Transcript #00007068

Transcript name transcript variant 1
Gene name GPRASP1 (G protein-coupled receptor associated sorting protein 1)
Chromosome X
Transcript - NCBI ID NM_014710.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_055525.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

90 entries on 1 page. Showing entries 1 - 90.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-35G>A r.(=) p.(=)
?/? c.21G>A r.(=) p.(=)
?/? c.55G>T r.(?) p.(Gly19Trp)
?/? c.64G>A r.(?) p.(Val22Ile)
?/? c.83T>C r.(?) p.(Ile28Thr)
?/? c.110G>A r.(?) p.(Arg37Lys)
?/? c.130G>C r.(?) p.(Ala44Pro)
?/? c.141G>A r.(?) p.(Met47Ile)
?/? c.259C>T r.(?) p.(Arg87*)
?/? c.345T>C r.(=) p.(=)
?/? c.368G>T r.(?) p.(Ser123Ile)
?/? c.379G>C r.(?) p.(Val127Leu)
?/? c.560C>G r.(?) p.(Ser187Cys)
?/? c.622G>A r.(?) p.(Glu208Lys)
?/? c.737A>G r.(?) p.(Tyr246Cys)
?/? c.758C>A r.(?) p.(Ser253Tyr)
?/? c.779C>T r.(?) p.(Thr260Ile)
?/? c.783C>G r.(=) p.(=)
?/? c.807C>T r.(=) p.(=)
?/? c.816G>T r.(?) p.(Trp272Cys)
?/? c.834T>G r.(?) p.(Asp278Glu)
?/? c.944C>G r.(?) p.(Ala315Gly)
?/? c.945C>T r.(=) p.(=)
?/? c.972G>A r.(=) p.(=)
?/? c.1108A>T r.(?) p.(Met370Leu)
?/? c.1169G>A r.(?) p.(Arg390Gln)
?/? c.1207G>T r.(?) p.(Ala403Ser)
?/? c.1239C>T r.(=) p.(=)
?/? c.1331A>G r.(?) p.(Glu444Gly)
?/? c.1547C>G r.(?) p.(Thr516Ser)
?/? c.1636G>A r.(?) p.(Glu546Lys)
?/? c.1678G>A r.(?) p.(Val560Ile)
?/? c.1685T>C r.(?) p.(Ile562Thr)
?/? c.1686A>G r.(?) p.(Ile562Met)
?/? c.1698C>T r.(=) p.(=)
?/? c.1754G>C r.(?) p.(Trp585Ser)
?/? c.1781G>A r.(?) p.(Cys594Tyr)
?/? c.1783A>G r.(?) p.(Arg595Gly)
?/? c.1852T>C r.(?) p.(Trp618Arg)
?/? c.1908G>A r.(=) p.(=)
?/? c.1928T>C r.(?) p.(Ile643Thr)
?/? c.1958G>A r.(?) p.(Ser653Asn)
?/? c.1976G>A r.(?) p.(Gly659Asp)
?/? c.2021A>C r.(?) p.(Lys674Thr)
?/? c.2117C>T r.(?) p.(Ser706Leu)
?/? c.2162G>A r.(?) p.(Gly721Glu)
?/? c.2332A>G r.(?) p.(Ile778Val)
?/? c.2372T>C r.(?) p.(Leu791Pro)
?/? c.2446G>T r.(?) p.(Gly816Trp)
?/? c.2479G>C r.(?) p.(Gly827Arg)
?/? c.2490C>A r.(?) p.(Ser830Arg)
?/? c.2496C>T r.(=) p.(=)
?/? c.2553G>A r.(=) p.(=)
?/? c.2663A>C r.(?) p.(Gln888Pro)
?/? c.2715C>A r.(=) p.(=)
?/? c.2747A>C r.(?) p.(Glu916Ala)
?/? c.2923G>C r.(?) p.(Ala975Pro)
?/? c.2939A>G r.(?) p.(Asp980Gly)
?/? c.3060C>G r.(=) p.(=)
?/? c.3137A>G r.(?) p.(Glu1046Gly)
?/? c.3154T>G r.(?) p.(Phe1052Val)
?/? c.3178G>C r.(?) p.(Val1060Leu)
?/? c.3213G>A r.(=) p.(=)
?/? c.3265A>G r.(?) p.(Met1089Val)
?/? c.3277C>T r.(?) p.(Pro1093Ser)
?/? c.3366C>G r.(=) p.(=)
?/? c.3423C>T r.(=) p.(=)
?/? c.3499C>T r.(?) p.(Arg1167Trp)
?/? c.3529A>C r.(?) p.(Ile1177Leu)
?/? c.3624G>T r.(=) p.(=)
?/? c.3634G>T r.(?) p.(Val1212Phe)
?/? c.3670_3671insC r.(?) p.(Pro1226Thrfs*14)
?/? c.3715A>C r.(?) p.(Lys1239Gln)
?/? c.3756G>A r.(=) p.(=)
?/? c.3810T>C r.(=) p.(=)
?/? c.3819G>C r.(=) p.(=)
?/? c.3822T>G r.(=) p.(=)
?/? c.3830A>G r.(?) p.(Tyr1277Cys)
?/? c.3840G>A r.(=) p.(=)
?/? c.3876A>T r.(=) p.(=)
?/? c.3896T>C r.(?) p.(Met1299Thr)
?/? c.3930A>G r.(=) p.(=)
?/? c.3957G>T r.(=) p.(=)
?/? c.3992C>A r.(?) p.(Thr1331Lys)
?/? c.4029G>C r.(?) p.(Glu1343Asp)
?/? c.4045A>G r.(?) p.(Ile1349Val)
?/? c.4059_4060del r.(?) p.(Phe1355Leufs*2)
?/? c.4084A>G r.(?) p.(Ile1362Val)
?/? c.4092G>A r.(=) p.(=)
?/? c.*9A>G r.(=) p.(=)
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