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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
AGPAT3
(V12M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
AGPAT3
(L45V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
AGPAT3
(R52C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
AGPAT3
(G113R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGPAT3
(T73M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGPAT3
(R152Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGPAT3
(R99C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGPAT3
(R161H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGPAT3
(E105K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGPAT3
(A161T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGPAT3
(K174Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGPAT3
(E269K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGPAT3
(P243A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
AGPAT3
Single nucleotide variant
(synonymous variant)
not specified
GLikely benign
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