Transcript #00000084 (NM_172250.2, MMAA gene)

Transcript name methylmalonic aciduria (cobalamin deficiency) cblA type
Gene name MMAA (methylmalonic aciduria (cobalamin deficiency) cblA type)
Chromosome 4
Transcript - NCBI ID NM_172250.2
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 01 c.-66+116G>A - -
./. 02 c.-65-249A>C - -
./. 02 c.-65-2_-65-1insG - -
./. 00 c.-56A>G - -
./. 02 c.64C>T - p.Arg22X
./. 02 c.64C>T - p.Arg22X
./. 02 c.64C>T - p.Arg22X
./. 02 c.64C>T - p.Arg22X
./. 02 c.64C>T - p.Arg22X
./. 02 c.138T>C - p.Ser46Ser
./. 02 c.161G>A - p.Trp54X
./. 02 c.259_260insATAAACTT - p.Asp87IlefsX10
./. 02 c.260_267dup - p.Tyr90IlefsX7
./. 02 c.260_267dupATAAACTT - p.Tyr90IlefsX7
./. 02 c.266T>C - p.Leu89Pro
./. 02 c.266T>C - p.Leu89Pro
./. 02 c.283C>T - p.Gln95X
./. 02 c.283C>T - p.Gln95X
./. 02 c.283C>T - p.Gln95X
./. 02 c.283C>T - p.Gln95X
./. 02 c.358C>T - p.Gln120X
./. 02 c.358C>T - p.Gln120X
./. 02 c.358C>T - p.Gln120X
./. 02 c.387C>A - p.Tyr129X
./. 02 c.387C>A - p.Tyr129X
./. 02 c.397C>T - p.Gln133X
./. 02 c.397C>T - p.Gln133X
./. 02 c.397C>T - p.Gln133X
./. 02 c.397C>T - p.Gln133X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.433C>T - p.Arg145X
./. 02 c.434G>A - p.Arg145Gln
./. 02 c.439+1_439+4del - -
./. 02 c.439+108A>G - -
./. 02 c.439+262C>T - -
./. 03 c.440-659_440-658insC - -
./. 03 c.440G>A - p.Glu147Gly
./. 03 c.450dupG - p.Pro151AlafsX19
./. 03 c.450dupG - p.Pro151AlafsX19
./. 03 c.450dupG - p.Pro151AlafsX19
./. 03 c.500T>C - p.Leu167Pro
./. 03 c.503delC - p.Thr168MetfsX10
./. 03 c.503delC - p.Thr168MetfsX10
./. 03 c.503delC - p.Thr168MetfsX10
./. 03 c.503delC - p.Thr168MetfsX10
./. 03 c.562+22_562+23insC - -
./. 04 c.563-71C>G - -
./. 04 c.592_595delACTG - p.Thr198SerfsX6
./. 04 c.592_595delACTG - p.Thr198SerfsX6
./. 04 c.592_595delACTG - p.Thr198SerfsX6
./. 04 c.592_595delACTG - p.Thr198SerfsX6
./. 04 c.592_595delACTG - p.Thr198SerfsX6
./. 04 c.592_595delACTG - p.Thr198SerfsX6
./. 04 c.592_595delACTG - p.Thr198SerfsX6
./. 04 c.594dupT - p.Glu199X
./. 04 c.594dupT - p.Glu199X
./. 04 c.594dupT - p.Glu199X
./. 04 c.620A>G - p.Tyr207Cys
./. 04 c.620A>G - p.Tyr207Cys
./. 04 c.620A>G - p.Tyr207Cys
./. 04 c.650T>A - p.Leu217X
./. 04 c.653G>A - p.Gly218Glu
./. 04 c.653G>A - p.Gly218Glu
./. 04 c.733G>A - p.Gly245Ser
./. 04 c.733G>A - p.Gly245Ser
./. 04 c.733G>A - p.Gly245Ser
./. 04 c.733+1G>A - -
./. 04 c.733+1G>A - -
./. 04 c.733+276T>G - -
./. 05 c.734-74G>A - -
./. 05 c.742C>T - p.Gln248X
./. 05 c.747G>A - p.Ser249Ser
./. 05 c.812_813dupAG - p.Leu272SerfsX9
./. 05 c.812_813dupAG - p.Leu272SerfsX9
./. 05 c.812_813dupAG - p.Leu272SerfsX9
./. 05 c.819+168C>G - -
./. 05 c.819+252C>T - -
./. 06 c.820-169T>C - -
./. 06 c.820-110A>G - -
./. 06 c.820-101T>C - -
./. 06 c.959G>A - p.Trp320X
./. 07 c.970-216A>T - -
./. 07 c.970-2A>T - -
./. 07 c.988C>T - p.Arg330X
./. 07 c.1075C>G - p.Arg359Gly
./. 07 c.1076G>A - p.Arg359Gln
./. 07 c.1076G>A - p.Arg359Gln
./. 07 c.1078C>T - p.Arg360Trp
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