All transcript variants in gene PAGE2

Information The variants shown are described using the NM_207339.2 transcript reference sequence.

24 entries on 1 page. Showing entries 1 - 24.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-8-49_-8-46del r.(=) p.(=) g.55116397_55116400del Copied from the Exome Variant Server PAGE2_000001 15/10148 10/6477 5/3671
?/? c.-8-34A>G r.(=) p.(=) g.55116412A>G Copied from the Exome Variant Server PAGE2_000002 1/10509 0/6721 1/3788
?/? c.-8-19_-8-17del r.(=) p.(=) g.55116427_55116429del Copied from the Exome Variant Server PAGE2_000003 22/10154 14/6478 8/3676
?/? c.-8-12T>G r.(=) p.(=) g.55116434T>G Copied from the Exome Variant Server PAGE2_000005 1/10514 1/6722 0/3792
?/? c.13C>G r.(?) p.(Leu5Val) g.55116466C>G Copied from the Exome Variant Server PAGE2_000007 9713/10516 6684/6722 3029/3794
?/? c.25T>A r.(?) p.(Ser9Thr) g.55116478T>A Copied from the Exome Variant Server PAGE2_000009 51/10516 49/6722 2/3794
?/? c.74G>T r.(?) p.(Gly25Val) g.55116527G>T Copied from the Exome Variant Server PAGE2_000011 2/10522 0/6722 2/3800
?/? c.84+7C>G r.(=) p.(=) g.55116544C>G Copied from the Exome Variant Server PAGE2_000013 1/10520 1/6722 0/3798
?/? c.84+20A>T r.(=) p.(=) g.55116557A>T Copied from the Exome Variant Server PAGE2_000015 1/10520 1/6722 0/3798
?/? c.85-24_85-23insCA r.(=) p.(=) g.55116911_55116912insCA Copied from the Exome Variant Server PAGE2_000017 17/10120 10/6443 7/3677
?/? c.108A>C r.(?) p.(Lys36Asn) g.55116958A>C Copied from the Exome Variant Server PAGE2_000019 1/10511 1/6715 0/3796
?/? c.135T>G r.(?) p.(Asp45Glu) g.55116985T>G Copied from the Exome Variant Server PAGE2_000022 1/10516 0/6720 1/3796
?/? c.164T>C r.(?) p.(Ile55Thr) g.55117014T>C Copied from the Exome Variant Server PAGE2_000024 1/10513 0/6717 1/3796
?/? c.165T>C r.(=) p.(=) g.55117015T>C Copied from the Exome Variant Server PAGE2_000004 5/10513 1/6717 4/3796
?/? c.186T>C r.(=) p.(=) g.55117036T>C Copied from the Exome Variant Server PAGE2_000006 1/10512 1/6716 0/3796
?/? c.193+11A>T r.(=) p.(=) g.55117054A>T Copied from the Exome Variant Server PAGE2_000008 32/10511 0/6714 32/3797
?/? c.193+17A>G r.(=) p.(=) g.55117060A>G Copied from the Exome Variant Server PAGE2_000010 2/10512 0/6714 2/3798
?/? c.193+29T>C r.(=) p.(=) g.55117072T>C Copied from the Exome Variant Server PAGE2_000012 1/10508 1/6712 0/3796
?/? c.194-52G>A r.(=) p.(=) g.55117713G>A Copied from the Exome Variant Server PAGE2_000014 129/4510 0/3103 129/1407
?/? c.194-24T>C r.(=) p.(=) g.55117741T>C Copied from the Exome Variant Server PAGE2_000016 1/10520 0/6721 1/3799
?/? c.241G>C r.(?) p.(Glu81Gln) g.55117812G>C Copied from the Exome Variant Server PAGE2_000018 1/10520 0/6721 1/3799
?/? c.269T>G r.(?) p.(Val90Gly) g.55117840T>G Copied from the Exome Variant Server PAGE2_000020 4/10520 0/6724 4/3796
?/? c.286del r.(?) p.(Thr97Leufs*16) g.55117857del Copied from the Exome Variant Server PAGE2_000021 1/10163 1/6477 0/3686
?/? c.291T>C r.(=) p.(=) g.55117862T>C Copied from the Exome Variant Server PAGE2_000023 4/10525 0/6725 4/3800
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