All transcript variants in gene CCND2

Information The variants shown are described using the NM_001759.3 transcript reference sequence.

32 entries on 1 page. Showing entries 1 - 32.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-49T>C r.(=) p.(=) g.4383158T>C Copied from the Exome Variant Server CCND2_000001 12543/12850 8504/8508 4039/4342
?/? c.-36G>T r.(=) p.(=) g.4383171G>T Copied from the Exome Variant Server CCND2_000002 66/12952 4/8562 62/4390
?/? c.22G>A r.(?) p.(Val8Met) g.4383228G>A Copied from the Exome Variant Server CCND2_000003 1/13000 1/8596 0/4404
?/? c.33C>T r.(=) p.(=) g.4383239C>T Copied from the Exome Variant Server CCND2_000004 1/13000 1/8596 0/4404
?/? c.36C>T r.(=) p.(=) g.4383242C>T Copied from the Exome Variant Server CCND2_000005 1/13002 1/8598 0/4404
?/? c.114T>G r.(=) p.(=) g.4383320T>G Copied from the Exome Variant Server CCND2_000006 9/13006 0/8600 9/4406
?/? c.195+7_195+8insG r.(=) p.(=) g.4383408_4383409insG Copied from the Exome Variant Server CCND2_000007 3/12510 2/8250 1/4260
?/? c.195+22G>T r.(=) p.(=) g.4383423G>T Copied from the Exome Variant Server CCND2_000008 4/13002 0/8598 4/4404
?/? c.406C>G r.(?) p.(Leu136Val) g.4385381C>G Copied from the Exome Variant Server CCND2_000009 1/13006 1/8600 0/4406
?/? c.411+7A>T r.(=) p.(=) g.4385393A>T Copied from the Exome Variant Server CCND2_000010 1/13006 0/8600 1/4406
?/? c.412-18T>C r.(=) p.(=) g.4387908T>C Copied from the Exome Variant Server CCND2_000011 1/13006 1/8600 0/4406
?/? c.450C>T r.(=) p.(=) g.4387964C>T Copied from the Exome Variant Server CCND2_000012 1/13006 0/8600 1/4406
?/? c.512G>A r.(?) p.(Arg171Gln) g.4388026G>A Copied from the Exome Variant Server CCND2_000014 1/13006 1/8600 0/4406
?/? c.524C>G r.(?) p.(Ser175Cys) g.4388038C>G Copied from the Exome Variant Server CCND2_000016 5/13006 5/8600 0/4406
?/? c.570C>G r.(=) p.(=) g.4388084C>G Copied from the Exome Variant Server CCND2_000018 4244/13006 3378/8600 866/4406
?/? c.571+51A>C r.(=) p.(=) g.4388136A>C Copied from the Exome Variant Server CCND2_000020 1/13004 0/8598 1/4406
?/? c.572-39C>T r.(=) p.(=) g.4397969C>T Copied from the Exome Variant Server CCND2_000022 1/13006 1/8600 0/4406
?/? c.572-38G>A r.(=) p.(=) g.4397970G>A Copied from the Exome Variant Server CCND2_000024 3/13006 3/8600 0/4406
?/? c.687T>G r.(=) p.(=) g.4398123T>G Copied from the Exome Variant Server CCND2_000026 4/13006 0/8600 4/4406
?/? c.702G>A r.(=) p.(=) g.4398138G>A Copied from the Exome Variant Server CCND2_000027 5/13006 3/8600 2/4406
?/? c.718G>A r.(?) p.(Val240Met) g.4398154G>A Copied from the Exome Variant Server CCND2_000028 1/13006 0/8600 1/4406
?/? c.720+15C>T r.(=) p.(=) g.4398171C>T Copied from the Exome Variant Server CCND2_000029 1/13006 0/8600 1/4406
?/? c.721-9T>C r.(=) p.(=) g.4409017T>C Copied from the Exome Variant Server CCND2_000030 1/13006 1/8600 0/4406
?/? c.747G>T r.(?) p.(Gln249His) g.4409052G>T Copied from the Exome Variant Server CCND2_000031 1/13006 1/8600 0/4406
?/? c.756G>A r.(=) p.(=) g.4409061G>A Copied from the Exome Variant Server CCND2_000032 13/13006 12/8600 1/4406
?/? c.785G>A r.(?) p.(Arg262His) g.4409090G>A Copied from the Exome Variant Server CCND2_000013 8/13006 4/8600 4/4406
?/? c.802G>A r.(?) p.(Gly268Arg) g.4409107G>A Copied from the Exome Variant Server CCND2_000015 1/13006 1/8600 0/4406
?/? c.813G>A r.(=) p.(=) g.4409118G>A Copied from the Exome Variant Server CCND2_000017 1/13006 0/8600 1/4406
?/? c.*20_*21del r.(=) p.(=) g.4409195_4409196del Copied from the Exome Variant Server CCND2_000019 25/12518 23/8254 2/4264
?/? c.*29C>T r.(=) p.(=) g.4409204C>T Copied from the Exome Variant Server CCND2_000021 1/13006 0/8600 1/4406
?/? c.*31C>T r.(=) p.(=) g.4409206C>T Copied from the Exome Variant Server CCND2_000023 25/13006 0/8600 25/4406
?/? c.*47_*49del r.(=) p.(=) g.4409222_4409224del Copied from the Exome Variant Server CCND2_000025 4/12518 0/8254 4/4264
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