Transcript #00025900 (NM_001122769.2, LCA5 gene)

Transcript name transcript variant 2
Gene name LCA5 (Leber congenital amaurosis 5)
Chromosome 6
Transcript - NCBI ID NM_001122769.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001116241.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2024-01-25 16:03:47 +01:00 (CET)
Date last edited N/A


Variants

81 entries on 1 page. Showing entries 1 - 81.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-192+62T>G r.(=) p.(=)
-/. - c.-191-6202C>T r.(=) p.(=)
+?/. - c.-191-5332_-191-3735del r.(=) p.(=)
+?/. - c.-191-5332_-191-3735del r.(=) p.(=)
+?/. - c.-191-5332_-191-3735del r.(=) p.(=)
+?/. - c.-191-5332_-191-3735del r.(=) p.(=)
+?/. - c.-191-5332_-191-3735del r.(=) p.(=)
-/. - c.-62A>G r.(?) p.(=)
-?/. - c.28A>G r.(?) p.(Thr10Ala)
+/. - c.69C>G r.(?) p.(Tyr23*)
?/. - c.71T>C r.(?) p.(Leu24Ser)
-/. - c.71T>C r.(?) p.(Leu24Ser)
-/. - c.71T>C r.(?) p.(Leu24Ser)
?/. - c.77A>C r.(?) p.(Asp26Ala)
-/. - c.77A>C r.(?) p.(Asp26Ala)
+/. - c.91C>T r.(?) p.(Gln31*)
?/. - c.103C>T r.(?) p.(Arg35*)
?/. - c.137T>A r.(?) p.(Val46Asp)
?/. - c.137T>A r.(?) p.(Val46Asp)
-/. - c.191-9del r.(=) p.(=)
-?/. - c.191-3del r.spl? p.?
+?/. - c.191del r.(?) p.(Pro65Leufs*46)
-/. - c.197G>A r.(?) p.(Arg66Gln)
-?/. - c.325C>T r.(?) p.(Leu109=)
?/. - c.338A>G r.(?) p.(Asn113Ser)
+?/. - c.401A>C r.(?) p.(Lys134Thr)
+?/. - c.514_517del r.(?) p.(Lys172Asnfs*3)
?/. - c.521G>A r.(?) p.(Arg174His)
?/. - c.547C>T r.(?) p.(Arg183Trp)
-/. - c.586C>T r.(?) p.(Leu196=)
+?/. - c.604T>C r.(?) p.(Ser202Pro)
+?/. - c.631_637del r.(?) p.(Glu211Aspfs*13)
+?/. - c.631_637del r.(?) p.(Glu211Aspfs*13)
+/. - c.633_639del r.(?) p.(Glu211Aspfs*13)
+?/. - c.634G>C r.(?) p.(Ala212Pro)
+?/. - c.634G>C r.(?) p.(Ala212Pro)
?/. - c.661T>G r.(?) p.(Leu221Val)
+/. - c.763C>T r.(?) p.(Arg255Ter)
+?/. - c.784del r.(?) p.(Arg263Glyfs*23)
+/. - c.795T>G r.(?) p.(Tyr265*)
+?/. - c.835C>T r.(?) p.(Gln279*)
+?/. - c.835C>T r.(?) p.(Gln279*)
+?/. - c.835C>T r.(?) p.(Gln279*)
+/. - c.838C>T r.(?) p.(Arg280*)
+?/. - c.838C>T r.(?) p.(Arg280*)
+?/. - c.838C>T r.(?) p.(Arg280*)
+/. - c.838C>T r.(?) p.(Arg280*)
+/. - c.838C>T r.(?) p.(Arg280*)
+/. - c.838C>T r.(?) p.(Arg280*)
-?/. - c.858+5G>C r.spl? p.?
?/. - c.858+77C>T r.(=) p.(=)
?/. - c.858+127_858+129del r.(=) p.(=)
-/. - c.859-12G>C r.(=) p.(=)
?/. - c.902G>A r.(?) p.(Arg301His)
?/. - c.955G>A r.(?) p.(Ala319Thr)
?/. - c.1097T>C r.(?) p.(Leu366Ser)
?/. - c.1098+3G>T r.spl? p.?
+?/. - c.1149del r.(?) p.(Pro384Glnfs*18)
-?/. - c.1215T>G r.(?) p.(Val405=)
-/. - c.1232-15T>A r.(=) p.(=)
+?/. - c.1243G>T r.(?) p.(Glu415*)
+?/. - c.1243G>T r.(?) p.(Glu415*)
+?/. - c.1243G>T r.(?) p.(Glu415*)
+?/. - c.1243G>T r.(?) p.(Glu415*)
-?/. - c.1260G>A r.(?) p.(Lys420=)
+?/. - c.1322A>G r.(?) p.(Tyr441Cys)
+?/. - c.1322A>G r.(?) p.(Tyr441Cys)
-?/. - c.1323C>T r.(?) p.(=)
?/. - c.1533C>A r.(?) p.(Phe511Leu)
-/. - c.1642C>T r.(?) p.(Pro548Ser)
-?/. - c.1642C>T r.(?) p.(Pro548Ser)
+/. - c.1676C>A r.(?) p.(Ser559*)
+/. - c.1676C>A r.(?) p.(Ser559*)
-/. - c.1746C>T r.(?) p.(Asn582=)
+/. - c.1756A>T r.(?) p.(Lys586*)
-/. - c.1967G>A r.(?) p.(Gly656Asp)
?/. - c.1967G>A r.(?) p.(Gly656Asp)
?/. - c.1967G>A r.(?) p.(Gly656Asp)
-/. - c.1967G>A r.(?) p.(Gly656Asp)
?/. - c.2036_2047del r.(?) p.(Val681_Ala684del)
?/. - c.2047G>C r.(?) p.(Ala683Pro)
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