Transcript #00009869

Transcript name transcript variant 3
Gene name MAGED1 (melanoma antigen family D, 1)
Chromosome X
Transcript - NCBI ID NM_001005332.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001005332.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

78 entries on 1 page. Showing entries 1 - 78.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-36-11C>T r.(=) p.(=)
?/? c.45+23C>T r.(=) p.(=)
?/? c.45+26C>T r.(=) p.(=)
?/? c.45+321C>T r.(=) p.(=)
?/? c.46-347C>T r.(=) p.(=)
?/? c.46-338_46-337insC r.(=) p.(=)
?/? c.46-308C>T r.(=) p.(=)
?/? c.46-303G>A r.(=) p.(=)
?/? c.46-266C>T r.(=) p.(=)
?/? c.46-44C>G r.(=) p.(=)
?/? c.46-23del r.(=) p.(=)
?/? c.46-17del r.(=) p.(=)
?/? c.172A>G r.(?) p.(Thr58Ala)
?/? c.175G>A r.(?) p.(Ala59Thr)
?/? c.214G>A r.(?) p.(Ala72Thr)
?/? c.275A>G r.(?) p.(Tyr92Cys)
?/? c.307G>A r.(?) p.(Val103Met)
?/? c.346A>C r.(?) p.(Asn116His)
?/? c.444C>T r.(=) p.(=)
?/? c.475G>A r.(?) p.(Ala159Thr)
?/? c.662C>G r.(?) p.(Pro221Arg)
?/? c.686C>T r.(?) p.(Ser229Leu)
?/? c.753+11T>C r.(=) p.(=)
?/? c.753+44T>G r.(=) p.(=)
?/? c.814G>A r.(?) p.(Ala272Thr)
?/? c.867C>T r.(=) p.(=)
?/? c.893C>T r.(?) p.(Thr298Met)
?/? c.913C>T r.(?) p.(Pro305Ser)
?/? c.949C>G r.(?) p.(Pro317Ala)
?/? c.959G>A r.(?) p.(Arg320His)
?/? c.1062G>A r.(=) p.(=)
?/? c.1170G>A r.(=) p.(=)
?/? c.1245T>C r.(=) p.(=)
?/? c.1251A>C r.(=) p.(=)
?/? c.1290C>T r.(=) p.(=)
?/? c.1327C>T r.(?) p.(Arg443Cys)
?/? c.1382G>A r.(?) p.(Gly461Asp)
?/? c.1393C>T r.(?) p.(Pro465Ser)
?/? c.1422+43C>G r.(=) p.(=)
?/? c.1423-15C>T r.(=) p.(=)
?/? c.1486+51G>A r.(=) p.(=)
?/? c.1487-41G>A r.(=) p.(=)
?/? c.1487-7C>T r.(=) p.(=)
?/? c.1542A>G r.(=) p.(=)
?/? c.1567-10G>T r.(=) p.(=)
?/? c.1567-4G>T r.spl? p.?
?/? c.1605A>G r.(=) p.(=)
?/? c.1632C>T r.(=) p.(=)
?/? c.1658+24C>T r.(=) p.(=)
?/? c.1658+33T>C r.(=) p.(=)
?/? c.1658+55del r.(=) p.(=)
?/? c.1659-35G>A r.(=) p.(=)
?/? c.1659-13T>G r.(=) p.(=)
?/? c.1659-7del r.(=) p.(=)
?/? c.1689C>T r.(=) p.(=)
?/? c.1726C>T r.(?) p.(Arg576Cys)
?/? c.1738+9C>A r.(=) p.(=)
?/? c.1738+21C>T r.(=) p.(=)
?/? c.1739-31G>A r.(=) p.(=)
?/? c.1781+7T>G r.(=) p.(=)
?/? c.1781+28C>G r.(=) p.(=)
?/? c.1781+30G>A r.(=) p.(=)
?/? c.1782-15T>G r.(=) p.(=)
?/? c.1795C>G r.(?) p.(Leu599Val)
?/? c.1844+29_1844+31del r.(=) p.(=)
?/? c.1844+43G>T r.(=) p.(=)
?/? c.1959+51T>C r.(=) p.(=)
?/? c.1960-33G>A r.(=) p.(=)
?/? c.1998C>T r.(=) p.(=)
?/? c.2025T>C r.(=) p.(=)
?/? c.2052C>T r.(=) p.(=)
?/? c.2059C>A r.(=) p.(=)
?/? c.2226C>T r.(=) p.(=)
?/? c.2243A>C r.(?) p.(Gln748Pro)
?/? c.2263A>G r.(?) p.(Ile755Val)
?/? c.2295C>T r.(=) p.(=)
?/? c.2307T>C r.(=) p.(=)
?/? c.*8+31G>C r.(=) p.(=)
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