Transcript #00015599 (NM_005493.2, RANBP9 gene)

Transcript name RAN binding protein 9
Gene name RANBP9 (RAN binding protein 9)
Chromosome 6
Transcript - NCBI ID NM_005493.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_005484.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-36G>A r.(=) p.(=)
?/? c.23_25dup r.(?) p.(Pro10dup)
?/? c.23_25del r.(?) p.(Pro10del)
?/? c.23_31del r.(?) p.(Pro8_Pro10del)
?/? c.400C>T r.(?) p.(Pro134Ser)
?/? c.457C>G r.(?) p.(Arg153Gly)
?/? c.459T>C r.(=) p.(=)
?/? c.462C>G r.(=) p.(=)
?/? c.465C>T r.(=) p.(=)
?/? c.471C>T r.(=) p.(=)
?/? c.510C>T r.(=) p.(=)
?/? c.516G>A r.(=) p.(=)
?/? c.519C>T r.(=) p.(=)
?/? c.525C>T r.(=) p.(=)
?/? c.534C>T r.(=) p.(=)
?/? c.537C>T r.(=) p.(=)
?/? c.540C>T r.(=) p.(=)
?/? c.552C>T r.(=) p.(=)
?/? c.563A>T r.(?) p.(His188Leu)
?/? c.571+9C>T r.(=) p.(=)
?/? c.571+45C>T r.(=) p.(=)
?/? c.600G>A r.(=) p.(=)
?/? c.683+27G>A r.(=) p.(=)
?/? c.683+31G>C r.(=) p.(=)
?/? c.683+35G>C r.(=) p.(=)
?/? c.683+49G>A r.(=) p.(=)
?/? c.684-42T>C r.(=) p.(=)
?/? c.684-22C>A r.(=) p.(=)
?/? c.684-15A>C r.(=) p.(=)
?/? c.694A>G r.(?) p.(Ile232Val)
?/? c.736+17A>G r.(=) p.(=)
?/? c.736+39G>A r.(=) p.(=)
?/? c.736+44T>A r.(=) p.(=)
?/? c.737-17C>T r.(=) p.(=)
?/? c.855T>C r.(=) p.(=)
?/? c.905-9dup r.(=) p.(=)
?/? c.905-9del r.(=) p.(=)
?/? c.927+14del r.(=) p.(=)
?/? c.928-14A>G r.(=) p.(=)
?/? c.994C>T r.(?) p.(His332Tyr)
?/? c.1002C>T r.(=) p.(=)
?/? c.1003G>A r.(?) p.(Val335Met)
?/? c.1064G>A r.(?) p.(Arg355Gln)
?/? c.1107A>G r.(?) p.(Ile369Met)
?/? c.1112+10A>T r.(=) p.(=)
?/? c.1112+21A>G r.(=) p.(=)
?/? c.1112+22T>C r.(=) p.(=)
?/? c.1112+28C>G r.(=) p.(=)
?/? c.1122A>G r.(=) p.(=)
?/? c.1225+19A>G r.(=) p.(=)
?/? c.1225+26A>T r.(=) p.(=)
?/? c.1225+28A>G r.(=) p.(=)
?/? c.1225+35T>A r.(=) p.(=)
?/? c.1225+47A>G r.(=) p.(=)
?/? c.1226-40T>C r.(=) p.(=)
?/? c.1226-14C>A r.(=) p.(=)
?/? c.1226-7T>C r.(=) p.(=)
?/? c.1243T>C r.(=) p.(=)
?/? c.1308A>G r.(=) p.(=)
?/? c.1315A>C r.(?) p.(Asn439His)
?/? c.1321C>T r.(?) p.(Leu441Phe)
?/? c.1334+22C>T r.(=) p.(=)
?/? c.1334+36_1334+42del r.(=) p.(=)
?/? c.1334+50G>C r.(=) p.(=)
?/? c.1335-34T>C r.(=) p.(=)
?/? c.1335-20del r.(=) p.(=)
?/? c.1338G>A r.(=) p.(=)
?/? c.1340G>A r.(?) p.(Arg447His)
?/? c.1380A>T r.(=) p.(=)
?/? c.1392A>T r.(=) p.(=)
?/? c.1416C>T r.(=) p.(=)
?/? c.1436G>A r.(?) p.(Arg479Gln)
?/? c.1493C>T r.(?) p.(Ala498Val)
?/? c.1508G>A r.(?) p.(Ser503Asn)
?/? c.1525+19C>T r.(=) p.(=)
?/? c.1525+20A>G r.(=) p.(=)
?/? c.1526-51A>G r.(=) p.(=)
?/? c.1526-35T>A r.(=) p.(=)
?/? c.1526-19G>A r.(=) p.(=)
?/? c.1538G>A r.(?) p.(Cys513Tyr)
?/? c.1586_1591del r.(?) p.(Ser529_Asn530del)
?/? c.1590_1592del r.(?) p.(Asn530del)
?/? c.1596C>T r.(=) p.(=)
?/? c.1640T>C r.(?) p.(Met547Thr)
?/? c.1659T>A r.(=) p.(=)
?/? c.1673+26C>G r.(=) p.(=)
?/? c.1673+40C>G r.(=) p.(=)
?/? c.1673+46A>T r.(=) p.(=)
?/? c.1733A>G r.(?) p.(Asn578Ser)
?/? c.1768G>A r.(?) p.(Glu590Lys)
?/? c.1770A>T r.(?) p.(Glu590Asp)
?/? c.1789G>A r.(?) p.(Glu597Lys)
?/? c.1795+24T>G r.(=) p.(=)
?/? c.1795+45A>G r.(=) p.(=)
?/? c.1796-28G>T r.(=) p.(=)
?/? c.1809T>A r.(?) p.(Ser603Arg)
?/? c.1815G>T r.(?) p.(Leu605Phe)
?/? c.1827G>T r.(?) p.(Leu609Phe)
?/? c.1831G>A r.(?) p.(Gly611Arg)
?/? c.1868T>A r.(?) p.(Phe623Tyr)
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