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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LEMD3
(A5T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LEMD3
Deletion
(inframe_deletion)
Dermatofibrosis lenticularis disseminata
+3 more
GLikely benign
LEMD3, LOC130008224
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LEMD3, LOC130008224
(L98F)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
LEMD3, LOC130008224
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign
LEMD3
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
LEMD3
(R288G)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LEMD3
(P296R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LEMD3
(G303C)
Single nucleotide variant
(missense variant)
not specified
+2 more
GLikely benign
LEMD3
(P444A)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
LEMD3
Single nucleotide variant
(intron variant)
not specified
+2 more
GBenign
LEMD3
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
LEMD3
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GLikely benign
LEMD3
Single nucleotide variant
(intron variant)
not provided
+1 more
GBenign/Likely benign
LEMD3
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
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