Full data view for gene CHST7

Information The variants shown are described using the NM_019886.2 transcript reference sequence.

18 entries on 1 page. Showing entries 1 - 18.
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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.-30_-29insC r.(=) p.(=) g.46433337_46433338insC Copied from the Exome Variant Server CHST7_000001 9/6837 0/4316 9/2521 - - - - - - -
?/? c.63C>T r.(=) p.(=) g.46433429C>T Copied from the Exome Variant Server CHST7_000002 156/9473 5/6080 151/3393 - - - - - - -
?/? c.213G>A r.(=) p.(=) g.46433579G>A Copied from the Exome Variant Server CHST7_000003 2/9773 0/6203 2/3570 - - - - - - -
?/? c.289G>A r.(?) p.(Val97Met) g.46433655G>A Copied from the Exome Variant Server CHST7_000004 1/10563 0/6728 1/3835 - - - - - - -
?/? c.298G>A r.(?) p.(Glu100Lys) g.46433664G>A Copied from the Exome Variant Server CHST7_000005 1/10563 1/6728 0/3835 - - - - - - -
?/? c.379G>T r.(?) p.(Val127Phe) g.46433745G>T Copied from the Exome Variant Server CHST7_000006 1/10563 1/6728 0/3835 - - - - - - -
?/? c.388T>G r.(?) p.(Leu130Val) g.46433754T>G Copied from the Exome Variant Server CHST7_000007 1/10563 1/6728 0/3835 - - - - - - -
?/? c.456G>T r.(=) p.(=) g.46433822G>T Copied from the Exome Variant Server CHST7_000008 1/10561 1/6726 0/3835 - - - - - - -
?/? c.516G>C r.(=) p.(=) g.46433882G>C Copied from the Exome Variant Server CHST7_000009 109/10404 0/6629 109/3775 - - - - - - -
?/? c.533C>T r.(?) p.(Ala178Val) g.46433899C>T Copied from the Exome Variant Server CHST7_000010 96/10052 0/6426 96/3626 - - - - - - -
?/? c.611C>T r.(?) p.(Pro204Leu) g.46433977C>T Copied from the Exome Variant Server CHST7_000011 1/10418 0/6624 1/3794 - - - - - - -
?/? c.654C>T r.(=) p.(=) g.46434020C>T Copied from the Exome Variant Server CHST7_000012 10/10533 3/6709 7/3824 - - - - - - -
?/? c.717C>A r.(=) p.(=) g.46434083C>A Copied from the Exome Variant Server CHST7_000013 1/10556 1/6727 0/3829 - - - - - - -
?/? c.760C>A r.(?) p.(Leu254Met) g.46434126C>A Copied from the Exome Variant Server CHST7_000014 1/10562 0/6728 1/3834 - - - - - - -
?/? c.798T>C r.(=) p.(=) g.46434164T>C Copied from the Exome Variant Server CHST7_000015 52/10563 1/6728 51/3835 - - - - - - -
?/? c.1364G>A r.(?) p.(Arg455His) g.46434730G>A Copied from the Exome Variant Server CHST7_000016 1/9742 0/6260 1/3482 - - - - - - -
?/? c.1381C>T r.(?) p.(Arg461Cys) g.46434747C>T Copied from the Exome Variant Server CHST7_000017 1/9960 1/6364 0/3596 - - - - - - -
?/? c.1446C>T r.(=) p.(=) g.46434812C>T Copied from the Exome Variant Server CHST7_000018 1/10156 1/6488 0/3668 - - - - - - -
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