Transcript #00025390 (NM_001008211.1, OPTN gene)

Transcript name transcript variant 1
Gene name OPTN (optineurin)
Chromosome 10
Transcript - NCBI ID NM_001008211.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001008212.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2019-03-09 15:08:13 +01:00 (CET)
Date last edited N/A


Variants

72 entries on 1 page. Showing entries 1 - 72.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.102G>A r.(?) p.(Thr34=)
-/. - c.102G>A r.(?) p.(Thr34=)
-/. - c.102G>A r.(?) p.(Thr34=)
-/. - c.102G>A r.(?) p.(Thr34=)
-/. - c.123G>A r.(?) p.(Leu41=)
-?/. - c.147C>T r.(?) p.(Thr49=)
+/. - c.160C>G r.spl p.(Leu54Val)
-/. - c.293T>A r.(?) p.(Met98Lys)
-/. - c.293T>A r.(?) p.(Met98Lys)
-?/. - c.293T>A r.(?) p.(Met98Lys)
-?/. 5 c.293T>A r.(?) p.(Met98Lys)
+/. - c.293T>A r.(?) p.(Met98Lys)
-/. - c.293T>A r.(?) p.(Met98Lys)
-?/. - c.295G>T r.(?) p.(Ala99Ser)
-/. - c.369+40del r.(=) p.(=)
+?/. - c.370-50_626+50del r.(?) p.(Asp124Glyfs*4)
+/. - c.381_382insAG r.(?) p.(Asp128Argfs*22)
+/. - c.381_382insAG r.(?) p.(Asp128Argfs*22)
+/. - c.381_382insAG r.(?) p.(Asp128Argfs*22)
+/. - c.381_382insAG r.(?) p.(Asp128Argfs*22)
-?/. - c.398G>A r.(?) p.(Arg133Lys)
-/. - c.402C>A r.(?) p.(Ala134=)
-?/. - c.403G>A r.(?) p.(Glu135Lys)
-?/. - c.404A>C r.(?) p.(Glu135Ala)
-?/. - c.447G>A r.(?) p.(Arg149=)
?/. - c.476G>T r.(?) p.(Gly159Val)
-?/. - c.489A>G r.(?) p.(Glu163=)
-?/. - c.489A>G r.(?) p.(Glu163=)
-?/. - c.489A>G r.(?) p.(Glu163=)
+/. - c.493C>T r.(?) p.(Gln165Ter)
+/. - c.493C>T r.(?) p.(Gln165Ter)
-?/. - c.553-10G>A r.(=) p.(=)
-?/. - c.553-10G>C r.(=) p.(=)
-/. - c.553-5C>T r.spl? p.?
-/. - c.553-5C>T r.spl? p.?
+?/. 6i c.553-5C>T r.spl? p.?
-/. - c.553-5C>T r.spl? p.?
-/. - c.553-5C>T r.spl? p.?
-?/. - c.627-10T>C r.(=) p.(=)
?/. - c.754G>A r.(?) p.(Val252Ile)
-?/. - c.758C>T r.(?) p.(Ala253Val)
-?/. - c.777A>T r.(?) p.(Glu259Asp)
-?/. - c.844A>C r.(?) p.(Thr282Pro)
+/. - c.872del r.(?) p.(Gly291AlafsTer12)
?/. - c.882+5G>C r.spl? p.?
?/. - c.882+5G>C r.spl? p.?
-?/. - c.891C>T r.(?) p.(Ser297=)
-?/. - c.909C>A r.(?) p.(Asn303Lys)
?/. - c.941A>T r.(?) p.(Gln314Leu)
-?/. - c.963C>T r.(?) p.(Ser321=)
-/. - c.964= r.(=) p.(Glu322=)
-/. - c.964= r.(=) p.(Glu322=)
-/. - c.964= r.(=) p.(Glu322=)
-/. - c.964= r.(=) p.(Glu322=)
-/. - c.964= r.(=) p.(Glu322=)
+?/. 10 c.964A>G r.(?) p.(Lys322Glu)
-?/. - c.1077A>G r.(?) p.(Lys359=)
+/. - c.1078_1079del r.(?) p.(Lys360ValfsTer18)
+/. - c.1078_1079del r.(?) p.(Lys360ValfsTer18)
+/. - c.1078_1079del r.(?) p.(Lys360ValfsTer18)
?/. - c.1229T>C r.(?) p.(Leu410Pro)
+/. - c.1242+1G>A r.spl? p.?
+/. - c.1242+1G>A r.spl? p.?
-?/. - c.1324C>T r.(?) p.(Leu442=)
?/. - c.1340T>A r.(?) p.(Met447Lys)
?/. - c.1401+4A>G r.spl? p.?
+/. 14 c.1433A>G r.(?) p.(Glu478Gly)
-?/. - c.1442C>T r.(?) p.(Ala481Val)
-/. - c.1612+10G>A r.(=) p.(=)
-?/. - c.1613-5C>T r.spl? p.?
?/. - c.1618G>C r.(?) p.(Glu540Gln)
-?/. - c.1634G>A r.(?) p.(Arg545Gln)
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