Transcript #00000968

Transcript name transcript variant 2
Gene name ARHGAP12 (Rho GTPase activating protein 12)
Chromosome 10
Transcript - NCBI ID NM_001270695.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001257624.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

134 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-34T>C r.(=) p.(=)
?/? c.-28A>T r.(=) p.(=)
?/? c.-5A>G r.(=) p.(=)
?/? c.16A>C r.(=) p.(=)
?/? c.24G>A r.(=) p.(=)
?/? c.97G>C r.(?) p.(Val33Leu)
?/? c.182C>T r.(?) p.(Ala61Val)
?/? c.220C>T r.(?) p.(Arg74Cys)
?/? c.221G>C r.(?) p.(Arg74Pro)
?/? c.236C>T r.(?) p.(Pro79Leu)
?/? c.238C>T r.(?) p.(Pro80Ser)
?/? c.265A>G r.(?) p.(Asn89Asp)
?/? c.310A>G r.(?) p.(Thr104Ala)
?/? c.348C>T r.(=) p.(=)
?/? c.370C>G r.(?) p.(Gln124Glu)
?/? c.388C>T r.(?) p.(Arg130Cys)
?/? c.434C>A r.(?) p.(Thr145Asn)
?/? c.454C>T r.(=) p.(=)
?/? c.486C>T r.(=) p.(=)
?/? c.542C>A r.(?) p.(Pro181His)
?/? c.575G>T r.(?) p.(Ser192Ile)
?/? c.590A>G r.(?) p.(Gln197Arg)
?/? c.624A>G r.(=) p.(=)
?/? c.628C>T r.(?) p.(His210Tyr)
?/? c.673G>C r.(?) p.(Glu225Gln)
?/? c.681A>C r.(=) p.(=)
?/? c.684+51T>C r.(=) p.(=)
?/? c.711G>A r.(=) p.(=)
?/? c.726C>G r.(=) p.(=)
?/? c.772C>G r.(?) p.(Pro258Ala)
?/? c.804T>C r.(=) p.(=)
?/? c.866A>G r.(?) p.(Gln289Arg)
?/? c.876T>C r.(=) p.(=)
?/? c.918A>G r.(=) p.(=)
?/? c.948+48T>C r.(=) p.(=)
?/? c.1039T>C r.(=) p.(=)
?/? c.1048C>T r.(?) p.(Arg350Cys)
?/? c.1066A>G r.(?) p.(Thr356Ala)
?/? c.1137A>G r.(=) p.(=)
?/? c.1155A>G r.(=) p.(=)
?/? c.1170+1G>A r.spl? p.?
?/? c.1170+18C>T r.(=) p.(=)
?/? c.1171-47A>G r.(=) p.(=)
?/? c.1205T>C r.(?) p.(Ile402Thr)
?/? c.1228C>T r.(?) p.(Arg410Trp)
?/? c.1254A>G r.(=) p.(=)
?/? c.1291G>A r.(?) p.(Asp431Asn)
?/? c.1296+3A>G r.spl? p.?
?/? c.1296+20T>C r.(=) p.(=)
?/? c.1297-4G>A r.spl? p.?
?/? c.1319C>T r.(?) p.(Pro440Leu)
?/? c.1325T>C r.(?) p.(Phe442Ser)
?/? c.1348T>A r.(?) p.(Ser450Thr)
?/? c.1359G>T r.(?) p.(Lys453Asn)
?/? c.1371+281A>G r.(=) p.(=)
?/? c.1371+291A>G r.(=) p.(=)
?/? c.1371+319C>T r.(=) p.(=)
?/? c.1371+348C>T r.(=) p.(=)
?/? c.1372-62G>A r.(=) p.(=)
?/? c.1372-28G>A r.(=) p.(=)
?/? c.1422G>A r.(=) p.(=)
?/? c.1432C>T r.(?) p.(Arg478*)
?/? c.1433+53del r.(=) p.(=)
?/? c.1433+53_1433+55del r.(=) p.(=)
?/? c.1434-34T>C r.(=) p.(=)
?/? c.1515+55C>T r.(=) p.(=)
?/? c.1516-36T>C r.(=) p.(=)
?/? c.1516-29A>T r.(=) p.(=)
?/? c.1516-18_1516-17insT r.(=) p.(=)
?/? c.1516-17C>T r.(=) p.(=)
?/? c.1525A>C r.(?) p.(Asn509His)
?/? c.1589A>G r.(?) p.(Asp530Gly)
?/? c.1617+38T>C r.(=) p.(=)
?/? c.1617+44A>G r.(=) p.(=)
?/? c.1617+48G>A r.(=) p.(=)
?/? c.1618-50T>C r.(=) p.(=)
?/? c.1618-37T>C r.(=) p.(=)
?/? c.1618-12T>C r.(=) p.(=)
?/? c.1628G>A r.(?) p.(Arg543His)
?/? c.1648A>G r.(?) p.(Ile550Val)
?/? c.1661A>G r.(?) p.(Asn554Ser)
?/? c.1668T>C r.(=) p.(=)
?/? c.1705A>G r.(?) p.(Ile569Val)
?/? c.1716+8G>T r.(=) p.(=)
?/? c.1716+27T>A r.(=) p.(=)
?/? c.1716+46C>A r.(=) p.(=)
?/? c.1717-29T>C r.(=) p.(=)
?/? c.1717-10T>C r.(=) p.(=)
?/? c.1754C>T r.(?) p.(Pro585Leu)
?/? c.1755G>A r.(=) p.(=)
?/? c.1766G>T r.(?) p.(Gly589Val)
?/? c.1815T>G r.(=) p.(=)
?/? c.1817G>A r.(?) p.(Arg606His)
?/? c.1820-44_1820-43insA r.(=) p.(=)
?/? c.1820-2A>C r.spl? p.?
?/? c.1862C>A r.(?) p.(Thr621Asn)
?/? c.1892G>A r.(?) p.(Arg631Gln)
?/? c.1899C>T r.(=) p.(=)
?/? c.1903T>G r.(?) p.(Leu635Val)
?/? c.1936+9_1936+11del r.(=) p.(=)
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