All transcript variants in gene MAGEC2

Information The variants shown are described using the NM_016249.3 transcript reference sequence.

45 entries on 1 page. Showing entries 1 - 45.
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Effect     

AscendingDNA change (cDNA)     

RNA change     

Protein     

DNA change (genomic) (hg19)     

Reference     

DB-ID     

Frequency     

Freq. EA     

Freq. AA     
?/? c.-31_-30insA r.(=) p.(=) g.141291803_141291804insT Copied from the Exome Variant Server MAGEC2_000025 1/10205 1/6484 0/3721
?/? c.-30C>A r.(=) p.(=) g.141291803G>T Copied from the Exome Variant Server MAGEC2_000024 1/10563 1/6728 0/3835
?/? c.-23C>T r.(=) p.(=) g.141291796G>A Copied from the Exome Variant Server MAGEC2_000023 2/10563 0/6728 2/3835
?/? c.10G>T r.(?) p.(Val4Phe) g.141291764C>A Copied from the Exome Variant Server MAGEC2_000022 1/10563 1/6728 0/3835
?/? c.18C>T r.(=) p.(=) g.141291756G>A Copied from the Exome Variant Server MAGEC2_000021 1/10563 0/6728 1/3835
?/? c.29G>A r.(?) p.(Arg10His) g.141291745C>T Copied from the Exome Variant Server MAGEC2_000020 1/10563 1/6728 0/3835
?/? c.54C>G r.(=) p.(=) g.141291720G>C Copied from the Exome Variant Server MAGEC2_000019 1/10563 0/6728 1/3835
?/? c.132C>T r.(=) p.(=) g.141291642G>A Copied from the Exome Variant Server MAGEC2_000018 1/10563 1/6728 0/3835
?/? c.144A>G r.(=) p.(=) g.141291630T>C Copied from the Exome Variant Server MAGEC2_000017 1/10563 1/6728 0/3835
?/? c.209_211del r.(?) p.(Glu70del) g.141291563_141291565del Copied from the Exome Variant Server MAGEC2_000016 33/10205 28/6484 5/3721
?/? c.257G>C r.(?) p.(Ser86Thr) g.141291517C>G Copied from the Exome Variant Server MAGEC2_000015 1/10563 1/6728 0/3835
?/? c.274_285del r.(?) p.(Pro92_Pro95del) g.141291489_141291500del Copied from the Exome Variant Server MAGEC2_000014 13/10205 5/6484 8/3721
?/? c.355C>G r.(?) p.(Gln119Glu) g.141291419G>C Copied from the Exome Variant Server MAGEC2_000013 2/10563 2/6728 0/3835
?/? c.357G>A r.(=) p.(=) g.141291417C>T Copied from the Exome Variant Server MAGEC2_000012 2/10563 0/6728 2/3835
?/? c.397A>C r.(?) p.(Ser133Arg) g.141291377T>G Copied from the Exome Variant Server MAGEC2_000011 1/10563 1/6728 0/3835
?/? c.409T>C r.(?) p.(Phe137Leu) g.141291365A>G Copied from the Exome Variant Server MAGEC2_000010 1/10563 1/6728 0/3835
?/? c.447G>A r.(=) p.(=) g.141291327C>T Copied from the Exome Variant Server MAGEC2_000009 1/10563 1/6728 0/3835
?/? c.453C>T r.(=) p.(=) g.141291321G>A Copied from the Exome Variant Server MAGEC2_000008 2/10563 0/6728 2/3835
?/? c.465A>C r.(?) p.(Lys155Asn) g.141291309T>G Copied from the Exome Variant Server MAGEC2_000007 1/10563 1/6728 0/3835
?/? c.467A>G r.(?) p.(Tyr156Cys) g.141291307T>C Copied from the Exome Variant Server MAGEC2_000006 1/10563 0/6728 1/3835
?/? c.574C>A r.(?) p.(Leu192Ile) g.141291200G>T Copied from the Exome Variant Server MAGEC2_000005 1/10563 1/6728 0/3835
?/? c.585T>C r.(=) p.(=) g.141291189A>G Copied from the Exome Variant Server MAGEC2_000004 1/10563 1/6728 0/3835
?/? c.586G>A r.(?) p.(Ala196Thr) g.141291188C>T Copied from the Exome Variant Server MAGEC2_000003 2/10563 2/6728 0/3835
?/? c.588C>T r.(=) p.(=) g.141291186G>A Copied from the Exome Variant Server MAGEC2_000002 1/10563 1/6728 0/3835
?/? c.607G>C r.(?) p.(Asp203His) g.141291167C>G Copied from the Exome Variant Server MAGEC2_000001 1/10563 1/6728 0/3835
?/? c.639C>T r.(=) p.(=) g.141291135G>A Copied from the Exome Variant Server MAGEC2_000042 1/10563 1/6728 0/3835
?/? c.676G>A r.(?) p.(Glu226Lys) g.141291098C>T Copied from the Exome Variant Server MAGEC2_000041 2/10563 2/6728 0/3835
?/? c.678G>C r.(?) p.(Glu226Asp) g.141291096C>G Copied from the Exome Variant Server MAGEC2_000040 2/10563 2/6728 0/3835
?/? c.685C>G r.(?) p.(Leu229Val) g.141291089G>C Copied from the Exome Variant Server MAGEC2_000039 1/10563 1/6728 0/3835
?/? c.733T>A r.(?) p.(Ser245Thr) g.141291041A>T Copied from the Exome Variant Server MAGEC2_000038 2/10563 2/6728 0/3835
?/? c.742G>A r.(?) p.(Val248Ile) g.141291032C>T Copied from the Exome Variant Server MAGEC2_000037 1/10563 1/6728 0/3835
?/? c.796G>A r.(?) p.(Val266Ile) g.141290978C>T Copied from the Exome Variant Server MAGEC2_000036 1/10563 1/6728 0/3835
?/? c.803G>A r.(?) p.(Gly268Glu) g.141290971C>T Copied from the Exome Variant Server MAGEC2_000035 1/10563 0/6728 1/3835
?/? c.824C>G r.(?) p.(Thr275Ser) g.141290950G>C Copied from the Exome Variant Server MAGEC2_000034 58/10563 53/6728 5/3835
?/? c.860G>A r.(?) p.(Arg287Gln) g.141290914C>T Copied from the Exome Variant Server MAGEC2_000033 2/10563 2/6728 0/3835
?/? c.865G>A r.(?) p.(Val289Met) g.141290909C>T Copied from the Exome Variant Server MAGEC2_000032 1/10563 0/6728 1/3835
?/? c.909G>A r.(=) p.(=) g.141290865C>T Copied from the Exome Variant Server MAGEC2_000031 7007/10563 4710/6728 2297/3835
?/? c.922G>A r.(?) p.(Glu308Lys) g.141290852C>T Copied from the Exome Variant Server MAGEC2_000030 2/10563 0/6728 2/3835
?/? c.994T>C r.(?) p.(Trp332Arg) g.141290780A>G Copied from the Exome Variant Server MAGEC2_000029 23/10563 0/6728 23/3835
?/? c.1027A>G r.(?) p.(Arg343Gly) g.141290747T>C Copied from the Exome Variant Server MAGEC2_000028 1/10563 0/6728 1/3835
?/? c.1049C>T r.(?) p.(Thr350Ile) g.141290725G>A Copied from the Exome Variant Server MAGEC2_000027 1/10563 0/6728 1/3835
?/? c.1050C>T r.(=) p.(=) g.141290724G>A Copied from the Exome Variant Server MAGEC2_000026 5/10563 5/6728 0/3835
?/? c.1059T>C r.(=) p.(=) g.141290715A>G Copied from the Exome Variant Server MAGEC2_000044 25/10563 0/6728 25/3835
?/? c.1065T>C r.(=) p.(=) g.141290709A>G Copied from the Exome Variant Server MAGEC2_000043 1/10563 0/6728 1/3835
?/? c.*15T>A r.(=) p.(=) g.141290637A>T Copied from the Exome Variant Server MAGEC2_000045 16/10563 0/6728 16/3835
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