Transcript #00009274 (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 NP_758454.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2014-01-21 10:29:30 +01:00 (CET)
Date last edited N/A


Variants

15 entries on 1 page. Showing entries 1 - 15.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-56A>G -56 r.(=) p.(=) - utr-5 -
./. - c.-14C>T -14 r.(=) p.(=) - utr-5 -
./. - c.138T>C 138 r.(?) p.(=) - coding-synonymous -
./. - c.747G>A 747 r.(?) p.(=) - coding-synonymous -
./. - c.747G>A 747 r.(?) p.(=) - coding-synonymous -
./. - c.747G>A 747 r.(?) p.(=) - coding-synonymous -
./. - c.747G>A 747 r.(?) p.(=) - coding-synonymous -
./. - c.1089G>C 1089 r.(?) p.(Gln363His) - missense -
./. - c.1089G>C 1089 r.(?) p.(Gln363His) - missense -
./. - c.1089G>C 1089 r.(?) p.(Gln363His) - missense -
./. - c.1089G>C 1089 r.(?) p.(Gln363His) - missense -
./. - c.1089G>C 1089 r.(?) p.(Gln363His) - missense -
./. - c.1089G>C 1089 r.(?) p.(Gln363His) - missense -
./. - c.1089G>C 1089 r.(?) p.(Gln363His) - missense -
./. - c.1089G>C 1089 r.(?) p.(Gln363His) - missense -
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