Transcript #00025980 (NM_001256715.1, DNAAF3 gene)

Transcript name transcript variant 3
Gene name DNAAF3 (dynein, axonemal, assembly factor 3)
Chromosome 19
Transcript - NCBI ID NM_001256715.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001243644.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks RefSeq select
Date created 2025-02-09 15:48:09 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-135C>G r.(?) p.(=)
-?/. - c.-5+5G>T r.spl? p.?
-?/. - c.-5+5G>T r.spl? p.?
-?/. - c.-4G>A r.(?) p.(=)
-/. - c.6C>T r.(?) p.(Thr2=)
-?/. - c.6C>T r.(?) p.(Thr2=)
?/. - c.72C>A r.(?) p.(Asp24Glu)
-?/. - c.228+63T>G r.(?) p.(=)
-?/. - c.228+80C>G r.(=) p.(=)
?/. - c.323-5C>A r.spl? p.?
-?/. - c.323-4del r.spl? p.?
-?/. - c.327A>G r.(?) p.(Arg109=)
-/. - c.327A>G r.(?) p.(Arg109=)
-/. - c.510A>G r.(?) p.(Val170=)
?/. - c.543_544dup r.(?) p.(Gln182Profs*6)
-/. - c.666T>C r.(?) p.(Ala222=)
-/. - c.666T>C r.(?) p.(Ala222=)
-/. - c.790-14C>T r.(=) p.(=)
-/. - c.790-14C>T r.(=) p.(=)
-?/. - c.831C>T r.(?) p.(Ile277=)
-?/. - c.832G>A r.(?) p.(Ala278Thr)
-?/. - c.832G>A r.(?) p.(Ala278Thr)
-?/. - c.832G>A r.(?) p.(Ala278Thr)
?/. - c.851C>A r.(?) p.(Ala284Asp)
?/. - c.853T>G r.(?) p.(Phe285Val)
-/. - c.875A>G r.(?) p.(Glu292Gly)
-/. - c.875A>G r.(?) p.(Glu292Gly)
?/. - c.890C>T r.(?) p.(Thr297Met)
?/. - c.912+5G>C r.spl? p.?
-?/. - c.913-8A>G r.(=) p.(=)
-?/. - c.927C>T r.(?) p.(Ile309=)
?/. - c.939C>A r.(?) p.(Asn313Lys)
?/. - c.960C>G r.(?) p.(Asp320Glu)
+/. - c.997dup r.(?) p.(Asp333Glyfs*64)
-?/. - c.997G>A r.(?) p.(Asp333Asn)
-?/. - c.1001T>C r.(?) p.(Leu334Pro)
-/. - c.1056G>A r.(?) p.(Pro352=)
-/. - c.1056G>A r.(?) p.(Pro352=)
-/. - c.1093= r.(=) p.(Asn365=)
-/. - c.1093= r.(=) p.(Asn365=)
-?/. - c.1163+10G>T r.(=) p.(=)
?/. - c.1163+10G>T r.(=) p.(=)
-/. - c.1164-116del r.(=) p.(=)
-/. - c.1164-14C>T r.(=) p.(=)
-/. - c.1239-8A>G r.(=) p.(=)
-/. - c.1239-8A>G r.(=) p.(=)
-?/. - NM_001256715.1:c.1255C>T r.(?) p.(Arg419Trp)
?/. - c.1256G>A r.(?) p.(Arg419Gln)
+?/. - c.1271dup r.(?) p.(Phe426IlefsTer52)
+/. - c.1271dup r.(?) p.(Phe426IlefsTer52)
-?/. - c.1284C>T r.(?) p.(Thr428=)
?/. - c.1294G>C r.(?) p.(Glu432Gln)
?/. - c.1354G>C r.(?) p.(Ala452Pro)
-?/. - c.1389C>A r.(?) p.(Gly463=)
-?/. - c.1405G>A r.(?) p.(Val469Met)
-?/. - c.1405G>A r.(?) p.(Val469Met)
-?/. - c.1414G>A r.(?) p.(Gly472Arg)
-?/. - c.1543G>A r.(?) p.(Gly515Ser)
-?/. - c.1589C>T r.(?) p.(Pro530Leu)
?/. - c.1618G>A r.(?) p.(Gly540Arg)
-?/. - c.*1291del r.(?) p.(=)
-?/. - c.*1357C>T r.(=) p.(=)
-/. - c.*1375C>A r.(=) p.(=)
-/. - c.*1426C>T r.(=) p.(=)
-/. - c.*1438C>A r.(=) p.(=)
+?/. - c.*1473A>G r.(=) p.(=)
+?/. - c.*1473A>G r.(=) p.(=)
-/. - c.*1611T>C r.(=) p.(=)
-/. - c.*1627A>G r.(=) p.(=)
-/. - c.*1704_*1707dup r.(=) p.(=)
-/. - c.*1708_*1711dup r.(=) p.(=)
-/. - c.*1726_*1727delinsT r.(=) p.(=)
-/. - c.*1747del r.(?) p.(=)
-?/. - c.*1747del r.(?) p.(=)
-/. - c.*1747del r.(?) p.(=)
-/. - c.*1901G>C r.(=) p.(=)
-/. - c.*1919C>G r.(=) p.(=)
-/. - c.*1921T>A r.(=) p.(=)
-/. - c.*1921T>A r.(=) p.(=)
-/. - c.*1921T>A r.(=) p.(=)
-/. - c.*1921T>A r.(=) p.(=)
-/. - c.*1925C>T r.(=) p.(=)
-?/. - c.*1925C>T r.(=) p.(=)
-?/. - c.*1925C>T r.(=) p.(=)
?/. - c.*1929G>T r.(=) p.(=)
?/. - c.*1941C>A r.(=) p.(=)
-?/. - c.*1949A>C r.(=) p.(=)
-?/. - c.*1959A>G r.(=) p.(=)
?/. - c.*1972C>G r.(=) p.(=)
?/. - c.*1987C>T r.(=) p.(=)
+?/. - c.*1992G>A r.(=) p.(=)
?/. - c.*1993C>A r.(=) p.(=)
?/. - c.*2020G>T r.(=) p.(=)
-?/. - c.*2025_*2026insG r.(=) p.(=)
-/. - c.*2033G>A r.(=) p.(=)
-/. - c.*2033G>A r.(=) p.(=)
-?/. - c.*2046C>T r.(=) p.(=)
-/. - c.*2101G>A r.(=) p.(=)
-/. - c.*2120G>C r.(=) p.(=)
-?/. - c.*2381C>T r.(=) p.(=)
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