Transcript #00015333 (NM_002832.3, PTPN7 gene)

Transcript name transcript variant 1
Gene name PTPN7 (protein tyrosine phosphatase, non-receptor type 7)
Chromosome 1
Transcript - NCBI ID NM_002832.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_002823.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.2T>C r.? p.?
?/? c.6C>T r.(=) p.(=)
?/? c.38G>T r.(?) p.(Gly13Val)
?/? c.41C>T r.(?) p.(Thr14Met)
?/? c.50_52del r.(?) p.(Trp17_Ala18delinsSer)
?/? c.97C>T r.(?) p.(Arg33Trp)
?/? c.98G>A r.(?) p.(Arg33Gln)
?/? c.110A>G r.(?) p.(Gln37Arg)
?/? c.264-99C>T r.(=) p.(=)
?/? c.264-50T>C r.(=) p.(=)
?/? c.264-19G>A r.(=) p.(=)
?/? c.264-12C>T r.(=) p.(=)
?/? c.273A>T r.(=) p.(=)
?/? c.282T>C r.(=) p.(=)
?/? c.295G>A r.(?) p.(Gly99Ser)
?/? c.306C>T r.(=) p.(=)
?/? c.307C>T r.(?) p.(His103Tyr)
?/? c.309C>A r.(?) p.(His103Gln)
?/? c.315C>T r.(=) p.(=)
?/? c.328C>T r.(?) p.(His110Tyr)
?/? c.336G>C r.(=) p.(=)
?/? c.338G>A r.(?) p.(Arg113His)
?/? c.352C>A r.(?) p.(Pro118Thr)
?/? c.376G>A r.(?) p.(Ala126Thr)
?/? c.393G>A r.(=) p.(=)
?/? c.405G>A r.(=) p.(=)
?/? c.424C>G r.(?) p.(Arg142Gly)
?/? c.425G>A r.(?) p.(Arg142Gln)
?/? c.437+30C>T r.(=) p.(=)
?/? c.437+50C>T r.(=) p.(=)
?/? c.437+51G>A r.(=) p.(=)
?/? c.438-3C>T r.spl? p.?
?/? c.440G>A r.(?) p.(Arg147Gln)
?/? c.468C>A r.(?) p.(Asp156Glu)
?/? c.473G>A r.(?) p.(Arg158Gln)
?/? c.487G>A r.(?) p.(Val163Ile)
?/? c.541C>T r.(?) p.(Arg181Cys)
?/? c.565C>T r.(?) p.(Arg189Cys)
?/? c.572C>T r.(?) p.(Ala191Val)
?/? c.621+27C>T r.(=) p.(=)
?/? c.621+28G>A r.(=) p.(=)
?/? c.621+29C>T r.(=) p.(=)
?/? c.621+38C>T r.(=) p.(=)
?/? c.621+40G>A r.(=) p.(=)
?/? c.622-36_622-32del r.(=) p.(=)
?/? c.622-12del r.(=) p.(=)
?/? c.627C>A r.(=) p.(=)
?/? c.672C>T r.(=) p.(=)
?/? c.673G>A r.(?) p.(Ala225Thr)
?/? c.706+50_706+51insA r.(=) p.(=)
?/? c.706+51G>A r.(=) p.(=)
?/? c.707-60T>C r.(=) p.(=)
?/? c.719G>A r.(?) p.(Arg240His)
?/? c.733C>T r.(?) p.(Arg245Trp)
?/? c.782G>A r.(?) p.(Arg261Gln)
?/? c.783+27C>T r.(=) p.(=)
?/? c.783+28G>A r.(=) p.(=)
?/? c.783+39del r.(=) p.(=)
?/? c.783+46C>T r.(=) p.(=)
?/? c.783+50C>T r.(=) p.(=)
?/? c.783+51G>A r.(=) p.(=)
?/? c.784-50G>C r.(=) p.(=)
?/? c.845C>T r.(?) p.(Ser282Leu)
?/? c.846G>A r.(=) p.(=)
?/? c.921+23A>G r.(=) p.(=)
?/? c.921+46G>A r.(=) p.(=)
?/? c.922-33C>T r.(=) p.(=)
?/? c.922-20C>T r.(=) p.(=)
?/? c.922-8C>G r.(=) p.(=)
?/? c.929T>G r.(?) p.(Val310Gly)
?/? c.989T>C r.(?) p.(Met330Thr)
?/? c.1016G>A r.(?) p.(Arg339Gln)
?/? c.1020G>C r.(?) p.(Gln340His)
?/? c.1032+8C>G r.(=) p.(=)
?/? c.1032+13C>T r.(=) p.(=)
?/? c.1032+18C>T r.(=) p.(=)
?/? c.1032+22G>A r.(=) p.(=)
?/? c.1032+31G>C r.(=) p.(=)
?/? c.1032+41C>T r.(=) p.(=)
?/? c.1032+42G>A r.(=) p.(=)
?/? c.1033-14T>C r.(=) p.(=)
?/? c.1033-7A>T r.(=) p.(=)
?/? c.1045C>T r.(?) p.(Arg349Cys)
?/? c.1046G>A r.(?) p.(Arg349His)
?/? c.1066C>G r.(?) p.(Leu356Val)
?/? c.1074G>A r.(=) p.(=)
?/? c.1089T>C r.(=) p.(=)
?/? c.1120C>T r.(?) p.(Arg374Cys)
?/? c.1122C>T r.(=) p.(=)
?/? c.1135G>A r.(?) p.(Val379Met)
?/? c.1149G>A r.(=) p.(=)
?/? c.1172C>T r.(?) p.(Pro391Leu)
?/? c.1175T>C r.(?) p.(Ile392Thr)
?/? c.1177G>A r.(?) p.(Val393Ile)
?/? c.1185C>T r.(=) p.(=)
?/? c.1190+5G>A r.spl? p.?
?/? c.1190+11C>T r.(=) p.(=)
?/? c.1190+27C>T r.(=) p.(=)
?/? c.1190+49C>G r.(=) p.(=)
?/? c.1190+50T>C r.(=) p.(=)
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