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Items: 6

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FMO3
(N61S +1 more)
Single nucleotide variant
(missense variant +1 more)
Trimethylaminuria
GLikely pathogenic
FMO3, LOC126805916
(P153L +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
FMO3, LOC126805916
(V187A +2 more)
Single nucleotide variant
(missense variant)
Trimethylaminuria
GPathogenic
FMO3, LOC126805916
(E308G +2 more)
Single nucleotide variant
(missense variant)
Trimethylaminuria, mild
+1 more
GPathogenic/Likely pathogenic
FMO3
(E305* +2 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
FMO3
(L360P +2 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
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