Transcript #00024186 (NM_144672.3, OTOA gene)

Transcript name transcript variant 1
Gene name OTOA (otoancorin)
Chromosome 16
Transcript - NCBI ID NM_144672.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_653273.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2016-10-14 18:12:04 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-375587_*144212del r.0? p.0?
./. - c.-159629_*7560384del r.0? p.0?
+/. _1_28_ c.-1_*189{0} r.0 p.0
+?/. _1_28_ c.(?_1)_(3420_?)del r.0? p.0?
+?/. _1_28_ c.(?_1)_(3420_?)del r.0? p.0?
-/. - c.44T>A r.(?) p.(Phe15Tyr)
?/. - c.91G>A r.(?) p.(Asp31Asn)
-/. - c.92-11C>A r.(=) p.(=)
+/. - c.92-1G>T r.spl? p.?
-?/. - c.120+10C>G r.(=) p.(=)
-?/-? 2i c.120+10C>G r.(=) p.(=)
?/? 3 c.131T>C r.(?) p.(Ile44Thr)
+/+ 3i c.151+1G>A r.spl? p.?
+?/. - c.235C>T r.(?) p.(Arg79Trp)
+?/. - c.267+1G>A r.spl? p.?
?/. - c.267+5G>A r.(?) p.(?)
+/. - c.399+2T>C r.spl? p.?
+/. - c.436C>T r.(?) p.(Arg146Ter)
+/. - c.593del r.(?) p.(Glu198GlyfsTer38)
?/. - c.616G>A r.(?) p.(Glu206Lys)
-?/-? 8 c.660C>T r.(=) p.(=)
?/. - c.674C>G r.(?) p.(Ala225Gly)
-?/-? 8i c.739+11A>G r.(=) p.(=)
-?/. - c.821C>T r.(?) p.(Thr274Met)
?/? 10 c.851T>C r.(?) p.(Phe284Ser)
?/. - c.900C>G r.(?) p.(Ile300Met)
-?/. - c.921G>A r.(?) p.(Ala307=)
+/. - c.928G>T r.(?) p.(Glu310*)
?/? 10i c.981-147A>G r.(=) p.(=)
+/+ 11 c.1025A>T r.(?) p.(Asp342Val)
+/. 11 c.1065del r.(?) p.(Lys355Asnfs*5)
-?/-? 11i c.1104+12G>C r.(=) p.(=)
-?/-? 11i c.1105-10C>T r.(=) p.(=)
?/? 12 c.1109A>G r.(?) p.(Lys370Arg)
-/. - c.1141C>G r.(?) p.(Gln381Glu)
?/. - c.1148C>T r.(?) p.(Ala707Val)
?/? 12 c.1172C>T r.(?) p.(Ser391Leu)
-?/. - c.1221C>T r.(?) p.(Pro407=)
?/. - c.1249C>T r.(?) p.(Leu417Phe)
+?/+? 12 c.1249C>T r.(?) p.(Leu417Phe)
+/. 12i c.1320+2T>C r.spl? p.?
+/+ 12i c.1320+2T>C r.spl? p.?
+/. - c.1320+5G>C r.spl? p.?
?/. - c.1334A>G r.(?) p.(Tyr445Cys)
+/. - c.1352G>A r.(?) p.(Gly451Asp)
+/+ 13 c.1352G>A r.(?) p.(Gly451Asp)
?/. - c.1429G>C r.(?) p.(Ala477Pro)
-?/. - c.1500G>C r.(?) p.(Ala500=)
-?/-? 14 c.1500G>C r.(=) p.(=)
-?/. - c.1522G>A r.(?) p.(Val508Met)
-?/. - c.1523T>C r.(?) p.(Val508Ala)
-/. - c.1630-5C>T r.spl? p.?
-/. - c.1630-5C>T r.spl? p.?
+/+ 15i c.1688+1G>T r.spl? p.?
+/. - c.1765del r.(?) p.(Gln589Argfs*55)
+?/+? 16 c.1765del r.(?) p.(Gln589Argfs*55)
+?/. - c.1771T>C r.(?) p.(Phe591Leu)
+/. - c.1807G>T r.(?) p.(Val603Phe)
?/. - c.1807G>T r.(?) p.(Val603Phe)
?/. - c.1820C>T r.(?) p.(Ala607Val)
+/+ 17 c.1879C>T r.(?) p.(Pro627Ser)
?/? 17 c.1880C>G r.(?) p.(Pro627Arg)
+/. - c.1880+1G>A r.spl? p.?
+/+ 17i c.1880+1G>A r.spl? p.?
+/+ 18 c.1939G>C r.(?) p.(Gly647Arg)
-?/. - c.1998G>A r.(?) p.(Arg666=)
-?/-? 19 c.2019C>T r.(=) p.(=)
-?/. - c.2020G>A r.(?) p.(Asp674Asn)
+/. 19 c.2102del r.(?) p.(Ile701Thrfs*27)
+/. - c.2102del r.(?) p.(Ile701Thrfs*27)
-/. - c.2120C>T r.(?) p.(Ala707Val)
-?/. - c.2120C>T r.(?) p.(Ala707Val)
-?/. - c.2121G>C r.(?) p.(Ala707=)
+/+ 19 c.2201A>G r.(?) p.(Gln734Arg)
+?/. - c.2207G>A r.(?) p.(Gly736Glu)
-?/-? 19i c.2207+9C>T r.(=) p.(=)
+/+ 19i c.2208-1G>A r.spl? p.?
?/? 20 c.2222G>C r.(?) p.(Trp741Ser)
+?/. 20 c.2223G>A r.(?) p.(Trp741*)
-?/. - c.2229C>T r.(?) p.(Ala743=)
-?/. - c.2229C>T r.(?) p.(Ala743=)
-/. - c.2353A>C r.(?) p.(Thr785Pro)
+/. - c.2359G>T r.(?) p.(Glu787Ter)
-?/. - c.2417A>C r.(?) p.(Tyr806Ser)
-?/. - c.2431+11T>C r.(=) p.(=)
?/. - c.2489A>G r.(?) p.(Asn830Ser)
?/. - c.2548G>C r.(?) p.(Val850Leu)
-?/. - c.2619+20G>A r.(=) p.(=)
?/. - c.2654A>G r.(?) p.(His885Arg)
?/. - c.2672G>T r.(?) p.(Arg891Leu)
+?/+? 24 c.2795G>C r.(?) p.(Gly932Ala)
?/. - c.2795G>C r.(?) p.(Gly932Ala)
+/. - c.2918+1G>A r.spl? p.?
?/. - c.2945T>C r.(?) p.(Leu982Pro)
+/. 23 c.2960_2961del r.(?) p.(His987Argfs*6)
?/. - c.3002G>A r.(?) p.(Gly1001Glu)
?/. - c.3055G>A r.(?) p.(Ala1019Thr)
-?/. - c.3075G>A r.(?) p.(Glu1025=)
-?/. - c.3281C>T r.(?) p.(Thr1094Ile)
?/. - c.3377T>C r.(?) p.(Leu1126Pro)
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