Full data view for gene CTAG2

Information The variants shown are described using the NM_020994.3 transcript reference sequence.

39 entries on 1 page. Showing entries 1 - 39.
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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.114_119del r.(?) p.(Ala39_Thr40del) g.153881671_153881676del Copied from the Exome Variant Server CTAG2_000024 78/6468 47/4438 31/2030 - - - - - - -
?/? c.162G>A r.(=) p.(=) g.153881628C>T Copied from the Exome Variant Server CTAG2_000023 172/9900 3/6324 169/3576 - - - - - - -
?/? c.212C>T r.(?) p.(Ala71Val) g.153881578G>A Copied from the Exome Variant Server CTAG2_000022 1/10536 0/6714 1/3822 - - - - - - -
?/? c.213G>A r.(=) p.(=) g.153881577C>T Copied from the Exome Variant Server CTAG2_000021 2/10533 1/6713 1/3820 - - - - - - -
?/? c.236G>T r.(?) p.(Gly79Val) g.153881554C>A Copied from the Exome Variant Server CTAG2_000020 1/10547 0/6721 1/3826 - - - - - - -
?/? c.238G>A r.(?) p.(Ala80Thr) g.153881552C>T Copied from the Exome Variant Server CTAG2_000019 113/10549 0/6723 113/3826 - - - - - - -
?/? c.244A>G r.(?) p.(Arg82Gly) g.153881546T>C Copied from the Exome Variant Server CTAG2_000018 71/10548 0/6724 71/3824 - - - - - - -
?/? c.252C>G r.(?) p.(Asp84Glu) g.153881538G>C Copied from the Exome Variant Server CTAG2_000017 1/10552 0/6724 1/3828 - - - - - - -
?/? c.254G>A r.(?) p.(Ser85Asn) g.153881536C>T Copied from the Exome Variant Server CTAG2_000016 1/10552 1/6724 0/3828 - - - - - - -
?/? c.259C>T r.(=) p.(=) g.153881531G>A Copied from the Exome Variant Server CTAG2_000015 125/10555 108/6725 17/3830 - - - - - - -
?/? c.265C>G r.(?) p.(Gln89Glu) g.153881525G>C Copied from the Exome Variant Server CTAG2_000014 5671/10555 2554/6725 3117/3830 - - - - - - -
?/? c.269+25G>A r.(=) p.(=) g.153881496C>T Copied from the Exome Variant Server CTAG2_000013 5/10554 5/6724 0/3830 - - - - - - -
?/? c.269+34G>T r.(=) p.(=) g.153881487C>A Copied from the Exome Variant Server CTAG2_000012 1/10550 1/6722 0/3828 - - - - - - -
?/? c.270-7C>G r.(=) p.(=) g.153880912G>C Copied from the Exome Variant Server CTAG2_000011 1/10551 1/6719 0/3832 - - - - - - -
?/? c.280A>G r.(?) p.(Met94Val) g.153880895T>C Copied from the Exome Variant Server CTAG2_000010 22/10560 0/6725 22/3835 - - - - - - -
?/? c.293C>T r.(?) p.(Ser98Leu) g.153880882G>A Copied from the Exome Variant Server CTAG2_000009 1/10560 1/6725 0/3835 - - - - - - -
?/? c.295C>G r.(?) p.(Pro99Ala) g.153880880G>C Copied from the Exome Variant Server CTAG2_000008 281/10561 0/6726 281/3835 - - - - - - -
?/? c.296C>T r.(?) p.(Pro99Leu) g.153880879G>A Copied from the Exome Variant Server CTAG2_000007 1/10561 1/6726 0/3835 - - - - - - -
?/? c.330C>T r.(=) p.(=) g.153880845G>A Copied from the Exome Variant Server CTAG2_000006 101/10561 0/6726 101/3835 - - - - - - -
?/? c.331C>A r.(=) p.(=) g.153880844G>T Copied from the Exome Variant Server CTAG2_000005 1/10561 0/6726 1/3835 - - - - - - -
?/? c.345T>G r.(=) p.(=) g.153880830A>C Copied from the Exome Variant Server CTAG2_000004 5935/10561 2555/6726 3380/3835 - - - - - - -
?/? c.392A>G r.(?) p.(Asn131Ser) g.153880783T>C Copied from the Exome Variant Server CTAG2_000003 1/10561 1/6726 0/3835 - - - - - - -
?/? c.413G>A r.(?) p.(Arg138Gln) g.153880762C>T Copied from the Exome Variant Server CTAG2_000002 1/10561 0/6726 1/3835 - - - - - - -
?/? c.462G>A r.(=) p.(=) g.153880713C>T Copied from the Exome Variant Server CTAG2_000001 2/10561 2/6726 0/3835 - - - - - - -
?/? c.496A>G r.(?) p.(Arg166Gly) g.153880679T>C Copied from the Exome Variant Server CTAG2_000034 1/10560 1/6725 0/3835 - - - - - - -
?/? c.511C>A r.(?) p.(Pro171Thr) g.153880664G>T Copied from the Exome Variant Server CTAG2_000033 1/10561 1/6726 0/3835 - - - - - - -
?/? c.522G>T r.(?) p.(Lys174Asn) g.153880653C>A Copied from the Exome Variant Server CTAG2_000032 1/10561 1/6726 0/3835 - - - - - - -
?/? c.541G>C r.(?) p.(Gly181Arg) g.153880634C>G Copied from the Exome Variant Server CTAG2_000031 278/10562 3/6727 275/3835 - - - - - - -
?/? c.565G>A r.(?) p.(Glu189Lys) g.153880610C>T Copied from the Exome Variant Server CTAG2_000030 6/10560 5/6725 1/3835 - - - - - - -
?/? c.595G>A r.(?) p.(Val199Ile) g.153880580C>T Copied from the Exome Variant Server CTAG2_000029 7/10562 7/6727 0/3835 - - - - - - -
?/? c.609G>A r.(=) p.(=) g.153880566C>T Copied from the Exome Variant Server CTAG2_000028 2/10561 0/6726 2/3835 - - - - - - -
?/? c.617C>T r.(?) p.(Ser206Phe) g.153880558G>A Copied from the Exome Variant Server CTAG2_000027 2/10561 0/6726 2/3835 - - - - - - -
?/? c.*9C>T r.(=) p.(=) g.153880533G>A Copied from the Exome Variant Server CTAG2_000026 3/10561 0/6726 3/3835 - - - - - - -
?/? c.*24G>A r.(=) p.(=) g.153880518C>T Copied from the Exome Variant Server CTAG2_000025 1/10555 1/6721 0/3834 - - - - - - -
?/? c.*28A>T r.(=) p.(=) g.153880514T>A Copied from the Exome Variant Server CTAG2_000039 9/10554 9/6721 0/3833 - - - - - - -
?/? c.*31G>C r.(=) p.(=) g.153880511C>G Copied from the Exome Variant Server CTAG2_000038 5/10552 0/6719 5/3833 - - - - - - -
?/? c.*47T>A r.(=) p.(=) g.153880495A>T Copied from the Exome Variant Server CTAG2_000037 1/10550 0/6717 1/3833 - - - - - - -
?/? c.*65T>C r.(=) p.(=) g.153880477A>G Copied from the Exome Variant Server CTAG2_000036 6/10550 0/6715 6/3835 - - - - - - -
?/? c.*145G>T r.(=) p.(=) g.153880397C>A Copied from the Exome Variant Server CTAG2_000035 1/10557 0/6723 1/3834 - - - - - - -
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