Transcript #00021708 (NM_001128228.2, TPRN gene)

Transcript name taperin
Gene name TPRN (taperin)
Chromosome 9
Transcript - NCBI ID NM_001128228.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001121700.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

65 entries on 1 page. Showing entries 1 - 65.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-4439dup r.(?) p.(=)
-?/. _1_4_ c.(?_1)_(*1_?)dup r.(=) p.(=)
-?/. - c.46C>T r.(?) p.(Pro16Ser)
+?/. - c.85A>T r.(?) p.(Lys29*)
-?/. - c.116C>T r.(?) p.(Pro39Leu)
?/. - c.176A>G r.(?) p.(Asn59Ser)
+/+ 1 c.225_235del r.(?) p.(Gly76Alafs*150)
+/. 1 c.225_235del r.(?) p.(Gly76Alafs*150)
+/. 1 c.225_235del r.(?) p.(Gly76Alafs*150)
+/. - c.225_235del r.(?) p.(Gly76AlafsTer150)
+/. - c.225_235del r.(?) p.(Gly76AlafsTer150)
+/. - c.225_235del r.(?) p.(Gly76AlafsTer150)
+/+ 1 c.227_237dup r.(?) p.(Leu80Glyfs*374)
+/. 1 c.227_237dup r.(?) p.(Leu80Glyfs*374)
-/. 1 c.229G>A r.(?) p.(Ala77Thr)
-?/. - c.229G>A r.(?) p.(Ala77Thr)
?/. - c.229G>A r.(?) p.(Ala77Thr)
-/. 1 c.229G>A r.(?) p.(Ala77Thr)
?/. - c.274C>T r.(?) p.(Leu92Phe)
-/. - c.559G>T r.(?) p.(Ala187Ser)
?/. - c.655C>A r.(?) p.(Arg219Ser)
?/. - c.655C>A r.(?) p.(Arg219Ser)
-?/. - c.663C>A r.(?) p.(Leu221=)
-?/. - c.669C>T r.(?) p.(Asn223=)
-?/. - c.674A>C r.(?) p.(His225Pro)
+/. - c.744G>A r.(?) p.(Trp248Ter)
?/. - c.787C>G r.(?) p.(Pro263Ala)
-?/. - c.823C>A r.(?) p.(Pro275Thr)
-?/. - c.891C>G r.(?) p.(Phe297Leu)
?/. - c.905C>A r.(?) p.(Ala302Asp)
+/+ 1 c.943dup r.(?) p.(Leu315Profs*32)
+/. - c.1056G>A p.(Trp352*) p.(Glu352=)
+/. - c.1056G>A p.(Trp352*) p.(Glu352=)
+/. - c.1056G>A p.(Trp352*) p.(Glu352=)
+/. - c.1056G>A p.(Trp352*) p.(Glu352=)
+/. - c.1056G>A p.(Trp352*) p.(Glu352=)
+/+ 1 c.1239G>A r.(?) p.(Trp413*)
+/. 1 c.1239G>A r.(?) p.(Trp413*)
-?/. - c.1261C>T r.(?) p.(Pro421Ser)
-?/. - c.1400C>G r.(?) p.(Pro467Arg)
+?/. - c.1402dup r.(?) p.(Gln468ProfsTer68)
+/. - c.1402dup r.(?) p.(Gln468ProfsTer68)
+/+ 1 c.1427del r.(?) p.(Pro476Argfs*67)
+/. 1 c.1427del r.(?) p.(Pro476Argfs*67)
+/+ 1 c.1530del r.(?) p.(Thr511Leufs*32)
+/. 1 c.1530del r.(?) p.(Thr511Leufs*32)
?/. - c.1573C>T r.(?) p.(Arg525Trp)
?/. - c.1579C>T r.(?) p.(Arg527Trp)
-?/. - c.1668C>T r.(?) p.(Gly556=)
+/+ 1i c.1725+5G>A r.spl? p.?
-?/. - c.1726-2198C>T r.(?) p.(?)
-?/. - c.1726-2198C>T r.(?) p.(?)
-?/. - c.1726-7C>T r.(=) p.(=)
-?/-? 2 c.1743C>T r.(=) p.(=)
-?/. - c.1748A>G r.(?) p.(Lys583Arg)
-?/. - c.1748A>G r.(?) p.(Lys583Arg)
-/. - c.1842_1844del r.(?) p.(Glu621del)
-/. - c.1842_1844del r.(?) p.(Glu621del)
-/. - c.1842_1844dup r.(?) p.(Glu621dup)
-/- 2 c.1845_1847del r.(?) p.(Glu621del)
?/. - c.2023G>A r.(?) p.(Ala675Thr)
-?/-? 3 c.2057C>T r.(?) p.(Pro686Leu)
-?/. - c.*4084C>T r.(=) p.(=)
-?/. - c.*4148A>G r.(=) p.(=)
-?/. - c.*4208A>G r.(=) p.(=)
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