Transcript #00000039 (NM_000199.3, SGSH gene)

Transcript name N-sulfoglucosamine sulfohydrolase
Gene name SGSH (N-sulfoglucosamine sulfohydrolase)
Chromosome 17
Transcript - NCBI ID NM_000199.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000190.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-05-11 13:11:54 +02:00 (CEST)
Date last edited N/A


Variants

345 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-2434G>T r.(?) p.(=)
?/. - c.-1315C>T r.(?) p.(=)
+/. _1_5i c.-687_664-23del r.0? p.0?
+/. _1_5i c.-687_664-23del r.0? p.0?
+?/. - c.1A>G r.(?) p.(Met1?)
+/. - c.2T>C r.(?) p.0?
+/. 1 c.2T>C r.? p.?
+/. 1 c.2T>C r.? p.?
+/. - c.29dup r.(?) p.(Leu11Alafs*22)
+/. 1 c.29dup r.(?) p.(Leu11Alafs*22)
+/. 1 c.29dup r.(?) p.(Leu11Alafs*22)
?/. 1 c.83T>C r.(?) p.(Leu28Pro)
?/. - c.88G>A r.(?) p.(Ala30Thr)
+?/. - c.88G>C r.(?) p.(Ala30Pro)
?/. - c.90G>A r.(?) p.(=)
+?/. 2 c.96C>A r.(?) p.(Asp32Glu)
+?/. - c.97G>A r.(?) p.(Gly33Arg)
+/. - c.111T>A r.(?) p.(Ser37Arg)
+?/. - c.149_169del r.(?) p.(Leu50_Ser57delinsArg)
?/. - c.163C>T r.(?) p.(Arg55Cys)
-?/. - c.177C>T r.(?) p.(Leu59=)
+/. 2 c.197C>G r.(?) p.(Ser66Trp)
+/. - c.197C>G r.(?) p.(Ser66Trp)
+/. - c.197C>G r.(?) p.(Ser66Trp)
+/. - c.197C>G r.(?) p.(Ser66Trp)
+/. - c.197C>G r.(?) p.(Ser66Trp)
+/. - c.197C>G r.(?) p.(Ser66Trp)
?/. - c.197C>G r.(?) p.(Ser66Trp)
+/. - c.197C>G r.(?) p.(Ser66Trp)
+/. 2 c.197C>G r.(?) p.(Ser66Trp)
+/. - c.220C>T r.(?) p.(Arg74Cys)
+/. - c.220C>T r.(?) p.(Arg74Cys)
?/. - c.220C>T r.(?) p.(Arg74Cys)
?/. - c.220C>T r.(?) p.(Arg74Cys)
+/. 2 c.220C>T r.(?) p.(Arg74Cys)
+/. - c.220C>T r.(?) p.(Arg74Cys)
+?/. - c.221G>A r.(?) p.(Arg74His)
?/. - c.235A>C r.(?) p.(Thr79Pro)
-/. - c.250-26C>T r.(=) p.(=)
+?/. - c.265_269del r.(?) p.(Tyr89AlafsTer45)
?/. - c.276C>G r.(?) p.(His92Gln)
+?/. - c.301_303del r.(?) p.(Phe101del)
?/. - c.308A>G r.(?) p.(Lys103Arg)
?/. - c.344G>T r.(?) p.(Gly115Val)
?/. - c.349C>T r.(?) p.(Arg117Cys)
?/. - c.350G>T r.(?) p.(Arg117Leu)
-?/. - c.356-6G>A r.(=) p.(=)
+/. - c.364G>A r.(?) p.(Gly122Arg)
+/. - c.364G>A r.(?) p.(Gly122Arg)
+/. - c.364G>A r.(?) p.(Gly122Arg)
+/. - c.376dup r.(?) p.(Val126GlyfsTer10)
+/. - c.376dup r.(?) p.(Val126GlyfsTer10)
?/. - c.391G>A r.(?) p.(Val131Met)
+?/. - c.408_444dup r.(?) p.(Gly149CysfsTer18)
-/. - c.411G>A r.(?) p.(Ala137=)
-?/. - c.411G>A r.(?) p.(Ala137=)
+/. - c.449G>A r.(?) p.(Arg150Gln)
-?/. - c.494C>G r.(?) p.(Thr165Ser)
?/. - c.506+3A>G r.spl? p.?
-?/. - c.507-7C>T r.(=) p.(=)
-?/. - c.507-7C>T r.(=) p.(=)
?/. - c.508C>G r.(?) p.(Pro170Ala)
-?/. - c.522C>T r.(?) p.(Tyr174=)
-/. - c.522C>T r.(?) p.(Tyr174=)
+/. 5 c.544C>T r.(?) p.(Arg182Cys)
?/. - c.545G>A r.(?) p.(Arg182His)
?/. - c.563C>T r.(?) p.(Pro188Leu)
+/. 5 c.571G>A r.(?) p.(Gly191Arg)
+/. - c.571G>A r.(?) p.(Gly191Arg)
+?/. 5 c.571G>A r.(?) p.(Gly191Arg)
+?/. - c.582T>A r.(?) p.(Cys194Ter)
?/. - c.598G>A r.(?) p.(Gly200Arg)
+?/. - c.614G>T r.(?) p.(Gly205Val)
-?/. - c.617G>A r.(?) p.(Arg206His)
?/. - c.641C>A r.(?) p.(Ala214Asp)
-?/. - c.641C>A r.(?) p.(Ala214Asp)
-?/. - c.658G>T r.(?) p.(Val220Leu)
?/. - c.658G>T r.(?) p.(Val220Leu)
-/. - c.663+17T>C r.(=) p.(=)
-/. - c.663+17T>C r.(=) p.(=)
-/. - c.663+17T>C r.(=) p.(=)
-/. - c.663+17T>C r.(=) p.(=)
-/. - c.663+17T>C r.(=) p.(=)
-/. - c.664-39_664-36delinsGC r.(=) p.(=)
-/. - c.701C>G r.(?) p.(Ala234Gly)
?/. - c.701C>G r.(?) p.(Ala234Gly)
?/. - c.701C>G r.(?) p.(Ala234Gly)
+/. - c.734G>A r.(?) p.(Arg245His)
+/. - c.734G>A r.(?) p.(Arg245His)
+/. - c.734G>A r.(?) p.(Arg245His)
+/. - c.734G>A r.(?) p.(Arg245His)
+/. - c.734G>A r.(?) p.(Arg245His)
+/. - c.734G>A r.(?) p.(Arg245His)
+/. - c.734G>A r.(?) p.(Arg245His)
+/. - c.734G>A r.(?) p.(Arg245His)
+/. - c.734G>A r.(?) p.(Arg245His)
+/. - c.734G>A r.(?) p.(Arg245His)
+/. 7 c.734G>A r.(?) p.(Arg245His)
?/. - c.734G>A r.(?) p.(Arg245His)
+/. - c.734G>A r.(?) p.(Arg245His)
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