Transcript #00017698 (NM_002921.3, RGR gene)

Transcript name transcript variant 1
Gene name RGR (retinal G protein coupled receptor)
Chromosome 10
Transcript - NCBI ID NM_002921.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_002912.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. 1 c.-111A>G r.(=) p.(=)
?/. - c.5C>T r.(?) p.(Ala2Val)
-/. - c.19C>T r.(?) p.(Leu7=)
-/. 1 c.19C>T r.(=) p.(=)
-/. - c.27T>C r.(?) p.(Thr9=)
-/. 1 c.27T>C r.(=) p.(=)
-/. - c.27T>C r.(?) p.(Thr9=)
?/. - c.34G>A r.(?) p.(Gly12Arg)
-?/. 1i c.79+59C>T r.(=) p.(=)
?/. - c.88G>A r.(?) p.(Gly30Ser)
?/. - c.110C>T r.(?) p.(Thr37Ile)
?/. 2 c.123C>T r.(=) p.(=)
-?/. - c.183G>A r.(?) p.(Ala61=)
-?/. - c.183G>A r.(?) p.(Ala61=)
+?/. - c.196A>C r.(?) p.(Ser66Arg)
+?/. - c.196A>C r.(?) p.(Ser66Arg)
+?/. 2 c.196A>C r.(?) p.(Ser66Arg)
?/. 2 c.196A>C r.(?) p.(Ser66Arg)
?/. 2 c.196A>C r.(?) p.(Ser66Arg)
+?/. 2 c.196A>C r.(?) p.(Ser66Arg)
?/. 2 c.196A>C r.(?) p.(Ser66Arg)
?/. 2 c.196A>C r.(?) p.(Ser66Arg)
?/. - c.196A>C r.(?) p.(Ser66Arg)
+?/. - c.196A>C r.(?) p.(Ser66Arg)
+?/. - c.196A>C r.(?) p.(Ser66Arg)
+?/. - c.196A>C r.(?) p.(Ser66Arg)
+?/. - c.196A>C r.(?) p.(Ser66Arg)
+?/. - c.196A>C r.(?) p.(Ser66Arg)
+?/. - c.196A>C r.(?) p.(Ser66Arg)
?/. - c.196A>C r.(?) p.(Ser66Arg)
?/. - c.196A>C r.(?) p.(Ser66Arg)
?/. - c.229C>T r.(?) p.(Leu77Phe)
+?/. 2 c.236G>A r.(?) p.(Arg79His)
+?/. 2 c.236G>A r.(?) p.(Arg79His)
?/. 2i_3i c.(236+1_237-1)_(370+1_371-1)del r.? p.?
?/. - c.262G>A r.(?) p.(Gly88Ser)
?/. - c.262G>A r.(?) p.(?)
-?/. - c.262G>A r.(?) p.(Gly88Ser)
+/. - c.266C>A r.(?) p.(Ser89Ter)
+?/. - c.266C>A r.(?) p.(Ser89*)
+?/. - c.266C>A r.(?) p.(Ser89*)
+?/. - c.266C>A r.(?) p.(Ser89*)
?/. - c.269A>G r.(?) p.(Asp90Gly)
?/. 3 c.286G>A r.(?) p.(Gly96Ser)
?/. - c.286G>A r.(?) p.(Gly96Ser)
-/. - c.330T>C r.(?) p.(Ser110=)
-?/. - c.330T>C r.(?) p.(Ser110=)
?/. - c.349C>T r.(?) p.(Arg117Cys)
?/. - c.350G>A r.(?) p.(Arg117His)
-?/. - c.371-15C>A r.(=) p.(=)
+/. 4 c.371G>A r.(?) p.(Arg124His)
+?/. - c.371G>A r.(?) p.(Arg124His)
?/. - c.397G>A r.(?) p.(Val133Ile)
?/. - c.404T>C r.(?) p.(Leu135Pro)
+?/. 4 c.454C>A r.(?) p.(Leu152Met)
+?/. - c.466C>A r.(?) p.(His156Asn)
-/. 4 c.466C>A r.(?) p.(His156Asn)
-/. 4 c.466C>A r.(?) p.(His156Asn)
-?/. - c.466C>A r.(?) p.(His156Asn)
+?/. 4 c.466C>A r.(?) p.(His156Asn)
-/. - c.471C>T r.(?) p.(Tyr157=)
-/. - c.471C>T r.(?) p.(Tyr157=)
-?/. 4 c.474C>T r.(=) p.(=)
?/. - c.500C>T r.(?) p.(Thr167Ile)
?/. - c.505G>T r.(?) p.(Asp169Tyr)
?/. - c.505G>T r.(?) p.(Asp169Tyr)
?/. - c.505G>T r.(?) p.(Asp169Tyr)
-?/. - c.544T>C r.(?) p.(Phe182Leu)
?/. - c.556_576del r.(?) p.(Phe186_Pro192del)
?/. - c.642+10C>T r.(=) p.(=)
-?/. 5i c.642+16G>A r.(?) p.?
-?/. - c.697A>C r.(?) p.(Ile233Leu)
+?/. - c.734C>T r.(?) p.(Ser245Phe)
+?/. 6 c.734C>T r.(?) p.(Ser245Phe)
-/. - c.734C>T r.(?) p.(Ser245Phe)
-/. - c.734C>T r.(?) p.(Ser245Phe)
+?/. - c.734_735del r.(?) p.(Ser245Tyrfs*29)
+?/. - c.734_735del r.(?) p.(Ser245Tyrfs*29)
+?/. - c.756+5A>G r.spl p.?
-/. 6i c.756+5A>G r.(spl?) p.(?)
-/. 6i c.756+5A>G r.(spl?) p.(?)
-?/. - c.756+5A>G r.spl? p.?
+?/. 6i c.756+5A>G r.spl? p.?
?/. - c.756+5A>G r.spl? p.(?)
-?/. 6i c.756+5A>G r.spl? p.?
-/. - c.756+5A>G r.spl? p.?
-/. 6i c.760-38C>T r.spl? p.?
-?/. - c.762C>A r.(?) p.(Pro254=)
?/. - c.821A>G r.(?) p.(Glu274Gly)
+/. - c.833_834insG r.(?) p.(Ile280Asnfs*78)
+/. - c.836dup r.(?) p.(Ile280Asnfs*78)
+/. - c.836dup r.(?) p.(Ile280Asnfs*78)
+?/. - c.836dup r.(?) p.(Ile280Asnfs*78)
+?/. - c.836dup r.(?) p.(Ile280Asnfs*78)
+?/. - c.836dup r.(?) p.(Ile280Asnfs*78)
+?/. - c.836dup r.(?) p.(Ile280Asnfs*78)
+?/. - c.836dup r.(?) p.(Ile280Asnfs*78)
+?/. - c.836dup r.(?) p.(Ile280Asnfs*78)
+?/. - c.836dup r.(?) p.(Ile280Asnfs*78)
+?/. - c.836dup r.(?) p.(Ile280Asnfs*78)
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