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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MTHFR
(L598R +1 more)
Single nucleotide variant
(missense variant)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency
GLikely pathogenic
MTHFR
(E511* +1 more)
Single nucleotide variant
(nonsense)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency
+1 more
GPathogenic
MTHFR
(L417fs +1 more)
Deletion
(frameshift variant)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency
GLikely pathogenic
MTHFR
(R377S +2 more)
Single nucleotide variant
(missense variant)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency
GUncertain significance
MTHFR
(A116T +1 more)
Single nucleotide variant
(missense variant)
Homocystinuria due to methylene tetrahydrofolate reductase deficiency
+1 more
GConflicting classifications of pathogenicity
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