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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MIR3976HG, TMEM200C
(S400I)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
MIR3976HG, TMEM200C
(S400R)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
MIR3976HG, TMEM200C
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
MIR3976HG, TMEM200C
Deletion
(inframe_deletion)
not provided
GLikely benign
MIR3976HG, TMEM200C
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
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