Transcript #00006521 (NM_018897.2, DNAH7 gene)

Transcript name dynein, axonemal, heavy chain 7
Gene name DNAH7 (dynein, axonemal, heavy chain 7)
Chromosome 2
Transcript - NCBI ID NM_018897.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_061720.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

63 entries on 1 page. Showing entries 1 - 63.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.415_416del r.(?) p.(Leu139ArgfsTer6)
-?/. - c.806A>T r.(?) p.(Asp269Val)
-?/. - c.1139T>G r.(?) p.(Met380Arg)
-/. - c.1139T>G r.(?) p.(Met380Arg)
?/. - c.1139T>G r.(?) p.(Met380Arg)
?/. - c.1173+4A>C r.spl? p.?
?/. - c.1448A>T r.(?) p.(Glu483Val)
-?/. - c.2023A>G r.(?) p.(Lys675Glu)
?/. - c.2072G>T r.(?) p.(Arg691Leu)
+/. 18 c.2479dup r.(?) p.(Val827Glyfs*20)
-?/. - c.2848A>G r.(?) p.(Met950Val)
?/. - c.2849T>C r.(?) p.(Met950Thr)
?/. - c.2929C>G r.(?) p.(Leu977Val)
?/. - c.2984G>T r.(?) p.(Ser995Ile)
-?/. - c.3007A>G r.(?) p.(Met1003Val)
?/. - c.3010C>T r.(?) p.(Pro1004Ser)
?/. - c.3038T>C r.(?) p.(Val1013Ala)
-?/. - c.4264C>A r.(?) p.(Pro1422Thr)
?/. - c.4451C>T r.(?) p.(Thr1484Met)
-?/. - c.4549-3del r.spl? p.?
-/. - c.4549-3dup r.spl? p.?
-?/. - c.4787dup r.(?) p.(Tyr1596Ter)
+?/. - c.4787dup r.(?) p.(Tyr1596Ter)
-/. - c.4897-9_4897-8del r.(=) p.(=)
-/. - c.4897-8del r.(=) p.(=)
?/. - c.4897-8del r.(=) p.(=)
?/. - c.5102A>C r.(?) p.(Glu1701Ala)
?/. - c.5212G>T r.(?) p.(Val1738Phe)
-?/. - c.5347A>T r.(?) p.(Met1783Leu)
-?/. - c.5352C>G r.(?) p.(Gly1784=)
?/. - c.5377T>G r.(?) p.(Ser1793Ala)
-?/. - c.5379G>A r.(?) p.(Ser1793=)
./. - c.5515C>T r.(?) p.(Arg1839*)
-/. - c.5560A>G r.(?) p.(Ile1854Val)
-/. - c.5560A>G r.(?) p.(Ile1854Val)
-?/. - c.5744A>T r.(?) p.(Asp1915Val)
?/. - c.5870G>A r.(?) p.(Arg1957Gln)
-?/. - c.6059T>C r.(?) p.(Met2020Thr)
-?/. - c.6161A>G r.(?) p.(Tyr2054Cys)
-?/. - c.6161A>G r.(?) p.(Tyr2054Cys)
?/. - c.6161A>G r.(?) p.(Tyr2054Cys)
-/. - c.6340A>G r.(?) p.(Thr2114Ala)
-/. - c.6340A>G r.(?) p.(Thr2114Ala)
-/. - c.6340A>G r.(?) p.(Thr2114Ala)
?/. - c.6878G>A r.(?) p.(Arg2293Gln)
?/. - c.6932T>C r.(?) p.(Met2311Thr)
?/. - c.6949C>T r.(?) p.(Arg2317Ter)
-?/. - c.7117A>G r.(?) p.(Thr2373Ala)
-?/. - c.7377C>G r.(?) p.(Asn2459Lys)
-?/. - c.7448G>A r.(?) p.(Arg2483Gln)
?/. - c.7565T>C r.(?) p.(Met2522Thr)
-?/. - c.7741G>A r.(?) p.(Val2581Ile)
+?/. - c.8624G>A r.(?) p.(Arg2875Gln)
?/. - c.9335A>G r.(?) p.(Asp3112Gly)
-?/. - c.9985G>A r.(?) p.(Asp3329Asn)
?/. - c.10697T>C r.(?) p.(Phe3566Ser)
?/. - c.10697T>C r.(?) p.(Phe3566Ser)
+?/. 58 c.10753T>C r.(?) p.(Phe3585Leu)
./. - c.11934T>A r.(?) p.(Tyr3978*)
?/. - c.11934T>A r.(?) p.(Tyr3978Ter)
+/. - c.11947C>T r.(?) p.(Arg3983Trp)
-/. - c.11947C>T r.(?) p.(Arg3983Trp)
?/. - c.11992_11995dup r.(?) p.(Ala3999AspfsTer8)
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