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Items: 35

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRD9
(Y582C +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(D603N +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(R516C +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(N554T +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(G489C +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(Q531R +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(N522T +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(D500A +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(V474L +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(M371V +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(T416R +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(D437V +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(D415N +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(E279D +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(T371M +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(L413V +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(A345T +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(D249E +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(G330R +8 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(L222F +7 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(D334H +7 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(E244Q +7 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(E200K +7 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(I181T +6 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(V155F +6 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(N245S +6 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
BRD9
(A116T +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(M128V +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(E139K +3 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BRD9
(P83L)
Single nucleotide variant
(missense variant +2 more)
not specified
GLikely benign
BRD9
(R77H)
Single nucleotide variant
(missense variant +3 more)
not specified
GLikely benign
BRD9
(E90K)
Single nucleotide variant
(synonymous variant +3 more)
not specified
GUncertain significance
BRD9
(L80V +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
BRD9
(H58Y)
Single nucleotide variant
(synonymous variant +3 more)
not specified
GUncertain significance
BRD9
(E17G)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
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