Transcript #00002639 (NM_003938.6, AP3D1 gene)

Transcript name transcript variant 2
Gene name AP3D1 (adaptor-related protein complex 3, delta 1 subunit)
Chromosome 19
Transcript - NCBI ID NM_003938.6
Transcript - Ensembl ID -
Protein - NCBI ID NP_003929.4
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.211G>A r.(?) p.(Asp71Asn)
-?/. - c.273+15C>T r.(=) p.(=)
-?/. - c.274-16A>C r.(=) p.(=)
-?/. - c.309C>T r.(?) p.(His103=)
-?/. - c.309C>T r.(?) p.(His103=)
-?/. - c.463-4G>A r.spl? p.?
-?/. - c.463-4G>A r.spl? p.?
-?/. - c.592+12dup r.(=) p.(=)
-?/. - c.593-6C>T r.(=) p.(=)
?/. - c.602C>T r.(?) p.(Ser201Leu)
-?/. - c.655C>T r.(?) p.(Leu219=)
?/. - c.703_705del r.(?) p.(Asn235del)
-?/. - c.732+13C>T r.(=) p.(=)
-/. - c.733-64_733-15del r.(=) p.(=)
-?/. - c.733-64_733-15del r.(=) p.(=)
-?/. - c.735C>T r.(?) p.(=)
-?/. - c.780C>T r.(?) p.(Ile260=)
-?/. - c.810G>A r.(?) p.(Thr270=)
-?/. - c.810G>A r.(?) p.(Thr270=)
-/. - c.857-3C>T r.spl? p.?
-/. - c.857-3C>T r.spl? p.?
?/. - c.868C>G r.(?) p.(Leu290Val)
?/. - c.906+19G>A r.(=) p.(=)
-/. - c.1011C>T r.(?) p.(Ser337=)
-?/. - c.1011C>T r.(?) p.(Ser337=)
-?/. - c.1012G>A r.(?) p.(Val338Met)
-/. - c.1101+7G>A r.(=) p.(=)
-?/. - c.1116C>T r.(?) p.(Asn372=)
-?/. - c.1197G>A r.(?) p.(Lys399=)
-?/. - c.1363G>A r.(?) p.(Ala455Thr)
?/. - c.1363G>A r.(?) p.(Ala455Thr)
?/. - c.1390G>A r.(?) p.(Asp464Asn)
?/. - c.1597A>G r.(?) p.(Ile533Val)
?/. - c.1768G>A r.(?) p.(Val590Met)
?/. - c.1786G>A r.(?) p.(Val596Ile)
-?/. - c.1869G>A r.(?) p.(Leu623=)
-?/. - c.1869G>A r.(?) p.(Leu623=)
?/. - c.1917G>T r.(?) p.(Glu639Asp)
-?/. - c.1929C>T r.(?) p.(Ala643=)
-?/. - c.1936C>T r.(?) p.(His646Tyr)
+?/. - c.1977del r.(?) p.(Ala660Argfs*54)
-?/. - c.1978G>T r.(?) p.(Ala660Ser)
-/. - c.1989A>G r.(?) p.(Glu663=)
-?/. - c.2001+10T>A r.(=) p.(=)
-/. - c.2002-3C>T r.spl? p.?
-/. - c.2002-3C>T r.spl? p.?
-?/. - c.2087C>A r.(?) p.(Thr696Asn)
-?/. - c.2109C>T r.(?) p.(Pro703=)
-?/. - c.2124C>T r.(?) p.(=)
?/. - c.2194C>T r.(?) p.(Arg732Trp)
-?/. - c.2201G>A r.(?) p.(Arg734Gln)
?/. - c.2201G>A r.(?) p.(Arg734Gln)
-/. - c.2254A>G r.(?) p.(Lys752Glu)
-?/. - c.2254A>G r.(?) p.(Lys752Glu)
?/. - c.2263C>T r.(?) p.(Arg755Cys)
-?/. - c.2292C>T r.(?) p.(Ser764=)
?/. - c.2329G>A r.(?) p.(Val777Ile)
-?/. - c.2349+8T>C r.(=) p.(=)
?/. - c.2473G>A r.(?) p.(Glu825Lys)
-?/. - c.2504C>G r.(?) p.(Pro835Arg)
?/. - c.2516A>G r.(?) p.(Lys839Arg)
-?/. - c.2580G>T r.(?) p.(Lys860Asn)
-?/. - c.2593_2598del r.(?) p.(Glu865_Lys866del)
-?/. - c.2593_2598del r.(?) p.(Glu865_Lys866del)
-?/. - c.2593_2598del r.(?) p.(Glu865_Lys866del)
-?/. - c.2593_2598del r.(?) p.(Glu865_Lys866del)
-?/. - c.2601+765C>T r.(=) p.(=)
-/. - c.2601+777C>T r.(=) p.(=)
-?/. - c.2602-1125G>A r.(=) p.(=)
-?/. - c.2602-1101C>T r.(=) p.(=)
-?/. - c.2602-1089C>T r.(=) p.(=)
?/. - c.2602-1081C>T r.(=) p.(=)
-?/. - c.2602-1017C>A r.(=) p.(=)
-?/. - c.2602-1017C>A r.(=) p.(=)
-/. - c.2602-1014C>T r.(=) p.(=)
-?/. - c.2602-1012A>G r.(=) p.(=)
-?/. - c.2638G>A r.(?) p.(Glu880Lys)
-?/. - c.2659G>A r.(?) p.(Gly887Ser)
-?/. - c.2706G>A r.(?) p.(Ala902=)
-?/. - c.2706G>A r.(?) p.(Ala902=)
-?/. - c.2706G>A r.(?) p.(Ala902=)
-?/. - c.2715G>A r.(?) p.(Pro905=)
-?/. - c.2751+12T>A r.(=) p.(=)
-/. - c.2752-8A>G r.(=) p.(=)
-?/. - c.2766C>T r.(?) p.(Tyr922=)
-?/. - c.2799+9C>T r.(=) p.(=)
-?/. - c.2799+17C>T r.(=) p.(=)
-?/. - c.3012T>C r.(?) p.(Tyr1004=)
?/. - c.3028A>C r.(?) p.(Ser1010Arg)
?/. - c.3028A>C r.(?) p.(Ser1010Arg)
-?/. - c.3047A>G r.(?) p.(Lys1016Arg)
-?/. - c.3079-13C>T r.(=) p.(=)
-?/. - c.3079-5C>T r.spl? p.?
-?/. - c.3099C>T r.(?) p.(His1033=)
-/. - c.3099C>T r.(?) p.(His1033=)
-?/. - c.3099C>T r.(?) p.(His1033=)
-?/. - c.3214A>C r.(?) p.(Ile1072Leu)
-?/. - c.3214A>C r.(?) p.(Ile1072Leu)
?/. - c.3218A>C r.(?) p.(Lys1073Thr)
-?/. - c.3233G>A r.(?) p.(Arg1078Gln)
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