Transcript #00000005 (NM_000046.3, ARSB gene)

Transcript name transcript variant 1
Gene name ARSB (arylsulfatase B)
Chromosome 5
Transcript - NCBI ID NM_000046.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000037.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

61 entries on 1 page. Showing entries 1 - 61.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Clinical classification     
./. - c.31C>T r.(?) p.(Arg11*) pathogenic
./. - c.31C>T r.(?) p.(Arg11*) pathogenic
./. - c.113_121delGCGCCGGGG r.(?) p.(Gly38_Gly40del) likely benign
./. - c.190G>C r.(?) p.(Gly64Arg) likely pathogenic
./. - c.235G>A r.(?) p.(Gly79Arg) likely pathogenic
./+ 1 c.235G>A r.(?) p.(Gly79Arg) likely pathogenic
./+ - c.274A>C r.(?) p.(Thr92Pro) likely pathogenic
./. - c.275C>A r.(?) p.(Thr92Lys) likely pathogenic
+/+ - c.275C>A r.(?) p.(Thr92Lys) likely pathogenic
./. - c.275C>A r.(?) p.(Thr92Lys) likely pathogenic
./. - c.281C>A r.(?) p.(Ser94*) pathogenic
./. - c.281C>A r.(?) p.(Ser94*) pathogenic
./. - c.281C>A r.(?) p.(Ser94*) pathogenic
./. - c.281C>A r.(?) p.(Ser94*) pathogenic
./+? - c.312G>C r.(?) p.(Gln104His) pathogenic
+/+ - c.427_460del r.(?) p.(Val143Asnfs*30) pathogenic
./. - c.430G>A r.(?) p.(Gly144Arg) pathogenic
./. - c.430G>A r.(?) p.(Gly144Arg) pathogenic
./. - c.430G>A r.(?) p.(Gly144Arg) pathogenic
./. - c.430G>A r.(?) p.(Gly144Arg) pathogenic
./. - c.430G>A r.(?) p.(Gly144Arg) pathogenic
+/+ - c.430G>A r.(?) p.(Gly144Arg) pathogenic
+/+ - c.430G>A r.(?) p.(Gly144Arg) pathogenic
./. - c.430G>A r.(?) p.(Gly144Arg) pathogenic
./+ - c.430G>A r.(?) p.(Gly144Arg) pathogenic
+/+ - c.430G>A r.(?) p.(Gly144Arg) pathogenic
./. - c.430G>A r.(?) p.(Gly144Arg) pathogenic
+/+ - c.430G>A r.(?) p.(Gly144Arg) pathogenic
./. - c.430G>A r.(?) p.(Gly144Arg) pathogenic
./. - c.430G>A r.(?) p.(Gly144Arg) pathogenic
./. - c.430G>A r.(?) p.(Gly144Arg) pathogenic
./. - c.478C>T r.(?) p.(Arg160*) pathogenic
./. - c.479G>A r.(?) p.(Arg160Gln) pathogenic
./. - c.532C>G r.(?) p.(His178Asp) likely pathogenic
./. - c.532C>G r.(?) p.(His178Asp) likely pathogenic
./. - c.571C>T r.(?) p.(Arg191*) pathogenic
+/+ - c.710C>A r.(?) p.(Ala237Asp) pathogenic
./. - c.710C>A r.(?) p.(Ala237Asp) likely pathogenic
./. - c.725A>G r.(?) p.(His242Arg) likely pathogenic
./. - c.753C>G r.(?) p.(Tyr251*) pathogenic
+/+ - c.753C>G r.(?) p.(Tyr251*) pathogenic
+/+ - c.753C>G r.(?) p.(Tyr251*) pathogenic
./. - c.898+1G>A r.spl? p.? pathogenic
./+ - c.904G>A r.(?) p.(Gly302Arg) pathogenic
./. - c.904G>A r.(?) p.(Gly302Arg) pathogenic
./. - c.934T>C r.(?) p.(Trp312Arg) likely pathogenic
+/+ - c.962T>C r.(?) p.(Leu321Pro) pathogenic
./. - c.962T>C r.(?) p.(Leu321Pro) pathogenic
+/+ - c.962T>C r.(?) p.(Leu321Pro) pathogenic
./. - c.962T>C r.(?) p.(Leu321Pro) pathogenic
./. - c.962T>C r.(?) p.(Leu321Pro) pathogenic
./. - c.962T>C r.(?) p.(Leu321Pro) pathogenic
./. - c.962T>C r.(?) p.(Leu321Pro) pathogenic
./. - c.979C>T r.(?) p.(Arg327*) pathogenic
./. - c.982G>C r.(?) p.(Gly328Arg) likely pathogenic
./. - c.982G>C r.(?) p.(Gly328Arg) likely pathogenic
+/+ - c.985del r.(?) p.(Val329Trpfs*9) pathogenic
./. - c.1142+2T>C r.spl? p.? pathogenic
./. - c.1178A>G r.(?) p.(His393Arg) likely pathogenic
./. - c.1339T>C r.(?) p.(Cys447Arg) likely pathogenic
./. - c.1601A>G r.(?) p.(*534Trpext*50) VUS
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