All transcript variants in gene ARHGAP32

Information The variants shown are described using the NM_014715.3 transcript reference sequence.

235 entries on 3 pages. Showing entries 1 - 100.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-31C>T r.(=) p.(=) g.128868350G>A Copied from the Exome Variant Server ARHGAP32_000235 1/12996 0/8594 1/4402
?/? c.-22C>T r.(=) p.(=) g.128868341G>A Copied from the Exome Variant Server ARHGAP32_000234 1/12996 1/8594 0/4402
?/? c.-16G>A r.(=) p.(=) g.128868335C>T Copied from the Exome Variant Server ARHGAP32_000233 3/12996 2/8594 1/4402
?/? c.6G>A r.(=) p.(=) g.128868314C>T Copied from the Exome Variant Server ARHGAP32_000232 1/12996 1/8594 0/4402
?/? c.81A>G r.(=) p.(=) g.128868239T>C Copied from the Exome Variant Server ARHGAP32_000231 8587/12996 5971/8594 2616/4402
?/? c.106+18A>G r.(=) p.(=) g.128868196T>C Copied from the Exome Variant Server ARHGAP32_000230 2/12996 2/8594 0/4402
?/? c.106+32A>T r.(=) p.(=) g.128868182T>A Copied from the Exome Variant Server ARHGAP32_000229 1/12996 1/8594 0/4402
?/? c.107-27A>G r.(=) p.(=) g.128858047T>C Copied from the Exome Variant Server ARHGAP32_000228 50/12992 43/8592 7/4400
?/? c.141T>C r.(=) p.(=) g.128857986A>G Copied from the Exome Variant Server ARHGAP32_000227 1/12996 0/8594 1/4402
?/? c.191C>T r.(?) p.(Ser64Phe) g.128857936G>A Copied from the Exome Variant Server ARHGAP32_000226 1/12996 0/8594 1/4402
?/? c.209+34del r.(=) p.(=) g.128857884del Copied from the Exome Variant Server ARHGAP32_000225 20/12514 14/8252 6/4262
?/? c.209+33_209+35del r.(=) p.(=) g.128857883_128857885del Copied from the Exome Variant Server ARHGAP32_000224 4386/12514 2945/8252 1441/4262
?/? c.210-52T>C r.(=) p.(=) g.128856615A>G Copied from the Exome Variant Server ARHGAP32_000223 1/7272 1/4618 0/2654
?/? c.210-26T>C r.(=) p.(=) g.128856589A>G Copied from the Exome Variant Server ARHGAP32_000222 3/12996 2/8594 1/4402
?/? c.210-25G>A r.(=) p.(=) g.128856588C>T Copied from the Exome Variant Server ARHGAP32_000221 198/12996 3/8594 195/4402
?/? c.210-5G>A r.spl? p.? g.128856568C>T Copied from the Exome Variant Server ARHGAP32_000220 2/12996 2/8594 0/4402
?/? c.210C>T r.(=) p.(=) g.128856563G>A Copied from the Exome Variant Server ARHGAP32_000219 9/12996 0/8594 9/4402
?/? c.232G>A r.(?) p.(Val78Ile) g.128856541C>T Copied from the Exome Variant Server ARHGAP32_000218 1/12996 0/8594 1/4402
?/? c.237C>T r.(=) p.(=) g.128856536G>A Copied from the Exome Variant Server ARHGAP32_000217 1/12996 1/8594 0/4402
?/? c.245C>T r.(?) p.(Thr82Met) g.128856528G>A Copied from the Exome Variant Server ARHGAP32_000216 1/12996 0/8594 1/4402
?/? c.255G>A r.(=) p.(=) g.128856518C>T Copied from the Exome Variant Server ARHGAP32_000215 1/12996 1/8594 0/4402
?/? c.403G>A r.(?) p.(Asp135Asn) g.128855932C>T Copied from the Exome Variant Server ARHGAP32_000214 1/12996 0/8594 1/4402
?/? c.437+43T>C r.(=) p.(=) g.128855855A>G Copied from the Exome Variant Server ARHGAP32_000212 1/12996 0/8594 1/4402
?/? c.437+56G>A r.(=) p.(=) g.128855842C>T Copied from the Exome Variant Server ARHGAP32_000211 2/4566 1/3182 1/1384
?/? c.438-51A>G r.(=) p.(=) g.128851882T>C Copied from the Exome Variant Server ARHGAP32_000208 1/12984 0/8590 1/4394
?/? c.445G>C r.(?) p.(Glu149Gln) g.128851824C>G Copied from the Exome Variant Server ARHGAP32_000206 1/12996 0/8594 1/4402
?/? c.482A>G r.(?) p.(Tyr161Cys) g.128851787T>C Copied from the Exome Variant Server ARHGAP32_000204 1/12996 1/8594 0/4402
?/? c.546-40C>G r.(=) p.(=) g.128851496G>C Copied from the Exome Variant Server ARHGAP32_000202 9/12996 9/8594 0/4402
?/? c.546-38A>G r.(=) p.(=) g.128851494T>C Copied from the Exome Variant Server ARHGAP32_000200 1/12996 1/8594 0/4402
?/? c.546-36C>T r.(=) p.(=) g.128851492G>A Copied from the Exome Variant Server ARHGAP32_000213 1/12996 0/8594 1/4402
?/? c.546-14T>C r.(=) p.(=) g.128851470A>G Copied from the Exome Variant Server ARHGAP32_000210 1/12996 1/8594 0/4402
?/? c.606T>G r.(?) p.(Ile202Met) g.128851396A>C Copied from the Exome Variant Server ARHGAP32_000209 1/12996 1/8594 0/4402
?/? c.691+11G>A r.(=) p.(=) g.128851300C>T Copied from the Exome Variant Server ARHGAP32_000207 2/12996 1/8594 1/4402
?/? c.692-41C>T r.(=) p.(=) g.128850684G>A Copied from the Exome Variant Server ARHGAP32_000205 17/12996 0/8594 17/4402
?/? c.692-21A>G r.(=) p.(=) g.128850664T>C Copied from the Exome Variant Server ARHGAP32_000203 2/12996 0/8594 2/4402
?/? c.726C>T r.(=) p.(=) g.128850609G>A Copied from the Exome Variant Server ARHGAP32_000201 4/12996 0/8594 4/4402
?/? c.748A>T r.(?) p.(Thr250Ser) g.128850587T>A Copied from the Exome Variant Server ARHGAP32_000199 2/12996 2/8594 0/4402
?/? c.767C>G r.(?) p.(Ala256Gly) g.128850568G>C Copied from the Exome Variant Server ARHGAP32_000198 1/12996 1/8594 0/4402
?/? c.776A>G r.(?) p.(Gln259Arg) g.128850559T>C Copied from the Exome Variant Server ARHGAP32_000197 2/12996 2/8594 0/4402
?/? c.787A>G r.(?) p.(Asn263Asp) g.128850548T>C Copied from the Exome Variant Server ARHGAP32_000196 2/12996 2/8594 0/4402
?/? c.796A>G r.(?) p.(Ile266Val) g.128850539T>C Copied from the Exome Variant Server ARHGAP32_000195 4/12996 4/8594 0/4402
?/? c.820G>A r.(?) p.(Glu274Lys) g.128850515C>T Copied from the Exome Variant Server ARHGAP32_000194 1/12996 1/8594 0/4402
?/? c.887+9T>C r.(=) p.(=) g.128850439A>G Copied from the Exome Variant Server ARHGAP32_000193 1/12996 1/8594 0/4402
?/? c.887+20A>G r.(=) p.(=) g.128850428T>C Copied from the Exome Variant Server ARHGAP32_000192 1/12996 1/8594 0/4402
?/? c.887+33A>G r.(=) p.(=) g.128850415T>C Copied from the Exome Variant Server ARHGAP32_000191 1/12996 1/8594 0/4402
?/? c.888-35_888-33del r.(=) p.(=) g.128848843_128848845del Copied from the Exome Variant Server ARHGAP32_000190 1/12518 1/8254 0/4264
?/? c.896C>G r.(?) p.(Pro299Arg) g.128848802G>C Copied from the Exome Variant Server ARHGAP32_000189 1/12996 0/8594 1/4402
?/? c.977G>A r.(?) p.(Arg326Gln) g.128848721C>T Copied from the Exome Variant Server ARHGAP32_000188 1/12996 1/8594 0/4402
?/? c.993T>A r.(?) p.(Asn331Lys) g.128848705A>T Copied from the Exome Variant Server ARHGAP32_000187 1/12996 0/8594 1/4402
?/? c.1033+37A>G r.(=) p.(=) g.128848628T>C Copied from the Exome Variant Server ARHGAP32_000186 1/12996 1/8594 0/4402
?/? c.1033+49G>A r.(=) p.(=) g.128848616C>T Copied from the Exome Variant Server ARHGAP32_000185 1/12996 1/8594 0/4402
?/? c.1034-47A>G r.(=) p.(=) g.128846576T>C Copied from the Exome Variant Server ARHGAP32_000184 9/12996 8/8594 1/4402
?/? c.1034-36A>G r.(=) p.(=) g.128846565T>C Copied from the Exome Variant Server ARHGAP32_000183 3/12996 2/8594 1/4402
?/? c.1034-18G>T r.(=) p.(=) g.128846547C>A Copied from the Exome Variant Server ARHGAP32_000182 8568/12996 5960/8594 2608/4402
?/? c.1035T>C r.(=) p.(=) g.128846528A>G Copied from the Exome Variant Server ARHGAP32_000181 3/12996 0/8594 3/4402
?/? c.1058G>A r.(?) p.(Arg353His) g.128846505C>T Copied from the Exome Variant Server ARHGAP32_000180 1/12996 0/8594 1/4402
?/? c.1086A>G r.(=) p.(=) g.128846477T>C Copied from the Exome Variant Server ARHGAP32_000179 70/12996 58/8594 12/4402
?/? c.1106-39C>T r.(=) p.(=) g.128844936G>A Copied from the Exome Variant Server ARHGAP32_000178 1/12816 1/8486 0/4330
?/? c.1106-38G>A r.(=) p.(=) g.128844935C>T Copied from the Exome Variant Server ARHGAP32_000177 1/12860 1/8518 0/4342
?/? c.1106-14T>C r.(=) p.(=) g.128844911A>G Copied from the Exome Variant Server ARHGAP32_000176 1/12978 1/8586 0/4392
?/? c.1124G>A r.(?) p.(Arg375Gln) g.128844879C>T Copied from the Exome Variant Server ARHGAP32_000175 1/12996 1/8594 0/4402
?/? c.1172A>G r.(?) p.(Asn391Ser) g.128844831T>C Copied from the Exome Variant Server ARHGAP32_000174 1/12996 0/8594 1/4402
?/? c.1181T>C r.(?) p.(Met394Thr) g.128844822A>G Copied from the Exome Variant Server ARHGAP32_000173 1/12996 1/8594 0/4402
?/? c.1191C>G r.(?) p.(Asn397Lys) g.128844812G>C Copied from the Exome Variant Server ARHGAP32_000172 1/12996 0/8594 1/4402
?/? c.1248G>C r.(=) p.(=) g.128844755C>G Copied from the Exome Variant Server ARHGAP32_000171 3/12996 0/8594 3/4402
?/? c.1316T>C r.(?) p.(Ile439Thr) g.128844687A>G Copied from the Exome Variant Server ARHGAP32_000170 1/12996 1/8594 0/4402
?/? c.1373C>A r.(?) p.(Ala458Asp) g.128844630G>T Copied from the Exome Variant Server ARHGAP32_000169 1/12996 0/8594 1/4402
?/? c.1384T>C r.(?) p.(Cys462Arg) g.128844619A>G Copied from the Exome Variant Server ARHGAP32_000168 1/12996 0/8594 1/4402
?/? c.1388_1389insCTC r.(?) p.(Leu463_Glu464insSer) g.128844614_128844615insGAG Copied from the Exome Variant Server ARHGAP32_000167 1/12518 1/8254 0/4264
?/? c.1468G>A r.(?) p.(Gly490Ser) g.128844535C>T Copied from the Exome Variant Server ARHGAP32_000166 2/12996 0/8594 2/4402
?/? c.1490C>T r.(?) p.(Pro497Leu) g.128844513G>A Copied from the Exome Variant Server ARHGAP32_000165 2/12996 1/8594 1/4402
?/? c.1523C>G r.(?) p.(Pro508Arg) g.128844480G>C Copied from the Exome Variant Server ARHGAP32_000164 1/12996 1/8594 0/4402
?/? c.1587T>C r.(=) p.(=) g.128844416A>G Copied from the Exome Variant Server ARHGAP32_000163 3/12996 0/8594 3/4402
?/? c.1599C>T r.(=) p.(=) g.128844404G>A Copied from the Exome Variant Server ARHGAP32_000162 378/12996 127/8594 251/4402
?/? c.1615G>A r.(?) p.(Val539Ile) g.128844388C>T Copied from the Exome Variant Server ARHGAP32_000161 2/12996 2/8594 0/4402
?/? c.1619A>G r.(?) p.(Tyr540Cys) g.128844384T>C Copied from the Exome Variant Server ARHGAP32_000160 1/12996 1/8594 0/4402
?/? c.1642C>T r.(?) p.(Arg548Trp) g.128844361G>A Copied from the Exome Variant Server ARHGAP32_000159 1/12996 1/8594 0/4402
?/? c.1649T>C r.(?) p.(Leu550Ser) g.128844354A>G Copied from the Exome Variant Server ARHGAP32_000157 1/12996 1/8594 0/4402
?/? c.1672A>T r.(?) p.(Ile558Leu) g.128844331T>A Copied from the Exome Variant Server ARHGAP32_000155 3/12996 3/8594 0/4402
?/? c.1706G>A r.(?) p.(Arg569Gln) g.128844297C>T Copied from the Exome Variant Server ARHGAP32_000158 1/12996 0/8594 1/4402
?/? c.1748A>C r.(?) p.(Gln583Pro) g.128844255T>G Copied from the Exome Variant Server ARHGAP32_000156 7/12996 5/8594 2/4402
?/? c.1783G>A r.(?) p.(Glu595Lys) g.128844220C>T Copied from the Exome Variant Server ARHGAP32_000154 2/12996 0/8594 2/4402
?/? c.1795G>A r.(?) p.(Ala599Thr) g.128844208C>T Copied from the Exome Variant Server ARHGAP32_000153 1/12996 0/8594 1/4402
?/? c.1868C>A r.(?) p.(Ser623Tyr) g.128844135G>T Copied from the Exome Variant Server ARHGAP32_000152 1/12996 1/8594 0/4402
?/? c.1878G>A r.(=) p.(=) g.128844125C>T Copied from the Exome Variant Server ARHGAP32_000151 1/12996 1/8594 0/4402
?/? c.1890G>C r.(?) p.(Gln630His) g.128844113C>G Copied from the Exome Variant Server ARHGAP32_000150 1/12996 0/8594 1/4402
?/? c.1936G>T r.(?) p.(Val646Phe) g.128844067C>A Copied from the Exome Variant Server ARHGAP32_000149 1/12996 0/8594 1/4402
?/? c.1984+27_1984+30del r.(=) p.(=) g.128843989_128843992del Copied from the Exome Variant Server ARHGAP32_000148 3/12518 2/8254 1/4264
?/? c.1984+34_1984+38del r.(=) p.(=) g.128843981_128843985del Copied from the Exome Variant Server ARHGAP32_000147 1/12518 0/8254 1/4264
?/? c.1985-47C>T r.(=) p.(=) g.128843374G>A Copied from the Exome Variant Server ARHGAP32_000146 1/12512 0/8410 1/4102
?/? c.1985-46G>A r.(=) p.(=) g.128843373C>T Copied from the Exome Variant Server ARHGAP32_000145 1/12544 1/8414 0/4130
?/? c.2016C>T r.(=) p.(=) g.128843296G>A Copied from the Exome Variant Server ARHGAP32_000144 12/12964 12/8586 0/4378
?/? c.2017G>A r.(?) p.(Val673Ile) g.128843295C>T Copied from the Exome Variant Server ARHGAP32_000143 2/12968 2/8586 0/4382
?/? c.2085G>A r.(=) p.(=) g.128843227C>T Copied from the Exome Variant Server ARHGAP32_000142 2/12994 2/8594 0/4400
?/? c.2102C>A r.(?) p.(Ser701Tyr) g.128843210G>T Copied from the Exome Variant Server ARHGAP32_000141 1/12994 1/8594 0/4400
?/? c.2180C>T r.(?) p.(Ala727Val) g.128843132G>A Copied from the Exome Variant Server ARHGAP32_000140 1/12996 1/8594 0/4402
?/? c.2181G>A r.(=) p.(=) g.128843131C>T Copied from the Exome Variant Server ARHGAP32_000139 1/12996 1/8594 0/4402
?/? c.2240C>A r.(?) p.(Ala747Asp) g.128843072G>T Copied from the Exome Variant Server ARHGAP32_000138 1/12996 1/8594 0/4402
?/? c.2372A>G r.(?) p.(Glu791Gly) g.128842940T>C Copied from the Exome Variant Server ARHGAP32_000137 80/12996 0/8594 80/4402
?/? c.2380C>T r.(?) p.(His794Tyr) g.128842932G>A Copied from the Exome Variant Server ARHGAP32_000136 1/12996 1/8594 0/4402
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