Transcript #00000647 (NM_138702.1, MAGEC3 gene)

Transcript name transcript variant 1
Gene name MAGEC3 (melanoma antigen family C, 3)
Chromosome X
Transcript - NCBI ID NM_138702.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_619647.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

50 entries on 1 page. Showing entries 1 - 50.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.200G>A r.(?) p.(Arg67Lys)
-?/. - c.221G>A r.(?) p.(Arg74Gln)
-?/. - c.230G>A r.(?) p.(Ser77Asn)
-?/. - c.269C>A r.(?) p.(Thr90Asn)
-?/. - c.279G>A r.(?) p.(Gly93=)
-?/. - c.305T>C r.(?) p.(Leu102Ser)
-?/. - c.361A>G r.(?) p.(Lys121Glu)
?/. - c.419A>T r.(?) p.(Asp140Val)
?/. - c.463T>C r.(?) p.(Ser155Pro)
?/. - c.493T>A r.(?) p.(Leu165Met)
-?/. - c.607G>A r.(?) p.(Glu203Lys)
-?/. - c.667C>T r.(?) p.(Pro223Ser)
-/. - c.683A>G r.(?) p.(Lys228Arg)
-?/. - c.689G>C r.(?) p.(Arg230Pro)
?/. - c.740del r.(?) p.(Asp247AlafsTer7)
?/. - c.887G>T r.(?) p.(Trp296Leu)
?/. - n.910-24A>G r.(?) p.(=)
?/. - n.910-24A>G r.(?) p.(=)
?/. - n.919G>A r.(?) p.(Ala307Thr)
?/. - n.919G>A r.(?) p.(Ala307Thr)
?/. - c.956C>T r.(?) p.(Ala319Val)
-?/. - c.991G>A r.(?) p.(Glu331Lys)
?/. - c.992del r.(?) p.(Glu331GlyfsTer13)
-?/. - c.1049-10G>A r.(=) p.(=)
-?/. - c.1049-7G>A r.(=) p.(=)
-?/. - c.1078C>T r.(?) p.(Arg360Cys)
-?/. - c.1097C>T r.(?) p.(Ala366Val)
?/. - c.1100C>T r.(?) p.(Ser367Phe)
?/. - n.1124-418C>T r.(?) p.(=)
?/. - n.1124-418C>T r.(?) p.(=)
-?/. - c.1124-225C>G r.(=) p.(=)
-?/. - c.1124-202C>T r.(=) p.(=)
-?/. - c.1124-178A>G r.(=) p.(=)
-/. - c.1124-156T>G r.(=) p.(=)
?/. - c.1176_1199dup r.(?) p.(Glu393_Pro400dup)
-?/. - c.1178A>C r.(?) p.(Glu393Ala)
-?/. - c.1190A>C r.(?) p.(Gln397Pro)
?/. - c.1213C>T r.(?) p.(Gln405Ter)
-?/. - c.1280G>A r.(?) p.(Arg427Gln)
-?/. - c.1456G>A r.(?) p.(Val486Ile)
-?/. - c.1459A>C r.(?) p.(Ile487Leu)
-?/. - c.1495G>A r.(?) p.(Gly499Arg)
-?/. - c.1554C>T r.(?) p.(Pro518=)
-?/. - c.1581C>T r.(?) p.(Asp527=)
-?/. - c.1598A>G r.(?) p.(Tyr533Cys)
-/. - c.1699G>T r.(?) p.(Val567Phe)
?/. - c.1699G>T r.(?) p.(Val567Phe)
-?/. - c.1728+46C>G r.(=) p.(=)
-?/. - c.1728+48G>T r.(=) p.(=)
-?/. - c.1728+59A>T r.(=) p.(=)
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