Transcript #00024113 (NM_014363.5, SACS gene)

Transcript name transcript variant 1
Gene name SACS (spastic ataxia of Charlevoix-Saguenay (sacsin))
Chromosome 13
Transcript - NCBI ID NM_014363.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_055178.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2016-03-18 16:41:06 +01:00 (CET)
Date last edited N/A


Variants

663 entries on 7 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-13A>G r.(?) p.(=)
-/. - c.-13A>G r.(?) p.(=)
+?/? _1_10_ c.(?_-1)_(-1_?)dup r.? p.?
+/? _1_10_ c.0 r.0 p.0
+/? _1_10_ c.0 r.0 p.0
+/? _1_10_ c.0 r.0 p.0
+/? _1_10_ c.0 r.0 p.0
+/? _1_10_ c.0 r.0 p.0
+/? _1_10_ c.0 r.(?) p.0
+/? _1_10_ c.0 r.0 p.0
+/? _1_10_ c.0 r.0 p.0
+/? _1_10_ c.0 r.0 p.0
+/? _1_10_ c.0 r.0 p.0
+/? _1_10_ c.0 r.0 p.0
+/? 8 c.1475ˆ1476G>A r.? p.(Trp492*)
-?/. - c.21-15C>T r.(=) p.(=)
+/? 2i_5i c.(20+1_21-1)_(345+1_346-1)dup r.(?) p.fs*
-?/. - c.90C>T r.(?) p.(Thr30=)
?/. - c.166C>T r.(?) p.(Arg56Cys)
+/. - c.171+1G>A r.spl? p.?
-/. - c.171+6C>T r.(=) p.(=)
-/. - c.171+6C>T r.(=) p.(=)
-?/. - c.171+13C>T r.(=) p.(=)
+/? 4 c.216del r.(?) p.(His73Ilefs*4)
+/? 4 c.237dup r.(?) p.(Ser80Ilefs*98)
+/? 4 c.237dup r.(?) p.(Ser80Ilefs*98)
+/. - c.262C>T r.(?) p.(Arg88Ter)
-/. - c.346-19del r.(=) p.(=)
+/? 6 c.414C>G r.(?) p.(Tyr138*)
+/? 6 c.414C>G r.(?) p.(Tyr138*)
+?/. - c.423_424del r.(?) p.(Glu141AspfsTer42)
?/. - c.432G>T r.(?) p.(Trp144Cys)
?/. - c.432G>T r.(?) p.(Trp144Cys)
+/. - c.457+1G>A r.spl? p.?
+/? 7 c.482del r.(?) p.(Asn161Thrfs*15)
+/? 7 c.482del r.(?) p.(Asn161Thrfs*15)
+/? 7 c.502G>T r.(?) p.(Asp168Tyr)
+/? 7_7i c.600_604+1del r.spl p.Thr201Cysfs*6
+/? 7 c.602C>A r.(?) p.(Thr201Lys)
?/. 7i c.605-3C>G r.spl p.?
+?/. 8 c.623G>A r.(?) p.(Ser208Asn)
?/. - c.639G>T r.(?) p.(Gly213=)
?/. - c.662T>C r.(?) p.(Leu221Pro)
-/. - c.696T>A r.(?) p.(Asn232Lys)
-/. - c.696T>A r.(?) p.(Asn232Lys)
-/. - c.696T>A r.(?) p.(Asn232Lys)
-?/. - c.744A>C r.(?) p.(Ala248=)
-?/. - c.810T>G r.(?) p.(Phe270Leu)
+/? 8 c.814C>T r.(?) p.(Arg272Cys)
+/? 8 c.814C>T r.(?) p.(Arg272Cys)
+/? 8 c.814C>T r.(?) p.(Arg272Cys)
+/? 8 c.814C>T r.(?) p.(Arg272Cys)
+/? 8 c.814C>T r.(?) p.(Arg272Cys)
+/? 8 c.814C>T r.(?) p.(Arg272Cys)
+/? 8 c.814C>T r.(?) p.(Arg272Cys)
+/? 8 c.814C>T r.(?) p.(Arg272Cys)
+/? 8 c.814C>T r.(?) p.(Arg272Cys)
+/? 8 c.814C>T r.(?) p.(Arg272Cys)
+/? 8 c.815G>A r.(?) p.(Arg272His)
+?/? 8 c.826C>T r.(?) p.(Arg276Cys)
+?/? 8 c.826C>T r.(?) p.(Arg276Cys)
+/? 8 c.832C>T r.(?) p.(Gln278*)
+/? 8 c.832C>T r.(?) p.(Gln278*)
-?/. - c.909A>G r.(=) p.(=)
-?/. - c.909A>G r.(=) p.(=)
-/. - c.909A>G r.(?) p.(Ala303=)
-/. - c.909A>G r.(?) p.(Ala303=)
+/? 8 c.922C>T r.(?) p.(Leu308Phe)
+/? 8 c.922C>T r.(?) p.(Leu308Phe)
+/? 8 c.922C>T r.(?) p.(Leu308Phe)
+/? 8 c.922C>T r.(?) p.(Leu308Phe)
?/. - c.956A>T r.(?) p.(Tyr319Phe)
+/? 8 c.961C>T r.(?) p.(Arg321*)
+/? 8 c.961C>T r.(?) p.(Arg321*)
+/? 8 c.961C>T r.(?) p.(Arg321*)
?/. - c.972C>A r.(?) p.(Asp324Glu)
?/. - c.973G>A r.(?) p.(Gly325Arg)
?/. - c.991_999del r.(?) p.(Phe331_Val333del)
?/. - c.1037C>T r.(?) p.(Pro346Leu)
?/. - c.1159G>A r.(?) p.(Ala387Thr)
+/? 8 c.1185_1194del r.(?) p.(Cys395Trpfs*13)
+/? 8 c.1189dup r.(?) p.(S397Kfs*405)
+/. - c.1201C>T r.(?) p.(Arg401Ter)
+/. - c.1201C>T r.(?) p.(Arg401Ter)
+/. - c.1201C>T r.(?) p.(Arg401Ter)
+/. - c.1201C>T r.(?) p.(Arg401Ter)
+/. 10 c.1201C>T r.(?) p.(Arg401*)
?/. - c.1219C>A r.(?) p.(Leu407Ile)
?/. - c.1219C>A r.(?) p.(Leu407Ile)
+/? 8 c.1228_1229del r.(?) p.(Leu410Serfs*2)
+/? 8 c.1229del r.(?) p.(Leu410*)
+/? 8 c.1229del r.(?) p.(Leu410*)
-?/. - c.1273C>A r.(?) p.(Pro425Thr)
?/. - c.1373C>T r.(?) p.(Thr458Ile)
-?/. - c.1373C>T r.(?) p.(Thr458Ile)
?/. - c.1373C>T r.(?) p.(Thr458Ile)
?/. - c.1373C>T r.(?) p.(Thr458Ile)
+/? 8 c.1373C>T r.(?) p.(Thr458Ile)
?/? 8 c.1373C>T r.(?) p.(Thr458Ile)
?/? 8 c.1373C>T r.(?) p.(Thr458Ile)
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