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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MS4A7
(C55W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
MS4A7
(S80P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
MS4A7
(M84T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
MS4A7
(G54E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MS4A7
(S100A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MS4A7
(I58V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MS4A7
(S105T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MS4A7
(S124N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MS4A7
(S80A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MS4A7
(S80F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MS4A7
(S146Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MS4A7
(D173V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MS4A7
(S218P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MS4A7
(S176L +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
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