T>G c.515T>G (p.Ile172Ser) c.188T>G (p.Ile63Ser) | |
5 | g.149978167T= | CA1590737436 | SLC26A2 | n.747T= c.515T= (p.Ile172=) c.188T= (p.Ile63=) | |
5 | g.149978168T>A | CA447402043 | SLC26A2 | n.748T>A c.516T>A (p.Ile172=) c.189T>A (p.Ile63=) | |
5 | g.149978168T>C | CA447402044 | SLC26A2 | n.748T>C c.516T>C (p.Ile172=) c.189T>C (p.Ile63=) | |
5 | g.149978168T>G | CA361705152 | SLC26A2 | n.748T>G c.516T>G (p.Ile172Met) c.189T>G (p.Ile63Met) | |
5 | g.149978169G>A | CA361705155 | SLC26A2 | n.749G>A c.517G>A (p.Gly173Ser) c.190G>A (p.Gly64Ser) | |
5 | g.149978169G>C | CA361705154 | SLC26A2 | n.749G>C c.517G>C (p.Gly173Arg) c.190G>C (p.Gly64Arg) | |
5 | g.149978169G>T | CA361705153 | SLC26A2 | n.749G>T c.517G>T (p.Gly173Cys) c.190G>T (p.Gly64Cys) | |
5 | g.149978170G>A | CA361705156 | SLC26A2 | n.750G>A c.518G>A (p.Gly173Asp) c.191G>A (p.Gly64Asp) | |
5 | g.149978170G>C | CA361705157 | SLC26A2 | n.750G>C c.518G>C (p.Gly173Ala) c.191G>C (p.Gly64Ala) | |
5 | g.149978170G>T | CA361705158 | SLC26A2 | n.750G>T c.518G>T (p.Gly173Val) c.191G>T (p.Gly64Val) | |
5 | g.149978171T>A | CA447402045 | SLC26A2 | n.751T>A c.519T>A (p.Gly173=) c.192T>A (p.Gly64=) | |
5 | g.149978171T>C | CA447402046 | SLC26A2 | n.751T>C c.519T>C (p.Gly173=) c.192T>C (p.Gly64=) | |
5 | g.149978171T>G | CA447402047 | SLC26A2 | n.751T>G c.519T>G (p.Gly173=) c.192T>G (p.Gly64=) | |
5 | g.149978172G>A | CA361705159 | SLC26A2 | n.752G>A c.520G>A (p.Glu174Lys) c.193G>A (p.Glu65Lys) | gnomAD v4 |
5 | g.149978172G>C | CA361705160 | SLC26A2 | n.752G>C c.520G>C (p.Glu174Gln) c.193G>C (p.Glu65Gln) | |
5 | g.149978172G>T | CA361705161 | SLC26A2 | n.752G>T c.520G>T (p.Glu174Ter) c.193G>T (p.Glu65Ter) | |
5 | g.149978173A>C | CA361705162 | SLC26A2 | n.753A>C c.521A>C (p.Glu174Ala) c.194A>C (p.Glu65Ala) | |
5 | g.149978173A>G | CA361705163 | SLC26A2 | n.753A>G c.521A>G (p.Glu174Gly) c.194A>G (p.Glu65Gly) | |
5 | g.149978173A>T | CA361705164 | SLC26A2 | n.753A>T c.521A>T (p.Glu174Val) c.194A>T (p.Glu65Val) | |
5 | g.149978174G>A | CA129082620 | SLC26A2 | n.754G>A c.522G>A (p.Glu174=) c.195G>A (p.Glu65=) | dbSNP |
5 | g.149978174G>C | CA361705165 | SLC26A2 | n.754G>C c.522G>C (p.Glu174Asp) c.195G>C (p.Glu65Asp) | |
5 | g.149978174G= | CA1590737437 | SLC26A2 | n.754G= c.522G= (p.Glu174=) c.195G= (p.Glu65=) | |
5 | g.149978174G>T | CA361705166 | SLC26A2 | n.754G>T c.522G>T (p.Glu174Asp) c.195G>T (p.Glu65Asp) | |
5 | g.149978175A>C | CA361705167 | SLC26A2 | n.755A>C c.523A>C (p.Thr175Pro) c.196A>C (p.Thr66Pro) | |
5 | g.149978175A>G | CA361705168 | SLC26A2 | n.755A>G c.523A>G (p.Thr175Ala) c.196A>G (p.Thr66Ala) | |
5 | g.149978175A>T | CA361705169 | SLC26A2 | n.755A>T c.523A>T (p.Thr175Ser) c.196A>T (p.Thr66Ser) | |
5 | g.149978176C>A | CA361705171 | SLC26A2 | n.756C>A c.524C>A (p.Thr175Lys) c.197C>A (p.Thr66Lys) | gnomAD v4 |
5 | g.149978176C= | CA1590737438 | SLC26A2 | n.756C= c.524C= (p.Thr175=) c.197C= (p.Thr66=) | |
5 | g.149978176C>G | CA361705172 | SLC26A2 | n.756C>G c.524C>G (p.Thr175Arg) c.197C>G (p.Thr66Arg) | dbSNP |
5 | g.149978176C>T | CA361705170 | SLC26A2 | n.756C>T c.524C>T (p.Thr175Ile) c.197C>T (p.Thr66Ile) | |
5 | g.149978177A= | CA1590737439 | SLC26A2 | n.757A= c.525A= (p.Thr175=) c.198A= (p.Thr66=) | |
5 | g.149978177A>C | CA447402048 | SLC26A2 | n.757A>C c.525A>C (p.Thr175=) c.198A>C (p.Thr66=) | |
5 | g.149978177A>G | CA447402049 | SLC26A2 | n.757A>G c.525A>G (p.Thr175=) c.198A>G (p.Thr66=) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
5 | g.149978177A>T | CA447402050 | SLC26A2 | n.757A>T c.525A>T (p.Thr175=) c.198A>T (p.Thr66=) | |
5 | g.149978178G>A | CA361705173 | SLC26A2 | n.758G>A c.526G>A (p.Val176Ile) c.199G>A (p.Val67Ile) | |
5 | g.149978178G>C | CA361705174 | SLC26A2 | n.758G>C c.526G>C (p.Val176Leu) c.199G>C (p.Val67Leu) | |
5 | g.149978178G>T | CA361705175 | SLC26A2 | n.758G>T c.526G>T (p.Val176Phe) c.199G>T (p.Val67Phe) | |
5 | g.149978179T>A | CA361705176 | SLC26A2 | n.759T>A c.527T>A (p.Val176Asp) c.200T>A (p.Val67Asp) | |
5 | g.149978179T>C | CA361705177 | SLC26A2 | n.759T>C c.527T>C (p.Val176Ala) c.200T>C (p.Val67Ala) | |
5 | g.149978179T>G | CA361705178 | SLC26A2 | n.759T>G c.527T>G (p.Val176Gly) c.200T>G (p.Val67Gly) | |
5 | g.149978180T>A | CA447402051 | SLC26A2 | n.760T>A c.528T>A (p.Val176=) c.201T>A (p.Val67=) | |
5 | g.149978180T>C | CA447402052 | SLC26A2 | n.760T>C c.528T>C (p.Val176=) c.201T>C (p.Val67=) | |
5 | g.149978180T>G | CA447402053 | SLC26A2 | n.760T>G c.528T>G (p.Val176=) c.201T>G (p.Val67=) | |
5 | g.149978181G>A | CA361705179 | SLC26A2 | n.761G>A c.529G>A (p.Asp177Asn) c.202G>A (p.Asp68Asn) | |
5 | g.149978181G>C | CA361705180 | SLC26A2 | n.761G>C c.529G>C (p.Asp177His) c.202G>C (p.Asp68His) | |
5 | g.149978181G>T | CA361705181 | SLC26A2 | n.761G>T c.529G>T (p.Asp177Tyr) c.202G>T (p.Asp68Tyr) | |
5 | g.149978182A>C | CA361705182 | SLC26A2 | n.762A>C c.530A>C (p.Asp177Ala) c.203A>C (p.Asp68Ala) | |
5 | g.149978182A>G | CA361705183 | SLC26A2 | n.762A>G c.530A>G (p.Asp177Gly) c.203A>G (p.Asp68Gly) | gnomAD v4 |
5 | g.149978182A>T | CA361705184 | SLC26A2 | n.762A>T c.530A>T (p.Asp177Val) c.203A>T (p.Asp68Val) | |
5 | g.149978183C>A | CA361705185 | SLC26A2 | n.763C>A c.531C>A (p.Asp177Glu) c.204C>A (p.Asp68Glu) | |
5 | g.149978183C>G | CA361705186 | SLC26A2 | n.763C>G c.531C>G (p.Asp177Glu) c.204C>G (p.Asp68Glu) | |
5 | g.149978183C>T | CA447402054 | SLC26A2 | n.763C>T c.531C>T (p.Asp177=) c.204C>T (p.Asp68=) | gnomAD v4 |
5 | g.149978184C>A | CA447402055 | SLC26A2 | n.764C>A c.532C>A (p.Arg178=) c.205C>A (p.Arg69=) | |
5 | g.149978184C= | CA1590737440 | SLC26A2 | n.764C= c.532C= (p.Arg178=) c.205C= (p.Arg69=) | |
5 | g.149978184C>G | CA361705187 | SLC26A2 | n.764C>G c.532C>G (p.Arg178Gly) c.205C>G (p.Arg69Gly) | |
5 | g.149978184C>T | CA259839 | SLC26A2 | n.764C>T c.532C>T (p.Arg178Ter) c.205C>T (p.Arg69Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978185G>A | CA3505268 | SLC26A2 | n.765G>A c.533G>A (p.Arg178Gln) c.206G>A (p.Arg69Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978185G>C | CA361705188 | SLC26A2 | n.765G>C c.533G>C (p.Arg178Pro) c.206G>C (p.Arg69Pro) | |
5 | g.149978185G= | CA1590737441 | SLC26A2 | n.765G= c.533G= (p.Arg178=) c.206G= (p.Arg69=) | |
5 | g.149978185G>T | CA361705189 | SLC26A2 | n.765G>T c.533G>T (p.Arg178Leu) c.206G>T (p.Arg69Leu) | gnomAD v4 |
5 | g.149978186A= | CA1590737442 | SLC26A2 | n.766A= c.534A= (p.Arg178=) c.207A= (p.Arg69=) | |
5 | g.149978186A>C | CA447402056 | SLC26A2 | n.766A>C c.534A>C (p.Arg178=) c.207A>C (p.Arg69=) | |
5 | g.149978186A>G | CA129082639 | SLC26A2 | n.766A>G c.534A>G (p.Arg178=) c.207A>G (p.Arg69=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978186A>T | CA447402057 | SLC26A2 | n.766A>T c.534A>T (p.Arg178=) c.207A>T (p.Arg69=) | |
5 | g.149978187G>A | CA3505269 | SLC26A2 | n.767G>A c.535G>A (p.Glu179Lys) c.208G>A (p.Glu70Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.149978187G>C | CA361705190 | SLC26A2 | n.767G>C c.535G>C (p.Glu179Gln) c.208G>C (p.Glu70Gln) | |
5 | g.149978187G= | CA1590737443 | SLC26A2 | n.767G= c.535G= (p.Glu179=) c.208G= (p.Glu70=) | |
5 | g.149978187G>T | CA361705191 | SLC26A2 | n.767G>T c.535G>T (p.Glu179Ter) c.208G>T (p.Glu70Ter) | COSMIC |
5 | g.149978188A>C | CA361705192 | SLC26A2 | n.768A>C c.536A>C (p.Glu179Ala) c.209A>C (p.Glu70Ala) | |
5 | g.149978188A>G | CA361705193 | SLC26A2 | n.768A>G c.536A>G (p.Glu179Gly) c.209A>G (p.Glu70Gly) | |
5 | g.149978188A>T | CA361705194 | SLC26A2 | n.768A>T c.536A>T (p.Glu179Val) c.209A>T (p.Glu70Val) | |
5 | g.149978189A>C | CA361705195 | SLC26A2 | n.769A>C c.537A>C (p.Glu179Asp) c.210A>C (p.Glu70Asp) | |
5 | g.149978189A>G | CA447402058 | SLC26A2 | n.769A>G c.537A>G (p.Glu179=) c.210A>G (p.Glu70=) | |
5 | g.149978189A>T | CA361705196 | SLC26A2 | n.769A>T c.537A>T (p.Glu179Asp) c.210A>T (p.Glu70Asp) | |
5 | g.149978190C>A | CA361705198 | SLC26A2 | n.770C>A c.538C>A (p.Leu180Ile) c.211C>A (p.Leu71Ile) | |
5 | g.149978190C>G | CA361705197 | SLC26A2 | n.770C>G c.538C>G (p.Leu180Val) c.211C>G (p.Leu71Val) | |
5 | g.149978190C>T | CA447402059 | SLC26A2 | n.770C>T c.538C>T (p.Leu180=) c.211C>T (p.Leu71=) | |
5 | g.149978191T>A | CA361705199 | SLC26A2 | n.771T>A c.539T>A (p.Leu180Gln) c.212T>A (p.Leu71Gln) | |
5 | g.149978191T>C | CA361705201 | SLC26A2 | n.771T>C c.539T>C (p.Leu180Pro) c.212T>C (p.Leu71Pro) | |
5 | g.149978191T>G | CA361705200 | SLC26A2 | n.771T>G c.539T>G (p.Leu180Arg) c.212T>G (p.Leu71Arg) | |
5 | g.149978192A>C | CA447402060 | SLC26A2 | n.772A>C c.540A>C (p.Leu180=) c.213A>C (p.Leu71=) | |
5 | g.149978192A>G | CA447402061 | SLC26A2 | n.772A>G c.540A>G (p.Leu180=) c.213A>G (p.Leu71=) | ClinVar |
5 | g.149978192A>T | CA447402062 | SLC26A2 | n.772A>T c.540A>T (p.Leu180=) c.213A>T (p.Leu71=) | |
5 | g.149978193C>A | CA361705202 | SLC26A2 | n.773C>A c.541C>A (p.Gln181Lys) c.214C>A (p.Gln72Lys) | |
5 | g.149978193C= | CA1590737444 | SLC26A2 | n.773C= c.541C= (p.Gln181=) c.214C= (p.Gln72=) | |
5 | g.149978193C>G | CA361705203 | SLC26A2 | n.773C>G c.541C>G (p.Gln181Glu) c.214C>G (p.Gln72Glu) | |
5 | g.149978193C>T | CA16040988 | SLC26A2 | n.773C>T c.541C>T (p.Gln181Ter) c.214C>T (p.Gln72Ter) | ClinVar dbSNP |
5 | g.149978194A>C | CA361705204 | SLC26A2 | n.774A>C c.542A>C (p.Gln181Pro) c.215A>C (p.Gln72Pro) | |
5 | g.149978194A>G | CA361705205 | SLC26A2 | n.774A>G c.542A>G (p.Gln181Arg) c.215A>G (p.Gln72Arg) | gnomAD v4 |
5 | g.149978194A>T | CA361705206 | SLC26A2 | n.774A>T c.542A>T (p.Gln181Leu) c.215A>T (p.Gln72Leu) | |
5 | g.149978195G>A | CA447402063 | SLC26A2 | n.775G>A c.543G>A (p.Gln181=) c.216G>A (p.Gln72=) | |
5 | g.149978195G>C | CA361705207 | SLC26A2 | n.775G>C c.543G>C (p.Gln181His) c.216G>C (p.Gln72His) | |
5 | g.149978195G>T | CA361705208 | SLC26A2 | n.775G>T c.543G>T (p.Gln181His) c.216G>T (p.Gln72His) | |
5 | g.149978196A>C | CA361705209 | SLC26A2 | n.776A>C c.544A>C (p.Lys182Gln) c.217A>C (p.Lys73Gln) | |
5 | g.149978196A>G | CA361705211 | SLC26A2 | n.776A>G c.544A>G (p.Lys182Glu) c.217A>G (p.Lys73Glu) | |
5 | g.149978196A>T | CA361705210 | SLC26A2 | n.776A>T c.544A>T (p.Lys182Ter) c.217A>T (p.Lys73Ter) | |
5 | g.149978200_149978296dup | CA2768879950 | SLC26A2 | n.780_876dup c.548_644dup (p.Cys216TrpfsTer3) c.221_317dup (p.Cys107TrpfsTer3) | |
5 | g.149978197A= | CA1590737445 | SLC26A2 | n.777A= c.545A= (p.Lys182=) c.218A= (p.Lys73=) | |
5 | g.149978197A>C | CA361705212 | SLC26A2 | n.777A>C c.545A>C (p.Lys182Thr) c.218A>C (p.Lys73Thr) | |
5 | g.149978197A>G | CA361705213 | SLC26A2 | n.777A>G c.545A>G (p.Lys182Arg) c.218A>G (p.Lys73Arg) | dbSNP gnomAD v3 gnomAD v4 |
5 | g.149978197A>T | CA361705214 | SLC26A2 | n.777A>T c.545A>T (p.Lys182Ile) c.218A>T (p.Lys73Ile) | |
5 | g.149978198A>C | CA361705215 | SLC26A2 | n.778A>C c.546A>C (p.Lys182Asn) c.219A>C (p.Lys73Asn) | |
5 | g.149978198A>G | CA447402064 | SLC26A2 | n.778A>G c.546A>G (p.Lys182=) c.219A>G (p.Lys73=) | gnomAD v4 |
5 | g.149978198A>T | CA361705216 | SLC26A2 | n.778A>T c.546A>T (p.Lys182Asn) c.219A>T (p.Lys73Asn) | |
5 | g.149978199G>A | CA361705217 | SLC26A2 | n.779G>A c.547G>A (p.Ala183Thr) c.220G>A (p.Ala74Thr) | dbSNP gnomAD v4 |
5 | g.149978199G>C | CA361705219 | SLC26A2 | n.779G>C c.547G>C (p.Ala183Pro) c.220G>C (p.Ala74Pro) | ClinVar dbSNP |
5 | g.149978199G= | CA1590737446 | SLC26A2 | n.779G= c.547G= (p.Ala183=) c.220G= (p.Ala74=) | |
5 | g.149978199G>T | CA361705218 | SLC26A2 | n.779G>T c.547G>T (p.Ala183Ser) c.220G>T (p.Ala74Ser) | gnomAD v4 |
5 | g.149978200C>A | CA361705220 | SLC26A2 | n.780C>A c.548C>A (p.Ala183Asp) c.221C>A (p.Ala74Asp) | |
5 | g.149978200C= | CA1590737447 | SLC26A2 | n.780C= c.548C= (p.Ala183=) c.221C= (p.Ala74=) | |
5 | g.149978200C>G | CA361705221 | SLC26A2 | n.780C>G c.548C>G (p.Ala183Gly) c.221C>G (p.Ala74Gly) | |
5 | g.149978200C>T | CA361705222 | SLC26A2 | n.780C>T c.548C>T (p.Ala183Val) c.221C>T (p.Ala74Val) | dbSNP gnomAD v4 |
5 | g.149978201T>A | CA447402067 | SLC26A2 | n.781T>A c.549T>A (p.Ala183=) c.222T>A (p.Ala74=) | |
5 | g.149978201T>C | CA447402066 | SLC26A2 | n.781T>C c.549T>C (p.Ala183=) c.222T>C (p.Ala74=) | |
5 | g.149978201T>G | CA447402065 | SLC26A2 | n.781T>G c.549T>G (p.Ala183=) c.222T>G (p.Ala74=) | |
5 | g.149978202G>A | CA361705223 | SLC26A2 | n.782G>A c.550G>A (p.Gly184Ser) c.223G>A (p.Gly75Ser) | |
5 | g.149978202G>C | CA361705224 | SLC26A2 | n.782G>C c.550G>C (p.Gly184Arg) c.223G>C (p.Gly75Arg) | |
5 | g.149978202G>T | CA361705225 | SLC26A2 | n.782G>T c.550G>T (p.Gly184Cys) c.223G>T (p.Gly75Cys) | |
5 | g.149978203G>A | CA361705226 | SLC26A2 | n.783G>A c.551G>A (p.Gly184Asp) c.224G>A (p.Gly75Asp) | |
5 | g.149978203G>C | CA361705227 | SLC26A2 | n.783G>C c.551G>C (p.Gly184Ala) c.224G>C (p.Gly75Ala) | |
5 | g.149978203G= | CA1590737448 | SLC26A2 | n.783G= c.551G= (p.Gly184=) c.224G= (p.Gly75=) | |
5 | g.149978203G>T | CA3505270 | SLC26A2 | n.783G>T c.551G>T (p.Gly184Val) c.224G>T (p.Gly75Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |