Transcript #00001219 (NM_182961.3, SYNE1 gene)

Transcript name transcript variant 1
Gene name SYNE1 (spectrin repeat containing, nuclear envelope 1)
Chromosome 6
Transcript - NCBI ID NM_182961.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_892006.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 13:19:22 +02:00 (CEST)
Date last edited N/A


Variants

2160 entries on 22 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.-529C>T r.(?) p.(=)
?/. 5' UTR c.-9G>T r.(?) p.(=)
?/. 6 c.? r.? p.?
?/. 104 c.? r.? p.?
?/. 77 c.? r.? p.?
?/. 127 c.? r.? p.?
?/. 140 c.? r.? p.?
?/. 134 c.? r.? p.?
+?/. 83 c.? r.? p.?
?/. 110 c.? r.? p.?
?/. 106 c.? r.? p.?
?/. - c.? r.? p.?
?/. 47 c.? r.? p.?
?/. 59 c.? r.? p.?
?/. 2 c.23C>T r.(?) p.(Ser8Phe)
?/. 2 c.23C>T r.(?) p.(Ser8Phe)
?/. 2 c.23C>T r.(?) p.(Ser8Phe)
?/. - c.25C>T r.(?) p.(Arg9Trp)
+/. - c.38del r.(?) p.(Asp13Valfs*5)
?/. 3 c.68A>G r.(?) p.(Asp23Gly)
-?/. - c.93A>G r.(?) p.(Arg31=)
?/. 3 c.116C>G r.(?) p.(Ser39Cys)
?/. 3 c.118C>T r.(?) p.(His40Tyr)
?/. - c.118C>T r.(?) p.(His40Tyr)
?/. - c.148G>T r.(?) p.(Val50Leu)
-?/. - c.156T>C r.(?) p.(Asp52=)
-/. - c.156T>C r.(?) p.(Asp52=)
-/. - c.156T>C r.(?) p.(Asp52=)
-?/. - c.181G>A r.(?) p.(Val61Ile)
-?/. - c.216G>A r.(?) p.(Gly72=)
-?/. - c.226-45T>C r.(=) p.(=)
?/. 4i c.226-2dup r.spl? p.?
?/. - c.226-2dup r.spl? p.?
+/. - c.226-2dup r.spl? p.?
?/. - c.226-2dup r.spl? p.?
?/. - c.242G>A r.(?) p.(Arg81His)
?/. - c.244C>T r.(?) p.(Arg82Trp)
-?/. - c.245G>T r.(?) p.(Arg82Leu)
?/. 5 c.245G>T r.(?) p.(Arg82Leu)
?/. 5 c.245G>T r.(?) p.(Arg82Leu)
+/. - c.253C>T r.(?) p.(Arg85Ter)
?/. 5 c.290A>G r.(?) p.(Lys97Arg)
+/. 6i c.309+1G>A r.spl p.?
-?/. - c.309+9_309+10del r.(=) p.(=)
?/. 6 c.310-469C>T r.(?) p.(=)
?/. - c.310-468G>A r.(=) p.(=)
+/. - c.323A>G r.(?) p.(Asn108Ser)
?/. 7 c.334A>T r.(?) p.(Thr112Ser)
?/. 7 c.337G>A r.(?) p.(Asp113Asn)
?/. 7 c.338A>G r.(?) p.(Asp113Gly)
?/. 7 c.340A>G r.(?) p.(Ile114Val)
+/. - c.352C>T r.(?) p.(Arg118Ter)
+/. - c.352C>T r.(?) p.(Arg118*)
+/. 7 c.374T>A r.0 p.0
?/. - c.379T>A r.(?) p.(Trp127Arg)
?/. - c.385A>G r.(?) p.(Ile129Val)
?/. 7 c.395A>G r.(?) p.(Tyr132Cys)
-/. - c.402+11A>G r.(=) p.(=)
+/. - c.482_483del r.(?) p.(Ser161*)
?/. 8 c.495C>A r.(?) p.(Ser165Arg)
?/. 8 c.508C>T r.(?) p.(Arg170Trp)
+?/. - c.532G>C r.(?) p.(Gly178Arg)
?/. - c.561G>T r.(?) p.(Trp187Cys)
?/. - c.561G>T r.(?) p.(Trp187Cys)
?/. - c.578G>A r.(?) p.(Gly193Asp)
?/. 9 c.590G>A r.(?) p.(Gly197Glu)
+/. 9 c.638T>C r.(?) p.(Phe213Ser)
?/. - c.646G>T r.(?) p.(Val216Phe)
+/. 9 c.661C>T r.(?) p.(Arg221*)
+/. 9 c.661C>T r.(?) p.(Arg221*)
+/. 9 c.706C>T r.(?) p.(Arg236*)
?/. - c.764T>C r.(?) p.(Leu255Pro)
?/. 10 c.781G>A r.(?) p.(Val261Ile)
-?/. - c.781G>A r.(?) p.(Val261Ile)
?/. 10 c.797C>A r.(?) p.(Pro266Gln)
?/. 10 c.862G>A r.(?) p.(Ala288Thr)
?/. - c.939G>C r.(?) p.(Lys313Asn)
?/. 11 c.939G>T r.(?) p.(Lys313Asn)
?/. - c.939+2T>C r.spl? p.?
?/. 12 c.941G>T r.(?) p.(Arg314Ile)
?/. - c.979A>G r.(?) p.(Ile327Val)
?/. 12 c.1038T>C r.(?) p.(=)
?/. 12 c.1038T>C r.(?) p.(=)
-/. - c.1047+4T>A r.spl? p.?
-/. - c.1047+4T>A r.spl? p.?
-/. - c.1047+4T>A r.spl? p.?
-/. - c.1047+4T>A r.spl? p.?
-?/. - c.1047+6G>A r.(=) p.(=)
+?/. 13 c.1053del r.(?) p.(Phe351Leufs*10)
-?/. - c.1086G>A r.(?) p.(Arg362=)
-?/. - c.1113A>G r.(?) p.(Pro371=)
-?/. - c.1141G>A r.(?) p.(Asp381Asn)
?/. - c.1141G>A r.(?) p.(Asp381Asn)
-?/. - c.1141G>A r.(?) p.(Asp381Asn)
?/. 13 c.1141G>A r.(?) p.(Asp381Asn)
?/. 13 c.1141G>A r.(?) p.(Asp381Asn)
?/. 13 c.1141G>A r.(?) p.(Asp381Asn)
?/. - c.1141G>A r.(?) p.(Asp381Asn)
?/. 13 c.1141G>A r.(?) p.(Asp381Asn)
?/. - c.1141G>A r.(?) p.(Asp381Asn)
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