All transcript variants in gene RAP2B

Information The variants shown are described using the NM_002886.2 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.-12G>C r.(=) p.(=) g.152880471G>C Copied from the Exome Variant Server RAP2B_000001 1/12996 1/8598 0/4398
?/? c.36C>T r.(=) p.(=) g.152880518C>T Copied from the Exome Variant Server RAP2B_000002 1/13006 0/8600 1/4406
?/? c.78C>T r.(=) p.(=) g.152880560C>T Copied from the Exome Variant Server RAP2B_000003 630/13006 1/8600 629/4406
?/? c.156G>A r.(=) p.(=) g.152880638G>A Copied from the Exome Variant Server RAP2B_000004 2/13006 0/8600 2/4406
?/? c.337C>T r.(=) p.(=) g.152880819C>T Copied from the Exome Variant Server RAP2B_000005 2/13006 0/8600 2/4406
?/? c.364G>C r.(?) p.(Gly122Arg) g.152880846G>C Copied from the Exome Variant Server RAP2B_000006 1/13006 1/8600 0/4406
?/? c.384C>T r.(=) p.(=) g.152880866C>T Copied from the Exome Variant Server RAP2B_000007 1/13006 0/8600 1/4406
?/? c.386G>A r.(?) p.(Gly129Glu) g.152880868G>A Copied from the Exome Variant Server RAP2B_000008 1/13006 1/8600 0/4406
?/? c.432G>A r.(=) p.(=) g.152880914G>A Copied from the Exome Variant Server RAP2B_000009 1/13006 1/8600 0/4406
?/? c.453C>T r.(=) p.(=) g.152880935C>T Copied from the Exome Variant Server RAP2B_000010 1/13004 1/8600 0/4404
?/? c.502G>T r.(?) p.(Ala168Ser) g.152880984G>T Copied from the Exome Variant Server RAP2B_000011 1/12964 0/8586 1/4378
?/? c.*11G>A r.(=) p.(=) g.152881045G>A Copied from the Exome Variant Server RAP2B_000012 12/12358 0/8204 12/4154
?/? c.*15G>T r.(=) p.(=) g.152881049G>T Copied from the Exome Variant Server RAP2B_000013 6/12326 0/8184 6/4142
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