Transcript #00001574 (NM_001372.3, DNAH9 gene)

Transcript name transcript variant 2
Gene name DNAH9 (dynein, axonemal, heavy chain 9)
Chromosome 17
Transcript - NCBI ID NM_001372.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_001363.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:40:35 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.28C>T r.(?) p.(Leu10Phe)
?/. - c.70C>G r.(?) p.(Arg24Gly)
?/. - c.253C>T r.(?) p.(Pro85Ser)
+?/. - c.308del r.(?) p.(Phe103Serfs*31)
+?/. - c.308del r.(?) p.(Phe103Serfs*31)
+/. - c.308dup r.(?) p.(Leu104Profs*45)
+/. - c.308dup r.(?) p.(Leu104ProfsTer45)
-?/. - c.394C>G r.(?) p.(His132Asp)
?/. - c.716C>G r.(?) p.(Pro239Arg)
?/. - c.793A>G r.(?) p.(Ile265Val)
-?/. - c.973A>G r.(?) p.(Asn325Asp)
+?/. - c.1010C>T r.(?) p.(Pro337Leu)
?/. - c.1181T>G r.(?) p.(Leu394Arg)
?/. - c.1298_1300del r.(?) p.(Ser433del)
?/. - c.1313G>A r.(?) p.(Arg438Gln)
?/. - c.1350+8C>G r.(=) p.(=)
?/. - c.1518+3A>G r.spl? p.?
?/. - c.1547A>C r.(?) p.(Asn516Thr)
-?/. - c.1547A>C r.(?) p.(Asn516Thr)
+?/. - c.1562A>T r.(?) p.(Asp521Val)
?/. - c.1571G>A r.(?) p.(Arg524Gln)
-?/. - c.1586T>G r.(?) p.(Ile529Ser)
?/. - c.1586T>G r.(?) p.(Ile529Ser)
-?/. - c.1788G>A r.(?) p.(=)
-?/. - c.1796C>T r.(?) p.(Pro599Leu)
-/. - c.1810A>G r.(?) p.(Met604Val)
-/. - c.1810A>G r.(?) p.(Met604Val)
-?/. - c.1830C>A r.(?) p.(Gly610=)
+/. - c.1970+4A>G r.spl p.?
?/. - c.1970+4A>G r.spl? p.?
+?/. - c.1995_1996insG r.(?) p.(Trp666Valfs*21)
+/. - c.1997G>A r.(?) p.(Trp666*)
+?/. - c.2002C>T r.(?) p.(Arg668Trp)
-?/. - c.2040A>G r.(?) p.(Gln680=)
?/. - c.2660T>C r.(?) p.(Ile887Thr)
?/. - c.2929-6C>G r.(=) p.(=)
?/. - c.3041C>T r.(?) p.(Ser1014Leu)
-?/. - c.3225G>A r.(?) p.(Leu1075=)
+?/. - c.3354-1del r.spl p.?
+/. - c.3354-1G>T r.spl p.?
?/. - c.3419_3421del r.(?) p.(Gly1140del)
-?/. - c.3661A>G r.(?) p.(Thr1221Ala)
-?/. - c.3743+5G>A r.spl? p.?
?/. - c.3919G>A r.(?) p.(Asp1307Asn)
?/. - c.3926T>G r.(?) p.(Ile1309Ser)
-?/. - c.4195A>G r.(?) p.(Met1399Val)
?/. - c.4231C>G r.(?) p.(Leu1411Val)
-?/. - c.4378C>A r.(?) p.(Pro1460Thr)
?/. - c.4536G>C r.(?) p.(Trp1512Cys)
+?/. - c.4549C>T r.(?) p.(Arg1517*)
?/. - c.4562A>G r.(?) p.(His1521Arg)
?/. - c.4778A>G r.(?) p.(Tyr1593Cys)
-?/. - c.4962C>T r.(?) p.(Leu1654=)
+/. - c.5020G>A r.(?) p.(Gly1674Arg)
?/. - c.5318G>A r.(?) p.(Arg1773Gln)
+?/. - c.5360G>A r.(?) p.(Arg1787Gln)
-?/. - c.5372C>T r.(?) p.(Ala1791Val)
-?/. - c.5403C>G r.(?) p.(Ala1801=)
-?/. - c.5403C>G r.(?) p.(Ala1801=)
?/. - c.5449G>A r.(?) p.(Glu1817Lys)
?/. - c.5561T>G r.(?) p.(Ile1854Ser)
+?/. - c.5605G>A r.(?) p.(Ala1869Thr)
+/. - c.5641A>G r.(?) p.(Lys1881Glu)
?/. - c.5644G>A r.(?) p.(Asp1882Asn)
?/. - c.5654G>A r.(?) p.(Arg1885His)
-?/. - c.5898C>T r.(?) p.(Val1966=)
?/. - c.5983A>G r.(?) p.(Met1995Val)
-?/. - c.6259A>G r.(?) p.(Met2087Val)
?/. - c.6283G>A r.(?) p.(Gly2095Arg)
+?/. - c.6298G>A r.(?) p.(Ala2100Thr)
-?/. - c.6405C>G r.(?) p.(Val2135=)
-?/. - c.6525C>T r.(?) p.(Pro2175=)
?/. - c.6641C>A r.(?) p.(Ala2214Asp)
?/. - c.6770C>T r.(?) p.(Pro2257Leu)
?/. - c.6847+5G>A r.spl? p.?
?/. - c.6895A>G r.(?) p.(Ser2299Gly)
?/. - c.7100A>G r.(?) p.(Lys2367Arg)
?/. - c.7150G>A r.(?) p.(Gly2384Arg)
-?/. - c.7171-1472_7171-1468del r.(=) p.(=)
?/. - c.7414C>T r.(?) p.(Arg2472Trp)
?/. - c.7456G>T r.(?) p.(Val2486Leu)
?/. - c.7520T>C r.(?) p.(Phe2507Ser)
?/. - c.7666G>A r.(?) p.(Gly2556Arg)
?/. - c.7787C>T r.(?) p.(Thr2596Met)
?/. - c.7901A>T r.(?) p.(His2634Leu)
-/. - c.7926G>A r.(?) p.(Ala2642=)
?/. - c.7949C>T r.(?) p.(Pro2650Leu)
-?/. - c.8196G>C r.(?) p.(Gln2732His)
+/. - c.8251C>T r.(?) p.(Gln2751*)
?/. - c.8366A>G r.(?) p.(Asn2789Ser)
?/. - c.8452C>T r.(?) p.(Arg2818Trp)
?/. - c.8453G>A r.(?) p.(Arg2818Gln)
+?/. - c.8614G>A r.(?) p.(Gly2872Arg)
?/. - c.8659G>C r.(?) p.(Val2887Leu)
+/. 45i c.8708-2A>G r.8708_8850del p.Glu2904Aspfs*53
+/. 45i c.8708-2A>G r.8708_8850del p.Glu2904Aspfs*53
-?/. - c.8736T>G r.(?) p.(Asp2912Glu)
-?/. - c.8749A>G r.(?) p.(Ile2917Val)
?/. - c.8754A>G r.(?) p.(Ile2918Met)
+?/. - c.8894G>A r.(?) p.(Arg2965His)
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