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Items: 23

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GMEB2
(E528K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(T515M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(Q488R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(V390I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(M371I)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
GMEB2
(E310Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(M305T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(S300G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(Q286R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(R276Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(M261I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(E256D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(E256V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(E256Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(A227T)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
GMEB2
(G209W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(R186C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(N173D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
GMEB2
(I90T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(A63S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(E49D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GMEB2
(A22T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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