3 | g.129530916G>A | CA435643776 | RHO | c.402G>A (p.Glu134=)
| dbSNP gnomAD v3 gnomAD v4 |
3 | g.129530916G>C | CA354498050 | RHO | c.402G>C (p.Glu134Asp)
| |
3 | g.129530916G>T | CA354498052 | RHO | c.402G>T (p.Glu134Asp)
| |
3 | g.129530917C>A | CA435643780 | RHO | c.403C>A (p.Arg135=)
| gnomAD v4 |
3 | g.129530917C= | CA1401209282 | RHO | c.403C= (p.Arg135=)
| |
3 | g.129530917C>G | CA354498053 | RHO | c.403C>G (p.Arg135Gly)
| ClinVar dbSNP |
3 | g.129530917C>T | CA122819 | RHO | c.403C>T (p.Arg135Trp)
| ClinVar dbSNP gnomAD v4 |
3 | g.129530917_129530919delinsTAC | CA2579758053 | RHO | c.403_405delinsTAC (p.Arg135Tyr)
| |
3 | g.129530918G>A | CA2607152 | RHO | c.404G>A (p.Arg135Gln)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530918G>C | CA354498057 | RHO | c.404G>C (p.Arg135Pro)
| ClinVar dbSNP |
3 | g.129530918G= | CA1401209302 | RHO | c.404G= (p.Arg135=)
| |
3 | g.129530918G>T | CA256671 | RHO | c.404G>T (p.Arg135Leu)
| ClinVar dbSNP |
3 | g.129530918_129530919delinsGG | CA1401209296 | RHO | c.404_405delinsGG (p.Arg135=)
| |
3 | g.129530918_129530919delinsTT | CA10602881 | RHO | c.404_405delinsTT (p.Arg135Leu)
| ClinVar dbSNP |
3 | g.129530919G>A | CA435643786 | RHO | c.405G>A (p.Arg135=)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530919G>C | CA435643788 | RHO | c.405G>C (p.Arg135=)
| |
3 | g.129530919G= | CA1401209310 | RHO | c.405G= (p.Arg135=)
| |
3 | g.129530919G>T | CA16604469 | RHO | c.405G>T (p.Arg135=)
| ClinVar dbSNP gnomAD v4 |
3 | g.129530920T>A | CA354498065 | RHO | c.406T>A (p.Tyr136Asn)
| |
3 | g.129530920T>C | CA354498064 | RHO | c.406T>C (p.Tyr136His)
| ClinVar dbSNP |
3 | g.129530920T>G | CA354498063 | RHO | c.406T>G (p.Tyr136Asp)
| |
3 | g.129530920T= | CA1401209319 | RHO | c.406T= (p.Tyr136=)
| |
3 | g.129530921A>C | CA354498067 | RHO | c.407A>C (p.Tyr136Ser)
| |
3 | g.129530921A>G | CA354498069 | RHO | c.407A>G (p.Tyr136Cys)
| |
3 | g.129530921A>T | CA354498072 | RHO | c.407A>T (p.Tyr136Phe)
| |
3 | g.129530922C>A | CA82648518 | RHO | c.408C>A (p.Tyr136Ter)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.129530922C= | CA1401209328 | RHO | c.408C= (p.Tyr136=)
| |
3 | g.129530922C>G | CA354498074 | RHO | c.408C>G (p.Tyr136Ter)
| dbSNP gnomAD v3 gnomAD v4 |
3 | g.129530922C>T | CA2607153 | RHO | c.408C>T (p.Tyr136=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530923_129530940del | CA2579758042 | RHO | c.409_426del (p.Val137_Pro142del)
| |
3 | g.129530923G>A | CA2607154 | RHO | c.409G>A (p.Val137Met)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.129530923G>C | CA354498078 | RHO | c.409G>C (p.Val137Leu)
| |
3 | g.129530923G= | CA1401209339 | RHO | c.409G= (p.Val137=)
| |
3 | g.129530923G>T | CA354498080 | RHO | c.409G>T (p.Val137Leu)
| |
3 | g.129530924T>A | CA354498081 | RHO | c.410T>A (p.Val137Glu)
| |
3 | g.129530924T>C | CA354498084 | RHO | c.410T>C (p.Val137Ala)
| |
3 | g.129530924T>G | CA354498086 | RHO | c.410T>G (p.Val137Gly)
| |
3 | g.129530925G>A | CA435643810 | RHO | c.411G>A (p.Val137=)
| |
3 | g.129530925G>C | CA435643812 | RHO | c.411G>C (p.Val137=)
| |
3 | g.129530925G>T | CA435643814 | RHO | c.411G>T (p.Val137=)
| |
3 | g.129530926G>A | CA354498093 | RHO | c.412G>A (p.Val138Met)
| |
3 | g.129530926G>C | CA354498090 | RHO | c.412G>C (p.Val138Leu)
| |
3 | g.129530926G>T | CA354498088 | RHO | c.412G>T (p.Val138Leu)
| |
3 | g.129530927T>A | CA354498097 | RHO | c.413T>A (p.Val138Glu)
| |
3 | g.129530927T>C | CA354498099 | RHO | c.413T>C (p.Val138Ala)
| gnomAD v4 |
3 | g.129530927T>G | CA354498101 | RHO | c.413T>G (p.Val138Gly)
| |
3 | g.129530928G>A | CA435643826 | RHO | c.414G>A (p.Val138=)
| dbSNP gnomAD v3 gnomAD v4 |
3 | g.129530928G>C | CA435643828 | RHO | c.414G>C (p.Val138=)
| dbSNP gnomAD v2 gnomAD v4 |
3 | g.129530928G= | CA1401209342 | RHO | c.414G= (p.Val138=)
| |
3 | g.129530928G>T | CA435643829 | RHO | c.414G>T (p.Val138=)
| |
3 | g.129530929G>A | CA354498103 | RHO | c.415G>A (p.Val139Met)
| |
3 | g.129530929G>C | CA354498105 | RHO | c.415G>C (p.Val139Leu)
| |
3 | g.129530929G>T | CA354498108 | RHO | c.415G>T (p.Val139Leu)
| |
3 | g.129530930T>A | CA354498111 | RHO | c.416T>A (p.Val139Glu)
| |
3 | g.129530930T>C | CA354498114 | RHO | c.416T>C (p.Val139Ala)
| |
3 | g.129530930T>G | CA354498116 | RHO | c.416T>G (p.Val139Gly)
| |
3 | g.129530931G>A | CA435643836 | RHO | c.417G>A (p.Val139=)
| dbSNP gnomAD v4 |
3 | g.129530931G>C | CA435643837 | RHO | c.417G>C (p.Val139=)
| gnomAD v4 |
3 | g.129530931G= | CA1401209347 | RHO | c.417G= (p.Val139=)
| |
3 | g.129530931G>T | CA435643840 | RHO | c.417G>T (p.Val139=)
| |
3 | g.129530932T>A | CA354498118 | RHO | c.418T>A (p.Cys140Ser)
| |
3 | g.129530932T>C | CA354498123 | RHO | c.418T>C (p.Cys140Arg)
| |
3 | g.129530932T>G | CA354498125 | RHO | c.418T>G (p.Cys140Gly)
| |
3 | g.129530933G>A | CA354498132 | RHO | c.419G>A (p.Cys140Tyr)
| |
3 | g.129530933G>C | CA354498130 | RHO | c.419G>C (p.Cys140Ser)
| ClinVar dbSNP gnomAD v4 |
3 | g.129530933G= | CA1401209351 | RHO | c.419G= (p.Cys140=)
| |
3 | g.129530933G>T | CA354498128 | RHO | c.419G>T (p.Cys140Phe)
| |
3 | g.129530934T>A | CA354498133 | RHO | c.420T>A (p.Cys140Ter)
| |
3 | g.129530934T>C | CA435643849 | RHO | c.420T>C (p.Cys140=)
| |
3 | g.129530934T>G | CA354498135 | RHO | c.420T>G (p.Cys140Trp)
| |
3 | g.129530935A>C | CA354498137 | RHO | c.421A>C (p.Lys141Gln)
| |
3 | g.129530935A>G | CA354498140 | RHO | c.421A>G (p.Lys141Glu)
| |
3 | g.129530935A>T | CA354498142 | RHO | c.421A>T (p.Lys141Ter)
| |
3 | g.129530935_129530938dup | CA2667616150 | RHO | c.421_424dup (p.Pro142GlnfsTer?)
| gnomAD v4 |
3 | g.129530936A>C | CA354498144 | RHO | c.422A>C (p.Lys141Thr)
| |
3 | g.129530936A>G | CA354498146 | RHO | c.422A>G (p.Lys141Arg)
| |
3 | g.129530936A>T | CA354498150 | RHO | c.422A>T (p.Lys141Met)
| |
3 | g.129530937G>A | CA435643858 | RHO | c.423G>A (p.Lys141=)
| COSMIC |
3 | g.129530937G>C | CA354498152 | RHO | c.423G>C (p.Lys141Asn)
| |
3 | g.129530937G>T | CA354498159 | RHO | c.423G>T (p.Lys141Asn)
| |
3 | g.129530938C>A | CA354498163 | RHO | c.424C>A (p.Pro142Thr)
| |
3 | g.129530938C= | CA1401209354 | RHO | c.424C= (p.Pro142=)
| |
3 | g.129530938C>G | CA354498165 | RHO | c.424C>G (p.Pro142Ala)
| |
3 | g.129530938C>T | CA354498167 | RHO | c.424C>T (p.Pro142Ser)
| dbSNP |
3 | g.129530939C>A | CA354498172 | RHO | c.425C>A (p.Pro142His)
| |
3 | g.129530939C>G | CA354498174 | RHO | c.425C>G (p.Pro142Arg)
| |
3 | g.129530939C>T | CA354498170 | RHO | c.425C>T (p.Pro142Leu)
| gnomAD v4 |
3 | g.129530940C>A | CA435643868 | RHO | c.426C>A (p.Pro142=)
| |
3 | g.129530940C>G | CA435643871 | RHO | c.426C>G (p.Pro142=)
| dbSNP |
3 | g.129530940C>T | CA435643873 | RHO | c.426C>T (p.Pro142=)
| ClinVar dbSNP |
3 | g.129530941A>C | CA354498180 | RHO | c.427A>C (p.Met143Leu)
| |
3 | g.129530941A>G | CA354498176 | RHO | c.427A>G (p.Met143Val)
| |
3 | g.129530941A>T | CA354498178 | RHO | c.427A>T (p.Met143Leu)
| |
3 | g.129530942T>A | CA2607155 | RHO | c.428T>A (p.Met143Lys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129530942T>C | CA354498185 | RHO | c.428T>C (p.Met143Thr)
| dbSNP gnomAD v4 |
3 | g.129530942T>G | CA2607156 | RHO | c.428T>G (p.Met143Arg)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129530942T= | CA1401209362 | RHO | c.428T= (p.Met143=)
| |
3 | g.129530943G>A | CA354498188 | RHO | c.429G>A (p.Met143Ile)
| dbSNP gnomAD v4 |
3 | g.129530943G>C | CA354498189 | RHO | c.429G>C (p.Met143Ile)
| |
3 | g.129530943G= | CA1401209365 | RHO | c.429G= (p.Met143=)
| |
3 | g.129530943G>T | CA354498190 | RHO | c.429G>T (p.Met143Ile)
| |
3 | g.129530944A>C | CA354498191 | RHO | c.430A>C (p.Ser144Arg)
| |
3 | g.129530944A>G | CA354498192 | RHO | c.430A>G (p.Ser144Gly)
| |
3 | g.129530944A>T | CA354498193 | RHO | c.430A>T (p.Ser144Cys)
| |
3 | g.129530945G>A | CA354498195 | RHO | c.431G>A (p.Ser144Asn)
| COSMIC |
3 | g.129530945G>C | CA354498196 | RHO | c.431G>C (p.Ser144Thr)
| |
3 | g.129530945G>T | CA354498198 | RHO | c.431G>T (p.Ser144Ile)
| |
3 | g.129530946C>A | CA354498202 | RHO | c.432C>A (p.Ser144Arg)
| |
3 | g.129530946C= | CA1401209367 | RHO | c.432C= (p.Ser144=)
| |
3 | g.129530946C>G | CA354498201 | RHO | c.432C>G (p.Ser144Arg)
| |
3 | g.129530946C>T | CA435643895 | RHO | c.432C>T (p.Ser144=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530947A>C | CA354498203 | RHO | c.433A>C (p.Asn145His)
| |
3 | g.129530947A>G | CA354498206 | RHO | c.433A>G (p.Asn145Asp)
| |
3 | g.129530947A>T | CA354498209 | RHO | c.433A>T (p.Asn145Tyr)
| |
3 | g.129530948A>C | CA354498211 | RHO | c.434A>C (p.Asn145Thr)
| |
3 | g.129530948A>G | CA354498213 | RHO | c.434A>G (p.Asn145Ser)
| |
3 | g.129530948A>T | CA354498215 | RHO | c.434A>T (p.Asn145Ile)
| |
3 | g.129530949C>A | CA354498217 | RHO | c.435C>A (p.Asn145Lys)
| |
3 | g.129530949C>G | CA354498219 | RHO | c.435C>G (p.Asn145Lys)
| |
3 | g.129530949C>T | CA435643902 | RHO | c.435C>T (p.Asn145=)
| |
3 | g.129530950T>A | CA354498221 | RHO | c.436T>A (p.Phe146Ile)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
3 | g.129530950T>C | CA354498223 | RHO | c.436T>C (p.Phe146Leu)
| |
3 | g.129530950T>G | CA354498226 | RHO | c.436T>G (p.Phe146Val)
| |
3 | g.129530950T= | CA1401209370 | RHO | c.436T= (p.Phe146=)
| |
3 | g.129530951T>A | CA354498229 | RHO | c.437T>A (p.Phe146Tyr)
| gnomAD v4 |
3 | g.129530951T>C | CA354498231 | RHO | c.437T>C (p.Phe146Ser)
| |
3 | g.129530951T>G | CA354498232 | RHO | c.437T>G (p.Phe146Cys)
| |
3 | g.129530952C>A | CA354498234 | RHO | c.438C>A (p.Phe146Leu)
| dbSNP gnomAD v3 gnomAD v4 |
3 | g.129530952C= | CA1401209376 | RHO | c.438C= (p.Phe146=)
| |
3 | g.129530952C>G | CA354498237 | RHO | c.438C>G (p.Phe146Leu)
| |
3 | g.129530952C>T | CA435643911 | RHO | c.438C>T (p.Phe146=)
| |
3 | g.129530953C>A | CA354498239 | RHO | c.439C>A (p.Arg147Ser)
| gnomAD v4 |
3 | g.129530953C= | CA1401209381 | RHO | c.439C= (p.Arg147=)
| |
3 | g.129530953C>G | CA354498242 | RHO | c.439C>G (p.Arg147Gly)
| |
3 | g.129530953C>T | CA2607157 | RHO | c.439C>T (p.Arg147Cys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530954G>A | CA2607158 | RHO | c.440G>A (p.Arg147His)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.129530954G>C | CA354498251 | RHO | c.440G>C (p.Arg147Pro)
| |
3 | g.129530954G= | CA1401209393 | RHO | c.440G= (p.Arg147=)
| |
3 | g.129530954G>T | CA354498253 | RHO | c.440G>T (p.Arg147Leu)
| |
3 | g.129530955C>A | CA435643918 | RHO | c.441C>A (p.Arg147=)
| |
3 | g.129530955C= | CA1401209395 | RHO | c.441C= (p.Arg147=)
| |
3 | g.129530955C>G | CA435643920 | RHO | c.441C>G (p.Arg147=)
| |
3 | g.129530955C>T | CA435643922 | RHO | c.441C>T (p.Arg147=)
| dbSNP |
3 | g.129530956T>A | CA354498260 | RHO | c.442T>A (p.Phe148Ile)
| |
3 | g.129530956T>C | CA354498258 | RHO | c.442T>C (p.Phe148Leu)
| |
3 | g.129530956T>G | CA354498256 | RHO | c.442T>G (p.Phe148Val)
| |
3 | g.129530957T>A | CA354498262 | RHO | c.443T>A (p.Phe148Tyr)
| |
3 | g.129530957T>C | CA354498263 | RHO | c.443T>C (p.Phe148Ser)
| ClinVar |
3 | g.129530957T>G | CA354498264 | RHO | c.443T>G (p.Phe148Cys)
| |
3 | g.129530958C>A | CA354498266 | RHO | c.444C>A (p.Phe148Leu)
| gnomAD v4 |
3 | g.129530958C= | CA1401209397 | RHO | c.444C= (p.Phe148=)
| |
3 | g.129530958C>G | CA354498268 | RHO | c.444C>G (p.Phe148Leu)
| gnomAD v4 |
3 | g.129530958C>T | CA2607159 | RHO | c.444C>T (p.Phe148=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.129530959G>A | CA2607160 | RHO | c.445G>A (p.Gly149Arg)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.129530959G>C | CA354498272 | RHO | c.445G>C (p.Gly149Arg)
| |
3 | g.129530959G= | CA1401209401 | RHO | c.445G= (p.Gly149=)
| |
3 | g.129530959G>T | CA354498271 | RHO | c.445G>T (p.Gly149Trp)
| dbSNP gnomAD v4 |
3 | g.129530962del | CA645514953 | RHO | c.448del (p.Glu150ArgfsTer?)
| COSMIC |
3 | g.129530960G>A | CA82648577 | RHO | c.446G>A (p.Gly149Glu)
| dbSNP gnomAD v2 gnomAD v4 |
3 | g.129530960G>C | CA354498275 | RHO | c.446G>C (p.Gly149Ala)
| |
3 | g.129530960G= | CA1401209405 | RHO | c.446G= (p.Gly149=)
| |
3 | g.129530960G>T | CA354498277 | RHO | c.446G>T (p.Gly149Val)
| |
3 | g.129530961G>A | CA435643939 | RHO | c.447G>A (p.Gly149=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.129530961G>C | CA435643942 | RHO | c.447G>C (p.Gly149=)
| |
3 | g.129530961G= | CA1401209410 | RHO | c.447G= (p.Gly149=)
| |
3 | g.129530961G>T | CA435643943 | RHO | c.447G>T (p.Gly149=)
| |
3 | g.129530962G>A | CA122824 | RHO | c.448G>A (p.Glu150Lys)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.129530962G>C | CA2607161 | RHO | c.448G>C (p.Glu150Gln)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530962G= | CA1401209417 | RHO | c.448G= (p.Glu150=)
| |
3 | g.129530962G>T | CA354498282 | RHO | c.448G>T (p.Glu150Ter)
| |
3 | g.129530963A>C | CA354498284 | RHO | c.449A>C (p.Glu150Ala)
| |
3 | g.129530963A>G | CA354498286 | RHO | c.449A>G (p.Glu150Gly)
| |
3 | g.129530963A>T | CA354498290 | RHO | c.449A>T (p.Glu150Val)
| |
3 | g.129530964G>A | CA435643952 | RHO | c.450G>A (p.Glu150=)
| |
3 | g.129530964G>C | CA354498294 | RHO | c.450G>C (p.Glu150Asp)
| ClinVar dbSNP gnomAD v4 |
3 | g.129530964G= | CA1401209423 | RHO | c.450G= (p.Glu150=)
| |
3 | g.129530964G>T | CA354498295 | RHO | c.450G>T (p.Glu150Asp)
| |
3 | g.129530965A>C | CA354498296 | RHO | c.451A>C (p.Asn151His)
| |
3 | g.129530965A>G | CA354498301 | RHO | c.451A>G (p.Asn151Asp)
| |
3 | g.129530965A>T | CA354498298 | RHO | c.451A>T (p.Asn151Tyr)
| |
3 | g.129530966A= | CA1401209428 | RHO | c.452A= (p.Asn151=)
| |
3 | g.129530966A>C | CA354498304 | RHO | c.452A>C (p.Asn151Thr)
| |
3 | g.129530966A>G | CA354498309 | RHO | c.452A>G (p.Asn151Ser)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530966A>T | CA354498306 | RHO | c.452A>T (p.Asn151Ile)
| |
3 | g.129530967C>A | CA354498312 | RHO | c.453C>A (p.Asn151Lys)
| |
3 | g.129530967C>G | CA354498315 | RHO | c.453C>G (p.Asn151Lys)
| |
3 | g.129530967C>T | CA435643964 | RHO | c.453C>T (p.Asn151=)
| dbSNP gnomAD v4 |
3 | g.129530968C>A | CA354498318 | RHO | c.454C>A (p.His152Asn)
| |
3 | g.129530968C= | CA1401209432 | RHO | c.454C= (p.His152=)
| |
3 | g.129530968C>G | CA354498321 | RHO | c.454C>G (p.His152Asp)
| |
3 | g.129530968C>T | CA354498322 | RHO | c.454C>T (p.His152Tyr)
| dbSNP gnomAD v2 gnomAD v4 |
3 | g.129530969A>C | CA354498324 | RHO | c.455A>C (p.His152Pro)
| |
3 | g.129530969A>G | CA354498330 | RHO | c.455A>G (p.His152Arg)
| gnomAD v4 |
3 | g.129530969A>T | CA354498336 | RHO | c.455A>T (p.His152Leu)
| |
3 | g.129530970T>A | CA354498340 | RHO | c.456T>A (p.His152Gln)
| |
3 | g.129530970T>C | CA435643976 | RHO | c.456T>C (p.His152=)
| dbSNP gnomAD v4 |
3 | g.129530970T>G | CA354498344 | RHO | c.456T>G (p.His152Gln)
| gnomAD v4 |
3 | g.129530971G>A | CA354498352 | RHO | c.457G>A (p.Ala153Thr)
| dbSNP gnomAD v2 |
3 | g.129530971G>C | CA354498357 | RHO | c.457G>C (p.Ala153Pro)
| |
3 | g.129530971G= | CA1401209436 | RHO | c.457G= (p.Ala153=)
| |
3 | g.129530971G>T | CA354498359 | RHO | c.457G>T (p.Ala153Ser)
| |
3 | g.129530972C>A | CA354498362 | RHO | c.458C>A (p.Ala153Asp)
| ClinVar dbSNP |
3 | g.129530972C= | CA1401209444 | RHO | c.458C= (p.Ala153=)
| |
3 | g.129530972C>G | CA354498365 | RHO | c.458C>G (p.Ala153Gly)
| COSMIC |
3 | g.129530972C>T | CA354498363 | RHO | c.458C>T (p.Ala153Val)
| ClinVar dbSNP gnomAD v3 gnomAD v4 |
3 | g.129530973C>A | CA435643986 | RHO | c.459C>A (p.Ala153=)
| gnomAD v4 |
3 | g.129530973C= | CA1401209449 | RHO | c.459C= (p.Ala153=)
| |
3 | g.129530973C>G | CA435643988 | RHO | c.459C>G (p.Ala153=)
| dbSNP gnomAD v2 gnomAD v4 |
3 | g.129530973C>T | CA435643990 | RHO | c.459C>T (p.Ala153=)
| dbSNP |
3 | g.129530974A>C | CA354498366 | RHO | c.460A>C (p.Ile154Leu)
| |
3 | g.129530974A>G | CA354498368 | RHO | c.460A>G (p.Ile154Val)
| gnomAD v4 |
3 | g.129530974A>T | CA354498370 | RHO | c.460A>T (p.Ile154Phe)
| |
3 | g.129530975T>A | CA354498371 | RHO | c.461T>A (p.Ile154Asn)
| |
3 | g.129530975T>C | CA354498373 | RHO | c.461T>C (p.Ile154Thr)
| |
3 | g.129530975T>G | CA354498375 | RHO | c.461T>G (p.Ile154Ser)
| |
3 | g.129530976C>A | CA435643999 | RHO | c.462C>A (p.Ile154=)
| |
3 | g.129530976C>G | CA354498376 | RHO | c.462C>G (p.Ile154Met)
| |
3 | g.129530976C>T | CA435644002 | RHO | c.462C>T (p.Ile154=)
| gnomAD v4 |
3 | g.129530977A= | CA1401209452 | RHO | c.463A= (p.Met155=)
| |
3 | g.129530977A>C | CA354498379 | RHO | c.463A>C (p.Met155Leu)
| |
3 | g.129530977A>G | CA2607162 | RHO | c.463A>G (p.Met155Val)
| dbSNP ExAC |
3 | g.129530977A>T | CA354498393 | RHO | c.463A>T (p.Met155Leu)
| |
3 | g.129530978T>A | CA354498399 | RHO | c.464T>A (p.Met155Lys)
| |
3 | g.129530978T>C | CA2607163 | RHO | c.464T>C (p.Met155Thr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129530978T>G | CA354498395 | RHO | c.464T>G (p.Met155Arg)
| |
3 | g.129530978T= | CA1401209457 | RHO | c.464T= (p.Met155=)
| |
3 | g.129530979G>A | CA354498402 | RHO | c.465G>A (p.Met155Ile)
| COSMIC |
3 | g.129530979G>C | CA354498404 | RHO | c.465G>C (p.Met155Ile)
| |
3 | g.129530979G>T | CA354498406 | RHO | c.465G>T (p.Met155Ile)
| |
3 | g.129530981del | CA2839192569 | RHO | c.467del (p.Gly156AlafsTer?)
| |
3 | g.129530980G>A | CA354498408 | RHO | c.466G>A (p.Gly156Ser)
| gnomAD v4 |
3 | g.129530980G>C | CA354498413 | RHO | c.466G>C (p.Gly156Arg)
| gnomAD v4 |
3 | g.129530980G>T | CA354498415 | RHO | c.466G>T (p.Gly156Cys)
| |
3 | g.129530981G>A | CA2607165 | RHO | c.467G>A (p.Gly156Asp)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530981G>C | CA354498419 | RHO | c.467G>C (p.Gly156Ala)
| dbSNP gnomAD v2 gnomAD v4 |
3 | g.129530981G= | CA1401209461 | RHO | c.467G= (p.Gly156=)
| |
3 | g.129530981G>T | CA2607164 | RHO | c.467G>T (p.Gly156Val)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129530982C>A | CA435644023 | RHO | c.468C>A (p.Gly156=)
| |
3 | g.129530982C= | CA1401209465 | RHO | c.468C= (p.Gly156=)
| |
3 | g.129530982C>G | CA435644024 | RHO | c.468C>G (p.Gly156=)
| |
3 | g.129530982C>T | CA2607166 | RHO | c.468C>T (p.Gly156=)
| dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530983G>A | CA2607167 | RHO | c.469G>A (p.Val157Ile)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530983G>C | CA354498423 | RHO | c.469G>C (p.Val157Leu)
| |
3 | g.129530983G= | CA1401209468 | RHO | c.469G= (p.Val157=)
| |
3 | g.129530983G>T | CA354498428 | RHO | c.469G>T (p.Val157Phe)
| |
3 | g.129530984T>A | CA354498443 | RHO | c.470T>A (p.Val157Asp)
| |
3 | g.129530984T>C | CA354498431 | RHO | c.470T>C (p.Val157Ala)
| |
3 | g.129530984T>G | CA354498438 | RHO | c.470T>G (p.Val157Gly)
| |
3 | g.129530985T>A | CA435644036 | RHO | c.471T>A (p.Val157=)
| |
3 | g.129530985T>C | CA435644038 | RHO | c.471T>C (p.Val157=)
| |
3 | g.129530985T>G | CA435644040 | RHO | c.471T>G (p.Val157=)
| dbSNP |
3 | g.129530986G>A | CA354498454 | RHO | c.472G>A (p.Ala158Thr)
| dbSNP |
3 | g.129530986G>C | CA354498455 | RHO | c.472G>C (p.Ala158Pro)
| |
3 | g.129530986G= | CA1401209471 | RHO | c.472G= (p.Ala158=)
| |
3 | g.129530986G>T | CA354498458 | RHO | c.472G>T (p.Ala158Ser)
| |
3 | g.129530987C>A | CA354498460 | RHO | c.473C>A (p.Ala158Asp)
| |
3 | g.129530987C>G | CA354498462 | RHO | c.473C>G (p.Ala158Gly)
| |
3 | g.129530987C>T | CA354498463 | RHO | c.473C>T (p.Ala158Val)
| dbSNP |
3 | g.129530988C>A | CA435644049 | RHO | c.474C>A (p.Ala158=)
| |
3 | g.129530988C>G | CA435644052 | RHO | c.474C>G (p.Ala158=)
| |
3 | g.129530988C>T | CA435644054 | RHO | c.474C>T (p.Ala158=)
| |
3 | g.129530989T>A | CA354498464 | RHO | c.475T>A (p.Phe159Ile)
| |
3 | g.129530989T>C | CA354498465 | RHO | c.475T>C (p.Phe159Leu)
| |
3 | g.129530989T>G | CA354498466 | RHO | c.475T>G (p.Phe159Val)
| |
3 | g.129530990T>A | CA354498469 | RHO | c.476T>A (p.Phe159Tyr)
| |
3 | g.129530990T>C | CA354498471 | RHO | c.476T>C (p.Phe159Ser)
| |
3 | g.129530990T>G | CA354498472 | RHO | c.476T>G (p.Phe159Cys)
| dbSNP |
3 | g.129530990T= | CA1401209475 | RHO | c.476T= (p.Phe159=)
| |
3 | g.129530991C>A | CA354498474 | RHO | c.477C>A (p.Phe159Leu)
| |
3 | g.129530991C>G | CA354498476 | RHO | c.477C>G (p.Phe159Leu)
| |
3 | g.129530991C>T | CA435644066 | RHO | c.477C>T (p.Phe159=)
| gnomAD v4 |
3 | g.129530991_129530992insTGGGACGAAAACGTCGAAGTCAAACCCGAAGAAGTCAGCGTACGCTTTGAAGAAGGCGTGCCGGTTGCATTGAACGGCAAAGAATACGCTGATCCTGTCGAACTCTTCCTCGA | CA2758363925 | RHO | c.477_478insTGGGACGAAAACGTCGAAGTCAAACCCGAAGAAGTCAGCGTACGCTTTGAAGAAGGCGTGCCGGTTGCATTGAACGGCAAAGAATACGCTGATCCTGTCGAACTCTTCCTCGA (p.Thr160TrpfsTer?)
| |
3 | g.129530992A>C | CA354498479 | RHO | c.478A>C (p.Thr160Pro)
| |
3 | g.129530992A>G | CA354498487 | RHO | c.478A>G (p.Thr160Ala)
| |
3 | g.129530992A>T | CA354498484 | RHO | c.478A>T (p.Thr160Ser)
| |
3 | g.129530993C>A | CA354498490 | RHO | c.479C>A (p.Thr160Asn)
| |
3 | g.129530993C= | CA1401209480 | RHO | c.479C= (p.Thr160=)
| |
3 | g.129530993C>G | CA354498492 | RHO | c.479C>G (p.Thr160Ser)
| |
3 | g.129530993C>T | CA82648613 | RHO | c.479C>T (p.Thr160Ile)
| dbSNP gnomAD v3 gnomAD v4 |
3 | g.129530994C>A | CA2607168 | RHO | c.480C>A (p.Thr160=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129530994C= | CA1401209486 | RHO | c.480C= (p.Thr160=)
| |
3 | g.129530994C>G | CA435644077 | RHO | c.480C>G (p.Thr160=)
| |
3 | g.129530994C>T | CA435644079 | RHO | c.480C>T (p.Thr160=)
| |
3 | g.129530995T>A | CA354498498 | RHO | c.481T>A (p.Trp161Arg)
| |
3 | g.129530995T>C | CA354498501 | RHO | c.481T>C (p.Trp161Arg)
| ClinVar dbSNP |
3 | g.129530995T>G | CA354498505 | RHO | c.481T>G (p.Trp161Gly)
| |
3 | g.129530996G>A | CA358695 | RHO | c.482G>A (p.Trp161Ter)
| ClinVar dbSNP gnomAD v2 gnomAD v4 |
3 | g.129530996G>C | CA354498515 | RHO | c.482G>C (p.Trp161Ser)
| |
3 | g.129530996G= | CA1401209491 | RHO | c.482G= (p.Trp161=)
| |
3 | g.129530996G>T | CA354498518 | RHO | c.482G>T (p.Trp161Leu)
| |
3 | g.129530997G>A | CA354498521 | RHO | c.483G>A (p.Trp161Ter)
| |
3 | g.129530997G>C | CA2607169 | RHO | c.483G>C (p.Trp161Cys)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129530997G= | CA1401209495 | RHO | c.483G= (p.Trp161=)
| |
3 | g.129530997G>T | CA354498523 | RHO | c.483G>T (p.Trp161Cys)
| |
3 | g.129530998G>A | CA354498525 | RHO | c.484G>A (p.Val162Ile)
| dbSNP |
3 | g.129530998G>C | CA82648646 | RHO | c.484G>C (p.Val162Leu)
| dbSNP gnomAD v4 |
3 | g.129530998G= | CA1401209497 | RHO | c.484G= (p.Val162=)
| |
3 | g.129530998G>T | CA354498528 | RHO | c.484G>T (p.Val162Phe)
| |
3 | g.129530999T>A | CA354498534 | RHO | c.485T>A (p.Val162Asp)
| |
3 | g.129530999T>C | CA354498538 | RHO | c.485T>C (p.Val162Ala)
| |
3 | g.129530999T>G | CA354498541 | RHO | c.485T>G (p.Val162Gly)
| |
3 | g.129531000C>A | CA435644102 | RHO | c.486C>A (p.Val162=)
| |
3 | g.129531000C= | CA1401209505 | RHO | c.486C= (p.Val162=)
| |
3 | g.129531000C>G | CA2607171 | RHO | c.486C>G (p.Val162=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129531000C>T | CA2607170 | RHO | c.486C>T (p.Val162=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129531001A= | CA1401209513 | RHO | c.487A= (p.Met163=)
| |
3 | g.129531001A>C | CA354498549 | RHO | c.487A>C (p.Met163Leu)
| |
3 | g.129531001A>G | CA354498550 | RHO | c.487A>G (p.Met163Val)
| |
3 | g.129531001A>T | CA354498554 | RHO | c.487A>T (p.Met163Leu)
| dbSNP |
3 | g.129531002T>A | CA354498555 | RHO | c.488T>A (p.Met163Lys)
| |
3 | g.129531002T>C | CA354498556 | RHO | c.488T>C (p.Met163Thr)
| |
3 | g.129531002T>G | CA354498558 | RHO | c.488T>G (p.Met163Arg)
| |
3 | g.129531003G>A | CA2607172 | RHO | c.489G>A (p.Met163Ile)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129531003G>C | CA354498564 | RHO | c.489G>C (p.Met163Ile)
| |
3 | g.129531003G= | CA1401209519 | RHO | c.489G= (p.Met163=)
| |
3 | g.129531003G>T | CA354498561 | RHO | c.489G>T (p.Met163Ile)
| COSMIC |
3 | g.129531004G>A | CA354498579 | RHO | c.490G>A (p.Ala164Thr)
| |
3 | g.129531004G>C | CA354498569 | RHO | c.490G>C (p.Ala164Pro)
| |
3 | g.129531004G>T | CA354498575 | RHO | c.490G>T (p.Ala164Ser)
| |
3 | g.129531005C>A | CA256689 | RHO | c.491C>A (p.Ala164Glu)
| ClinVar dbSNP |
3 | g.129531005C= | CA1401209527 | RHO | c.491C= (p.Ala164=)
| |
3 | g.129531005C>G | CA354498584 | RHO | c.491C>G (p.Ala164Gly)
| |
3 | g.129531005C>T | CA16616904 | RHO | c.491C>T (p.Ala164Val)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129531006G>A | CA82648684 | RHO | c.492G>A (p.Ala164=)
| ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.129531006G>C | CA435644123 | RHO | c.492G>C (p.Ala164=)
| |
3 | g.129531006G= | CA1401209537 | RHO | c.492G= (p.Ala164=)
| |
3 | g.129531006G>T | CA435644125 | RHO | c.492G>T (p.Ala164=)
| gnomAD v4 |
3 | g.129531007C>A | CA354498601 | RHO | c.493C>A (p.Leu165Met)
| |
3 | g.129531007C>G | CA354498604 | RHO | c.493C>G (p.Leu165Val)
| |
3 | g.129531007C>T | CA435644133 | RHO | c.493C>T (p.Leu165=)
| dbSNP |
3 | g.129531008T>A | CA354498606 | RHO | c.494T>A (p.Leu165Gln)
| |
3 | g.129531008T>C | CA354498614 | RHO | c.494T>C (p.Leu165Pro)
| dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129531008T>G | CA354498612 | RHO | c.494T>G (p.Leu165Arg)
| |
3 | g.129531008T= | CA1401209541 | RHO | c.494T= (p.Leu165=)
| |
3 | g.129531009G>A | CA435644135 | RHO | c.495G>A (p.Leu165=)
| |
3 | g.129531009G>C | CA435644136 | RHO | c.495G>C (p.Leu165=)
| |
3 | g.129531009G= | CA1401209546 | RHO | c.495G= (p.Leu165=)
| |
3 | g.129531009G>T | CA2607173 | RHO | c.495G>T (p.Leu165=)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129531010G>A | CA354498619 | RHO | c.496G>A (p.Ala166Thr)
| |
3 | g.129531010G>C | CA354498621 | RHO | c.496G>C (p.Ala166Pro)
| |
3 | g.129531010G>T | CA354498626 | RHO | c.496G>T (p.Ala166Ser)
| |
3 | g.129531011C>A | CA354498629 | RHO | c.497C>A (p.Ala166Asp)
| |
3 | g.129531011C= | CA1401209554 | RHO | c.497C= (p.Ala166=)
| |
3 | g.129531011C>G | CA354498636 | RHO | c.497C>G (p.Ala166Gly)
| |
3 | g.129531011C>T | CA354498630 | RHO | c.497C>T (p.Ala166Val)
| ClinVar dbSNP |
3 | g.129531012C>A | CA435644150 | RHO | c.498C>A (p.Ala166=)
| |
3 | g.129531012C>G | CA435644151 | RHO | c.498C>G (p.Ala166=)
| |
3 | g.129531012C>T | CA435644154 | RHO | c.498C>T (p.Ala166=)
| |
3 | g.129531013T>A | CA354498637 | RHO | c.499T>A (p.Cys167Ser)
| |
3 | g.129531013T>C | CA354498638 | RHO | c.499T>C (p.Cys167Arg)
| |
3 | g.129531013T>G | CA354498642 | RHO | c.499T>G (p.Cys167Gly)
| |
3 | g.129531013_129531018delinsTGCGCC | CA1401209559 | RHO | c.499_504delinsTGCGCC (p.Cys167=)
| |
3 | g.129531014G>A | CA354498646 | RHO | c.500G>A (p.Cys167Tyr)
| |
3 | g.129531014G>C | CA354498651 | RHO | c.500G>C (p.Cys167Ser)
| |
3 | g.129531014G>T | CA354498653 | RHO | c.500G>T (p.Cys167Phe)
| |
3 | g.129531016_129531020del | CA898752188 | RHO | c.502_506del (p.Ala168ThrfsTer?)
| dbSNP |
3 | g.129531015C>A | CA354498655 | RHO | c.501C>A (p.Cys167Ter)
| dbSNP |
3 | g.129531015C= | CA1401209566 | RHO | c.501C= (p.Cys167=)
| |
3 | g.129531015C>G | CA354498662 | RHO | c.501C>G (p.Cys167Trp)
| ClinVar dbSNP |
3 | g.129531015C>T | CA2607174 | RHO | c.501C>T (p.Cys167=)
| dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.129531016G>A | CA2607175 | RHO | c.502G>A (p.Ala168Thr)
| ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.129531016G>C | CA354498673 | RHO | c.502G>C (p.Ala168Pro)
| ClinVar |
3 | g.129531016G= | CA1401209573 | RHO | c.502G= (p.Ala168=)
| |
3 | g.129531016G>T | CA354498675 | RHO | c.502G>T (p.Ala168Ser)
| |