Transcript #00002306 (NM_005751.4, AKAP9 gene)

Transcript name transcript variant 2
Gene name AKAP9 (A kinase (PRKA) anchor protein (yotiao) 9)
Chromosome 7
Transcript - NCBI ID NM_005751.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_005742.4
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

466 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-6G>T r.(?) p.(=)
-?/. - c.48+19A>G r.(=) p.(=)
-?/. - c.54C>A r.(?) p.(Ala18=)
-/. - c.54C>A r.(?) p.(Ala18=)
-/. - c.80C>T r.(?) p.(Ser27Leu)
-?/. - c.80C>T r.(?) p.(Ser27Leu)
-?/. - c.80C>T r.(?) p.(Ser27Leu)
-?/. - c.80C>T r.(?) p.(Ser27Leu)
-/. - c.80C>T r.(?) p.(Ser27Leu)
?/. - c.83A>G r.(?) p.(Asp28Gly)
?/. - c.136A>G r.(?) p.(Lys46Glu)
-?/. - c.139C>T r.(?) p.(His47Tyr)
-/. - c.139C>T r.(?) p.(His47Tyr)
-/. - c.139C>T r.(?) p.(His47Tyr)
-?/. - c.158A>G r.(?) p.(His53Arg)
-/. - c.171T>C r.(?) p.(Ile57=)
?/. - c.205A>G r.(?) p.(Ser69Gly)
?/. - c.285T>A r.(?) p.(His95Gln)
?/. - c.287A>C r.(?) p.(Glu96Ala)
?/. - c.288G>T r.(?) p.(Glu96Asp)
?/. - c.289C>G r.(?) p.(Gln97Glu)
-?/. - c.307-7G>T r.(=) p.(=)
-/. - c.351+12T>C r.(=) p.(=)
?/. - c.375G>A r.(?) p.(Met125Ile)
-?/. - c.441A>G r.(?) p.(Glu147=)
?/. - c.452A>C r.(?) p.(Gln151Pro)
-?/. - c.510G>C r.(?) p.(Glu170Asp)
-?/. - c.510G>C r.(?) p.(Glu170Asp)
-/. - c.510G>C r.(?) p.(Glu170Asp)
-/. - c.510G>C r.(?) p.(Glu170Asp)
-?/. - c.576+3A>G r.spl? p.?
-?/. - c.610G>A r.(?) p.(Asp204Asn)
-/. - c.645A>G r.(?) p.(Gln215=)
?/. - c.674T>C r.(?) p.(Met225Thr)
-?/. - c.714A>G r.(?) p.(Leu238=)
-/. - c.732+15T>C r.(=) p.(=)
?/. - c.743G>A r.(?) p.(Ser248Asn)
-/. - c.747A>G r.(?) p.(Glu249=)
-?/. - c.753G>A r.(?) p.(Leu251=)
-?/. - c.931-8dup r.(=) p.(=)
-/. - c.948A>G r.(?) p.(Val316=)
-?/. - c.948A>G r.(?) p.(Val316=)
-?/. - c.948A>G r.(?) p.(Val316=)
?/. - c.971T>C r.(?) p.(Ile324Thr)
-/. - c.1053A>G r.(?) p.(Lys351=)
-?/. - c.1099G>A r.(?) p.(Val367Met)
-?/. - c.1099G>A r.(?) p.(Val367Met)
?/. - c.1204G>A r.(?) p.(Glu402Lys)
-?/. - c.1259A>G r.(?) p.(Gln420Arg)
-?/. - c.1259A>G r.(?) p.(Gln420Arg)
?/. - c.1259A>G r.(?) p.(Gln420Arg)
?/. - c.1262G>A r.(?) p.(Arg421Gln)
?/. - c.1262G>A r.(?) p.(Arg421Gln)
-/. - c.1301G>A r.(?) p.(Arg434Gln)
?/. - c.1334T>C r.(?) p.(Ile445Thr)
-/. - c.1372G>C r.(?) p.(Ala458Pro)
-/. - c.1372G>C r.(?) p.(Ala458Pro)
-/. - c.1389G>T r.(?) p.(Met463Ile)
-/. - c.1389G>T r.(?) p.(Met463Ile)
-/. - c.1389G>T r.(?) p.(Met463Ile)
-?/. - c.1397G>A r.(?) p.(Arg466Gln)
-?/. - c.1397G>A r.(?) p.(Arg466Gln)
-/. - c.1398G>A r.(?) p.(Arg466=)
?/. - c.1434T>C r.(?) p.(Tyr478=)
?/. - c.1457A>T r.(?) p.(Asp486Val)
-?/. - c.1508A>G r.(?) p.(Gln503Arg)
-?/. - c.1514C>G r.(?) p.(Thr505Ser)
-/. - c.1524A>G r.(?) p.(Gln508=)
-?/. - c.1536C>T r.(?) p.(Leu512=)
-/. - c.1536C>T r.(?) p.(Leu512=)
-/. - c.1536C>T r.(?) p.(Leu512=)
?/. - c.1570T>C r.(?) p.(Cys524Arg)
-/. - c.1575T>C r.(?) p.(Ala525=)
-?/. - c.1599T>G r.(?) p.(Leu533=)
?/. - c.1631_1636del r.(?) p.(Ile544_Gln545del)
?/. - c.1651A>G r.(?) p.(Ile551Val)
-?/. - c.1685A>G r.(?) p.(His562Arg)
-?/. - c.1737T>G r.(?) p.(Ser579=)
-?/. - c.1737T>G r.(?) p.(Ser579=)
?/. - c.1826C>A r.(?) p.(Ala609Asp)
-?/. - c.1890A>G r.(?) p.(Leu630=)
?/. - c.1900G>A r.(?) p.(Glu634Lys)
-?/. - c.1946G>A r.(?) p.(Arg649Gln)
?/. - c.1946G>A r.(?) p.(Arg649Gln)
?/. - c.2003A>C r.(?) p.(Asp668Ala)
-/. - c.2058C>T r.(?) p.(Asp686=)
?/. - c.2113T>G r.(?) p.(Leu705Val)
-?/. - c.2311G>A r.(?) p.(Ala771Thr)
-?/. - c.2377A>G r.(?) p.(Ile793Val)
-?/. - c.2425A>G r.(?) p.(Ile809Val)
?/. - c.2438C>T r.(?) p.(Ser813Phe)
-/. - c.2475T>G r.(?) p.(Leu825=)
-?/. - c.2511T>C r.(?) p.(Ile837=)
?/. - c.2512C>G r.(?) p.(Gln838Glu)
-?/. - c.2554T>C r.(?) p.(Phe852Leu)
?/. - c.2554T>C r.(?) p.(Phe852Leu)
-?/. - c.2559T>C r.(?) p.(Ala853=)
?/. - c.2581T>C r.(?) p.(Tyr861His)
-?/. - c.2589G>A r.(?) p.(Glu863=)
?/. - c.2609G>A r.(?) p.(Cys870Tyr)
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