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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NRBF2
(L22V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NRBF2
(A37T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NRBF2
(A38T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
NRBF2
(A43T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NRBF2
(E71K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NRBF2
(A84V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
NRBF2
(A176T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NRBF2
(E178D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NRBF2
(L192V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NRBF2
(I201V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
NRBF2
(K213E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NRBF2
(D206N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NRBF2
(A243G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NRBF2
(N250K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NRBF2
(F274I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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