Transcript #00000083 (NM_015272.2, RPGRIP1L gene)

Transcript name RPGRIP1-like, transcript variant 1
Gene name RPGRIP1L (RPGRIP1-like)
Chromosome 16
Transcript - NCBI ID NM_015272.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_056087.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-05-11 13:12:02 +02:00 (CEST)
Date last edited N/A


Variants

267 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-393T>C r.(?) p.(=)
?/. - c.19G>A r.(?) p.(Glu7Lys)
+/. - c.86-2A>G r.86_230del p.?
-?/. - c.106A>G r.(?) p.(Met36Val)
-?/. - c.123A>G r.(?) p.(Ala41=)
?/. - c.140G>A r.(?) p.(Arg47His)
?/. - c.144G>C r.(?) p.(Glu48Asp)
?/. - c.167G>A r.(?) p.(Arg56His)
+?/. - c.171G>T r.(?) p.(Leu57Phe)
?/. - c.171G>T r.(?) p.(Leu57Phe)
?/. - c.196C>A r.(?) p.(Gln66Lys)
+/. - c.196C>T r.(?) p.(Gln66Ter)
-?/. - c.206G>A r.(?) p.(Arg69His)
-?/. - c.230+711A>T r.(=) p.(=)
-?/. - c.230+820T>C r.(=) p.(=)
+/. - c.231-2A>G r.231_529del p.?
?/. - c.287G>A r.(?) p.(Gly96Asp)
-?/. - c.324G>C r.(?) p.(Met108Ile)
+/. - c.394A>T r.(?) p.(Arg132Ter)
+/. - c.394A>T r.(?) p.(Arg132*)
+/. - c.394A>T r.(?) p.(Arg132*)
+/. 4 c.394A>T r.(394a>u) p.(Arg132*)
?/. - c.418C>T r.(?) p.(Leu140Phe)
-?/. - c.444T>C r.(?) p.(Thr148=)
?/. - c.466C>T r.(?) p.(Arg156Cys)
-?/. - c.482G>A r.(?) p.(Arg161His)
-/. - c.529+17G>A r.(=) p.(=)
-/. - c.529+64C>A r.(=) p.(=)
-/. - c.529+64del r.(=) p.(=)
-/. - c.530-15T>C r.(=) p.(=)
-?/. - c.530-15T>C r.(=) p.(=)
-/. - c.532A>G r.(?) p.(Ile178Val)
-?/. - c.532A>G r.(?) p.(Ile178Val)
?/. - c.628A>G r.(?) p.(Asn210Asp)
+?/. - c.628A>G r.(?) p.(Asn210Asp)
-/. - c.632+16del r.(=) p.(=)
-?/. - c.633-14G>C r.(=) p.(=)
-?/. - c.640G>A r.(?) p.(Val214Ile)
-?/. - c.659G>A r.(?) p.(Gly220Asp)
+?/. - c.671_677del r.(?) p.(Gln224Glyfs*7)
+/. 6 c.671_677del r.(?) p.(Glu224Glyfs*7)
?/. - c.685G>A r.(?) p.(Ala229Thr)
-?/. - c.685G>A r.(?) p.(Ala229Thr)
-?/. - c.685G>A r.(?) p.(Ala229Thr)
-/. - c.685G>A r.(?) p.(Ala229Thr)
?/. - c.685G>A r.(?) p.(Ala229Thr)
-?/. - c.685G>A r.(?) p.(Ala229Thr)
-/. - c.685G>A r.(?) p.(Ala229Thr)
-?/. - c.685G>A r.(?) p.(Ala229Thr)
+/. - c.697A>T r.(?) p.(Lys233*)
+?/. 6 c.712del r.(?) p.(Arg238Glufs*29)
+/. - c.712del r.(?) p.(Arg238GlufsTer29)
+/. 6 c.721_724delAATG r.(?) p.(Asn241Lysfs*25)
+/+ 6 c.723_726del r.(723_726del) p.(Asn241Lysfs*25)
+/. - c.757C>T r.(?) p.(Gln253*)
?/. - c.788G>A r.(?) p.(Arg263Gln)
?/. - c.821A>T r.(?) p.(Gln274Leu)
?/. - c.949C>T r.(?) p.(Leu317Phe)
-?/. - c.960G>A r.(?) p.(=)
-?/. - c.961C>T r.(?) p.(Arg321Cys)
?/. - c.962G>A r.(?) p.(Arg321His)
+/. - c.962G>A r.(?) p.(Arg321His)
?/. 8 c.972C>G r.(?) p.(Cys324Trp)
+/. - c.986_987del r.(?) p.(Lys329ThrfsTer9)
+/. - c.986_987del r.(?) p.(Lys329ThrfsTer9)
?/. - c.1029+3A>C r.spl? p.?
-/. - c.1030-58del r.(=) p.(=)
+/. - c.1033C>T r.(?) p.(Gln345*)
+/. 9 c.1033C>T r.(1033c>u) p.(Gln345*)
-/. - c.1072T>C r.(?) p.(Leu358=)
-?/. - c.1072T>C r.(?) p.(Leu358=)
-?/. - c.1072T>C r.(?) p.(Leu358=)
-?/. - c.1085A>G r.(?) p.(Tyr362Cys)
-?/. - c.1103+15C>T r.(=) p.(=)
+/. - c.1132del r.(?) p.(Trp378Glyfs*3)
?/. - c.1156A>G r.(?) p.(Lys386Glu)
-?/. - c.1156A>G r.(?) p.(Lys386Glu)
-/. - c.1165A>G r.(?) p.(Ile389Val)
-?/. - c.1165A>G r.(?) p.(Ile389Val)
-?/. - c.1165A>G r.(?) p.(Ile389Val)
+/. 10 c.1177G>A r.(?) p.(Glu393Lys)
+/. - c.1243+1G>A r.spl? p.?
+/. - c.1243+1530G>C r.1243_1244ins1243+1459_1243+1532 p.Gln416IlefsTer55
-?/. - c.1331G>A r.(?) p.(Arg444His)
?/. 11 c.1331G>A r.(?) p.(Arg444His)
-?/. - c.1335A>T r.(?) p.(Ile445=)
-?/. - c.1340T>C r.(?) p.(Leu447Ser)
-/. - c.1340T>C r.(?) p.(Leu447Ser)
+?/. 11 c.1340T>C r.(?) p.(Leu447Ser)
+/. 11 c.1340T>C r.(?) p.(Leu447Ser)
-/. - c.1340T>C r.(?) p.(Leu447Ser)
-?/. - c.1340T>C r.(?) p.(Leu447Ser)
-?/. - c.1340T>C r.(?) p.(Leu447Ser)
-/. - c.1341G>A r.(?) p.(Leu447=)
?/. 11i c.1351-11A>G r.spl p.?
?/. - c.1397T>G r.(?) p.(Ile466Arg)
?/. - c.1419A>C r.(?) p.(Lys473Asn)
?/. - c.1496A>C r.(?) p.(Gln499Pro)
+/. - c.1555C>T r.(?) p.(Gln519Ter)
-?/. - c.1558C>G r.(?) p.(His520Asp)
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