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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126863330, RBMX
(R369C)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
LOC126863330, RBMX
(T297A)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
LOC126863330, RBMX
(I161S +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
RBMX
(G132C)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
RBMX
(R101K)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
RBMX
(P99L)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
RBMX
(A26T)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
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