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Items: 55

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EFS
(A560S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(S389R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(Q428K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(G528S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(A326P +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(V318A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(V487F +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(R314H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(V302M +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(L469F +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(P298Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(N295T +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(S322N +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(G262R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(V428A +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(P228A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(N201S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(G256V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(R174H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(R343C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(R335L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(R166W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(P233S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(R135L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(R304H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(R135C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(S298P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(P204S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(R295W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(H123L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(S194R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(A169S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(T155S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(N231S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(L130V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(P121H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(P119L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(R117Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(P109S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(A93V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(E183K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(P180S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(A167T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(D143E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(P131S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(S123C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(P22A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
EFS
(E96K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(N61D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(G53S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(G45S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(A40V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(R33W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(S20C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
EFS
(R11W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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