All transcript variants in gene PIM2

Information The variants shown are described using the NM_006875.3 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.-46C>T r.(=) p.(=) g.48776157G>A Copied from the Exome Variant Server PIM2_000032 2/9992 0/6487 2/3505
?/? c.-6A>T r.(=) p.(=) g.48776117T>A Copied from the Exome Variant Server PIM2_000031 1/10433 1/6654 0/3779
?/? c.14C>T r.(?) p.(Pro5Leu) g.48776098G>A Copied from the Exome Variant Server PIM2_000030 2/10443 0/6658 2/3785
?/? c.24G>A r.(=) p.(=) g.48776088C>T Copied from the Exome Variant Server PIM2_000029 18/10430 18/6659 0/3771
?/? c.33G>A r.(=) p.(=) g.48776079C>T Copied from the Exome Variant Server PIM2_000028 1/10416 1/6653 0/3763
?/? c.38C>G r.(?) p.(Pro13Arg) g.48776074G>C Copied from the Exome Variant Server PIM2_000027 6/10401 6/6644 0/3757
?/? c.39del r.(?) p.(Thr15Profs*48) g.48776073del Copied from the Exome Variant Server PIM2_000026 33/9876 14/6318 19/3558
?/? c.61+11C>T r.(=) p.(=) g.48776040G>A Copied from the Exome Variant Server PIM2_000025 2/10517 2/6700 0/3817
?/? c.135C>G r.(=) p.(=) g.48775849G>C Copied from the Exome Variant Server PIM2_000024 6/10563 0/6728 6/3835
?/? c.171+14G>T r.(=) p.(=) g.48775799C>A Copied from the Exome Variant Server PIM2_000023 1/10562 1/6727 0/3835
?/? c.171+29C>G r.(=) p.(=) g.48775784G>C Copied from the Exome Variant Server PIM2_000022 1/10560 1/6726 0/3834
?/? c.171+47G>T r.(=) p.(=) g.48775766C>A Copied from the Exome Variant Server PIM2_000021 66/10531 57/6713 9/3818
?/? c.223-13C>T r.(=) p.(=) g.48772682G>A Copied from the Exome Variant Server PIM2_000020 44/10559 40/6727 4/3832
?/? c.246C>T r.(=) p.(=) g.48772646G>A Copied from the Exome Variant Server PIM2_000019 3/10561 0/6727 3/3834
?/? c.330G>C r.(?) p.(Glu110Asp) g.48772562C>G Copied from the Exome Variant Server PIM2_000018 1/10563 1/6728 0/3835
?/? c.363C>T r.(=) p.(=) g.48772529G>A Copied from the Exome Variant Server PIM2_000017 1/10563 0/6728 1/3835
?/? c.413G>A r.(?) p.(Gly138Asp) g.48772479C>T Copied from the Exome Variant Server PIM2_000016 3/10563 3/6728 0/3835
?/? c.596-15_596-14insCCC r.(=) p.(=) g.48771862_48771863insGGG Copied from the Exome Variant Server PIM2_000015 1/10204 1/6483 0/3721
?/? c.596-11C>G r.(=) p.(=) g.48771859G>C Copied from the Exome Variant Server PIM2_000014 1/10562 1/6727 0/3835
?/? c.609C>T r.(=) p.(=) g.48771835G>A Copied from the Exome Variant Server PIM2_000013 2/10563 2/6728 0/3835
?/? c.644A>G r.(?) p.(His215Arg) g.48771800T>C Copied from the Exome Variant Server PIM2_000012 2/10563 0/6728 2/3835
?/? c.651C>T r.(=) p.(=) g.48771793G>A Copied from the Exome Variant Server PIM2_000011 5/10563 5/6728 0/3835
?/? c.654G>A r.(=) p.(=) g.48771790C>T Copied from the Exome Variant Server PIM2_000010 1/10563 0/6728 1/3835
?/? c.681C>T r.(=) p.(=) g.48771763G>A Copied from the Exome Variant Server PIM2_000009 1/10563 1/6728 0/3835
?/? c.772+26G>C r.(=) p.(=) g.48771646C>G Copied from the Exome Variant Server PIM2_000008 2/10563 2/6728 0/3835
?/? c.772+43C>T r.(=) p.(=) g.48771629G>A Copied from the Exome Variant Server PIM2_000007 1/10563 1/6728 0/3835
?/? c.773-35C>G r.(=) p.(=) g.48771606G>C Copied from the Exome Variant Server PIM2_000006 1/10562 1/6727 0/3835
?/? c.773-7C>A r.(=) p.(=) g.48771578G>T Copied from the Exome Variant Server PIM2_000005 1/10563 1/6728 0/3835
?/? c.846G>T r.(=) p.(=) g.48771498C>A Copied from the Exome Variant Server PIM2_000004 1/10549 1/6718 0/3831
?/? c.849C>T r.(=) p.(=) g.48771495G>A Copied from the Exome Variant Server PIM2_000003 1/10548 1/6718 0/3830
?/? c.870C>T r.(=) p.(=) g.48771474G>A Copied from the Exome Variant Server PIM2_000002 71/10524 60/6709 11/3815
?/? c.*19_*23del r.(=) p.(=) g.48771385_48771389del Copied from the Exome Variant Server PIM2_000001 27/9019 7/5679 20/3340
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