Transcript #00005304

Transcript name transcript variant 2
Gene name ENOX2 (ecto-NOX disulfide-thiol exchanger 2)
Chromosome X
Transcript - NCBI ID NM_182314.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_872114.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

75 entries on 1 page. Showing entries 1 - 75.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-40-10_-40-9del r.(=) p.(=)
?/? c.-16A>G r.(=) p.(=)
?/? c.33C>T r.(=) p.(=)
?/? c.46G>T r.(?) p.(Ala16Ser)
?/? c.49+35T>C r.(=) p.(=)
?/? c.49+63A>G r.(=) p.(=)
?/? c.50-51G>A r.(=) p.(=)
?/? c.52G>A r.(?) p.(Asp18Asn)
?/? c.88A>G r.(?) p.(Met30Val)
?/? c.153G>T r.(=) p.(=)
?/? c.158G>C r.(?) p.(Gly53Ala)
?/? c.165C>T r.(=) p.(=)
?/? c.184+33A>G r.(=) p.(=)
?/? c.184+51G>A r.(=) p.(=)
?/? c.235A>G r.(?) p.(Met79Val)
?/? c.321G>A r.(=) p.(=)
?/? c.340+37A>G r.(=) p.(=)
?/? c.447G>A r.(=) p.(=)
?/? c.472C>T r.(?) p.(Arg158Cys)
?/? c.473G>A r.(?) p.(Arg158His)
?/? c.547+42G>A r.(=) p.(=)
?/? c.612C>T r.(=) p.(=)
?/? c.727C>G r.(?) p.(Pro243Ala)
?/? c.781+10G>A r.(=) p.(=)
?/? c.781+38C>G r.(=) p.(=)
?/? c.782-51T>C r.(=) p.(=)
?/? c.782-49G>A r.(=) p.(=)
?/? c.782-22T>A r.(=) p.(=)
?/? c.782-19A>C r.(=) p.(=)
?/? c.900C>A r.(=) p.(=)
?/? c.902G>A r.(?) p.(Arg301His)
?/? c.905G>A r.(?) p.(Arg302His)
?/? c.941T>C r.(?) p.(Met314Thr)
?/? c.950C>G r.(?) p.(Ala317Gly)
?/? c.966G>C r.(?) p.(Lys322Asn)
?/? c.995-26A>G r.(=) p.(=)
?/? c.1023C>T r.(=) p.(=)
?/? c.1013_1042del r.(?) p.(Val338_Trp348delinsGly)
?/? c.1044G>A r.(?) p.(Trp348*)
?/? c.1086G>A r.(?) p.(Trp362*)
?/? c.1101+30T>C r.(=) p.(=)
?/? c.1101+32G>A r.(=) p.(=)
?/? c.1101+36G>A r.(=) p.(=)
?/? c.1101+36_1101+37insG r.(=) p.(=)
?/? c.1216+6G>A r.(=) p.(=)
?/? c.1216+39A>G r.(=) p.(=)
?/? c.1217-12A>G r.(=) p.(=)
?/? c.1232C>T r.(?) p.(Ala411Val)
?/? c.1264C>T r.(?) p.(Arg422Cys)
?/? c.1371G>A r.(=) p.(=)
?/? c.1389A>G r.(=) p.(=)
?/? c.1399-40C>T r.(=) p.(=)
?/? c.1483A>G r.(?) p.(Met495Val)
?/? c.1490A>G r.(?) p.(Glu497Gly)
?/? c.1506+6T>C r.(=) p.(=)
?/? c.1506+47T>C r.(=) p.(=)
?/? c.1507-39A>G r.(=) p.(=)
?/? c.1507-3C>T r.spl? p.?
?/? c.1525C>A r.(?) p.(Leu509Met)
?/? c.1548C>A r.(?) p.(Ser516Arg)
?/? c.1549G>A r.(?) p.(Glu517Lys)
?/? c.1552T>A r.(?) p.(Tyr518Asn)
?/? c.1557T>C r.(=) p.(=)
?/? c.1598G>A r.(?) p.(Arg533His)
?/? c.1607T>G r.(?) p.(Leu536Arg)
?/? c.1615+28G>A r.(=) p.(=)
?/? c.1616-50C>G r.(=) p.(=)
?/? c.1616-48C>G r.(=) p.(=)
?/? c.1616-13C>T r.(=) p.(=)
?/? c.1701+7G>A r.(=) p.(=)
?/? c.1702-4A>G r.spl? p.?
?/? c.1723T>C r.(?) p.(Cys575Arg)
?/? c.1728C>G r.(=) p.(=)
?/? c.1813G>A r.(?) p.(Glu605Lys)
?/? c.*3C>A r.(=) p.(=)
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