Transcript #00007954 (NM_025135.2, FHOD3 gene)

Transcript name formin homology 2 domain containing 3
Gene name FHOD3 (formin homology 2 domain containing 3)
Chromosome 18
Transcript - NCBI ID NM_025135.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_079411.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

243 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.61A>G r.(?) p.(Asn21Asp)
-?/. - c.132G>A r.(?) p.(Ala44=)
-?/. - c.238C>T r.(?) p.(Arg80Trp)
?/. - c.238C>T r.(?) p.(Arg80Trp)
?/. - c.238C>T r.(?) p.(Arg80Trp)
?/. - c.238C>T r.(?) p.(Arg80Trp)
?/. - c.274C>T r.(?) p.(Arg92Trp)
?/. - c.274C>T r.(?) p.(Arg92Trp)
-/. - c.285G>A r.(?) p.(=)
?/. - c.305C>T r.(?) p.(Thr102Met)
-?/. - c.345A>G r.(?) p.(=)
-/. - c.357C>T r.(?) p.(=)
?/. - c.409G>A r.(?) p.(Asp137Asn)
-?/. - c.423G>A r.(?) p.(Val141=)
-/. - c.511+13T>G r.(=) p.(=)
-?/. - c.537G>A r.(?) p.(Val179=)
-?/. - c.563G>A r.(?) p.(Arg188His)
-?/. - c.573C>T r.(?) p.(Thr191=)
-/. - c.595A>G r.(?) p.(Ile199Val)
-?/. - c.606+8del r.(=) p.(=)
-?/. - c.606+8del r.(=) p.(=)
-?/. - c.606+8del r.(=) p.(=)
-?/. - c.606+19T>C r.(=) p.(=)
-/. - c.607-20G>A r.(=) p.(=)
?/. - c.646G>A r.(?) p.(Val216Ile)
-?/. - c.663G>A r.(?) p.(Ser221=)
-/. - c.663G>A r.(?) p.(Ser221=)
-?/. - c.673G>A r.(?) p.(Ala225Thr)
-?/. - c.673G>A r.(?) p.(Ala225Thr)
?/. - c.676C>T r.(?) p.(Pro226Ser)
-?/. - c.719-20G>T r.(=) p.(=)
-?/. - c.777G>A r.(?) p.(Thr259=)
-?/. - c.777G>A r.(?) p.(Thr259=)
-/. - c.781C>T r.(?) p.(=)
-/. - c.795A>G r.(?) p.(=)
-?/. - c.807G>A r.(?) p.(=)
-?/. - c.814-6T>C r.(=) p.(=)
-?/. - c.849C>T r.(?) p.(Tyr283=)
-?/. - c.850G>A r.(?) p.(Asp284Asn)
?/. - c.877G>A r.(?) p.(Gly293Ser)
?/. - c.877G>A r.(?) p.(Gly293Ser)
-/. - c.918G>A r.(?) p.(=)
?/. - c.928G>A r.(?) p.(Asp310Asn)
-?/. - c.958-17G>A r.(=) p.(=)
-/. - c.958-4C>T r.spl? p.?
-?/. - c.958-4C>T r.spl? p.?
-/. - c.963G>A r.(?) p.(=)
?/. - c.972C>G r.(?) p.(His324Gln)
?/. - c.972C>G r.(?) p.(His324Gln)
?/. - c.992C>G r.(?) p.(Thr331Arg)
-/. - c.1004C>G r.(?) p.(Pro335Arg)
-?/. - c.1004C>G r.(?) p.(Pro335Arg)
-/. - c.1005C>A r.(?) p.(Pro335=)
?/. - c.1010G>A r.(?) p.(Gly337Glu)
-/. - c.1035C>T r.(?) p.(Ser345=)
?/. - c.1036G>A r.(?) p.(Val346Met)
-?/. - c.1044C>T r.(?) p.(Ser348=)
-/. - c.1050C>T r.(?) p.(Gly350=)
-/. - c.1064G>A r.(?) p.(Arg355Gln)
?/. - c.1088G>A r.(?) p.(Arg363His)
-?/. - c.1139C>T r.(?) p.(Pro380Leu)
?/. - c.1153G>C r.(?) p.(Ala385Pro)
?/. - c.1172A>G r.(?) p.(Asn391Ser)
?/. - c.1180C>G r.(?) p.(Arg394Gly)
?/. - c.1197-8760G>A r.(=) p.(=)
?/. - c.1197-8760G>A r.(=) p.(=)
?/. - c.1197-8747_1197-8745dup r.(=) p.(=)
?/. - c.1197-8727C>T r.(=) p.(=)
-?/. - c.1197-8726G>A r.(=) p.(=)
-?/. - c.1197-8708A>G r.(=) p.(=)
-/. - c.1197-8708A>G r.(=) p.(=)
?/. - c.1197-8698G>A r.(=) p.(=)
?/. - c.1197-8680G>A r.(=) p.(=)
-?/. - c.1197-8680G>A r.(=) p.(=)
+?/. - c.1197-8668del r.(=) p.(=)
-/. - c.1197-5495G>A r.(=) p.(=)
-/. - c.1197-5428C>T r.(=) p.(=)
-/. - c.1197-5411G>A r.(=) p.(=)
-/. - c.1197-5402C>T r.(=) p.(=)
-?/. - c.1197-5402C>T r.(=) p.(=)
?/. - c.1197-5384G>C r.(=) p.(=)
-/. - c.1197-5381G>A r.(=) p.(=)
-/. - c.1197-5303C>T r.(=) p.(=)
-?/. - c.1197-5303C>T r.(=) p.(=)
-?/. - c.1197-5295C>T r.(=) p.(=)
?/. - c.1197-5257T>C r.(=) p.(=)
-/. - c.1197-5241C>T r.(=) p.(=)
-?/. - c.1197-5235C>T r.(=) p.(=)
?/. - c.1197-5233A>G r.(=) p.(=)
?/. - c.1197-5212C>T r.(=) p.(=)
-/. - c.1197-5172G>A r.(=) p.(=)
-?/. - c.1197-4682C>G r.(=) p.(=)
-?/. - c.1197-4679C>A r.(=) p.(=)
?/. - c.1197-4679C>A r.(=) p.(=)
?/. - c.1197-4674C>G r.(=) p.(=)
-?/. - c.1197-4655G>A r.(=) p.(=)
-/. - c.1214A>G r.(?) p.(Asn405Ser)
-?/. - c.1214A>G r.(?) p.(Asn405Ser)
-?/. - c.1221T>C r.(?) p.(Ser407=)
-?/. - c.1221T>C r.(?) p.(Ser407=)
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