Transcript #00007261

Transcript name guanylate cyclase 2F, retinal
Gene name GUCY2F (guanylate cyclase 2F, retinal)
Chromosome X
Transcript - NCBI ID NM_001522.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001513.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-43C>T r.(=) p.(=)
?/? c.-23A>G r.(=) p.(=)
?/? c.2_3insTAT r.? p.?
?/? c.112C>T r.(?) p.(Leu38Phe)
?/? c.119C>G r.(?) p.(Ser40Cys)
?/? c.220G>C r.(?) p.(Val74Leu)
?/? c.256G>C r.(?) p.(Asp86His)
?/? c.309C>T r.(=) p.(=)
?/? c.315G>C r.(?) p.(Gln105His)
?/? c.479T>A r.(?) p.(Ile160Asn)
?/? c.505C>T r.(?) p.(Leu169Phe)
?/? c.521G>A r.(?) p.(Arg174Gln)
?/? c.542A>G r.(?) p.(Lys181Arg)
?/? c.587A>G r.(?) p.(Asp196Gly)
?/? c.612A>G r.(=) p.(=)
?/? c.628C>T r.(?) p.(Arg210Trp)
?/? c.636C>T r.(=) p.(=)
?/? c.668G>A r.(?) p.(Gly223Glu)
?/? c.688C>T r.(?) p.(Arg230Trp)
?/? c.698T>C r.(?) p.(Leu233Pro)
?/? c.714G>C r.(?) p.(Gln238His)
?/? c.730+13T>C r.(=) p.(=)
?/? c.766G>A r.(?) p.(Gly256Arg)
?/? c.851T>C r.(?) p.(Leu284Pro)
?/? c.887G>A r.(?) p.(Arg296Gln)
?/? c.913C>T r.(?) p.(Arg305Trp)
?/? c.923A>G r.(?) p.(Tyr308Cys)
?/? c.930A>G r.(=) p.(=)
?/? c.969C>A r.(?) p.(Phe323Leu)
?/? c.970T>C r.(?) p.(Tyr324His)
?/? c.974A>G r.(?) p.(Gln325Arg)
?/? c.994del r.(?) p.(Ala332Glnfs*32)
?/? c.1014G>A r.(=) p.(=)
?/? c.1021G>C r.(?) p.(Glu341Gln)
?/? c.1026C>T r.(=) p.(=)
?/? c.1027G>A r.(?) p.(Asp343Asn)
?/? c.1031A>G r.(?) p.(Gln344Arg)
?/? c.1032+12T>G r.(=) p.(=)
?/? c.1032+23T>C r.(=) p.(=)
?/? c.1032+25A>G r.(=) p.(=)
?/? c.1033-47G>A r.(=) p.(=)
?/? c.1033-40G>A r.(=) p.(=)
?/? c.1033-2A>G r.spl? p.?
?/? c.1048G>A r.(?) p.(Gly350Arg)
?/? c.1077C>T r.(=) p.(=)
?/? c.1134G>T r.(=) p.(=)
?/? c.1140G>T r.(?) p.(Gln380His)
?/? c.1272G>A r.(=) p.(=)
?/? c.1294C>T r.(?) p.(Arg432Cys)
?/? c.1299C>T r.(=) p.(=)
?/? c.1300G>A r.(?) p.(Gly434Arg)
?/? c.1308C>T r.(=) p.(=)
?/? c.1323T>A r.(=) p.(=)
?/? c.1355G>T r.(?) p.(Cys452Phe)
?/? c.1383T>C r.(=) p.(=)
?/? c.1387+3A>C r.spl? p.?
?/? c.1388-34A>G r.(=) p.(=)
?/? c.1392C>T r.(=) p.(=)
?/? c.1436C>T r.(?) p.(Ala479Val)
?/? c.1472G>A r.(?) p.(Arg491Lys)
?/? c.1475G>A r.(?) p.(Arg492His)
?/? c.1478G>A r.(?) p.(Arg493His)
?/? c.1483A>C r.(?) p.(Asn495His)
?/? c.1541C>T r.(?) p.(Thr514Met)
?/? c.1542G>A r.(=) p.(=)
?/? c.1569G>C r.(?) p.(Lys523Asn)
?/? c.1569+29C>G r.(=) p.(=)
?/? c.1650A>G r.(=) p.(=)
?/? c.1692G>A r.(=) p.(=)
?/? c.1701+22T>G r.(=) p.(=)
?/? c.1702-32A>G r.(=) p.(=)
?/? c.1720A>C r.(?) p.(Lys574Gln)
?/? c.1791+4T>C r.spl? p.?
?/? c.1791+10A>C r.(=) p.(=)
?/? c.1791+16G>A r.(=) p.(=)
?/? c.1791+40A>G r.(=) p.(=)
?/? c.1792-46T>G r.(=) p.(=)
?/? c.1838T>A r.(?) p.(Phe613Tyr)
?/? c.1848G>C r.(=) p.(=)
?/? c.1883G>A r.(?) p.(Arg628Gln)
?/? c.1887G>T r.(=) p.(=)
?/? c.1932G>T r.(?) p.(Trp644Cys)
?/? c.2029G>C r.(?) p.(Val677Leu)
?/? c.2041C>T r.(?) p.(Arg681Cys)
?/? c.2050C>T r.(=) p.(=)
?/? c.2068G>A r.(?) p.(Gly690Ser)
?/? c.2119A>G r.(?) p.(Met707Val)
?/? c.2126-30T>C r.(=) p.(=)
?/? c.2126-29G>T r.(=) p.(=)
?/? c.2129T>A r.(?) p.(Leu710Gln)
?/? c.2138C>T r.(?) p.(Thr713Met)
?/? c.2144C>T r.(?) p.(Pro715Leu)
?/? c.2239G>T r.(?) p.(Gly747Cys)
?/? c.2275+36A>G r.(=) p.(=)
?/? c.2275+41G>A r.(=) p.(=)
?/? c.2275+44C>T r.(=) p.(=)
?/? c.2275+45G>A r.(=) p.(=)
?/? c.2276-40_2276-39insT r.(=) p.(=)
?/? c.2276-25C>T r.(=) p.(=)
?/? c.2280C>T r.(=) p.(=)
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