Transcript #00000041 (NM_015506.2, MMACHC gene)

Transcript name methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria
Gene name MMACHC (methylmalonic aciduria (cobalamin deficiency) cblC type, with homocystinuria)
Chromosome 1
Transcript - NCBI ID NM_015506.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_056321.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-05-11 13:11:54 +02:00 (CEST)
Date last edited N/A


Variants

117 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/. - c.-103943_*536033dup r.0? p.0?
-/. _1 - r.(=) p.(=)
-/. _1 - r.0 p.0
-/. _1 - r.(=) p.(=)
+/. - - r.0 p.0
+/. - - r.0 p.0
+/. - - r.0 p.0
+/. - c.1A>G r.(?) p.(Met1?)
+/. - c.1A>G r.(?) p.(Met1?)
+/. - c.3G>A r.(?) p.(Met1?)
?/. - c.8C>G r.(?) p.(Pro3Arg)
?/. - c.47T>C r.(?) p.(Leu16Pro)
?/. - c.67G>T r.(?) p.(Val23Phe)
?/. - c.67G>T r.(?) p.(Val23Phe)
?/. - c.67G>T r.(?) p.(Val23Phe)
?/. - c.67G>T r.(?) p.(Val23Phe)
+/. - c.80A>G r.(?) p.(Gln27Arg)
+/. - c.81G>A r.spl p.?
+?/. - c.82-2A>G r.(?) p.(?)
?/. - c.82G>A r.(?) p.(Val28Met)
-?/. - c.126G>A r.(?) p.(Pro42=)
-?/. - c.126G>A r.(?) p.(Pro42=)
-?/. - c.126G>A r.(?) p.(Pro42=)
-?/. - c.126G>A r.(?) p.(Pro42=)
?/. - c.145G>T r.(?) p.(Ala49Ser)
?/. - c.157C>T r.(?) p.(Leu53Phe)
+/. - c.158T>C r.(?) p.(Leu53Pro)
-?/. - c.165G>A r.(?) p.(=)
-/. - c.178G>C r.(?) p.(Asp60His)
-/. - c.178G>C r.(?) p.(Asp60His)
?/. - c.181C>T r.(?) p.(Arg61Trp)
-?/. - c.181C>T r.(?) p.(Arg61Trp)
?/. - c.181C>T r.(?) p.(Arg61Trp)
?/. - c.181C>T r.(?) p.(Arg61Trp)
+/. - c.217C>T r.(?) p.(Arg73*)
+/. - c.271dup r.(?) p.(Arg91LysfsTer14)
+/. - c.271dup r.(?) p.(Arg91LysfsTer14)
+/. - c.271dup r.(?) p.(Arg91LysfsTer14)
?/. - c.271dup r.(?) p.(Arg91Lysfs*14)
?/. - c.271dup r.(?) p.(Arg91Lysfs*14)
+/. - c.271dup r.271dup p.Arg91Lysfs*14
+/. - c.271dup r.(?) p.(Arg91LysfsTer14)
+/. - c.271dup r.(?) p.(Arg91LysfsTer14)
+?/. - c.271dup r.(?) p.(Arg91LysfsTer14)
+?/. - c.276G>T r.(?) p.(Glu92Asp)
-?/. - c.276+6del r.(=) p.(=)
-?/. - c.276+17T>A r.(=) p.(=)
-?/. - c.277-8_277-3dup r.spl? p.?
-?/. - c.277-4C>G r.spl? p.?
?/. - c.316G>A r.(?) p.(Glu106Lys)
?/. - c.316G>A r.(?) p.(Glu106Lys)
?/. - c.316G>A r.(?) p.(Glu106Lys)
-?/. - c.316G>A r.(?) p.(Glu106Lys)
-/. - c.321G>A r.(?) p.(Val107=)
-/. - c.321G>A r.(?) p.(Val107=)
-/. - c.321G>A r.(?) p.(Val107=)
+/. - c.331C>T r.(?) p.(Arg111Ter)
?/. - c.332G>A r.(?) p.(Arg111Gln)
?/. - c.334C>T r.(?) p.(Arg112Cys)
+?/. - c.347T>C r.(?) p.(Leu116Pro)
+?/. - c.347T>C r.(?) p.(Leu116Pro)
+/. - c.388T>C r.(?) p.(Tyr130His)
+?/. - c.389A>G r.(?) p.(Tyr130Cys)
?/. - c.389A>G r.(?) p.(Tyr130Cys)
+/. - c.389A>G r.(?) p.(Tyr130Cys)
+/. 3 c.394C>T r.(?) p.(Arg132Ter)
+/. - c.394C>T r.(?) p.(Arg132*)
+/. - c.394C>T r.(?) p.(Arg132*)
+/. - c.394C>T r.(?) p.(Arg132*)
+/. - c.394C>T r.(?) p.(Arg132Ter)
-?/. - c.405G>A r.(?) p.(Val135=)
?/. - c.433A>G r.(?) p.(Ile145Val)
?/. - c.433A>G r.(?) p.(Ile145Val)
-?/. - c.433A>T r.(?) p.(Ile145Leu)
-?/. - c.433A>T r.(?) p.(Ile145Leu)
?/. - c.433A>T r.(?) p.(Ile145Leu)
+?/. - c.440G>C r.(?) p.(Gly147Ala)
+/. - c.440G>C r.(?) p.(Gly147Ala)
+/. - c.440G>C r.(?) p.(Gly147Ala)
+/. - c.440G>C r.(?) p.(Gly147Ala)
+/. - c.440G>C r.(?) p.(Gly147Ala)
+?/. - c.440G>C r.(?) p.(Gly147Ala)
?/. - c.458G>C r.(?) p.(Arg153Pro)
+?/. - c.463G>C r.(?) p.(Gly155Arg)
?/. - c.472T>C r.(?) p.(Phe158Leu)
?/. - c.472T>C r.(?) p.(Phe158Leu)
+?/. - c.472T>C r.(?) p.(Phe158Leu)
+/. - c.482G>A r.(?) p.(Arg161Gln)
+/. - c.566G>A r.(?) p.(Arg189His)
+/. - c.567dup r.(?) p.(Ile190TyrfsTer13)
?/. - c.569T>C r.(?) p.(Ile190Thr)
-?/. - c.584G>C r.(?) p.(Gly195Ala)
-?/. - c.584G>C r.(?) p.(Gly195Ala)
+/. - c.609G>A r.(?) p.(Trp203*)
+/. - c.609G>A r.(?) p.(Trp203*)
+/. - c.609G>A r.(?) p.(Trp203Ter)
-?/. - c.631C>A r.(?) p.(Pro211Thr)
?/. - c.641G>A r.(?) p.(Arg214His)
+/. - c.658_660del r.(?) p.(Lys220del)
+/. - c.658_660del r.(?) p.(Lys220del)
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