Transcript #00024040 (NM_025137.3, SPG11 gene)

Transcript name transcript variant 1
Gene name SPG11 (spastic paraplegia 11 (autosomal recessive))
Chromosome 15
Transcript - NCBI ID NM_025137.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_079413.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2015-06-15 11:30:40 +02:00 (CEST)
Date last edited N/A


Variants

468 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.16G>A r.(?) p.(Gly6Arg)
?/. - c.16G>A r.(?) p.(Gly6Arg)
-?/. - c.16G>A r.(?) p.(Gly6Arg)
-/. - c.23C>G r.(?) p.(Ala8Gly)
-?/. - c.23C>G r.(?) p.(Ala8Gly)
?/. - c.28G>A r.(?) p.(Ala10Thr)
-/. - c.43G>A r.(?) p.(Gly15Ser)
?/. - c.44G>A r.(?) p.(Gly15Asp)
-?/. - c.48C>T r.(?) p.(Ser16=)
?/. - c.66G>A r.(?) p.(Met22Ile)
-?/. - c.176C>T r.(?) p.(Ala59Val)
-?/. - c.176C>T r.(?) p.(Ala59Val)
-?/. - c.196C>T r.(?) p.(Leu66Phe)
?/+? 1 c.255G>A r.(?) p.(Trp85*)
-?/. - c.257+13G>A r.(=) p.(=)
-?/. - c.257+13G>A r.(=) p.(=)
-?/. - c.257+13G>A r.(=) p.(=)
-?/. - c.257+15A>G r.(=) p.(=)
-?/. - c.257+17A>G r.(=) p.(=)
-/. - c.258-6del r.(=) p.(=)
?/. - c.258-6del r.(=) p.(=)
?/. - c.278G>A r.(?) p.(Arg93His)
?/. - c.304C>T r.(?) p.(Pro102Ser)
+/. - c.315del r.(?) p.(Ala106Leufs*15)
-?/. - c.328A>G r.(?) p.(Asn110Asp)
-?/. - c.395G>A r.(?) p.(Ser132Asn)
-?/. - c.395G>A r.(?) p.(Ser132Asn)
-?/. - c.395G>A r.(?) p.(Ser132Asn)
-?/. - c.395G>A r.(?) p.(Ser132Asn)
-?/. - c.440T>C r.(?) p.(Ile147Thr)
-?/. - c.440T>C r.(?) p.(Ile147Thr)
+/. - c.442+1G>A r.(?) p.(?)
+/. - c.442+1G>C r.spl p.?
-?/. - c.528T>C r.(?) p.(Ile176=)
-?/. - c.529A>C r.(?) p.(Ile177Leu)
-?/. - c.535C>T r.(?) p.(Pro179Ser)
-?/. - c.545A>T r.(?) p.(Asp182Val)
+/. - c.575del r.(?) p.(Thr192AsnfsTer11)
+/. 4 c.733_734del r.(?) p.(Met245Valfs*2)
+/. - c.733_734del r.(?) p.(Met245ValfsTer2)
+/. - c.733_734del r.(?) p.(Met245ValfsTer2)
-?/. - c.763A>G r.(?) p.(Lys255Glu)
+/. - c.777_781del r.(?) p.(Ser261Glufs*22)
?/. - c.779C>A r.(?) p.(Thr260Asn)
-/. - c.808G>A r.(?) p.(Val270Ile)
-/. - c.808G>A r.(?) p.(Val270Ile)
-?/. - c.808G>A r.(?) p.(Val270Ile)
-?/. - c.808G>A r.(?) p.(Val270Ile)
-/. - c.808G>A r.(?) p.(Val270Ile)
-?/. - c.808G>A r.(?) p.(Val270Ile)
-?/. - c.833A>G r.(?) p.(Asn278Ser)
-/. - c.833A>G r.(?) p.(Asn278Ser)
-?/. - c.833A>G r.(?) p.(Asn278Ser)
-?/. - c.833A>G r.(?) p.(Asn278Ser)
?/. - c.833A>T r.(?) p.(Asn278Ile)
?/. - c.844G>C r.(?) p.(Ala282Pro)
?/. - c.844G>C r.(?) p.(Ala282Pro)
+/. - c.869+1G>A r.spl p.?
?/. - c.934G>T r.(?) p.(Gly312Cys)
-/. - c.993C>T r.(?) p.(Ser331=)
-?/. - c.993C>T r.(?) p.(Ser331=)
-/. - c.993C>T r.(?) p.(Ser331=)
-?/. - c.1002T>A r.(?) p.(Ile334=)
?/. - c.1084T>C r.(?) p.(Trp362Arg)
+/. - c.1085G>A r.(?) p.(Trp362Ter)
-/. - c.1108G>A r.(?) p.(Glu370Lys)
-/. - c.1108G>A r.(?) p.(Glu370Lys)
-/. - c.1108G>A r.(?) p.(Glu370Lys)
-/. - c.1108G>A r.(?) p.(Glu370Lys)
-/. - c.1108G>A r.(?) p.(Glu370Lys)
-?/. - c.1108G>A r.(?) p.(Glu370Lys)
-?/. - c.1168G>A r.(?) p.(Asp390Asn)
+/. 6 c.1214A>C r.(?) p.(Lys405Thr)
-?/. - c.1218C>G r.(?) p.(Thr406=)
+/. 6 c.1235C>G r.(?) p.(Ser412*)
+/. - c.1235C>G r.(?) p.(Ser412Ter)
+/. 6 c.1235C>G r.(?) p.(Ser412*)
?/. - c.1238G>A r.(?) p.(Trp413Ter)
-?/. - c.1248G>T r.(?) p.(Met416Ile)
-?/. - c.1251C>T r.(?) p.(His417=)
+/. 6 c.1275dup r.(?) p.(Glu426Argfs*3)
-?/. - c.1276G>A r.(?) p.(Glu426Lys)
-/. - c.1347C>T r.(?) p.(Thr449=)
-/. - c.1347C>T r.(?) p.(Thr449=)
-/. - c.1348A>G r.(?) p.(Ile450Val)
-/. - c.1348A>G r.(?) p.(Ile450Val)
-/. - c.1348A>G r.(?) p.(Ile450Val)
+/. - c.1348dup r.(?) p.(Ile450AsnfsTer26)
?/. - c.1384T>C r.(?) p.(Cys462Arg)
-/. - c.1388T>C r.(?) p.(Phe463Ser)
-/. - c.1388T>C r.(?) p.(Phe463Ser)
-/. - c.1388T>C r.(?) p.(Phe463Ser)
-/. - c.1388T>C r.(?) p.(Phe463Ser)
+/. - c.1432C>T r.(?) p.(Gln478Ter)
?/. - c.1435C>A r.(?) p.(Gln479Lys)
-?/. - c.1457-4A>G r.spl? p.?
+/. - c.1457-2A>G r.spl? p.?
+/. 7 c.1492C>T r.(?) p.(Gln498*)
+/. 7 c.1492C>T r.(?) p.(Gln498*)
?/. - c.1529G>A r.(?) p.(Ser510Asn)
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