Transcript #00006522 (NM_001206927.1, DNAH8 gene)

Transcript name dynein, axonemal, heavy chain 8
Gene name DNAH8 (dynein, axonemal, heavy chain 8)
Chromosome 6
Transcript - NCBI ID NM_001206927.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001193856.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

68 entries on 1 page. Showing entries 1 - 68.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.265G>A r.(?) p.(Ala89Thr)
-?/. - c.301C>T r.(?) p.(Leu101=)
+/. - c.380_381del r.(?) p.(Lys127Argfs*7)
?/. - c.384G>C r.(?) p.(Glu128Asp)
?/. - c.668T>C r.(?) p.(Ile223Thr)
?/. - c.863A>G r.(?) p.(Asn288Ser)
?/. - c.872C>A r.(?) p.(Ala291Asp)
?/. - c.872C>A r.(?) p.(Ala291Asp)
?/. - c.872C>T r.(?) p.(Ala291Val)
?/. - c.952+2dup r.spl? p.?
?/. - c.1525_1529del r.(?) p.(Gln509GlyfsTer5)
-/. - c.1549T>C r.(?) p.(Tyr517His)
-/. - c.1549T>C r.(?) p.(Tyr517His)
?/. - c.2111A>G r.(?) p.(Tyr704Cys)
?/. - c.2174C>G r.(?) p.(Ala725Gly)
-?/. - c.2174C>G r.(?) p.(Ala725Gly)
+?/? ? c.2419C>T r.(?) p.(Arg807*)
-/. - c.2620G>A r.(?) p.(Val874Met)
-/. - c.2620G>A r.(?) p.(Val874Met)
-?/. - c.3061A>G r.(?) p.(Ser1021Gly)
-?/. - c.3289A>G r.(?) p.(Ile1097Val)
?/. - c.3289A>G r.(?) p.(Ile1097Val)
?/. - c.3311T>C r.(?) p.(Val1104Ala)
?/. - c.3703C>T r.(?) p.(Arg1235Cys)
?/. - c.3776A>G r.(?) p.(Tyr1259Cys)
-/. - c.4300T>C r.(=) p.(.Leu4373=)
-/. - c.5196T>C r.(=) p.(Pro1732=)
-?/. - c.5376G>C r.(?) p.(Lys1792Asn)
-?/. - c.5490C>A r.(?) p.(Asp1830Glu)
-/. - c.5490C>A r.(?) p.(Asp1830Glu)
?/. - c.5530C>A r.(?) p.(Arg1844Ser)
-/. - c.5541C>T r.(?) p.(Ala1847=)
-?/. - c.5789G>A r.(?) p.(Arg1930His)
?/. - c.5828A>T r.(?) p.(Asn1943Ile)
+/. - c.6689A>G r.(?) p.(Lys2230Arg)
?/. - c.6856A>G r.(?) p.(Ser2286Gly)
+/. - c.6962_6968del r.(?) p.(His2321Profs*4)
?/. - c.7123A>C r.(?) p.(Asn2375His)
?/. - c.7177A>C r.(?) p.(Asn2393His)
+?/. - c.7774C>T r.(?) p.(Arg2592Trp)
-/. - c.7982C>A r.(?) p.(Thr2661Asn)
?/. - c.8221_8223del r.(?) p.(Asp2741del)
+?/. - c.9194+1G>A r.spl? p.?
+/. - c.9427C>T r.(?) p.(Arg3143Cys)
?/. - c.9739A>G r.(?) p.(Arg3247Gly)
-/. - c.10141-4del r.(?) p.(=)
?/. - c.10238A>G r.(?) p.(Lys3413Arg)
?/. - c.10678G>A r.(?) p.(Ala3560Thr)
?/. - c.11048C>T r.(?) p.(Pro3683Leu)
?/. - c.11182C>T r.(?) p.(Pro3728Ser)
?/. - c.11274+3G>T r.spl? p.?
-?/. - c.11274+10G>T r.(=) p.(=)
?/. - c.11374A>G r.(?) p.(Lys3792Glu)
?/. - c.11771C>T r.(?) p.(Thr3924Met)
+/. - c.11771C>T r.(?) p.(Thr3924Met)
?/. - c.11819C>A r.(?) p.(Ser3940Tyr)
?/. - c.11894_11895del r.(?) p.(Ser3965Cysfs*21)
?/. - c.11980C>T r.(?) p.(His3994Tyr)
-?/. - c.12525+3A>T r.spl? p.?
?/. - c.12617A>C r.(?) p.(Asp4206Ala)
+/. - c.12721G>A r.(?) p.(Ala4241Thr)
?/. - c.12914T>A r.(?) p.(Phe4305Tyr)
-/. - c.12968C>T r.(?) p.(Thr4323Met)
-/. - c.13119A>G r.(=) p.(Leu4373=)
?/. - c.13462A>G r.(?) p.(Ile4488Val)
?/. - c.13996G>T r.(?) p.(Val4666Leu)
?/. - c.14059C>T r.(?) p.(Arg4687*)
?/. - c.14059C>T r.(?) p.(Arg4687*)
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