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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SLC19A3
(T418P +1 more)
Single nucleotide variant
(missense variant)
Biotin-responsive basal ganglia disease
GLikely pathogenic
SLC19A3
(T422A)
Single nucleotide variant
(missense variant)
Biotin-responsive basal ganglia disease
+3 more
GPathogenic
SLC19A3
(V61fs +1 more)
Duplication
(frameshift variant)
Biotin-responsive basal ganglia disease
GUncertain significance
SLC19A3
(L46P)
Single nucleotide variant
(missense variant +1 more)
Biotin-responsive basal ganglia disease
GUncertain significance
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