Full data view for gene NYX

Information The variants shown are described using the NM_022567.2 transcript reference sequence.

27 entries on 1 page. Showing entries 1 - 27.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     

Template     

Technique     

Disease     

Reference     

Remarks     

Panel size     

Owner     
?/? c.-8C>G r.(=) p.(=) g.41307135C>G Copied from the Exome Variant Server NYX_000001 2/10563 0/6728 2/3835 - - - - - - -
?/? c.10C>T r.(?) p.(Arg4*) g.41307152C>T Copied from the Exome Variant Server NYX_000002 1/10563 1/6728 0/3835 - - - - - - -
?/? c.37+16G>A r.(=) p.(=) g.41307195G>A Copied from the Exome Variant Server NYX_000003 157/10563 149/6728 8/3835 - - - - - - -
?/? c.37+44G>A r.(=) p.(=) g.41307223G>A Copied from the Exome Variant Server NYX_000004 18/10563 0/6728 18/3835 - - - - - - -
?/? c.222G>A r.(=) p.(=) g.41332928G>A Copied from the Exome Variant Server NYX_000005 127/9783 2/6208 125/3575 - - - - - - -
?/? c.239G>A r.(?) p.(Arg80Gln) g.41332945G>A Copied from the Exome Variant Server NYX_000006 1/9716 1/6198 0/3518 - - - - - - -
?/? c.761G>A r.(?) p.(Arg254Gln) g.41333467G>A Copied from the Exome Variant Server NYX_000007 1/9854 1/6188 0/3666 - - - - - - -
?/? c.773C>T r.(?) p.(Thr258Met) g.41333479C>T Copied from the Exome Variant Server NYX_000008 55/10306 0/6531 55/3775 - - - - - - -
?/? c.802C>G r.(?) p.(Arg268Gly) g.41333508C>G Copied from the Exome Variant Server NYX_000009 1/10512 1/6696 0/3816 - - - - - - -
?/? c.811C>T r.(?) p.(Arg271Cys) g.41333517C>T Copied from the Exome Variant Server NYX_000010 2/10536 2/6713 0/3823 - - - - - - -
?/? c.843G>A r.(=) p.(=) g.41333549G>A Copied from the Exome Variant Server NYX_000011 35/10557 31/6725 4/3832 - - - - - - -
?/? c.871G>A r.(?) p.(Ala291Thr) g.41333577G>A Copied from the Exome Variant Server NYX_000012 1/10559 0/6727 1/3832 - - - - - - -
?/? c.877G>C r.(?) p.(Val293Leu) g.41333583G>C Copied from the Exome Variant Server NYX_000013 1/10560 0/6728 1/3832 - - - - - - -
?/? c.910C>G r.(?) p.(Leu304Val) g.41333616C>G Copied from the Exome Variant Server NYX_000014 1/10561 1/6727 0/3834 - - - - - - -
?/? c.1035G>A r.(=) p.(=) g.41333741G>A Copied from the Exome Variant Server NYX_000015 7/10558 6/6724 1/3834 - - - - - - -
?/? c.1170G>C r.(?) p.(Glu390Asp) g.41333876G>C Copied from the Exome Variant Server NYX_000016 1/10547 1/6715 0/3832 - - - - - - -
?/? c.1180C>T r.(?) p.(Leu394Phe) g.41333886C>T Copied from the Exome Variant Server NYX_000017 41/10542 0/6714 41/3828 - - - - - - -
?/? c.1186A>T r.(?) p.(Thr396Ser) g.41333892A>T Copied from the Exome Variant Server NYX_000018 1/10543 1/6715 0/3828 - - - - - - -
?/? c.1198G>A r.(?) p.(Gly400Ser) g.41333904G>A Copied from the Exome Variant Server NYX_000019 2/10539 0/6709 2/3830 - - - - - - -
?/? c.1203G>A r.(=) p.(=) g.41333909G>A Copied from the Exome Variant Server NYX_000020 17/10538 0/6712 17/3826 - - - - - - -
?/? c.1217C>G r.(?) p.(Ala406Gly) g.41333923C>G Copied from the Exome Variant Server NYX_000021 75/10523 1/6703 74/3820 - - - - - - -
?/? c.1244G>A r.(?) p.(Ser415Asn) g.41333950G>A Copied from the Exome Variant Server NYX_000022 41/10487 0/6681 41/3806 - - - - - - -
?/? c.1251C>T r.(=) p.(=) g.41333957C>T Copied from the Exome Variant Server NYX_000023 43/10475 0/6673 43/3802 - - - - - - -
?/? c.1316A>G r.(?) p.(Asn439Ser) g.41334022A>G Copied from the Exome Variant Server NYX_000024 1/10455 0/6661 1/3794 - - - - - - -
?/? c.1394G>T r.(?) p.(Cys465Phe) g.41334100G>T Copied from the Exome Variant Server NYX_000025 2/10214 2/6501 0/3713 - - - - - - -
?/? c.1420G>A r.(?) p.(Val474Met) g.41334126G>A Copied from the Exome Variant Server NYX_000026 2/10035 0/6385 2/3650 - - - - - - -
?/? c.*12G>T r.(=) p.(=) g.41334164G>T Copied from the Exome Variant Server NYX_000027 4/9736 0/6195 4/3541 - - - - - - -
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