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Items: 1 to 100 of 111

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(G26S)
Single nucleotide variant
(missense variant)
not provided
GBenign
LIPG
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LIPG
(K37N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(K39Q)
Single nucleotide variant
(missense variant)
not provided
GBenign
LIPG
(V45I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(R54C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(H61D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(P73L)
Single nucleotide variant
(missense variant)
not provided
GBenign
LIPG
(C77R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(G91R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(intron variant)
not provided
GBenign
LIPG
(M94I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(V106M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(T111I)
Single nucleotide variant
(missense variant)
not provided
GBenign
LIPG
(R112G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(A116T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(N117S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(V119I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(M148I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(intron variant)
not provided
GBenign
LIPG
Single nucleotide variant
(splice acceptor variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(G161R)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
LIPG
(G167S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GBenign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LIPG
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LIPG
(D203N)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LIPG
(P210L)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
LIPG
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LIPG
(R224H)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LIPG
(V236L)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LIPG
(N244fs)
Deletion
(frameshift variant +1 more)
not provided
GUncertain significance
LIPG
(P243L)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LIPG
(V257I)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(intron variant)
not provided
GBenign
LIPG
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(splice acceptor variant)
not provided
GUncertain significance
LIPG
(A203D +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(V204I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(L285fs +1 more)
Microsatellite
(frameshift variant)
not provided
GUncertain significance
LIPG
(D289G +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(P217L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(T224S +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
LIPG
(R302C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LIPG
(M287T +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(V370I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(I386T +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(splice donor variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(intron variant)
not provided
GBenign
LIPG
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(intron variant)
not provided
GBenign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(E317K +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
LIPG
(N322S +1 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(E330K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(L410V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(T341I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(R431C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(R438C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(N365S +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
(R368W +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
LIPG
(R374C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(R376W +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(V377M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
(R384W +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LIPG
Microsatellite
(intron variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(intron variant)
not provided
GBenign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LIPG
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
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