Transcript #00001472 (NM_000484.3, APP gene)

Transcript name transcript variant 1
Gene name APP (amyloid beta (A4) precursor protein)
Chromosome 21
Transcript - NCBI ID NM_000484.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000475.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:34:50 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. 1 c.47G>A r.(?) p.(Arg16Gln)
?/. 2 c.144G>T r.(?) p.(Gln48His)
-?/. - c.225+19C>G r.(=) p.(=)
-?/. - c.225+19C>G r.(=) p.(=)
-?/. - c.355+9G>A r.(=) p.(=)
-?/. - c.355+9G>A r.(=) p.(=)
?/. - c.433G>A r.(?) p.(Glu145Lys)
?/. - c.440A>G r.(?) p.(His147Arg)
+?/. - c.440A>G r.(?) p.(His147Arg)
-?/. - c.469-4G>A r.spl? p.?
-?/. - c.602C>T r.(?) p.(Ala201Val)
?/. 5 c.622G>T r.(?) p.(Val208Phe)
?/. 5 c.635G>T r.(?) p.(Gly212Val)
-?/. - c.663-9C>A r.(=) p.(=)
?/. - c.722_724del r.(?) p.(Glu241del)
?/. - c.830C>T r.(?) p.(Thr277Ile)
-?/. - c.885C>T r.(?) p.(Ala295=)
?/. - c.890C>T r.(?) p.(Thr297Met)
?/. - c.916C>T r.(?) p.(Arg306Cys)
?/. 7 c.923A>G r.(?) p.(Tyr308Cys)
?/. - c.952C>G r.(?) p.(Pro318Ala)
-?/. - c.975C>T r.(?) p.(=)
?/. - c.982C>T r.(?) p.(Arg328Trp)
?/. 7 c.982C>T r.(?) p.(Arg328Trp)
-?/. - c.1017C>T r.(?) p.(Ala339=)
-?/. - c.1034-6C>G r.(=) p.(=)
?/. 8i c.1090+194G>A r.(=) p.(=)
?/. 9 c.1103C>A r.(?) p.(Ala368Glu)
-?/. - c.1224+16C>T r.(=) p.(=)
-?/. - c.1224+20C>T r.(=) p.(=)
-?/. - c.1299+9T>C r.(=) p.(=)
-?/. - c.1305C>T r.(?) p.(Phe435=)
?/. - c.1343A>G r.(?) p.(Asn448Ser)
?/. - c.1406G>A r.(?) p.(Arg469His)
?/. - c.1408C>T r.(?) p.(Arg470Cys)
-?/. - c.1416C>T r.(?) p.(Ala472=)
?/. 11 c.1433C>A r.(?) p.(Thr478Asn)
?/. - c.1435G>A r.(?) p.(Ala479Thr)
?/. 12 c.1546C>A r.(?) p.(Arg516Ser)
-?/. - c.1614T>C r.(?) p.(Tyr538=)
-?/. - c.1614T>C r.(?) p.(Tyr538=)
?/. - c.1659A>G r.(?) p.(Ala553=)
-?/. - c.1665C>T r.(?) p.(Ala555=)
?/. - c.1689T>C r.(?) p.(Asp563=)
?/. - c.1751C>A r.(?) p.(Pro584Gln)
-?/. - c.1794C>T r.(?) p.(Thr598=)
-?/. - c.1795G>A r.(?) p.(Glu599Lys)
?/. 14 c.1795G>A r.(?) p.(Glu599Lys)
-?/. - c.1795G>A r.(?) p.(Glu599Lys)
-?/. - c.1815G>A r.(?) p.(Glu605=)
-?/. - c.1824C>T r.(?) p.(Pro608=)
?/. 15 c.1941C>A r.(?) p.(Asp647Glu)
-/? 16 c.1995G>C r.(?) p.(Glu665Asp)
+/+ 16 c.2010G>T r.(?) -
+/+ 16 c.2011A>C r.(?) -
-/? 16 c.(2017G>A) r.(?) p.(Ala673Thr)
?/. 16 c.2017G>A r.(?) p.(Ala673Thr)
+/+ 17 c.(2018C>G) r.(?) p.(Ala673Gly)
+/+ 17 c.(2018C>G) r.(?) p.(Ala673Gly)
+/+ 17 c.(2020G>A) r.(?) p.(Glu674Lys)
+/+ 17 c.(2020G>A) r.(?) p.(Glu674Lys)
+/+ 17 c.(2020G>A) r.(?) p.(Glu674Lys)
+/+ 17 c.2020G>C r.(?) p.(Glu674Gln)
+/+ 17 c.2020G>C r.(?) p.(Glu674Gln)
+/+ 17 c.2020G>C r.(?) p.(Glu674Gln)
+/+ 17 c.2020G>C r.(?) p.(Glu674Gln)
+/+ 17 c.(2021A>G) r.(?) p.(Glu674Gly)
+/+ 17 c.(2021A>G) r.(?) p.(Glu674Gly)
-/- 16 c.(2030A>G) r.(?) p.(His677Arg)
+/+ 16 c.(2032G>A) r.(?) p.(Asp678Asn)
+/+ 16 c.(2044G>A) r.(?) p.(Glu682Lys)
-?/. - c.2064+4C>T r.spl? p.?
-?/. - c.2064+11T>C r.(=) p.(=)
+/. - c.2077G>C r.(?) p.(Glu693Gln)
+/+ 17 c.(2079_2081del) r.(?) p.(Glu693del)
+/+ 17 c.(2079_2081del) r.(?) p.(Glu693del)
+/+ 17 c.(2080G>A) r.(?) p.(Asp694Asn)
+/+ 17 c.(2080G>A) r.(?) p.(Asp694Asn)
+/+ 17 c.(2113C>G) r.(?) p.(Leu705Val)
-/? 17 c.(2124C>T) r.(?) p.(=)
-/. - c.2124C>T r.(?) p.(Gly708=)
-?/. - c.2124C>T r.(?) p.(Gly708=)
-?/. - c.2124C>T r.(?) p.(Gly708=)
?/. - c.2125G>A r.(?) p.(Gly709Ser)
?/. 17 c.2128G>A r.(?) p.(Val710Ile)
-?/. - c.2133C>A r.(?) p.(Val711=)
-?/. - c.2133C>A r.(?) p.(Val711=)
+/+ 17 c.(2137G>A) r.(?) p.(Ala713Thr)
+/+ 17 c.(2137G>A) r.(?) p.(Ala713Thr)
+/+ 17 c.(2137G>A) r.(?) p.(Ala713Thr)
+/+ 17 c.(2137G>A) r.(?) p.(Ala713Thr)
+/+ 17 c.(2137G>A) r.(?) p.(Ala713Thr)
+/? 17 c.2137G>A r.(?) p.(Ala713Thr)
-/? 17 c.(2138C>T) r.(?) p.(Ala713Val)
?/. - c.2138C>T r.(?) p.(Ala713Val)
?/. 17 c.2138C>T r.(?) p.(Ala713Val)
+/+ 17 c.(2140A>G) r.(?) p.(Thr714Ala)
+/+ 17 c.(2140A>G) r.(?) p.(Thr714Ala)
+/+ 17 c.(2140A>G) r.(?) p.(Thr714Ala)
+/+ 17 c.(2141C>T) r.(?) p.(Thr714Ile)
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