UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.97601889G>A | CA203959 | HOGA1 | c.733G>A (p.Val245Ile) c.143G>A c.244G>A (p.Val82Ile) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601889G>C | CA377981033 | HOGA1 | c.733G>C (p.Val245Leu) c.143G>C c.244G>C (p.Val82Leu) | |
| 10 | g.97601889G= | CA1930508660 | HOGA1 | c.733G= (p.Val245=) c.143G= c.244G= (p.Val82=) | |
| 10 | g.97601889G>T | CA5634231 | HOGA1 | c.733G>T (p.Val245Phe) c.143G>T c.244G>T (p.Val82Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601890T>A | CA377981054 | HOGA1 | c.734T>A (p.Val245Asp) c.144T>A c.245T>A (p.Val82Asp) | gnomAD v4 |
| 10 | g.97601890T>C | CA377981057 | HOGA1 | c.734T>C (p.Val245Ala) c.144T>C c.245T>C (p.Val82Ala) | |
| 10 | g.97601890T>G | CA377981061 | HOGA1 | c.734T>G (p.Val245Gly) c.144T>G c.245T>G (p.Val82Gly) | |
| 10 | g.97601891C>A | CA471092386 | HOGA1 | c.735C>A (p.Val245=) c.145C>A c.246C>A (p.Val82=) | gnomAD v4 |
| 10 | g.97601891C>G | CA471092387 | HOGA1 | c.735C>G (p.Val245=) c.145C>G c.246C>G (p.Val82=) | |
| 10 | g.97601891C>T | CA471092388 | HOGA1 | c.735C>T (p.Val245=) c.145C>T c.246C>T (p.Val82=) | |
| 10 | g.97601892C>A | CA377981063 | HOGA1 | c.736C>A (p.Leu246Met) c.146C>A c.247C>A (p.Leu83Met) | |
| 10 | g.97601892C>G | CA377981062 | HOGA1 | c.736C>G (p.Leu246Val) c.146C>G c.247C>G (p.Leu83Val) | |
| 10 | g.97601892C>T | CA471092389 | HOGA1 | c.736C>T (p.Leu246=) c.146C>T c.247C>T (p.Leu83=) | |
| 10 | g.97601893T>A | CA377981064 | HOGA1 | c.737T>A (p.Leu246Gln) c.147T>A c.248T>A (p.Leu83Gln) | |
| 10 | g.97601893T>C | CA377981070 | HOGA1 | c.737T>C (p.Leu246Pro) c.147T>C c.248T>C (p.Leu83Pro) | |
| 10 | g.97601893T>G | CA377981066 | HOGA1 | c.737T>G (p.Leu246Arg) c.147T>G c.248T>G (p.Leu83Arg) | |
| 10 | g.97601894G>A | CA471092392 | HOGA1 | c.738G>A (p.Leu246=) c.148G>A c.249G>A (p.Leu83=) | |
| 10 | g.97601894G>C | CA471092391 | HOGA1 | c.738G>C (p.Leu246=) c.148G>C c.249G>C (p.Leu83=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.97601894G= | CA1930508667 | HOGA1 | c.738G= (p.Leu246=) c.148G= c.249G= (p.Leu83=) | |
| 10 | g.97601894G>T | CA471092390 | HOGA1 | c.738G>T (p.Leu246=) c.148G>T c.249G>T (p.Leu83=) | |
| 10 | g.97601895G>A | CA377981074 | HOGA1 | c.739G>A (p.Gly247Arg) c.149G>A c.250G>A (p.Gly84Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.97601895G>C | CA377981078 | HOGA1 | c.739G>C (p.Gly247Arg) c.149G>C c.250G>C (p.Gly84Arg) | |
| 10 | g.97601895G= | CA1930508674 | HOGA1 | c.739G= (p.Gly247=) c.149G= c.250G= (p.Gly84=) | |
| 10 | g.97601895G>T | CA377981076 | HOGA1 | c.739G>T (p.Gly247Trp) c.149G>T c.250G>T (p.Gly84Trp) | |
| 10 | g.97601896G>A | CA377981082 | HOGA1 | c.740G>A (p.Gly247Glu) c.150G>A c.251G>A (p.Gly84Glu) | |
| 10 | g.97601896G>C | CA377981090 | HOGA1 | c.740G>C (p.Gly247Ala) c.150G>C c.251G>C (p.Gly84Ala) | |
| 10 | g.97601896G>T | CA377981086 | HOGA1 | c.740G>T (p.Gly247Val) c.150G>T c.251G>T (p.Gly84Val) | |
| 10 | g.97601897G>A | CA471092393 | HOGA1 | c.741G>A (p.Gly247=) c.151G>A c.252G>A (p.Gly84=) | |
| 10 | g.97601897G>C | CA471092394 | HOGA1 | c.741G>C (p.Gly247=) c.151G>C c.252G>C (p.Gly84=) | |
| 10 | g.97601897G>T | CA471092395 | HOGA1 | c.741G>T (p.Gly247=) c.151G>T c.252G>T (p.Gly84=) | |
| 10 | g.97601898G>A | CA377981095 | HOGA1 | c.742G>A (p.Ala248Thr) c.152G>A c.253G>A (p.Ala85Thr) | |
| 10 | g.97601898G>C | CA377981105 | HOGA1 | c.742G>C (p.Ala248Pro) c.152G>C c.253G>C (p.Ala85Pro) | |
| 10 | g.97601898G= | CA1930508678 | HOGA1 | c.742G= (p.Ala248=) c.152G= c.253G= (p.Ala85=) | |
| 10 | g.97601898G>T | CA377981108 | HOGA1 | c.742G>T (p.Ala248Ser) c.152G>T c.253G>T (p.Ala85Ser) | dbSNP |
| 10 | g.97601898_97601899delinsGC | CA1930508677 | HOGA1 | c.742_743delinsGC (p.Ala248=) c.152_153delinsGC c.253_254delinsGC (p.Ala85=) | |
| 10 | g.97601899del | CA5634232 | HOGA1 | c.743del (p.Ala248ValfsTer?) c.153del c.254del (p.Ala85ValfsTer?) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.97601899C>A | CA377981116 | HOGA1 | c.743C>A (p.Ala248Asp) c.153C>A c.254C>A (p.Ala85Asp) | |
| 10 | g.97601899C= | CA1930508683 | HOGA1 | c.743C= (p.Ala248=) c.153C= c.254C= (p.Ala85=) | |
| 10 | g.97601899C>G | CA377981119 | HOGA1 | c.743C>G (p.Ala248Gly) c.153C>G c.254C>G (p.Ala85Gly) | |
| 10 | g.97601899C>T | CA377981122 | HOGA1 | c.743C>T (p.Ala248Val) c.153C>T c.254C>T (p.Ala85Val) | dbSNP |
| 10 | g.97601900T>A | CA471092396 | HOGA1 | c.744T>A (p.Ala248=) c.154T>A c.255T>A (p.Ala85=) | |
| 10 | g.97601900T>C | CA471092397 | HOGA1 | c.744T>C (p.Ala248=) c.154T>C c.255T>C (p.Ala85=) | gnomAD v4 |
| 10 | g.97601900T>G | CA471092398 | HOGA1 | c.744T>G (p.Ala248=) c.154T>G c.255T>G (p.Ala85=) | |
| 10 | g.97601901C>A | CA377981128 | HOGA1 | c.745C>A (p.Gln249Lys) c.155C>A c.256C>A (p.Gln86Lys) | |
| 10 | g.97601901C= | CA1930508691 | HOGA1 | c.745C= (p.Gln249=) c.155C= c.256C= (p.Gln86=) | |
| 10 | g.97601901C>G | CA203930 | HOGA1 | c.745C>G (p.Gln249Glu) c.155C>G c.256C>G (p.Gln86Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601901C>T | CA377981129 | HOGA1 | c.745C>T (p.Gln249Ter) c.155C>T c.256C>T (p.Gln86Ter) | |
| 10 | g.97601902A>C | CA377981131 | HOGA1 | c.746A>C (p.Gln249Pro) c.156A>C c.257A>C (p.Gln86Pro) | |
| 10 | g.97601902A>G | CA377981134 | HOGA1 | c.746A>G (p.Gln249Arg) c.156A>G c.257A>G (p.Gln86Arg) | |
| 10 | g.97601902A>T | CA377981144 | HOGA1 | c.746A>T (p.Gln249Leu) c.156A>T c.257A>T (p.Gln86Leu) | |
| 10 | g.97601903G>A | CA471092399 | HOGA1 | c.747G>A (p.Gln249=) c.157G>A c.258G>A (p.Gln86=) | |
| 10 | g.97601903G>C | CA212675216 | HOGA1 | c.747G>C (p.Gln249His) c.157G>C c.258G>C (p.Gln86His) | dbSNP gnomAD v4 |
| 10 | g.97601903G= | CA1930508701 | HOGA1 | c.747G= (p.Gln249=) c.157G= c.258G= (p.Gln86=) | |
| 10 | g.97601903G>T | CA377981154 | HOGA1 | c.747G>T (p.Gln249His) c.157G>T c.258G>T (p.Gln86His) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601904G>A | CA377981157 | HOGA1 | c.748G>A (p.Val250Met) c.158G>A c.259G>A (p.Val87Met) | dbSNP gnomAD v4 |
| 10 | g.97601904G>C | CA377981159 | HOGA1 | c.748G>C (p.Val250Leu) c.158G>C c.259G>C (p.Val87Leu) | |
| 10 | g.97601904G= | CA1930508706 | HOGA1 | c.748G= (p.Val250=) c.158G= c.259G= (p.Val87=) | |
| 10 | g.97601904G>T | CA377981162 | HOGA1 | c.748G>T (p.Val250Leu) c.158G>T c.259G>T (p.Val87Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.97601905T>A | CA377981166 | HOGA1 | c.749T>A (p.Val250Glu) c.159T>A c.260T>A (p.Val87Glu) | |
| 10 | g.97601905T>C | CA377981167 | HOGA1 | c.749T>C (p.Val250Ala) c.159T>C c.260T>C (p.Val87Ala) | |
| 10 | g.97601905T>G | CA377981168 | HOGA1 | c.749T>G (p.Val250Gly) c.159T>G c.260T>G (p.Val87Gly) | |
| 10 | g.97601906G>A | CA212675222 | HOGA1 | c.750G>A (p.Val250=) c.160G>A c.261G>A (p.Val87=) | dbSNP |
| 10 | g.97601906G>C | CA471092400 | HOGA1 | c.750G>C (p.Val250=) c.160G>C c.261G>C (p.Val87=) | |
| 10 | g.97601906G= | CA1930508713 | HOGA1 | c.750G= (p.Val250=) c.160G= c.261G= (p.Val87=) | |
| 10 | g.97601906G>T | CA471092401 | HOGA1 | c.750G>T (p.Val250=) c.160G>T c.261G>T (p.Val87=) | |
| 10 | g.97601907T>A | CA377981172 | HOGA1 | c.751T>A (p.Cys251Ser) c.161T>A c.262T>A (p.Cys88Ser) | |
| 10 | g.97601907T>C | CA377981174 | HOGA1 | c.751T>C (p.Cys251Arg) c.161T>C c.262T>C (p.Cys88Arg) | |
| 10 | g.97601907T>G | CA212675227 | HOGA1 | c.751T>G (p.Cys251Gly) c.161T>G c.262T>G (p.Cys88Gly) | dbSNP |
| 10 | g.97601907T= | CA1930508719 | HOGA1 | c.751T= (p.Cys251=) c.161T= c.262T= (p.Cys88=) | |
| 10 | g.97601908G>A | CA377981191 | HOGA1 | c.752G>A (p.Cys251Tyr) c.162G>A c.263G>A (p.Cys88Tyr) | gnomAD v4 |
| 10 | g.97601908G>C | CA10637006 | HOGA1 | c.752G>C (p.Cys251Ser) c.162G>C c.263G>C (p.Cys88Ser) | ClinVar dbSNP gnomAD v4 |
| 10 | g.97601908G= | CA1930508729 | HOGA1 | c.752G= (p.Cys251=) c.162G= c.263G= (p.Cys88=) | |
| 10 | g.97601908G>T | CA377981179 | HOGA1 | c.752G>T (p.Cys251Phe) c.162G>T c.263G>T (p.Cys88Phe) | |
| 10 | g.97601909C>A | CA377981192 | HOGA1 | c.753C>A (p.Cys251Ter) c.163C>A c.264C>A (p.Cys88Ter) | |
| 10 | g.97601909C>G | CA377981193 | HOGA1 | c.753C>G (p.Cys251Trp) c.163C>G c.264C>G (p.Cys88Trp) | |
| 10 | g.97601909C>T | CA471092402 | HOGA1 | c.753C>T (p.Cys251=) c.163C>T c.264C>T (p.Cys88=) | |
| 10 | g.97601910C>A | CA377981194 | HOGA1 | c.754C>A (p.Gln252Lys) c.164C>A c.265C>A (p.Gln89Lys) | |
| 10 | g.97601910C= | CA1930508732 | HOGA1 | c.754C= (p.Gln252=) c.164C= c.265C= (p.Gln89=) | |
| 10 | g.97601910C>G | CA377981196 | HOGA1 | c.754C>G (p.Gln252Glu) c.164C>G c.265C>G (p.Gln89Glu) | |
| 10 | g.97601910C>T | CA377981200 | HOGA1 | c.754C>T (p.Gln252Ter) c.164C>T c.265C>T (p.Gln89Ter) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.97601911A>C | CA377981202 | HOGA1 | c.755A>C (p.Gln252Pro) c.165A>C c.266A>C (p.Gln89Pro) | |
| 10 | g.97601911A>G | CA377981204 | HOGA1 | c.755A>G (p.Gln252Arg) c.165A>G c.266A>G (p.Gln89Arg) | |
| 10 | g.97601911A>T | CA377981206 | HOGA1 | c.755A>T (p.Gln252Leu) c.165A>T c.266A>T (p.Gln89Leu) | |
| 10 | g.97601912G>A | CA471092403 | HOGA1 | c.756G>A (p.Gln252=) c.166G>A c.267G>A (p.Gln89=) | dbSNP gnomAD v4 |
| 10 | g.97601912G>C | CA377981210 | HOGA1 | c.756G>C (p.Gln252His) c.166G>C c.267G>C (p.Gln89His) | |
| 10 | g.97601912G= | CA1930508736 | HOGA1 | c.756G= (p.Gln252=) c.166G= c.267G= (p.Gln89=) | |
| 10 | g.97601912G>T | CA377981213 | HOGA1 | c.756G>T (p.Gln252His) c.166G>T c.267G>T (p.Gln89His) | |
| 10 | g.97601913C>A | CA377981219 | HOGA1 | c.757C>A (p.Leu253Met) c.167C>A c.268C>A (p.Leu90Met) | |
| 10 | g.97601913C>G | CA377981224 | HOGA1 | c.757C>G (p.Leu253Val) c.167C>G c.268C>G (p.Leu90Val) | |
| 10 | g.97601913C>T | CA471092404 | HOGA1 | c.757C>T (p.Leu253=) c.167C>T c.268C>T (p.Leu90=) | |
| 10 | g.97601914T>A | CA377981238 | HOGA1 | c.758T>A (p.Leu253Gln) c.168T>A c.269T>A (p.Leu90Gln) | |
| 10 | g.97601914T>C | CA377981234 | HOGA1 | c.758T>C (p.Leu253Pro) c.168T>C c.269T>C (p.Leu90Pro) | gnomAD v4 |
| 10 | g.97601914T>G | CA377981231 | HOGA1 | c.758T>G (p.Leu253Arg) c.168T>G c.269T>G (p.Leu90Arg) | |
| 10 | g.97601915G>A | CA471092407 | HOGA1 | c.759G>A (p.Leu253=) c.169G>A c.270G>A (p.Leu90=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601915G>C | CA471092406 | HOGA1 | c.759G>C (p.Leu253=) c.169G>C c.270G>C (p.Leu90=) | |
| 10 | g.97601915G= | CA1930508741 | HOGA1 | c.759G= (p.Leu253=) c.169G= c.270G= (p.Leu90=) | |
| 10 | g.97601915G>T | CA471092405 | HOGA1 | c.759G>T (p.Leu253=) c.169G>T c.270G>T (p.Leu90=) | |
| 10 | g.97601916G>A | CA377981243 | HOGA1 | c.760G>A (p.Glu254Lys) c.170G>A c.271G>A (p.Glu91Lys) | |
| 10 | g.97601916G>C | CA377981247 | HOGA1 | c.760G>C (p.Glu254Gln) c.170G>C c.271G>C (p.Glu91Gln) | gnomAD v4 |
| 10 | g.97601916G>T | CA377981251 | HOGA1 | c.760G>T (p.Glu254Ter) c.170G>T c.271G>T (p.Glu91Ter) | |
| 10 | g.97601917A>C | CA377981252 | HOGA1 | c.761A>C (p.Glu254Ala) c.171A>C c.272A>C (p.Glu91Ala) | |
| 10 | g.97601917A>G | CA377981253 | HOGA1 | c.761A>G (p.Glu254Gly) c.171A>G c.272A>G (p.Glu91Gly) | |
| 10 | g.97601917A>T | CA377981254 | HOGA1 | c.761A>T (p.Glu254Val) c.171A>T c.272A>T (p.Glu91Val) | gnomAD v4 |
| 10 | g.97601918G>A | CA471092408 | HOGA1 | c.762G>A (p.Glu254=) c.172G>A c.273G>A (p.Glu91=) | |
| 10 | g.97601918G>C | CA377981255 | HOGA1 | c.762G>C (p.Glu254Asp) c.172G>C c.273G>C (p.Glu91Asp) | |
| 10 | g.97601918G>T | CA377981257 | HOGA1 | c.762G>T (p.Glu254Asp) c.172G>T c.273G>T (p.Glu91Asp) | |
| 10 | g.97601919C>A | CA471092409 | HOGA1 | c.763C>A (p.Arg255=) c.173C>A c.274C>A (p.Arg92=) | ClinVar dbSNP gnomAD v4 |
| 10 | g.97601919C= | CA1930508747 | HOGA1 | c.763C= (p.Arg255=) c.173C= c.274C= (p.Arg92=) | |
| 10 | g.97601919C>G | CA377981261 | HOGA1 | c.763C>G (p.Arg255Gly) c.173C>G c.274C>G (p.Arg92Gly) | |
| 10 | g.97601919C>T | CA203961 | HOGA1 | c.763C>T (p.Arg255Ter) c.173C>T c.274C>T (p.Arg92Ter) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601920G>A | CA5634233 | HOGA1 | c.764G>A (p.Arg255Gln) c.174G>A c.275G>A (p.Arg92Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601920G>C | CA377981273 | HOGA1 | c.764G>C (p.Arg255Pro) c.174G>C c.275G>C (p.Arg92Pro) | gnomAD v4 |
| 10 | g.97601920G= | CA1930508753 | HOGA1 | c.764G= (p.Arg255=) c.174G= c.275G= (p.Arg92=) | |
| 10 | g.97601920G>T | CA377981278 | HOGA1 | c.764G>T (p.Arg255Leu) c.174G>T c.275G>T (p.Arg92Leu) | gnomAD v4 |
| 10 | g.97601921A>C | CA471092410 | HOGA1 | c.765A>C (p.Arg255=) c.175A>C c.276A>C (p.Arg92=) | |
| 10 | g.97601921A>G | CA471092412 | HOGA1 | c.765A>G (p.Arg255=) c.175A>G c.276A>G (p.Arg92=) | |
| 10 | g.97601921A>T | CA471092411 | HOGA1 | c.765A>T (p.Arg255=) c.175A>T c.276A>T (p.Arg92=) | |
| 10 | g.97601922C>A | CA377981292 | HOGA1 | c.766C>A (p.Leu256Met) c.176C>A c.277C>A (p.Leu93Met) | |
| 10 | g.97601922C>G | CA377981280 | HOGA1 | c.766C>G (p.Leu256Val) c.176C>G c.277C>G (p.Leu93Val) | |
| 10 | g.97601922C>T | CA471092413 | HOGA1 | c.766C>T (p.Leu256=) c.176C>T c.277C>T (p.Leu93=) | gnomAD v4 |
| 10 | g.97601922_97601924delinsCTG | CA1930508759 | HOGA1 | c.766_768delinsCTG (p.Leu256=) c.176_178delinsCTG c.277_279delinsCTG (p.Leu93=) | |
| 10 | g.97601923T>A | CA377981296 | HOGA1 | c.767T>A (p.Leu256Gln) c.177T>A c.278T>A (p.Leu93Gln) | |
| 10 | g.97601923T>C | CA377981297 | HOGA1 | c.767T>C (p.Leu256Pro) c.177T>C c.278T>C (p.Leu93Pro) | |
| 10 | g.97601923T>G | CA377981298 | HOGA1 | c.767T>G (p.Leu256Arg) c.177T>G c.278T>G (p.Leu93Arg) | |
| 10 | g.97601925_97601926del | CA5634234 | HOGA1 | c.769_770del (p.Cys257LeufsTer17) c.179_180del c.280_281del (p.Cys94LeufsTer17) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.97601924G>A | CA471092416 | HOGA1 | c.768G>A (p.Leu256=) c.178G>A c.279G>A (p.Leu93=) | |
| 10 | g.97601924G>C | CA471092414 | HOGA1 | c.768G>C (p.Leu256=) c.178G>C c.279G>C (p.Leu93=) | |
| 10 | g.97601924G>T | CA471092415 | HOGA1 | c.768G>T (p.Leu256=) c.178G>T c.279G>T (p.Leu93=) | ClinVar |
| 10 | g.97601925T>A | CA377981301 | HOGA1 | c.769T>A (p.Cys257Ser) c.179T>A c.280T>A (p.Cys94Ser) | |
| 10 | g.97601925T>C | CA377981304 | HOGA1 | c.769T>C (p.Cys257Arg) c.179T>C c.280T>C (p.Cys94Arg) | |
| 10 | g.97601925T>G | CA113818 | HOGA1 | c.769T>G (p.Cys257Gly) c.179T>G c.280T>G (p.Cys94Gly) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601925T= | CA1930508768 | HOGA1 | c.769T= (p.Cys257=) c.179T= c.280T= (p.Cys94=) | |
| 10 | g.97601926G>A | CA377981322 | HOGA1 | c.770G>A (p.Cys257Tyr) c.180G>A c.281G>A (p.Cys94Tyr) | ClinVar dbSNP COSMIC COSMIC |
| 10 | g.97601926G>C | CA377981318 | HOGA1 | c.770G>C (p.Cys257Ser) c.180G>C c.281G>C (p.Cys94Ser) | |
| 10 | g.97601926G>T | CA377981319 | HOGA1 | c.770G>T (p.Cys257Phe) c.180G>T c.281G>T (p.Cys94Phe) | |
| 10 | g.97601927C>A | CA377981323 | HOGA1 | c.771C>A (p.Cys257Ter) c.181C>A c.282C>A (p.Cys94Ter) | |
| 10 | g.97601927C= | CA1930508776 | HOGA1 | c.771C= (p.Cys257=) c.181C= c.282C= (p.Cys94=) | |
| 10 | g.97601927C>G | CA377981326 | HOGA1 | c.771C>G (p.Cys257Trp) c.181C>G c.282C>G (p.Cys94Trp) | |
| 10 | g.97601927C>T | CA5634235 | HOGA1 | c.771C>T (p.Cys257=) c.181C>T c.282C>T (p.Cys94=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601928T>A | CA377981332 | HOGA1 | c.772T>A (p.Cys258Ser) c.182T>A c.283T>A (p.Cys95Ser) | |
| 10 | g.97601928T>C | CA377981340 | HOGA1 | c.772T>C (p.Cys258Arg) c.182T>C c.283T>C (p.Cys95Arg) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601928T>G | CA377981342 | HOGA1 | c.772T>G (p.Cys258Gly) c.182T>G c.283T>G (p.Cys95Gly) | |
| 10 | g.97601928T= | CA1930508785 | HOGA1 | c.772T= (p.Cys258=) c.182T= c.283T= (p.Cys95=) | |
| 10 | g.97601928_97601934delinsTGCACGG | CA1930508783 | HOGA1 | c.772_778delinsTGCACGG (p.Cys258=) c.182_188delinsTGCACGG c.283_289delinsTGCACGG (p.Cys95=) | |
| 10 | g.97601929G>A | CA377981347 | HOGA1 | c.773G>A (p.Cys258Tyr) c.183G>A c.284G>A (p.Cys95Tyr) | |
| 10 | g.97601929G>C | CA377981354 | HOGA1 | c.773G>C (p.Cys258Ser) c.183G>C c.284G>C (p.Cys95Ser) | |
| 10 | g.97601929G>T | CA377981349 | HOGA1 | c.773G>T (p.Cys258Phe) c.183G>T c.284G>T (p.Cys95Phe) | gnomAD v4 |
| 10 | g.97601930_97601935del | CA1930508787 | HOGA1 | c.774_779del (p.Cys258_Gly260delinsTrp) c.184_189del c.285_290del (p.Cys95_Gly97delinsTrp) | dbSNP |
| 10 | g.97601930C>A | CA377981357 | HOGA1 | c.774C>A (p.Cys258Ter) c.184C>A c.285C>A (p.Cys95Ter) | gnomAD v4 |
| 10 | g.97601930C>G | CA377981361 | HOGA1 | c.774C>G (p.Cys258Trp) c.184C>G c.285C>G (p.Cys95Trp) | |
| 10 | g.97601930C>T | CA471092417 | HOGA1 | c.774C>T (p.Cys258=) c.184C>T c.285C>T (p.Cys95=) | ClinVar |
| 10 | g.97601931A= | CA1930508790 | HOGA1 | c.775A= (p.Thr259=) c.185A= c.286A= (p.Thr96=) | |
| 10 | g.97601931A>C | CA377981365 | HOGA1 | c.775A>C (p.Thr259Pro) c.185A>C c.286A>C (p.Thr96Pro) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.97601931A>G | CA377981369 | HOGA1 | c.775A>G (p.Thr259Ala) c.185A>G c.286A>G (p.Thr96Ala) | gnomAD v4 |
| 10 | g.97601931A>T | CA377981375 | HOGA1 | c.775A>T (p.Thr259Ser) c.185A>T c.286A>T (p.Thr96Ser) | |
| 10 | g.97601932C>A | CA377981379 | HOGA1 | c.776C>A (p.Thr259Lys) c.186C>A c.287C>A (p.Thr96Lys) | |
| 10 | g.97601932C= | CA1930508800 | HOGA1 | c.776C= (p.Thr259=) c.186C= c.287C= (p.Thr96=) | |
| 10 | g.97601932C>G | CA212675281 | HOGA1 | c.776C>G (p.Thr259Arg) c.186C>G c.287C>G (p.Thr96Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601932C>T | CA5634236 | HOGA1 | c.776C>T (p.Thr259Met) c.186C>T c.287C>T (p.Thr96Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601933G>A | CA5634237 | HOGA1 | c.777G>A (p.Thr259=) c.187G>A c.288G>A (p.Thr96=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601933G>C | CA471092418 | HOGA1 | c.777G>C (p.Thr259=) c.187G>C c.288G>C (p.Thr96=) | gnomAD v4 |
| 10 | g.97601933G= | CA1930508809 | HOGA1 | c.777G= (p.Thr259=) c.187G= c.288G= (p.Thr96=) | |
| 10 | g.97601933G>T | CA471092419 | HOGA1 | c.777G>T (p.Thr259=) c.187G>T c.288G>T (p.Thr96=) | |
| 10 | g.97601934G>A | CA212675289 | HOGA1 | c.778G>A (p.Gly260Arg) c.188G>A c.289G>A (p.Gly97Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 10 | g.97601934G>C | CA377981399 | HOGA1 | c.778G>C (p.Gly260Arg) c.188G>C c.289G>C (p.Gly97Arg) | |
| 10 | g.97601934G= | CA1930508820 | HOGA1 | c.778G= (p.Gly260=) c.188G= c.289G= (p.Gly97=) | |
| 10 | g.97601934G>T | CA377981403 | HOGA1 | c.778G>T (p.Gly260Trp) c.188G>T c.289G>T (p.Gly97Trp) | |
| 10 | g.97601935G>A | CA377981408 | HOGA1 | c.779G>A (p.Gly260Glu) c.189G>A c.290G>A (p.Gly97Glu) | dbSNP |
| 10 | g.97601935G>C | CA377981415 | HOGA1 | c.779G>C (p.Gly260Ala) c.189G>C c.290G>C (p.Gly97Ala) | |
| 10 | g.97601935G= | CA1930508828 | HOGA1 | c.779G= (p.Gly260=) c.189G= c.290G= (p.Gly97=) | |
| 10 | g.97601935G>T | CA377981411 | HOGA1 | c.779G>T (p.Gly260Val) c.189G>T c.290G>T (p.Gly97Val) | COSMIC COSMIC |
| 10 | g.97601936G>A | CA5634239 | HOGA1 | c.780G>A (p.Gly260=) c.190G>A c.291G>A (p.Gly97=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601936G>C | CA5634238 | HOGA1 | c.780G>C (p.Gly260=) c.190G>C c.291G>C (p.Gly97=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601936G= | CA1930508835 | HOGA1 | c.780G= (p.Gly260=) c.190G= c.291G= (p.Gly97=) | |
| 10 | g.97601936G>T | CA471092420 | HOGA1 | c.780G>T (p.Gly260=) c.190G>T c.291G>T (p.Gly97=) | |
| 10 | g.97601937C>A | CA212675306 | HOGA1 | c.781C>A (p.Gln261Lys) c.191C>A c.292C>A (p.Gln98Lys) | dbSNP gnomAD v4 |
| 10 | g.97601937C= | CA1930508841 | HOGA1 | c.781C= (p.Gln261=) c.191C= c.292C= (p.Gln98=) | |
| 10 | g.97601937C>G | CA377981434 | HOGA1 | c.781C>G (p.Gln261Glu) c.191C>G c.292C>G (p.Gln98Glu) | |
| 10 | g.97601937C>T | CA377981438 | HOGA1 | c.781C>T (p.Gln261Ter) c.191C>T c.292C>T (p.Gln98Ter) | dbSNP |
| 10 | g.97601938A>C | CA377981444 | HOGA1 | c.782A>C (p.Gln261Pro) c.192A>C c.293A>C (p.Gln98Pro) | |
| 10 | g.97601938A>G | CA377981446 | HOGA1 | c.782A>G (p.Gln261Arg) c.192A>G c.293A>G (p.Gln98Arg) | |
| 10 | g.97601938A>T | CA377981454 | HOGA1 | c.782A>T (p.Gln261Leu) c.192A>T c.293A>T (p.Gln98Leu) | |
| 10 | g.97601939A= | CA1930508847 | HOGA1 | c.783A= (p.Gln261=) c.193A= c.294A= (p.Gln98=) | |
| 10 | g.97601939A>C | CA377981460 | HOGA1 | c.783A>C (p.Gln261His) c.193A>C c.294A>C (p.Gln98His) | |
| 10 | g.97601939A>G | CA471092421 | HOGA1 | c.783A>G (p.Gln261=) c.193A>G c.294A>G (p.Gln98=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601939A>T | CA377981464 | HOGA1 | c.783A>T (p.Gln261His) c.193A>T c.294A>T (p.Gln98His) | |
| 10 | g.97601940T>A | CA377981471 | HOGA1 | c.784T>A (p.Trp262Arg) c.194T>A c.295T>A (p.Trp99Arg) | gnomAD v4 |
| 10 | g.97601940T>C | CA5634240 | HOGA1 | c.784T>C (p.Trp262Arg) c.194T>C c.295T>C (p.Trp99Arg) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.97601940T>G | CA377981478 | HOGA1 | c.784T>G (p.Trp262Gly) c.194T>G c.295T>G (p.Trp99Gly) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601940T= | CA1930508852 | HOGA1 | c.784T= (p.Trp262=) c.194T= c.295T= (p.Trp99=) | |
| 10 | g.97601941G>A | CA5634241 | HOGA1 | c.785G>A (p.Trp262Ter) c.195G>A c.296G>A (p.Trp99Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601941G>C | CA377981482 | HOGA1 | c.785G>C (p.Trp262Ser) c.195G>C c.296G>C (p.Trp99Ser) | |
| 10 | g.97601941G= | CA1930508858 | HOGA1 | c.785G= (p.Trp262=) c.195G= c.296G= (p.Trp99=) | |
| 10 | g.97601941G>T | CA377981485 | HOGA1 | c.785G>T (p.Trp262Leu) c.195G>T c.296G>T (p.Trp99Leu) | |
| 10 | g.97601942G>A | CA377981492 | HOGA1 | c.786G>A (p.Trp262Ter) c.196G>A c.297G>A (p.Trp99Ter) | |
| 10 | g.97601942G>C | CA377981494 | HOGA1 | c.786G>C (p.Trp262Cys) c.196G>C c.297G>C (p.Trp99Cys) | |
| 10 | g.97601942G>T | CA377981498 | HOGA1 | c.786G>T (p.Trp262Cys) c.196G>T c.297G>T (p.Trp99Cys) | |
| 10 | g.97601943G>A | CA377981504 | HOGA1 | c.787G>A (p.Glu263Lys) c.197G>A c.298G>A (p.Glu100Lys) | gnomAD v4 |
| 10 | g.97601943G>C | CA377981508 | HOGA1 | c.787G>C (p.Glu263Gln) c.197G>C c.298G>C (p.Glu100Gln) | |
| 10 | g.97601943G= | CA1930508863 | HOGA1 | c.787G= (p.Glu263=) c.197G= c.298G= (p.Glu100=) | |
| 10 | g.97601943G>T | CA5634242 | HOGA1 | c.787G>T (p.Glu263Ter) c.197G>T c.298G>T (p.Glu100Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.97601944A>C | CA377981513 | HOGA1 | c.788A>C (p.Glu263Ala) c.198A>C c.299A>C (p.Glu100Ala) | |
| 10 | g.97601944A>G | CA377981518 | HOGA1 | c.788A>G (p.Glu263Gly) c.198A>G c.299A>G (p.Glu100Gly) | |
| 10 | g.97601944A>T | CA377981525 | HOGA1 | c.788A>T (p.Glu263Val) c.198A>T c.299A>T (p.Glu100Val) | |
| 10 | g.97601945A= | CA1930508868 | HOGA1 | c.789A= (p.Glu263=) c.199A= c.300A= (p.Glu100=) | |
| 10 | g.97601945A>C | CA377981530 | HOGA1 | c.789A>C (p.Glu263Asp) c.199A>C c.300A>C (p.Glu100Asp) | |
| 10 | g.97601945A>G | CA471092422 | HOGA1 | c.789A>G (p.Glu263=) c.199A>G c.300A>G (p.Glu100=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.97601945A>T | CA377981533 | HOGA1 | c.789A>T (p.Glu263Asp) c.199A>T c.300A>T (p.Glu100Asp) | |
| 10 | g.97601946G>A | CA377981538 | HOGA1 | c.790G>A (p.Asp264Asn) c.200G>A c.301G>A (p.Asp101Asn) | |
| 10 | g.97601946G>C | CA377981545 | HOGA1 | c.790G>C (p.Asp264His) c.200G>C c.301G>C (p.Asp101His) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.97601946G= | CA1930508872 | HOGA1 | c.790G= (p.Asp264=) c.200G= c.301G= (p.Asp101=) | |
| 10 | g.97601946G>T | CA377981541 | HOGA1 | c.790G>T (p.Asp264Tyr) c.200G>T c.301G>T (p.Asp101Tyr) | |
| 10 | g.97601947A= | CA1930508878 | HOGA1 | c.791A= (p.Asp264=) c.201A= c.302A= (p.Asp101=) | |
| 10 | g.97601947A>C | CA377981551 | HOGA1 | c.791A>C (p.Asp264Ala) c.201A>C c.302A>C (p.Asp101Ala) | |
| 10 | g.97601947A>G | CA377981554 | HOGA1 | c.791A>G (p.Asp264Gly) c.201A>G c.302A>G (p.Asp101Gly) | |
| 10 | g.97601947A>T | CA5634243 | HOGA1 | c.791A>T (p.Asp264Val) c.201A>T c.302A>T (p.Asp101Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601948T>A | CA377981569 | HOGA1 | c.792T>A (p.Asp264Glu) c.202T>A c.303T>A (p.Asp101Glu) | |
| 10 | g.97601948T>C | CA471092423 | HOGA1 | c.792T>C (p.Asp264=) c.202T>C c.303T>C (p.Asp101=) | |
| 10 | g.97601948T>G | CA377981573 | HOGA1 | c.792T>G (p.Asp264Glu) c.202T>G c.303T>G (p.Asp101Glu) | |
| 10 | g.97601949G>A | CA377981577 | HOGA1 | c.793G>A (p.Ala265Thr) c.203G>A c.304G>A (p.Ala102Thr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.97601949G>C | CA377981581 | HOGA1 | c.793G>C (p.Ala265Pro) c.203G>C c.304G>C (p.Ala102Pro) | |
| 10 | g.97601949G= | CA1930508885 | HOGA1 | c.793G= (p.Ala265=) c.203G= c.304G= (p.Ala102=) | |
| 10 | g.97601949G>T | CA377981584 | HOGA1 | c.793G>T (p.Ala265Ser) c.203G>T c.304G>T (p.Ala102Ser) | COSMIC COSMIC |
| 10 | g.97601950C>A | CA377981589 | HOGA1 | c.794C>A (p.Ala265Asp) c.204C>A c.305C>A (p.Ala102Asp) | |
| 10 | g.97601950C>G | CA377981591 | HOGA1 | c.794C>G (p.Ala265Gly) c.204C>G c.305C>G (p.Ala102Gly) | |
| 10 | g.97601950C>T | CA377981596 | HOGA1 | c.794C>T (p.Ala265Val) c.204C>T c.305C>T (p.Ala102Val) | gnomAD v4 |
| 10 | g.97601951C>A | CA5634244 | HOGA1 | c.795C>A (p.Ala265=) c.205C>A c.306C>A (p.Ala102=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601951C= | CA1930508891 | HOGA1 | c.795C= (p.Ala265=) c.205C= c.306C= (p.Ala102=) | |
| 10 | g.97601951C>G | CA471092424 | HOGA1 | c.795C>G (p.Ala265=) c.205C>G c.306C>G (p.Ala102=) | |
| 10 | g.97601951C>T | CA5634245 | HOGA1 | c.795C>T (p.Ala265=) c.205C>T c.306C>T (p.Ala102=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 10 | g.97601952C>A | CA377981619 | HOGA1 | c.796C>A (p.Gln266Lys) c.206C>A c.307C>A (p.Gln103Lys) | |
| 10 | g.97601952C= | CA1930508900 | HOGA1 | c.796C= (p.Gln266=) c.206C= c.307C= (p.Gln103=) | |
| 10 | g.97601952C>G | CA377981618 | HOGA1 | c.796C>G (p.Gln266Glu) c.206C>G c.307C>G (p.Gln103Glu) | |
| 10 | g.97601952C>T | CA5634246 | HOGA1 | c.796C>T (p.Gln266Ter) c.206C>T c.307C>T (p.Gln103Ter) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.97601953A>C | CA377981620 | HOGA1 | c.797A>C (p.Gln266Pro) c.207A>C c.308A>C (p.Gln103Pro) | |
| 10 | g.97601953A>G | CA377981621 | HOGA1 | c.797A>G (p.Gln266Arg) c.207A>G c.308A>G (p.Gln103Arg) | |
| 10 | g.97601953A>T | CA377981623 | HOGA1 | c.797A>T (p.Gln266Leu) c.207A>T c.308A>T (p.Gln103Leu) | |
| 10 | g.97601954G>A | CA471092425 | HOGA1 | c.798G>A (p.Gln266=) c.208G>A c.309G>A (p.Gln103=) | |
| 10 | g.97601954G>C | CA377981627 | HOGA1 | c.798G>C (p.Gln266His) c.208G>C c.309G>C (p.Gln103His) | |
| 10 | g.97601954G>T | CA377981630 | HOGA1 | c.798G>T (p.Gln266His) c.208G>T c.309G>T (p.Gln103His) | |
| 10 | g.97601955A>C | CA377981634 | HOGA1 | c.799A>C (p.Lys267Gln) c.209A>C c.310A>C (p.Lys104Gln) | |
| 10 | g.97601955A>G | CA377981637 | HOGA1 | c.799A>G (p.Lys267Glu) c.209A>G c.310A>G (p.Lys104Glu) | |
| 10 | g.97601955A>T | CA377981638 | HOGA1 | c.799A>T (p.Lys267Ter) c.209A>T c.310A>T (p.Lys104Ter) | |
| 10 | g.97601956A>C | CA377981642 | HOGA1 | c.800A>C (p.Lys267Thr) c.210A>C c.311A>C (p.Lys104Thr) | gnomAD v4 |
| 10 | g.97601956A>G | CA377981645 | HOGA1 | c.800A>G (p.Lys267Arg) c.210A>G c.311A>G (p.Lys104Arg) | |
| 10 | g.97601956A>T | CA377981647 | HOGA1 | c.800A>T (p.Lys267Ile) c.210A>T c.311A>T (p.Lys104Ile) | |
| 10 | g.97601957A>C | CA377981652 | HOGA1 | c.801A>C (p.Lys267Asn) c.211A>C c.312A>C (p.Lys104Asn) | |
| 10 | g.97601957A>G | CA471092427 | HOGA1 | c.801A>G (p.Lys267=) c.211A>G c.312A>G (p.Lys104=) | |
| 10 | g.97601957A>T | CA377981654 | HOGA1 | c.801A>T (p.Lys267Asn) c.211A>T c.312A>T (p.Lys104Asn) | |
| 10 | g.97601957_97601960delinsACTG | CA1930508907 | HOGA1 | c.801_804delinsACTG (p.Lys267=) c.211_214delinsACTG c.312_315delinsACTG (p.Lys104=) | |
| 10 | g.97601958C>A | CA377981666 | HOGA1 | c.802C>A (p.Leu268Met) c.212C>A c.313C>A (p.Leu105Met) | |
| 10 | g.97601958C= | CA1930508918 | HOGA1 | c.802C= (p.Leu268=) c.212C= c.313C= (p.Leu105=) | |
| 10 | g.97601958C>G | CA377981663 | HOGA1 | c.802C>G (p.Leu268Val) c.212C>G c.313C>G (p.Leu105Val) | |
| 10 | g.97601958C>T | CA5634247 | HOGA1 | c.802C>T (p.Leu268=) c.212C>T c.313C>T (p.Leu105=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601959_97601961del | CA203984 | HOGA1 | c.803_805del (p.Leu268del) c.213_215del c.314_316del (p.Leu105del) | ClinVar dbSNP gnomAD v4 |
| 10 | g.97601959T>A | CA377981669 | HOGA1 | c.803T>A (p.Leu268Gln) c.213T>A c.314T>A (p.Leu105Gln) | |
| 10 | g.97601959T>C | CA377981673 | HOGA1 | c.803T>C (p.Leu268Pro) c.213T>C c.314T>C (p.Leu105Pro) | |
| 10 | g.97601959T>G | CA377981676 | HOGA1 | c.803T>G (p.Leu268Arg) c.213T>G c.314T>G (p.Leu105Arg) | |
| 10 | g.97601960G>A | CA471092428 | HOGA1 | c.804G>A (p.Leu268=) c.214G>A c.315G>A (p.Leu105=) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.97601960G>C | CA471092429 | HOGA1 | c.804G>C (p.Leu268=) c.214G>C c.315G>C (p.Leu105=) | |
| 10 | g.97601960G= | CA1930508929 | HOGA1 | c.804G= (p.Leu268=) c.214G= c.315G= (p.Leu105=) | |
| 10 | g.97601960G>T | CA471092430 | HOGA1 | c.804G>T (p.Leu268=) c.214G>T c.315G>T (p.Leu105=) | |
| 10 | g.97601961C>A | CA377981680 | HOGA1 | c.805C>A (p.Gln269Lys) c.215C>A c.316C>A (p.Gln106Lys) | |
| 10 | g.97601961C>G | CA377981684 | HOGA1 | c.805C>G (p.Gln269Glu) c.215C>G c.316C>G (p.Gln106Glu) | |
| 10 | g.97601961C>T | CA377981690 | HOGA1 | c.805C>T (p.Gln269Ter) c.215C>T c.316C>T (p.Gln106Ter) | |
| 10 | g.97601962A= | CA1930508934 | HOGA1 | c.806A= (p.Gln269=) c.216A= c.317A= (p.Gln106=) | |
| 10 | g.97601962A>C | CA377981704 | HOGA1 | c.806A>C (p.Gln269Pro) c.216A>C c.317A>C (p.Gln106Pro) | |
| 10 | g.97601962A>G | CA377981696 | HOGA1 | c.806A>G (p.Gln269Arg) c.216A>G c.317A>G (p.Gln106Arg) | dbSNP gnomAD v2 |
| 10 | g.97601962A>T | CA377981699 | HOGA1 | c.806A>T (p.Gln269Leu) c.216A>T c.317A>T (p.Gln106Leu) | gnomAD v4 |
| 10 | g.97601963G>A | CA471092431 | HOGA1 | c.807G>A (p.Gln269=) c.217G>A c.318G>A (p.Gln106=) | ClinVar dbSNP |
| 10 | g.97601963G>C | CA377981708 | HOGA1 | c.807G>C (p.Gln269His) c.217G>C c.318G>C (p.Gln106His) | |
| 10 | g.97601963G>T | CA377981711 | HOGA1 | c.807G>T (p.Gln269His) c.217G>T c.318G>T (p.Gln106His) | |
| 10 | g.97601964C>A | CA377981717 | HOGA1 | c.808C>A (p.His270Asn) c.218C>A c.319C>A (p.His107Asn) | |
| 10 | g.97601964C>G | CA377981718 | HOGA1 | c.808C>G (p.His270Asp) c.218C>G c.319C>G (p.His107Asp) | |
| 10 | g.97601964C>T | CA377981719 | HOGA1 | c.808C>T (p.His270Tyr) c.218C>T c.319C>T (p.His107Tyr) | gnomAD v4 |
| 10 | g.97601965A>C | CA377981720 | HOGA1 | c.809A>C (p.His270Pro) c.219A>C c.320A>C (p.His107Pro) | |
| 10 | g.97601965A>G | CA377981725 | HOGA1 | c.809A>G (p.His270Arg) c.219A>G c.320A>G (p.His107Arg) | |
| 10 | g.97601965A>T | CA377981721 | HOGA1 | c.809A>T (p.His270Leu) c.219A>T c.320A>T (p.His107Leu) | |
| 10 | g.97601966C>A | CA212675358 | HOGA1 | c.810C>A (p.His270Gln) c.220C>A c.321C>A (p.His107Gln) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601966C= | CA1930508939 | HOGA1 | c.810C= (p.His270=) c.220C= c.321C= (p.His107=) | |
| 10 | g.97601966C>G | CA377981730 | HOGA1 | c.810C>G (p.His270Gln) c.220C>G c.321C>G (p.His107Gln) | |
| 10 | g.97601966C>T | CA471092436 | HOGA1 | c.810C>T (p.His270=) c.220C>T c.321C>T (p.His107=) | |
| 10 | g.97601967C>A | CA377981732 | HOGA1 | c.811C>A (p.Arg271Ser) c.221C>A c.322C>A (p.Arg108Ser) | dbSNP |
| 10 | g.97601967C= | CA1930508943 | HOGA1 | c.811C= (p.Arg271=) c.221C= c.322C= (p.Arg108=) | |
| 10 | g.97601967C>G | CA377981735 | HOGA1 | c.811C>G (p.Arg271Gly) c.221C>G c.322C>G (p.Arg108Gly) | gnomAD v4 |
| 10 | g.97601967C>T | CA5634248 | HOGA1 | c.811C>T (p.Arg271Cys) c.221C>T c.322C>T (p.Arg108Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601968G>A | CA5634249 | HOGA1 | c.812G>A (p.Arg271His) c.222G>A c.323G>A (p.Arg108His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601968G>C | CA377981736 | HOGA1 | c.812G>C (p.Arg271Pro) c.222G>C c.323G>C (p.Arg108Pro) | |
| 10 | g.97601968G= | CA1930508949 | HOGA1 | c.812G= (p.Arg271=) c.222G= c.323G= (p.Arg108=) | |
| 10 | g.97601968G>T | CA377981737 | HOGA1 | c.812G>T (p.Arg271Leu) c.222G>T c.323G>T (p.Arg108Leu) | |
| 10 | g.97601969C>A | CA471092437 | HOGA1 | c.813C>A (p.Arg271=) c.223C>A c.324C>A (p.Arg108=) | |
| 10 | g.97601969C>G | CA471092439 | HOGA1 | c.813C>G (p.Arg271=) c.223C>G c.324C>G (p.Arg108=) | |
| 10 | g.97601969C>T | CA471092438 | HOGA1 | c.813C>T (p.Arg271=) c.223C>T c.324C>T (p.Arg108=) | |
| 10 | g.97601970C>A | CA377981741 | HOGA1 | c.814C>A (p.Leu272Ile) c.224C>A c.325C>A (p.Leu109Ile) | |
| 10 | g.97601970C>G | CA377981743 | HOGA1 | c.814C>G (p.Leu272Val) c.224C>G c.325C>G (p.Leu109Val) | ClinVar |
| 10 | g.97601970C>T | CA377981744 | HOGA1 | c.814C>T (p.Leu272Phe) c.224C>T c.325C>T (p.Leu109Phe) | gnomAD v4 |
| 10 | g.97601971T>A | CA377981747 | HOGA1 | c.815T>A (p.Leu272His) c.225T>A c.326T>A (p.Leu109His) | |
| 10 | g.97601971T>C | CA377981753 | HOGA1 | c.815T>C (p.Leu272Pro) c.225T>C c.326T>C (p.Leu109Pro) | |
| 10 | g.97601971T>G | CA377981750 | HOGA1 | c.815T>G (p.Leu272Arg) c.225T>G c.326T>G (p.Leu109Arg) | |
| 10 | g.97601972C>A | CA471092442 | HOGA1 | c.816C>A (p.Leu272=) c.226C>A c.327C>A (p.Leu109=) | |
| 10 | g.97601972C>G | CA471092443 | HOGA1 | c.816C>G (p.Leu272=) c.226C>G c.327C>G (p.Leu109=) | |
| 10 | g.97601972C>T | CA471092444 | HOGA1 | c.816C>T (p.Leu272=) c.226C>T c.327C>T (p.Leu109=) | |
| 10 | g.97601973A>C | CA377981757 | HOGA1 | c.817A>C (p.Ile273Leu) c.227A>C c.328A>C (p.Ile110Leu) | |
| 10 | g.97601973A>G | CA377981765 | HOGA1 | c.817A>G (p.Ile273Val) c.227A>G c.328A>G (p.Ile110Val) | |
| 10 | g.97601973A>T | CA377981763 | HOGA1 | c.817A>T (p.Ile273Phe) c.227A>T c.328A>T (p.Ile110Phe) | |
| 10 | g.97601974T>A | CA377981768 | HOGA1 | c.818T>A (p.Ile273Asn) c.228T>A c.329T>A (p.Ile110Asn) | |
| 10 | g.97601974T>C | CA5634250 | HOGA1 | c.818T>C (p.Ile273Thr) c.228T>C c.329T>C (p.Ile110Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601974T>G | CA377981771 | HOGA1 | c.818T>G (p.Ile273Ser) c.228T>G c.329T>G (p.Ile110Ser) | gnomAD v4 |
| 10 | g.97601974T= | CA1930508953 | HOGA1 | c.818T= (p.Ile273=) c.228T= c.329T= (p.Ile110=) | |
| 10 | g.97601975T>A | CA471092445 | HOGA1 | c.819T>A (p.Ile273=) c.229T>A c.330T>A (p.Ile110=) | |
| 10 | g.97601975T>C | CA471092446 | HOGA1 | c.819T>C (p.Ile273=) c.229T>C c.330T>C (p.Ile110=) | |
| 10 | g.97601975T>G | CA5634251 | HOGA1 | c.819T>G (p.Ile273Met) c.229T>G c.330T>G (p.Ile110Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.97601975T= | CA1930508955 | HOGA1 | c.819T= (p.Ile273=) c.229T= c.330T= (p.Ile110=) | |
| 10 | g.97601976G>A | CA377981777 | HOGA1 | c.820G>A (p.Glu274Lys) c.230G>A c.331G>A (p.Glu111Lys) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.97601976G>C | CA377981779 | HOGA1 | c.820G>C (p.Glu274Gln) c.230G>C c.331G>C (p.Glu111Gln) | |
| 10 | g.97601976G= | CA1930508957 | HOGA1 | c.820G= (p.Glu274=) c.230G= c.331G= (p.Glu111=) | |
| 10 | g.97601976G>T | CA377981780 | HOGA1 | c.820G>T (p.Glu274Ter) c.230G>T c.331G>T (p.Glu111Ter) | |
| 10 | g.97601977A>C | CA377981781 | HOGA1 | c.821A>C (p.Glu274Ala) c.231A>C c.332A>C (p.Glu111Ala) | |
| 10 | g.97601977A>G | CA377981782 | HOGA1 | c.821A>G (p.Glu274Gly) c.231A>G c.332A>G (p.Glu111Gly) | gnomAD v4 |
| 10 | g.97601977A>T | CA377981785 | HOGA1 | c.821A>T (p.Glu274Val) c.231A>T c.332A>T (p.Glu111Val) | |
| 10 | g.97601978G>A | CA471092447 | HOGA1 | c.822G>A (p.Glu274=) c.232G>A c.333G>A (p.Glu111=) | ClinVar dbSNP |
| 10 | g.97601978G>C | CA377981788 | HOGA1 | c.822G>C (p.Glu274Asp) c.232G>C c.333G>C (p.Glu111Asp) | |
| 10 | g.97601978G>T | CA377981791 | HOGA1 | c.822G>T (p.Glu274Asp) c.232G>T c.333G>T (p.Glu111Asp) | |
| 10 | g.97601979C>A | CA377981795 | HOGA1 | c.823C>A (p.Pro275Thr) c.233C>A c.334C>A (p.Pro112Thr) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.97601979C= | CA1930508961 | HOGA1 | c.823C= (p.Pro275=) c.233C= c.334C= (p.Pro112=) | |
| 10 | g.97601979C>G | CA377981803 | HOGA1 | c.823C>G (p.Pro275Ala) c.233C>G c.334C>G (p.Pro112Ala) | |
| 10 | g.97601979C>T | CA377981797 | HOGA1 | c.823C>T (p.Pro275Ser) c.233C>T c.334C>T (p.Pro112Ser) | |
| 10 | g.97601980C>A | CA377981805 | HOGA1 | c.824C>A (p.Pro275Gln) c.234C>A c.335C>A (p.Pro112Gln) | |
| 10 | g.97601980C>G | CA377981807 | HOGA1 | c.824C>G (p.Pro275Arg) c.234C>G c.335C>G (p.Pro112Arg) | gnomAD v4 |
| 10 | g.97601980C>T | CA377981822 | HOGA1 | c.824C>T (p.Pro275Leu) c.234C>T c.335C>T (p.Pro112Leu) | |
| 10 | g.97601981A>C | CA471092449 | HOGA1 | c.825A>C (p.Pro275=) c.235A>C c.336A>C (p.Pro112=) | |
| 10 | g.97601981A>G | CA471092450 | HOGA1 | c.825A>G (p.Pro275=) c.235A>G c.336A>G (p.Pro112=) | gnomAD v4 |
| 10 | g.97601981A>T | CA471092451 | HOGA1 | c.825A>T (p.Pro275=) c.235A>T c.336A>T (p.Pro112=) | |
| 10 | g.97601982A>C | CA377981825 | HOGA1 | c.826A>C (p.Asn276His) c.236A>C c.337A>C (p.Asn113His) | |
| 10 | g.97601982A>G | CA377981828 | HOGA1 | c.826A>G (p.Asn276Asp) c.236A>G c.337A>G (p.Asn113Asp) | |
| 10 | g.97601982A>T | CA377981831 | HOGA1 | c.826A>T (p.Asn276Tyr) c.236A>T c.337A>T (p.Asn113Tyr) | |
| 10 | g.97601983A>C | CA377981835 | HOGA1 | c.827A>C (p.Asn276Thr) c.237A>C c.338A>C (p.Asn113Thr) | |
| 10 | g.97601983A>G | CA377981836 | HOGA1 | c.827A>G (p.Asn276Ser) c.237A>G c.338A>G (p.Asn113Ser) | |
| 10 | g.97601983A>T | CA377981839 | HOGA1 | c.827A>T (p.Asn276Ile) c.237A>T c.338A>T (p.Asn113Ile) | |
| 10 | g.97601984C>A | CA5634253 | HOGA1 | c.828C>A (p.Asn276Lys) c.238C>A c.339C>A (p.Asn113Lys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.97601984C= | CA1930508968 | HOGA1 | c.828C= (p.Asn276=) c.238C= c.339C= (p.Asn113=) | |
| 10 | g.97601984C>G | CA377981847 | HOGA1 | c.828C>G (p.Asn276Lys) c.238C>G c.339C>G (p.Asn113Lys) | |
| 10 | g.97601984C>T | CA5634252 | HOGA1 | c.828C>T (p.Asn276=) c.238C>T c.339C>T (p.Asn113=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601985G>A | CA5634254 | HOGA1 | c.829G>A (p.Ala277Thr) c.239G>A c.340G>A (p.Ala114Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
| 10 | g.97601985G>C | CA377981853 | HOGA1 | c.829G>C (p.Ala277Pro) c.239G>C c.340G>C (p.Ala114Pro) | |
| 10 | g.97601985G= | CA1930508977 | HOGA1 | c.829G= (p.Ala277=) c.239G= c.340G= (p.Ala114=) | |
| 10 | g.97601985G>T | CA377981856 | HOGA1 | c.829G>T (p.Ala277Ser) c.239G>T c.340G>T (p.Ala114Ser) | gnomAD v4 |
| 10 | g.97601986C>A | CA377981862 | HOGA1 | c.830C>A (p.Ala277Asp) c.240C>A c.341C>A (p.Ala114Asp) | |
| 10 | g.97601986C>G | CA377981867 | HOGA1 | c.830C>G (p.Ala277Gly) c.240C>G c.341C>G (p.Ala114Gly) | |
| 10 | g.97601986C>T | CA377981870 | HOGA1 | c.830C>T (p.Ala277Val) c.240C>T c.341C>T (p.Ala114Val) | |
| 10 | g.97601987T>A | CA471092455 | HOGA1 | c.831T>A (p.Ala277=) c.241T>A c.342T>A (p.Ala114=) | |
| 10 | g.97601987T>C | CA471092456 | HOGA1 | c.831T>C (p.Ala277=) c.241T>C c.342T>C (p.Ala114=) | gnomAD v4 |
| 10 | g.97601987T>G | CA471092457 | HOGA1 | c.831T>G (p.Ala277=) c.241T>G c.342T>G (p.Ala114=) | |
| 10 | g.97601988G>A | CA5634255 | HOGA1 | c.832G>A (p.Ala278Thr) c.242G>A c.343G>A (p.Ala115Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601988G>C | CA377981876 | HOGA1 | c.832G>C (p.Ala278Pro) c.242G>C c.343G>C (p.Ala115Pro) | |
| 10 | g.97601988G= | CA1930508984 | HOGA1 | c.832G= (p.Ala278=) c.242G= c.343G= (p.Ala115=) | |
| 10 | g.97601988G>T | CA377981879 | HOGA1 | c.832G>T (p.Ala278Ser) c.242G>T c.343G>T (p.Ala115Ser) | gnomAD v4 |
| 10 | g.97601989C>A | CA377981882 | HOGA1 | c.833C>A (p.Ala278Glu) c.243C>A c.344C>A (p.Ala115Glu) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.97601989C= | CA1930508991 | HOGA1 | c.833C= (p.Ala278=) c.243C= c.344C= (p.Ala115=) | |
| 10 | g.97601989C>G | CA377981884 | HOGA1 | c.833C>G (p.Ala278Gly) c.243C>G c.344C>G (p.Ala115Gly) | |
| 10 | g.97601989C>T | CA377981887 | HOGA1 | c.833C>T (p.Ala278Val) c.243C>T c.344C>T (p.Ala115Val) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |