Transcript #00000757 (NM_144666.2, DNHD1 gene)

Transcript name transcript variant 1
Gene name DNHD1 (dynein heavy chain domain 1)
Chromosome 11
Transcript - NCBI ID NM_144666.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_653267.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 12:51:32 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-529+9T>C r.(=) p.(=)
-?/. - c.85T>C r.(?) p.(Leu29=)
+/. - c.425_428del r.(?) p.(Asp142ValfsTer35)
-?/. - c.480C>T r.(?) p.(Pro160=)
?/. - c.497C>G r.(?) p.(Pro166Arg)
+/. - c.522_525del r.(?) p.(Arg174SerfsTer3)
?/. - c.556C>T r.(?) p.(Arg186*)
./. - c.746+1G>T r.spl? p.?
-/. - c.890A>G r.(?) p.(Tyr297Cys)
?/. - c.898G>A r.(?) p.(Val300Met)
+/. - c.911G>A r.(?) p.(Arg304Gln)
?/. - c.1292A>G r.(?) p.(Tyr431Cys)
?/. - c.1345C>T r.(?) p.(Arg449Trp)
?/. - c.1348C>T r.(?) p.(Leu450=)
?/. - c.1387C>T r.(?) p.(Arg463*)
?/. - c.1606_1611del r.(?) p.(Leu536_Glu537del)
?/. - c.1903G>A r.(?) p.(Asp635Asn)
-?/. - c.1938A>T r.(?) p.(Gly646=)
?/. - c.2027A>G r.(?) p.(Tyr676Cys)
-?/. - c.2085A>G r.(?) p.(Ile695Met)
-?/. - c.2089C>G r.(?) p.(Gln697Glu)
-?/. - c.2394A>G r.(?) p.(Gln798=)
?/. - c.2545C>T r.(?) p.(Arg849Ter)
-/. - c.2561G>A r.(?) p.(Arg854Gln)
?/. - c.2581C>T r.(?) p.(Arg861Cys)
?/. - c.2839G>T r.(?) p.(Glu947*)
?/. - c.2909C>A r.(?) p.(Thr970Asn)
-?/. - c.3233G>A r.(?) p.(Arg1078His)
?/. - c.3323G>A r.(?) p.(Arg1108His)
?/. - c.3365C>T r.(?) p.(Thr1122Met)
-?/. - c.3492G>A r.(?) p.(Ala1164=)
?/. - c.3523dup r.(?) p.(His1175ProfsTer29)
-?/. - c.3534C>T r.(?) p.(Tyr1178=)
-?/. - c.3740T>C r.(?) p.(Ile1247Thr)
-?/. - c.4041C>T r.(?) p.(Ser1347=)
+/. - c.4072C>T r.(?) p.(Arg1358Cys)
+/. - c.4141C>T r.(?) p.(Gln1381Ter)
+?/. - c.4510C>T r.(?) p.(Gln1504*)
-?/. - c.4654G>T r.(?) p.(Ala1552Ser)
?/. - c.4767A>C r.(?) p.(Glu1589Asp)
-/. - c.5264G>A r.(?) p.(Arg1755His)
+/. - c.5347del r.(?) p.(Gln1783SerfsTer28)
+/. - c.5560C>T r.(?) p.(Arg1854Cys)
-?/. - c.5617C>A r.(?) p.(Arg1873Ser)
?/. - c.5676G>C r.(?) p.(Lys1892Asn)
-?/. - c.5839A>G r.(?) p.(Met1947Val)
?/. - c.5989G>A r.(?) p.(Gly1997Ser)
-?/. - c.6064G>C r.(?) p.(Gly2022Arg)
?/. - c.6109A>G r.(?) p.(Ser2037Gly)
?/. - c.6395C>T r.(?) p.(Thr2132Ile)
+/. - c.6498T>G r.(?) p.(Tyr2166Ter)
-?/. - c.6616G>A r.(?) p.(Gly2206Arg)
?/. - c.6616G>A r.(?) p.(Gly2206Arg)
?/. - c.6617G>A r.(?) p.(Gly2206Glu)
-?/. - c.6617G>A r.(?) p.(Gly2206Glu)
-?/. - c.6618G>A r.(?) p.(Gly2206=)
-?/. - c.6681G>C r.(?) p.(Leu2227=)
-/. - c.6697C>T r.(?) p.(Arg2233Cys)
-?/. - c.6971C>T r.(?) p.(Pro2324Leu)
?/. - c.7372C>T r.(?) p.(His2458Tyr)
?/. - c.7387+3621T>C r.(=) p.(=)
?/. - c.7387+3737A>G r.(=) p.(=)
?/. - c.7387+3737A>G r.(=) p.(=)
+?/. - c.7818C>T r.(?) p.(Asn2606=)
?/. - c.7888C>T r.(?) p.(Arg2630Ter)
-?/. - c.8116C>A r.(?) p.(Pro2706Thr)
-?/. - c.8319C>G r.(?) p.(Gly2773=)
?/. - c.8782C>T r.(?) p.(Arg2928Ter)
+/. - c.8782C>T r.(?) p.(Arg2928Ter)
?/. - c.8881G>A r.(?) p.(Ala2961Thr)
-?/. - c.8904C>A r.(?) p.(Gly2968=)
+/. - c.8909A>G r.(?) p.(Tyr2970Cys)
?/. - c.8971C>T r.(?) p.(Gln2991*)
+/. - c.9649C>T r.(?) p.(Arg3217Ter)
?/. - c.9724G>C r.(?) p.(Glu3242Gln)
?/. - c.9740G>C r.(?) p.(Arg3247Pro)
?/. - c.10078G>T r.(?) p.(Glu3360*)
-?/. - c.10153G>A r.(?) p.(Val3385Met)
?/. - c.10261C>T r.(?) p.(Arg3421Cys)
?/. - c.10348T>C r.(?) p.(Tyr3450His)
?/. - c.10624C>T r.(?) p.(Arg3542*)
-?/. - c.10704G>A r.(?) p.(Pro3568=)
?/. - c.10723C>T r.(?) p.(Arg3575*)
+?/. - c.11207-9_11207del r.spl? p.?
?/. - c.11207-2A>G r.spl? p.?
-?/. - c.11622C>T r.(?) p.(Phe3874=)
?/. - c.11894C>T r.(?) p.(Pro3965Leu)
?/. - c.12142C>T r.(?) p.(Arg4048*)
+/. - c.12347dup r.(?) p.(Gln4117Alafs*14)
?/. - c.12355C>T r.(?) p.(Gln4119Ter)
+/. - c.12453G>A r.(?) p.(Trp4151Ter)
+/. - c.12473A>G r.(?) p.(His4158Arg)
?/. - c.12491C>T r.(?) p.(Pro4164Leu)
?/. - c.12539-1G>A r.spl? p.?
-?/. - c.12684G>A r.(?) p.(Met4228Ile)
?/. - c.12728T>C r.(?) p.(Ile4243Thr)
-?/. - c.12885G>A r.(?) p.(Gln4295=)
?/. - c.12931del r.(?) p.(Arg4311ValfsTer26)
?/. - c.13172A>C r.(?) p.(Glu4391Ala)
?/. - c.13611G>A r.(?) p.(Trp4537Ter)
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