Transcript #00004130

Transcript name chromosome X open reading frame 23
Gene name CXorf23 (chromosome X open reading frame 23)
Chromosome X
Transcript - NCBI ID NM_198279.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_938020.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

70 entries on 1 page. Showing entries 1 - 70.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.28A>G r.(?) p.(Arg10Gly)
?/? c.41+32T>A r.(=) p.(=)
?/? c.97G>A r.(?) p.(Gly33Arg)
?/? c.110G>A r.(?) p.(Cys37Tyr)
?/? c.142G>A r.(?) p.(Ala48Thr)
?/? c.197G>A r.(?) p.(Arg66His)
?/? c.222T>C r.(=) p.(=)
?/? c.227A>G r.(?) p.(His76Arg)
?/? c.235C>A r.(?) p.(Pro79Thr)
?/? c.351A>G r.(=) p.(=)
?/? c.471G>A r.(=) p.(=)
?/? c.475A>G r.(?) p.(Ile159Val)
?/? c.489T>C r.(=) p.(=)
?/? c.581A>G r.(?) p.(Asp194Gly)
?/? c.612-30G>T r.(=) p.(=)
?/? c.642T>C r.(=) p.(=)
?/? c.669C>T r.(=) p.(=)
?/? c.698C>T r.(?) p.(Ala233Val)
?/? c.703A>G r.(?) p.(Asn235Asp)
?/? c.783T>C r.(=) p.(=)
?/? c.868G>A r.(?) p.(Asp290Asn)
?/? c.882C>T r.(=) p.(=)
?/? c.887C>G r.(?) p.(Ser296Cys)
?/? c.946G>A r.(?) p.(Gly316Ser)
?/? c.1011A>C r.(?) p.(Gln337His)
?/? c.1031C>T r.(?) p.(Pro344Leu)
?/? c.1062T>C r.(=) p.(=)
?/? c.1088G>A r.(?) p.(Arg363Gln)
?/? c.1097A>G r.(?) p.(Asn366Ser)
?/? c.1157C>T r.(?) p.(Ser386Phe)
?/? c.1180C>A r.(?) p.(Gln394Lys)
?/? c.1234A>C r.(?) p.(Thr412Pro)
?/? c.1274+23A>G r.(=) p.(=)
?/? c.1275-39T>C r.(=) p.(=)
?/? c.1275-33C>T r.(=) p.(=)
?/? c.1450+16A>G r.(=) p.(=)
?/? c.1450+21C>T r.(=) p.(=)
?/? c.1450+22G>A r.(=) p.(=)
?/? c.1451-51T>G r.(=) p.(=)
?/? c.1451-22A>C r.(=) p.(=)
?/? c.1566-22del r.(=) p.(=)
?/? c.1592T>C r.(?) p.(Leu531Pro)
?/? c.1609G>A r.(?) p.(Val537Met)
?/? c.1623G>A r.(=) p.(=)
?/? c.1629+12C>T r.(=) p.(=)
?/? c.1629+37T>C r.(=) p.(=)
?/? c.1629+53G>A r.(=) p.(=)
?/? c.1630-34T>C r.(=) p.(=)
?/? c.1649A>G r.(?) p.(Asp550Gly)
?/? c.1651C>T r.(?) p.(Pro551Ser)
?/? c.1695G>T r.(=) p.(=)
?/? c.1745+26G>T r.(=) p.(=)
?/? c.1745+30T>C r.(=) p.(=)
?/? c.1766T>C r.(?) p.(Phe589Ser)
?/? c.1774-37_1774-36insA r.(=) p.(=)
?/? c.1805C>T r.(?) p.(Thr602Ile)
?/? c.1826_1828del r.(?) p.(Glu609del)
?/? c.1853G>C r.(?) p.(Arg618Thr)
?/? c.1864-10_1864-9insT r.(=) p.(=)
?/? c.1928A>G r.(?) p.(Tyr643Cys)
?/? c.1934A>G r.(?) p.(Gln645Arg)
?/? c.1966C>T r.(?) p.(Pro656Ser)
?/? c.1984C>T r.(?) p.(His662Tyr)
?/? c.1989G>A r.(=) p.(=)
?/? c.2019+27A>G r.(=) p.(=)
?/? c.2020-4A>G r.spl? p.?
?/? c.2032G>A r.(?) p.(Val678Ile)
?/? c.*10G>C r.(=) p.(=)
?/? c.*34G>A r.(=) p.(=)
?/? c.*58_*59del r.(=) p.(=)
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