Transcript #00026049 (NM_001374736.1, DST gene)

Transcript name transcript variant 4 (removed from reference sequence) (removed from reference sequence)
Gene name DST (dystonin)
Chromosome 6
Transcript - NCBI ID NM_001374736.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001361665.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks MANE select
Date created 2026-02-24 20:07:44 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.1024T>C r.(?) p.(Trp342Arg)
-?/. - c.1779-303_1779-301del r.(?) p.(=)
+/. - c.1779-264del r.(?) p.(=)
-?/. - c.1779-261C>T r.(?) p.(=)
?/. - c.1779-261C>T r.(?) p.(=)
-?/. - c.1779-261C>T r.(?) p.(=)
+/. - c.1779-222C>T r.(?) p.(=)
-?/. - c.1779-202T>C r.(?) p.(=)
-/. - c.1779-188T>C r.(?) p.(=)
-/. - c.1779-188T>C r.(?) p.(=)
-/. - c.1779-188T>C r.(?) p.(=)
-?/. - c.1779-144G>A r.(?) p.(=)
-?/. - c.1988T>C r.(?) p.(Ile663Thr)
?/. - c.2125A>G r.(?) p.(Met709Val)
-?/. - c.2256A>T r.(?) p.(Ser752=)
-?/. - c.2256A>T r.(?) p.(Ser752=)
-/. - c.2256A>T r.(?) p.(Ser752=)
-?/. - c.2270G>T r.(?) p.(Arg757Leu)
-?/. - c.2350C>G r.(?) p.(Pro784Ala)
-?/. - c.2350C>G r.(?) p.(Pro784Ala)
-?/. - c.2350C>G r.(?) p.(Pro784Ala)
-?/. - c.2350C>G r.(?) p.(Pro784Ala)
-/. - c.2368T>C r.(?) p.(Leu790=)
-/. - c.2368T>C r.(?) p.(Leu790=)
-/. - c.2368T>C r.(?) p.(Leu790=)
?/. - c.2387G>A r.(?) p.(Arg796Gln)
-?/. - c.2406T>G r.(?) p.(Ser802=)
-?/. - c.2491-6C>T r.(?) p.(=)
?/. - c.2504G>A r.(?) p.(Arg835His)
-/. - c.2520A>C r.(?) p.(Ser840=)
?/. - c.2534T>G r.(?) p.(Val845Gly)
?/. - c.2555A>G r.(?) p.(His852Arg)
-?/. - c.2589A>G r.(?) p.(Glu863=)
?/. - c.2629A>G r.(?) p.(Thr877Ala)
?/. - c.2629A>G r.(?) p.(Thr877Ala)
?/. - c.2630C>T r.(?) p.(Thr877Ile)
-?/. - c.2697+16del r.(?) p.(=)
-/. - c.2697+16dup r.(?) p.(=)
?/. - c.2701A>G r.(?) p.(Thr901Ala)
?/. - c.2705C>G r.(?) p.(Ser902Cys)
-?/. - c.2705C>G r.(?) p.(Ser902Cys)
?/. - c.2705C>G r.(?) p.(Ser902Cys)
?/. - c.2705C>G r.(?) p.(Ser902Cys)
?/. - c.2705C>G r.(?) p.(Ser902Cys)
?/. - c.2759C>G r.(?) p.(Thr920Ser)
?/. - c.2848G>A r.(?) p.(Asp950Asn)
?/. - c.2851T>A r.(?) p.(Tyr951Asn)
-?/. - c.2950C>T r.(?) p.(Arg984Trp)
-?/. - c.2951G>A r.(?) p.(Arg984Gln)
?/. - c.2951G>T r.(?) p.(Arg984Leu)
-?/. - c.2964+16G>A r.(?) p.(=)
-?/. - c.2976G>A r.(?) p.(Ala992=)
?/. - c.2987C>T r.(?) p.(Thr996Met)
?/. - c.3121C>T r.(?) p.(Arg1041Trp)
-?/. - c.3126G>A r.(?) p.(Lys1042=)
-/. - c.3126G>A r.(?) p.(Lys1042=)
?/. - c.3389G>A r.(?) p.(Arg1130His)
-/. - c.3492C>T r.(?) p.(Asn1164=)
-/. - c.3495-17T>C r.(?) p.(=)
-/. - c.3557G>A r.(?) p.(Ser1186Asn)
-?/. - c.3557G>A r.(?) p.(Ser1186Asn)
-/. - c.3564A>G r.(?) p.(Val1188=)
-?/. - c.3600T>C r.(?) p.(Ile1200=)
?/. - c.3647A>G r.(?) p.(His1216Arg)
-?/. - c.3805+17C>T r.(?) p.(=)
-?/. - c.3963+7G>A r.(?) p.(=)
-/. - c.4062C>T r.(?) p.(Val1354=)
-/. - c.4143-15A>G r.(?) p.?
-/. - c.4200A>G r.(?) p.(Lys1400=)
?/. - c.4211C>T r.(?) p.(Thr1404Ile)
?/. - c.4229_4231del r.(?) p.(Glu1410del)
?/. - c.4283A>G r.(?) p.(Gln1428Arg)
-?/. - c.4330G>A r.(?) p.(Glu1444Lys)
-/. - c.4452T>C r.(?) p.(Asn1484=)
-?/. - c.4452T>C r.(?) p.(Asn1484=)
-?/. - c.4452T>C r.(?) p.(Asn1484=)
?/. - c.4470C>A r.(?) p.(Asp1490Glu)
-/. - c.4475+15T>A r.(?) p.(=)
-/. - c.4590T>G r.(?) p.(Asn1530Lys)
-?/. - c.4638+7A>T r.(?) p.?
-?/. - c.4638+7A>T r.(?) p.?
-/. - c.4638+16T>A r.(?) p.(=)
-?/. - c.4701A>G r.(?) p.(Glu1567=)
?/. - c.4727A>G r.(?) p.(Tyr1576Cys)
?/. - c.4750C>T r.(?) p.(Arg1584Trp)
-?/. - c.4831-3C>A r.spl? p.?
-?/. - c.4831-3C>A r.spl? p.?
-/. - c.4831-3C>A r.spl? p.?
?/. - c.4840C>G r.(?) p.(Leu1614Val)
-/. - c.4845G>A r.(?) p.(Arg1615=)
-/. - c.4845G>A r.(=) p.(Arg1615=)
?/. - c.4850G>A r.(?) p.(Arg1617Gln)
-?/. - c.4906T>C r.(?) p.(Leu1636=)
-?/. - c.4929+3811G>A r.spl? p.?
-?/. - c.4929+3832G>C r.(?) p.(=)
?/. - c.4929+3832G>C r.(?) p.(=)
-?/. - c.4929+3832G>C r.(?) p.(=)
-/. - c.4929+3842C>T r.(?) p.(=)
+/. - c.4929+3866C>T r.(?) p.(=)
-?/. - c.4929+3870G>C r.(?) p.(=)
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