Transcript #00006594 (NM_004408.2, DNM1 gene)

Transcript name transcript variant 1
Gene name DNM1 (dynamin 1)
Chromosome 9
Transcript - NCBI ID NM_004408.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_004399.2
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-37139G>A r.(?) p.(=)
-?/. - c.-37139G>A r.(?) p.(=)
?/. - c.-34366C>T r.(?) p.(=)
-?/. - c.-34078G>A r.(?) p.(=)
-/. - c.-33352_-33351del r.(?) p.(=)
?/. - c.-24975A>G r.(?) p.(=)
-?/. - c.-24629T>C r.(?) p.(=)
-/. - c.-24616G>A r.(?) p.(=)
-?/. - c.-24444G>C r.(?) p.(=)
-?/. - c.-24434C>A r.(?) p.(=)
-?/. - c.-24434C>A r.(?) p.(=)
-?/. - c.-24373T>C r.(?) p.(=)
-?/. - c.-24339T>C r.(?) p.(=)
-?/. - c.-24197G>C r.(?) p.(=)
?/. - c.-24193C>T r.(?) p.(=)
-?/. - c.-24156G>A r.(?) p.(=)
-?/. - c.-24059T>G r.(?) p.(=)
-?/. - c.-23018A>G r.(?) p.(=)
-?/. - c.-13038G>A r.(?) p.(=)
?/. - c.-12705_-12703dup r.(?) p.(=)
-?/. - c.-11600C>T r.(?) p.(=)
-?/. - c.-11576C>A r.(?) p.(=)
-?/. - c.-11576C>A r.(?) p.(=)
?/. - c.-11565G>A r.(?) p.(=)
?/. - c.109G>T r.(?) p.(Val37Leu)
+/. - c.112_120delinsAGCGGCCAC r.(?) p.(Gly38_Gln40delinsSerGlyHis)
+?/. - c.123C>A r.(?) p.(Ser41Arg)
+/. - c.193A>C r.(?) p.(Thr65Pro)
-?/. - c.224A>G r.(?) p.(Asn75Ser)
-?/. - c.235+8C>T r.(=) p.(=)
?/. - c.394C>A r.(?) p.(Leu132Met)
-?/. - c.450C>G r.(?) p.(Pro150=)
+/. - c.457G>A r.(?) p.(Glu153Lys)
?/. - c.520G>A r.(?) p.(Val174Met)
?/. - c.599C>T r.(?) p.(Thr200Ile)
+/. 6 c.709C>T r.(?) p.(Arg237Trp)
+/. - c.709C>T r.(?) p.(Arg237Trp)
./. - c.709C>T r.(?) p.(Arg237Trp)
+/. - c.727_744del r.(?) p.(Asp243_Ile248del)
?/. - c.775T>C r.(?) p.(Phe259Leu)
?/. - c.796C>T r.(?) p.(Arg266Cys)
-?/. - c.797G>A r.(?) p.(Arg266His)
+?/. - c.811C>T r.(?) p.(Arg271Cys)
?/. - c.812G>A r.(?) p.(Arg271His)
./. - c.865A>T r.(?) p.(Ile289Phe)
-?/. - c.890G>A r.(?) p.(Arg297Gln)
?/. - c.926A>G r.(?) p.(Lys309Arg)
?/. - c.953G>A r.(?) p.(Arg318His)
-/. - c.1008C>T r.(?) p.(Phe336=)
+?/. - c.1037G>A r.(?) p.(Gly346Asp)
+?/. - c.1081C>G r.(?) p.(Arg361Gly)
?/. - c.1091G>T r.(?) p.(Arg364Leu)
+?/. - c.1099C>G r.(?) p.(His367Asp)
-?/. - c.1128+5G>A r.spl? p.?
+?/. - c.1168T>G r.(?) p.(Tyr390Asp)
./. - c.1186C>G r.(?) p.(His396Asp)
+?/. - c.1190G>A r.(?) p.(Gly397Asp)
+/. 9 c.1195A>T r.(?) p.(Arg399Ter)
+/. 10b c.1214C>T r.(?) p.(Pro405Leu)
?/. - c.1261C>T r.(?) p.(Arg421*)
?/. 10i c.1335+1600C>G r.1335_1336= p.Lys445_Leu446=
+/. 9i c.1335+1638G>A r.(?) p.(=)
+/. 9i c.1335+1638G>A r.(?) p.(=)
+/. 9i c.1335+1638G>A r.(?) p.(=)
+/. 9i c.1335+1638G>A r.(?) p.(=)
+/. 9i c.1335+1638G>A r.(?) p.(=)
+/. 9i c.1335+1638G>A r.(?) p.(=)
+/. 9i c.1335+1638G>A r.(?) p.(=)
+/. 9i c.1335+1638G>A r.(?) p.(=)
+/. - c.1335+1638G>A r.(=) p.(=)
?/. - c.1335+1638G>A r.(?) p.(=)
?/. - c.1335+1638G>A r.(?) p.(=)
+/. 9i c.1335+1651G>A r.(?) p.(=)
-?/. - c.1335+1722A>G r.(=) p.(=)
-?/. - c.1343A>G r.(?) p.(Gln448Arg)
?/. - c.1378G>C r.(?) p.(Val460Leu)
-?/. - c.1422+7C>A r.(=) p.(=)
-?/. - c.1422+7C>A r.(=) p.(=)
?/. - c.1422+9C>T r.(=) p.(=)
-?/. - c.1493+3G>A r.spl? p.?
+?/. - c.1498C>T r.(?) p.(Gln500Ter)
-?/. - c.1558-47G>T r.(=) p.(=)
?/. - c.1586A>G r.(?) p.(Asn529Ser)
?/. - c.1690A>G r.(?) p.(Met564Val)
-?/. - c.1707C>T r.(?) p.(Asn569=)
-?/. - c.1707C>T r.(?) p.(Asn569=)
?/. - c.1742C>G r.(?) p.(Ser581Trp)
?/. - c.1852G>T r.(?) p.(Ala618Ser)
-?/. - c.1932C>T r.(?) p.(Ser644=)
?/. - c.2009T>C r.(?) p.(Met670Thr)
?/. - c.2011G>A r.(?) p.(Ala671Thr)
-?/. - c.2138C>T r.(?) p.(Thr713Met)
?/. - c.2164G>T r.(?) p.(Ala722Ser)
?/. 20 c.2170C>T r.(?) p.(Arg724Trp)
?/. - c.2201C>T r.(?) p.(Ala734Val)
?/. - c.2318+1G>A r.spl? p.?
?/. - c.2415T>G r.(?) p.(Ala805=)
-?/. - c.2420C>G r.(?) p.(Ser807Cys)
?/. - c.2460G>A r.(?) p.(Gly820=)
-?/. - c.2535-1556C>G r.(=) p.(=)
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