Transcript #00000570 (NM_000276.3, OCRL gene)

Transcript name transcript variant a
Gene name OCRL (oculocerebrorenal syndrome of Lowe)
Chromosome X
Transcript - NCBI ID NM_000276.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000267.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 12:33:16 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.(2139+1_2140-1)_(2581+1_2582-1) r.(?) p.(?)
?/. - c.16C>G r.(?) p.(Pro6Ala)
?/. - c.40-90del r.(=) p.(=)
-?/. - c.40-5C>T r.spl? p.?
-?/. - c.40-5C>T r.spl? p.?
-?/. - c.40A>G r.(?) p.(Thr14Ala)
?/. - c.40A>G r.(?) p.(Thr14Ala)
-?/. - c.41C>T r.(?) p.(Thr14Ile)
-/. - c.41C>T r.(?) p.(Thr14Ile)
-?/. - c.41C>T r.(?) p.(Thr14Ile)
-?/. - c.41C>T r.(?) p.(Thr14Ile)
+/. - c.112C>T r.(?) p.(Gln38*)
?/. - c.120-28T>G r.(=) p.(=)
-?/. - c.152A>G r.(?) p.(His51Arg)
-/. - c.152A>G r.(?) p.(His51Arg)
?/. - c.176A>G r.(?) p.(Asn59Ser)
-/. - c.199+16C>G r.(=) p.(=)
-/. - c.199+16C>G r.(=) p.(=)
-?/. - c.200-7dup r.(=) p.(=)
-/. - c.238+11T>C r.(=) p.(=)
+/. 4i c.239-4023A>G r.c.238_239ins[g;239-4022_239-3958] p.Gly81Lysfs*2
-?/. - c.239-20T>C r.(=) p.(=)
?/. - c.253C>T r.(?) p.(Arg85Trp)
+/. - c.260_261del r.(?) p.(Gln87ArgfsTer10)
+/. - c.270G>A r.(?) p.(Trp90Ter)
-/. - c.349+14C>T r.(=) p.(=)
-?/. - c.349+14C>T r.(=) p.(=)
?/. - c.350C>T r.(?) p.(Ala117Val)
?/. - c.351T>G r.(?) p.(Ala117=)
-/. - c.375G>T r.(?) p.(Glu125Asp)
?/. 6i c.439+3A>G r.spl p.?
?/. - c.439+3A>G r.spl p.?
-/. - c.439+3A>G r.spl? p.?
-?/. - c.439+3A>G r.spl? p.?
-?/. - c.439+3A>G r.spl? p.?
-?/. - c.439+3A>G r.spl? p.?
-?/. - c.441G>A r.(?) p.(Gly147=)
-?/. - c.481G>A r.(?) p.(Asp161Asn)
?/. - c.599C>G r.(?) p.(Pro200Arg)
-?/. - c.633A>G r.(?) p.(Val211=)
+/. - c.688C>T r.(?) p.(Arg230Ter)
+/. - c.723-2A>C r.723_824del p.Phe243_Phe276del
+?/. - c.808G>A r.(?) p.(Asp270Asn)
+/. - c.821T>C r.(?) p.(Ile274Thr)
+?/. 10 c.827T>C r.(?) p.(Phe276Ser)
+/. - c.891G>A r.(?) p.(Trp297Ter)
-/. - c.940-12C>T r.(=) p.(=)
+/. - c.940-11G>A r.(=) p.(=)
+/. - c.940-11G>A r.spl p.?
?/. - c.956T>C r.(?) p.(Leu319Pro)
?/. - c.961G>T r.(?) p.(Gly321Trp)
+/. - c.1000C>T r.(?) p.(Arg334Ter)
+?/. - c.1040G>A r.(?) p.(Gly347Glu)
?/. - c.1063A>G r.(?) p.(Lys355Glu)
-?/. - c.1110C>T r.(?) p.(Cys370=)
-?/. - c.1128G>T r.(?) p.(Leu376=)
?/. - c.1184C>T r.(?) p.(Ala395Val)
-/. - c.1245-68C>T r.(?) p.(=)
./. - c.1254T>G r.(?) p.(Ile418Met)
-?/. - c.1275T>C r.(?) p.(Tyr425=)
-?/. - c.1291G>A r.(?) p.(Asp431Asn)
?/. - c.1351G>A r.(?) p.(Asp451Asn)
-?/. - c.1416G>A r.(?) p.(Lys472=)
+/. - c.1431T>G r.(?) p.(Tyr477Ter)
+/. - c.1432_1437del r.(?) p.(Lys478_Tyr479del)
?/. - c.1454G>A r.(?) p.(Arg485Gln)
+/. - c.1466+1G>A r.spl? p.?
?/. - c.1467-4dup r.spl? p.?
+/. - c.1498C>T r.(?) p.(Arg500Ter)
?/. - c.1514G>T r.(?) p.(Gly505Val)
?/. - c.1541G>A r.(?) p.(Arg514Gln)
+?/. - c.1568A>C r.(?) p.(Asp523Ala)
-?/. - c.1602+7A>G r.(=) p.(=)
?/. - c.1603-207G>T r.(=) p.(=)
?/. - c.1603-207G>T r.(=) p.(=)
+/. - c.1621C>T r.(?) p.(Arg541Ter)
+/. - c.1621C>T r.(?) p.(Arg541Ter)
+/. - c.1691_1694dup r.(?) p.(Leu565PhefsTer12)
+/. - c.1737del r.(?) p.(Arg580GlyfsTer64)
?/. - c.1738C>T r.(?) p.(Arg580Trp)
+/. - c.1842G>A r.(?) p.(Trp614Ter)
?/. - c.1868A>G r.(?) p.(Tyr623Cys)
-?/. - c.1880-4T>C r.spl? p.?
+?/. - c.1919_1920del r.(?) p.(Lys640ArgfsTer12)
-?/. - c.1944G>A r.(?) p.(Ser648=)
-?/. - c.1944G>A r.(?) p.(Ser648=)
-?/. - c.1988G>A r.(?) p.(Arg663Gln)
?/. - c.2017G>A r.(?) p.(Gly673Arg)
+/. - c.2098dup r.(?) p.(Thr700AsnfsTer26)
-?/. - c.2116-9C>T r.(=) p.(=)
-?/. - c.2144A>T r.(?) p.(Lys715Ile)
+/. - c.2200del r.(?) p.(Val734PhefsTer8)
+/. - c.2257-2A>G r.spl? p.?
+/. - c.2313_2316del r.(?) p.(Cys771TrpfsTer53)
-?/. - c.2341+1G>A r.spl? p.?
?/. - c.2341+3A>G r.spl? p.?
?/. - c.2368_2370dup r.(?) p.(Ala790dup)
+/. - c.2414dup r.(?) p.(Tyr805*)
+/. - c.2464C>T r.(?) p.(Arg822Ter)
?/. - c.2469+2T>G r.spl? p.?
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