Full data view for gene RAP2C

Information The variants shown are described using the NM_021183.4 transcript reference sequence.

18 entries on 1 page. Showing entries 1 - 18.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     

Template     

Technique     

Disease     

Reference     

Remarks     

Panel size     

Owner     
?/? c.-32C>G r.(=) p.(=) g.131351328G>C Copied from the Exome Variant Server RAP2C_000018 46/10508 7/6683 39/3825 - - - - - - -
?/? c.-31C>A r.(=) p.(=) g.131351327G>T Copied from the Exome Variant Server RAP2C_000017 2/10515 0/6685 2/3830 - - - - - - -
?/? c.146C>T r.(?) p.(Ser49Phe) g.131351151G>A Copied from the Exome Variant Server RAP2C_000016 1/10563 0/6728 1/3835 - - - - - - -
?/? c.228A>G r.(=) p.(=) g.131351069T>C Copied from the Exome Variant Server RAP2C_000015 1/10563 0/6728 1/3835 - - - - - - -
?/? c.241G>A r.(?) p.(Val81Ile) g.131351056C>T Copied from the Exome Variant Server RAP2C_000014 2/10563 2/6728 0/3835 - - - - - - -
?/? c.273+36G>A r.(=) p.(=) g.131350988C>T Copied from the Exome Variant Server RAP2C_000013 1/10563 0/6728 1/3835 - - - - - - -
?/? c.273+47C>G r.(=) p.(=) g.131350977G>C Copied from the Exome Variant Server RAP2C_000012 1/10563 1/6728 0/3835 - - - - - - -
?/? c.274-52G>A r.(=) p.(=) g.131348526C>T Copied from the Exome Variant Server RAP2C_000011 2/5982 0/3585 2/2397 - - - - - - -
?/? c.274-36T>C r.(=) p.(=) g.131348510A>G Copied from the Exome Variant Server RAP2C_000010 551/10542 509/6713 42/3829 - - - - - - -
?/? c.274-5A>G r.spl? p.? g.131348479T>C Copied from the Exome Variant Server RAP2C_000009 1/10561 1/6726 0/3835 - - - - - - -
?/? c.318T>C r.(=) p.(=) g.131348430A>G Copied from the Exome Variant Server RAP2C_000008 2/10563 2/6728 0/3835 - - - - - - -
?/? c.396A>T r.(?) p.(Arg132Ser) g.131348352T>A Copied from the Exome Variant Server RAP2C_000007 1/10563 0/6728 1/3835 - - - - - - -
?/? c.438G>A r.(=) p.(=) g.131348310C>T Copied from the Exome Variant Server RAP2C_000006 8/10563 0/6728 8/3835 - - - - - - -
?/? c.466C>G r.(?) p.(Leu156Val) g.131348282G>C Copied from the Exome Variant Server RAP2C_000005 4/10563 0/6728 4/3835 - - - - - - -
?/? c.534A>C r.(=) p.(=) g.131348214T>G Copied from the Exome Variant Server RAP2C_000004 4/10562 4/6727 0/3835 - - - - - - -
?/? c.537T>C r.(=) p.(=) g.131348211A>G Copied from the Exome Variant Server RAP2C_000003 1/10562 1/6727 0/3835 - - - - - - -
?/? c.*7T>C r.(=) p.(=) g.131348189A>G Copied from the Exome Variant Server RAP2C_000002 72/10562 71/6727 1/3835 - - - - - - -
?/? c.*27C>T r.(=) p.(=) g.131348169G>A Copied from the Exome Variant Server RAP2C_000001 1/10563 0/6728 1/3835 - - - - - - -
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