Transcript #00024096 (NM_001277269.1, OTOG gene)

Transcript name otogelin
Gene name OTOG (otogelin)
Chromosome 11
Transcript - NCBI ID NM_001277269.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001264198.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2016-01-11 17:56:50 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-3093G>A r.(?) p.(=)
+/. - c.? r.? p.?
-?/. - c.93C>T r.(?) p.(Leu31=)
?/. - c.209C>T r.(?) p.(Ala70Val)
-?/. - c.274G>A r.(?) p.(Val92Met)
+?/. - c.330C>G r.(?) p.(Tyr110*)
-?/. - c.354C>T r.(?) p.(Gly118=)
?/. - c.421G>A r.(?) p.(Val141Met)
-?/. - c.421G>A r.(?) p.(Val141Met)
+/. - c.422-2A>G r.spl? p.?
?/. - c.433G>A r.(?) p.(Gly145Ser)
?/. - c.433G>A r.(?) p.(Gly145Ser)
?/. - c.437C>G r.(?) p.(Pro146Arg)
?/. - c.553G>A r.(?) p.(Glu185Lys)
-/. - c.570C>T r.(?) p.(Ser190=)
?/. - c.586G>A r.(?) p.(Asp196Asn)
?/. - c.586G>A r.(?) p.(Asp196Asn)
?/. - c.639_641del r.(?) p.(Phe214del)
-?/. - c.715A>G r.(?) p.(Met239Val)
?/. - c.849G>T r.(?) p.(Gly283=)
-?/. - c.879G>A r.(?) p.(Lys293=)
-?/. - c.918C>T r.(?) p.(Asp306=)
?/. - c.935A>G r.(?) p.(His312Arg)
?/. - c.952G>A r.(?) p.(Ala318Thr)
-/. - c.953C>A r.(?) p.(Ala318Asp)
-/. - c.953C>A r.(?) p.(Ala318Asp)
-?/. - c.970G>A r.(?) p.(Gly324Arg)
-?/. - c.1002G>A r.(?) p.(Pro334=)
+/. - c.1009C>T r.(?) p.(Gln337Ter)
-/. - c.1033-35A>C r.(=) p.(=)
-?/. - c.1086C>T r.(?) p.(His362=)
-/. - c.1123A>T r.(?) p.(Thr375Ser)
-?/. - c.1140-4A>C r.spl? p.?
?/. - c.1211G>A r.(?) p.(Arg404Gln)
?/. - c.1321C>T r.(?) p.(Arg441Trp)
?/. - c.1322G>A r.(?) p.(Arg441Gln)
-?/. - c.1389C>A r.(?) p.(Phe463Leu)
?/. - c.1414G>C r.(?) p.(Ala472Pro)
?/. - c.1433T>G r.(?) p.(Phe478Cys)
?/. - c.1438G>A r.(?) p.(Gly480Arg)
?/. - c.1490C>T r.(?) p.(Thr497Ile)
+/. - c.1535-2del r.spl? p.?
-?/. - c.1664A>G r.(?) p.(Asn555Ser)
-?/. - c.1842C>T r.(?) p.(Ser614=)
?/. - c.1876C>T r.(?) p.(Arg626Trp)
?/. - c.1991+61T>A r.(=) p.(=)
?/. - c.2020C>T r.(?) p.(Pro674Ser)
-/. - c.2074T>C r.(?) p.(Ser692Pro)
-/. - c.2074T>C r.(?) p.(Ser692Pro)
-?/. - c.2082C>T r.(?) p.(Ser694=)
?/. - c.2098G>A r.(?) p.(Asp700Asn)
-?/. - c.2117-9C>T r.(=) p.(=)
+/. - c.2126_2148dup r.(?) p.(Thr717GlnfsTer20)
?/. - c.2207A>G r.(?) p.(Gln736Arg)
+/. - c.2207del r.(?) p.(Gln736Argfs*79)
+/. - c.2228del r.(?) p.(Arg743ProfsTer72)
-?/. - c.2250C>T r.(?) p.(Cys750=)
?/. - c.2285G>A r.(?) p.(Arg762His)
-?/. - c.2314C>G r.(?) p.(Arg772Gly)
-/. - c.2376G>A r.(?) p.(Pro792=)
-/. - c.2434G>A r.(?) p.(Asp812Asn)
+/. - c.2500C>T r.(?) p.(Gln834Ter)
?/. - c.2561C>A r.(?) p.(Pro854His)
-/. - c.2597+10G>A r.(=) p.(=)
-/. - c.2597+10G>A r.(=) p.(=)
-/. - c.2597+14G>A r.(=) p.(=)
-/. - c.2597+14G>A r.(=) p.(=)
-?/. - c.2693C>T r.(?) p.(Thr898Met)
-/. - c.2755G>A r.(?) p.(Ala919Thr)
-/. - c.2755G>A r.(?) p.(Ala919Thr)
-?/. - c.2759G>T r.(?) p.(Arg920Leu)
-?/. - c.2781C>T r.(?) p.(Cys927=)
?/. - c.2984G>A r.(?) p.(Arg995His)
?/. - c.3177+3A>G r.spl? p.?
?/. - c.3178A>G r.(?) p.(Ser1060Gly)
?/. - c.3179G>A r.(?) p.(Ser1060Asn)
-/. - c.3224G>A r.(?) p.(Arg1075Gln)
-/. - c.3224G>A r.(?) p.(Arg1075Gln)
-?/. - c.3265A>G r.(?) p.(Ile1089Val)
-?/. 26 c.3265A>G r.(?) p.(Ile1089Val)
-?/. - c.3265A>G r.(?) p.(Ile1089Val)
-?/. - c.3336G>A r.(?) p.(Ala1112=)
-?/. - c.3371A>G r.(?) p.(Asn1124Ser)
?/. - c.3371A>G r.(?) p.(Asn1124Ser)
-/. - c.3444+15C>T r.(=) p.(=)
-/. - c.3444+15C>T r.(=) p.(=)
-/. - c.3459C>T r.(?) p.(Leu1153=)
-/. - c.3561+10C>A r.(=) p.(=)
?/. - c.3685G>A r.(?) p.(Val1229Met)
?/. - c.3685G>A r.(?) p.(Val1229Met)
-?/. - c.3700C>A r.(?) p.(Arg1234=)
+/. - c.3700C>T r.(?) p.(Arg1234*)
-/. - c.3710G>A r.(?) p.(Arg1237His)
-/. - c.3710G>A r.(?) p.(Arg1237His)
+/. - c.3718+1G>A r.spl? p.?
+/. - c.3718+2T>C r.spl? p.?
?/. - c.3719C>T r.(?) p.(Pro1240Leu)
?/. - c.3719C>T r.(?) p.(Pro1240Leu)
+?/+? 31 c.3763T>C r.(?) p.(Tyr1255His)
?/. - c.3997A>G r.(?) p.(Lys1333Glu)
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