Transcript #00001111

Transcript name transcript variant 2
Gene name ARSF (arylsulfatase F)
Chromosome X
Transcript - NCBI ID NM_001201538.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001188467.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

126 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-28-14G>A r.(=) p.(=)
?/? c.-28-3A>G r.(=) p.(=)
?/? c.-17_-16insTATT r.(=) p.(=)
?/? c.-1A>C r.(=) p.(=)
?/? c.11+10G>A r.(=) p.(=)
?/? c.12-28A>G r.(=) p.(=)
?/? c.16C>T r.(?) p.(Pro6Ser)
?/? c.17C>G r.(?) p.(Pro6Arg)
?/? c.18C>G r.(=) p.(=)
?/? c.64G>A r.(?) p.(Ala22Thr)
?/? c.145G>A r.(?) p.(Gly49Ser)
?/? c.161+7C>T r.(=) p.(=)
?/? c.161+45G>C r.(=) p.(=)
?/? c.161+48C>T r.(=) p.(=)
?/? c.162-51C>T r.(=) p.(=)
?/? c.162-50_162-49insCCC r.(=) p.(=)
?/? c.162-39T>C r.(=) p.(=)
?/? c.162-7C>A r.(=) p.(=)
?/? c.165G>A r.(=) p.(=)
?/? c.175G>C r.(?) p.(Asp59His)
?/? c.240A>G r.(=) p.(=)
?/? c.244C>T r.(?) p.(Arg82Trp)
?/? c.249C>T r.(=) p.(=)
?/? c.252G>A r.(=) p.(=)
?/? c.276C>A r.(=) p.(=)
?/? c.277C>T r.(?) p.(Arg93*)
?/? c.283+12G>T r.(=) p.(=)
?/? c.283+15G>A r.(=) p.(=)
?/? c.283+33C>T r.(=) p.(=)
?/? c.283+35C>G r.(=) p.(=)
?/? c.284-49C>A r.(=) p.(=)
?/? c.284-40C>T r.(=) p.(=)
?/? c.286A>G r.(?) p.(Met96Val)
?/? c.289G>C r.(?) p.(Val97Leu)
?/? c.327A>C r.(=) p.(=)
?/? c.333C>T r.(=) p.(=)
?/? c.362del r.(?) p.(Ala122Glnfs*4)
?/? c.395C>T r.(?) p.(Thr132Met)
?/? c.397G>T r.(?) p.(Gly133Trp)
?/? c.404T>C r.(?) p.(Ile135Thr)
?/? c.406+7C>T r.(=) p.(=)
?/? c.406+46T>C r.(=) p.(=)
?/? c.407-23T>C r.(=) p.(=)
?/? c.432C>T r.(=) p.(=)
?/? c.444T>C r.(=) p.(=)
?/? c.486C>T r.(=) p.(=)
?/? c.507C>T r.(=) p.(=)
?/? c.535C>T r.(?) p.(Arg179Cys)
?/? c.543G>A r.(=) p.(=)
?/? c.598A>G r.(?) p.(Ile200Val)
?/? c.636C>A r.(=) p.(=)
?/? c.704C>G r.(?) p.(Ser235Cys)
?/? c.716C>A r.(?) p.(Ser239Tyr)
?/? c.746G>T r.(?) p.(Arg249Leu)
?/? c.753C>G r.(?) p.(His251Gln)
?/? c.761C>T r.(?) p.(Thr254Met)
?/? c.772A>G r.(?) p.(Met258Val)
?/? c.779C>T r.(?) p.(Ala260Val)
?/? c.784C>G r.(?) p.(Arg262Gly)
?/? c.810A>G r.(=) p.(=)
?/? c.821T>C r.(?) p.(Phe274Ser)
?/? c.827A>G r.(?) p.(Glu276Gly)
?/? c.830G>A r.(?) p.(Arg277Lys)
?/? c.830+38A>G r.(=) p.(=)
?/? c.831-29C>T r.(=) p.(=)
?/? c.831-15T>C r.(=) p.(=)
?/? c.874G>A r.(?) p.(Val292Met)
?/? c.886C>A r.(?) p.(Leu296Ile)
?/? c.962T>C r.(?) p.(Met321Thr)
?/? c.967+1G>T r.spl? p.?
?/? c.967+34C>T r.(=) p.(=)
?/? c.968-34A>G r.(=) p.(=)
?/? c.968-14G>A r.(=) p.(=)
?/? c.987C>T r.(=) p.(=)
?/? c.1004G>A r.(?) p.(Arg335Lys)
?/? c.1011C>G r.(?) p.(Asn337Lys)
?/? c.1038C>T r.(=) p.(=)
?/? c.1086G>T r.(?) p.(Trp362Cys)
?/? c.1097A>G r.(?) p.(Tyr366Cys)
?/? c.1102+5G>A r.spl? p.?
?/? c.1102+42G>A r.(=) p.(=)
?/? c.1103-17A>C r.(=) p.(=)
?/? c.1103-5T>C r.spl? p.?
?/? c.1138C>T r.(?) p.(Arg380Cys)
?/? c.1139G>A r.(?) p.(Arg380His)
?/? c.1140C>T r.(=) p.(=)
?/? c.1183C>T r.(?) p.(Arg395Trp)
?/? c.1184G>A r.(?) p.(Arg395Gln)
?/? c.1202C>T r.(?) p.(Thr401Ile)
?/? c.1265+8_1265+9insA r.(=) p.(=)
?/? c.1265+11A>G r.(=) p.(=)
?/? c.1266-25A>G r.(=) p.(=)
?/? c.1271T>C r.(?) p.(Ile424Thr)
?/? c.1275C>T r.(=) p.(=)
?/? c.1278C>T r.(=) p.(=)
?/? c.1307A>G r.(?) p.(Asn436Ser)
?/? c.1308C>T r.(=) p.(=)
?/? c.1357C>T r.(=) p.(=)
?/? c.1365C>T r.(=) p.(=)
?/? c.1386C>T r.(=) p.(=)
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