Transcript #00000532 (NM_014599.4, MAGED2 gene)

Transcript name transcript variant 1
Gene name MAGED2 (melanoma antigen family D, 2)
Chromosome X
Transcript - NCBI ID NM_014599.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_055414.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 12:28:25 +02:00 (CEST)
Date last edited N/A


Variants

57 entries on 1 page. Showing entries 1 - 57.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-30+91A>C r.(=) p.(=)
?/. - c.-30+91A>C r.(=) p.(=)
?/. - c.-29-3C>A r.spl? p.?
-?/. - c.-29-3C>A r.spl? p.?
-?/. - c.128C>T r.(?) p.(Pro43Leu)
-?/. - c.130A>G r.(?) p.(Lys44Glu)
-?/. - c.130A>G r.(?) p.(Lys44Glu)
-?/. 3 c.252A>G r.(?) p.(=)
?/. - c.252A>G r.(?) p.(=)
?/. - c.252A>G r.(?) p.(=)
+/. - c.274dup r.(?) p.(Thr92Asnfs*7)
-?/. - c.375G>A r.(?) p.(Lys125=)
+/. - c.386_387del r.(?) p.(Val129Glyfs*2)
+/. - c.386_387del r.(?) p.(Val129Glyfs*2)
-?/. 3 c.396A>G r.(?) p.(=)
?/. - c.396A>G r.(?) p.(=)
?/. - c.396A>G r.(?) p.(=)
+/. - c.397A>T r.(?) p.(Lys133*)
-?/. 4 c.624C>T r.(?) p.(=)
?/. - c.624C>T r.(?) p.(=)
?/. - c.624C>T r.(?) p.(=)
-?/. - c.680G>A r.(?) p.(Arg227His)
+/. - c.847-9C>G r.(846_847insucugccag) p.(Trp283Serfs*11)
?/. - c.887C>T r.(?) p.(Thr296Met)
-?/. - c.887C>T r.(?) p.(Thr296Met)
-?/. 6 c.981C>T r.(?) p.(=)
?/. - c.981C>T r.(?) p.(=)
?/. - c.981C>T r.(?) p.(=)
?/. - c.991-238C>A r.(=) p.(=)
?/. - c.991-238C>A r.(=) p.(=)
?/. - c.991-153G>A r.(=) p.(=)
?/. - c.991-153G>A r.(=) p.(=)
+/. - c.991-2A>G r.spl p.?
+/. - c.991-2A>G r.spl p.?
+/. - c.991-2A>G r.spl p.?
+/. - c.1038C>G r.(?) p.(Tyr346*)
+/. - c.1038C>G r.(?) p.(Tyr346*)
+/. - c.1038C>G r.(?) p.(Tyr346*)
-?/. - c.1191G>A r.(?) p.(Lys397=)
-?/. - c.1209-3C>T r.spl? p.?
?/. - c.1271+30C>T r.(=) p.(=)
?/. - c.1271+30C>T r.(=) p.(=)
+/. - c.1336C>T r.(?) p.(Arg446Cys)
?/. - c.1387-224G>A r.(=) p.(=)
?/. - c.1387-224G>A r.(=) p.(=)
-?/. - c.1431G>A r.(?) p.(Glu477=)
-?/. 12 c.1443G>A r.(?) p.(=)
?/. - c.1443G>A r.(?) p.(=)
?/. - c.1443G>A r.(?) p.(=)
+/. - c.1464_1475del r.(?) p.(Ala490_Ala493del)
+/. - c.1464_1475del r.(?) p.(Ala490_Ala493del)
+/. - c.1484C>G r.(1484_*8del) p.(Ala495_Lys606delinsAspIleValAsnProAlaSerLeuSerLeuGlnAlaArgValHisProGlnLysProThrGlnHisSerThrLeuGlySerHisTyrGlnSerIleGluValAspThrLeuHis)
+?/. - c.1598C>T r.(?) p.(Ala533Val)
-?/. - c.1670A>G r.(?) p.(Asn557Ser)
?/. - c.1670A>G r.(?) p.(Asn557Ser)
-?/. - c.1729G>A r.(?) p.(Ala577Thr)
-?/. - c.1729G>A r.(?) p.(Ala577Thr)
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