Transcript #00025686 (NM_001127453.1, DFNA5 gene)

Transcript name transcript variant 2
Gene name DFNA5 (deafness, autosomal dominant 5)
Chromosome 7
Transcript - NCBI ID NM_001127453.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001120925.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2022-01-28 16:06:43 +01:00 (CET)
Date last edited N/A


Variants

57 entries on 1 page. Showing entries 1 - 57.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. - c.-8135039_*1550995del r.0? p.0?
+?/. - c.119dup r.(?) p.(Lys41Glufs*113)
-/. - c.405-15G>A r.(=) p.(=)
-/. - c.424C>A r.(?) p.(Pro142Thr)
-/. - c.447A>G r.(?) p.(Glu149=)
-/. - c.489G>A r.(?) p.(Thr163=)
-?/. - c.521T>C r.(?) p.(Met174Thr)
?/? 4 c.553G>A r.(?) p.(Gly185Ser)
-?/. - c.559C>T r.(?) p.(Gln187Ter)
-?/. - c.587C>T r.(?) p.(Thr196Met)
-?/. - c.612C>T r.(?) p.(Asp204=)
-/. - c.619G>A r.(?) p.(Val207Met)
-/- 5 c.642dup r.(?) p.(Thr215Hisfs*9)
+?/. - c.675C>G r.(?) p.(Tyr225*)
?/. - c.686dup r.(?) p.(Asp229GlufsTer23)
?/. - c.712C>T r.(?) p.(Arg238Ter)
-?/. - c.712C>T r.(?) p.(Arg238Ter)
+?/+? 6 c.781C>T r.(?) p.(Arg261*)
-?/-? 6 c.826T>C r.(?) p.(Ser276Pro)
-?/-? 6i c.862+11_862+12insG r.(=) p.(=)
+/. - c.863-1G>A r.spl? p.?
-?/. - c.864G>A r.(?) p.(Ala288=)
-?/. - c.939C>T r.(?) p.(Ile313=)
-?/-? 7 c.969A>G r.(=) p.(=)
+/. 7i_8i c.[990+793_1007del;1029_1183+1376del] r.? p.?
+/. 7i_8 c.991-60_1095del r.991_1183del p.?
+/. - c.991-15_991-13del r.(=) p.(=)
+?/. - c.991-15_991-13del r.(?) p.?
+/+ 7i c.991-15_991-13del r.(=) p.(=)
?/. - c.991-15_991-13del r.(991_1183del) p.(Cys331fs)
+/+ 7i c.991-6C>G r.(=) p.(=)
+/. - c.991-6C>G r.(=) p.(=)
+/+ 7i c.991-2A>G r.spl? p.?
?/? 8 c.991T>C r.(?) p.(Cys331Arg)
?/. - c.1008C>T r.(?) p.(Ser336=)
-?/. - c.1061A>C r.(?) p.(Gln354Pro)
-?/. - c.1086_1099del r.(?) p.(Val363ThrfsTer32)
+/+ 8 c.1102C>G r.(?) p.(Gln368Glu)
-?/. - c.1111T>G r.(?) p.(Cys371Gly)
-?/. - c.1116G>A r.(?) p.(Pro372=)
?/? 8 c.1118G>A r.(?) p.(Gly373Asp)
-?/-? 8 c.1122C>T r.(=) p.(=)
?/. - c.1162T>C r.(?) p.Phe388Leu
?/. - c.1162T>C r.(?) p.(Phe388Leu)
?/. - c.1182A>C r.(?) p.(Ala394=)
+/. - c.1183G>A r.(?) p.(Glu395Lys)
+?/. - c.1183G>T r.(?) p.(Glu395Ter)
+/+ 8i c.1183+4A>G r.spl? p.?
+?/. - c.1183+5G>A r.991_1183del p.Cys331Lysfs*42
-?/. - c.1198G>A r.(?) p.(Ala400Thr)
-?/. - c.1199C>T r.(?) p.(Ala400Val)
-/. - c.1199_1200inv r.(?) p.(Ala400Val)
?/. - c.1277_1279del r.(?) p.(Asp426del)
?/. - c.1348C>T r.(?) p.(Arg450Cys)
?/? 10 c.1355T>C r.(?) p.(Phe452Ser)
-?/-? 10 c.1416G>A r.(=) p.(=)
?/. - c.1490G>C r.(?) p.(*497Serext*4)
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