Transcript #00005382 (NM_001297.4, CNGB1 gene)

Transcript name transcript variant 1
Gene name CNGB1 (cyclic nucleotide gated channel beta 1)
Chromosome 16
Transcript - NCBI ID NM_001297.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_001288.3
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

766 entries on 8 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. 29 c.? r.(?) p.?
+/. 29 c.? r.(?) p.?
+?/. - c.1A>T r.(?) p.(Met1?)
+/. - c.1A>T r.(?) p.(Met1?)
?/. - c.1A>T r.(?) p.(Met1?)
?/. - c.46C>G r.(?) p.(Pro16Ala)
+/. 2 c.60del r.(?) p.(Met21Cysfs*75)
-?/. - c.90G>A r.(?) p.(Glu30=)
?/. - c.105G>A r.(=) p.(=)
?/. - c.106G>A r.(?) p.(Glu36Lys)
-/. - c.123G>A r.(?) p.(Pro41=)
?/. - c.139G>A r.(?) p.(Glu47Lys)
?/. 2i c.159+5G>A r.spl? p.?
?/. 2i c.159+5G>A r.spl? p.?
-/. - c.159+14C>T r.(=) p.(=)
?/. - c.161C>G r.(?) p.(Pro54Arg)
?/. - c.165C>T r.(?) p.(Pro55=)
?/. - c.190G>T r.(?) p.(Val64Leu)
?/. 3i c.217+5G>A r.spl? p.(?)
?/. 3i c.217+5G>A r.spl? p.?
?/. 3i c.217+5G>C r.spl? p.?
?/. - c.217+5G>C r.spl? p.?
+?/. - c.217+5G>C r.spl? p.?
?/. 3i c.217+5G>C r.spl? p.?
?/. 3i c.217+5G>C r.spl? p.?
+?/. - c.217+5G>C r.spl? p.?
+/. - c.217+5G>C r.spl p.?
?/. - c.217+5G>C r.spl? p.?
-/. 3i c.217+46G>A r.(?) p.(=)
+?/. - c.218-2A>G r.spl? p.?
?/. - c.232G>A r.(?) p.(Ala78Thr)
-?/. - c.256C>T r.(?) p.(Arg86Trp)
-/. - c.257G>C r.(?) p.(Arg86Pro)
+/. 4 c.262C>T r.(?) p.(Gln88*)
+/. 4 c.262C>T r.(?) p.(Gln88*)
+/. 4 c.262C>T r.(?) p.(Gln88*)
+?/. 4 c.262C>T r.(?) p.(Gln88*)
+/. - c.262C>T r.(?) p.(Gln88Ter)
?/. - c.262C>T r.(?) p.(Gln88*)
+/. - c.262C>T r.(?) p.(Gln88*)
+/. - c.290+2T>C r.spl? p.?
+/. - c.290+2T>C r.spl? p.?
+?/. - c.292C>T r.(?) p.(Pro98Ser)
-/. - c.299G>A r.(?) p.(Arg100His)
-/. - c.299G>A r.(?) p.(Arg100His)
-/. 5 c.299G>A r.(?) p.(Arg100His)
-/. - c.299G>A r.(?) p.(Arg100His)
-/. - c.299G>A r.(?) p.(Arg100His)
+?/. - c.315G>A r.(?) p.(Trp105*)
+/. 5 c.315G>A r.(?) p.(Trp105*)
+/. 5 c.315G>A r.(?) p.(Trp105*)
-/. - c.327C>T r.(?) p.(Gly109=)
-/. - c.327C>T r.(?) p.(Gly109=)
-/. 5 c.327C>T r.(?) p.(Gly109=)
+/. 5 c.346C>T r.(?) p.(Gln116*)
+/. 5 c.346C>T r.(?) p.(Gln116*)
+/. 5 c.346C>T r.(?) p.(Gln116*)
+/. - c.346C>T r.(?) p.(Gln116*)
?/. - c.358A>G r.(?) p.(Ser120Gly)
+?/. 5 c.367G>T r.(?) p.(Glu123*)
+/. 6 c.385del r.(?) p.(Leu129Trpfs*148)
+/. - c.385del r.(?) p.(Leu129Trpfs*148)
-?/. - c.412+8C>A r.(=) p.(=)
+?/. - c.412+8C>A r.(=) p.(=)
-/. - c.412+8C>A r.(=) p.(=)
+?/. 6i c.413-1G>A r.(?) p.(?)
+/. - c.413-1G>A r.spl p.?
+/. 6i c.413-1G>A r.spl p.(Cys139Alafs*138)
+/. 6i c.413-1G>A r.spl? p.(?)
+/. 6i c.413-1G>A r.spl p.?
+/. 6i c.413-1G>A r.spl? p.?
+/. - c.413-1G>A r.spl p.?
+/. - c.413-1G>A r.spl p.?
+/. 6i c.413-1G>A r.spl p.(Cys139Alafs*138)
+/. - c.413-1G>A r.spl p.?
+/. - c.413-1G>A r.(?) p.?
+/. - c.413-1G>A r.spl? p.?
+?/. - c.413-1G>A r.spl p.(?)
+?/. 6i c.413-1G>A r.spl p.?
+/. - c.413-1G>A r.spl? p.?
+/. - c.413-1G>A r.spl p.(?)
+/. - c.413-1G>A r.spl p.?
+/. - c.413-1G>A r.spl p.?
+/. - c.413-1G>A r.spl p.?
+/. - c.413-1G>A r.spl p.?
?/. 7 c.451G>C r.(?) p.(Asp151His)
-/. - c.458+7C>T r.(=) p.(=)
?/. - c.458+8C>T r.(?) p.?
?/. - c.479T>C r.(?) p.(Leu160Pro)
+/. 8 c.522dup r.(?) p.(Lys175Glnfs*4)
+/. - c.522dup r.(?) p.(Lys175Glnfs*4)
+/. - c.522dup r.(?) p.(Lys175Glnfs*4)
+/. - c.522dup r.(?) p.(Lys175GlnfsTer4)
+/. - c.522dup r.(?) p.(Lys175GlnfsTer4)
+/. 8i c.534+1G>A r.spl p.?
+/. 8i c.534+1G>A r.spl p.?
+/. - c.583+2T>C r.spl p.?
+/. - c.583+2T>C r.(535_583del) p.(Val179Argfs*82)
+/. - c.583+2T>C r.spl p.?
-?/. - c.584-9G>A r.(=) p.(=)
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