Transcript #00018508 (NM_005626.4, SRSF4 gene)

Transcript name serine/arginine-rich splicing factor 4
Gene name SRSF4 (serine/arginine-rich splicing factor 4)
Chromosome 1
Transcript - NCBI ID NM_005626.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_005617.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

81 entries on 1 page. Showing entries 1 - 81.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-4C>T r.(=) p.(=)
?/? c.15C>T r.(=) p.(=)
?/? c.45G>A r.(=) p.(=)
?/? c.69G>A r.(=) p.(=)
?/? c.107+28G>C r.(=) p.(=)
?/? c.107+45A>G r.(=) p.(=)
?/? c.108-27A>G r.(=) p.(=)
?/? c.108-7C>A r.(=) p.(=)
?/? c.108-4C>G r.spl? p.?
?/? c.111T>C r.(=) p.(=)
?/? c.133C>T r.(=) p.(=)
?/? c.250+34C>T r.(=) p.(=)
?/? c.250+35G>A r.(=) p.(=)
?/? c.250+47T>C r.(=) p.(=)
?/? c.251-25T>C r.(=) p.(=)
?/? c.251-24C>G r.(=) p.(=)
?/? c.251-20T>C r.(=) p.(=)
?/? c.251-13G>A r.(=) p.(=)
?/? c.339T>G r.(?) p.(Ser113Arg)
?/? c.363+47_363+48insA r.(=) p.(=)
?/? c.364-14T>C r.(=) p.(=)
?/? c.364-8del r.(=) p.(=)
?/? c.364-8_364-7del r.(=) p.(=)
?/? c.405T>C r.(=) p.(=)
?/? c.578+20T>C r.(=) p.(=)
?/? c.578+40A>G r.(=) p.(=)
?/? c.579-41C>T r.(=) p.(=)
?/? c.579-3del r.spl? p.?
?/? c.583C>T r.(?) p.(Arg195Cys)
?/? c.642T>A r.(?) p.(Ser214Arg)
?/? c.643C>A r.(?) p.(His215Asn)
?/? c.669-35A>G r.(=) p.(=)
?/? c.669-21C>T r.(=) p.(=)
?/? c.680G>A r.(?) p.(Arg227His)
?/? c.704G>A r.(?) p.(Arg235Gln)
?/? c.704_709del r.(?) p.(Arg235_Ser236del)
?/? c.713_714insCCAGAG r.(?) p.(Gln237_Ser238dup)
?/? c.716G>A r.(?) p.(Arg239Gln)
?/? c.722G>A r.(?) p.(Arg241Gln)
?/? c.759A>C r.(?) p.(Glu253Asp)
?/? c.779A>G r.(?) p.(His260Arg)
?/? c.780T>C r.(=) p.(=)
?/? c.865C>T r.(?) p.(Arg289Trp)
?/? c.878G>A r.(?) p.(Arg293Lys)
?/? c.885A>G r.(=) p.(=)
?/? c.924A>G r.(=) p.(=)
?/? c.948T>C r.(=) p.(=)
?/? c.949G>A r.(?) p.(Val317Met)
?/? c.983G>A r.(?) p.(Arg328His)
?/? c.991C>T r.(?) p.(Arg331Trp)
?/? c.1013G>C r.(?) p.(Gly338Ala)
?/? c.1021A>C r.(=) p.(=)
?/? c.1066G>A r.(?) p.(Gly356Ser)
?/? c.1095C>T r.(=) p.(=)
?/? c.1099C>T r.(?) p.(Arg367Cys)
?/? c.1104_1109del r.(?) p.(Arg371_Ser372del)
?/? c.1111C>T r.(?) p.(Arg371Cys)
?/? c.1186_1188del r.(?) p.(Lys396del)
?/? c.1202G>A r.(?) p.(Arg401His)
?/? c.1207C>G r.(?) p.(Gln403Glu)
?/? c.1209G>T r.(?) p.(Gln403His)
?/? c.1226_1228del r.(?) p.(Arg409_Ser410delinsPro)
?/? c.1230C>T r.(=) p.(=)
?/? c.1231G>A r.(?) p.(Val411Met)
?/? c.1248A>C r.(?) p.(Glu416Asp)
?/? c.1252G>A r.(?) p.(Ala418Thr)
?/? c.1321C>T r.(?) p.(Arg441Trp)
?/? c.1325C>G r.(?) p.(Ser442Cys)
?/? c.1335A>C r.(?) p.(Arg445Ser)
?/? c.1350G>A r.(=) p.(=)
?/? c.1387A>C r.(?) p.(Lys463Gln)
?/? c.1393G>C r.(?) p.(Ala465Pro)
?/? c.1419G>C r.(?) p.(Lys473Asn)
?/? c.1442G>C r.(?) p.(Arg481Thr)
?/? c.1443A>G r.(=) p.(=)
?/? c.1446G>A r.(=) p.(=)
?/? c.1448C>G r.(?) p.(Pro483Arg)
?/? c.1454G>C r.(?) p.(Arg485Pro)
?/? c.*36_*41del r.(=) p.(=)
?/? c.*41G>C r.(=) p.(=)
?/? c.*37_*43del r.(=) p.(=)
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