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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BCS1L
(D210N +2 more)
Single nucleotide variant
(missense variant +1 more)
Mitochondrial complex III deficiency nuclear type 1
+5 more
GBenign/Likely benign
BCS1L
Single nucleotide variant
(intron variant)
GRACILE syndrome
+3 more
GBenign
BCS1L
Single nucleotide variant
(synonymous variant +1 more)
Mitochondrial complex III deficiency nuclear type 1
+5 more
GBenign
BCS1L
Single nucleotide variant
(synonymous variant +1 more)
Mitochondrial complex III deficiency nuclear type 1
+5 more
GBenign
BCS1L
(P240fs +2 more)
Deletion
(frameshift variant +1 more)
Mitochondrial complex III deficiency nuclear type 1
+2 more
GUncertain significance
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