All transcript variants in gene PRAF2

Information The variants shown are described using the NM_007213.1 transcript reference sequence.

13 entries on 1 page. Showing entries 1 - 13.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-13A>G r.(=) p.(=) g.48931659T>C Copied from the Exome Variant Server PRAF2_000010 1/10500 0/6688 1/3812
?/? c.108C>T r.(=) p.(=) g.48931539G>A Copied from the Exome Variant Server PRAF2_000008 2/10563 2/6728 0/3835
?/? c.120C>T r.(=) p.(=) g.48931527G>A Copied from the Exome Variant Server PRAF2_000013 1/10563 0/6728 1/3835
?/? c.123C>G r.(=) p.(=) g.48931524G>C Copied from the Exome Variant Server PRAF2_000012 1/10563 1/6728 0/3835
?/? c.166C>T r.(?) p.(Leu56Phe) g.48931481G>A Copied from the Exome Variant Server PRAF2_000011 54/10563 47/6728 7/3835
?/? c.387G>A r.(=) p.(=) g.48930102C>T Copied from the Exome Variant Server PRAF2_000009 14/10374 14/6629 0/3745
?/? c.398-34T>G r.(=) p.(=) g.48929701A>C Copied from the Exome Variant Server PRAF2_000007 3/10563 0/6728 3/3835
?/? c.407T>C r.(?) p.(Val136Ala) g.48929658A>G Copied from the Exome Variant Server PRAF2_000006 1/10563 0/6728 1/3835
?/? c.411C>T r.(=) p.(=) g.48929654G>A Copied from the Exome Variant Server PRAF2_000005 1/10563 1/6728 0/3835
?/? c.443A>G r.(?) p.(Lys148Arg) g.48929622T>C Copied from the Exome Variant Server PRAF2_000004 6/10563 0/6728 6/3835
?/? c.445A>C r.(?) p.(Ile149Leu) g.48929620T>G Copied from the Exome Variant Server PRAF2_000003 2/10563 2/6728 0/3835
?/? c.451A>C r.(?) p.(Asn151His) g.48929614T>G Copied from the Exome Variant Server PRAF2_000002 2/10563 2/6728 0/3835
?/? c.463A>C r.(?) p.(Ser155Arg) g.48929602T>G Copied from the Exome Variant Server PRAF2_000001 1/10563 0/6728 1/3835
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