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Items: 31

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LAMC3
Single nucleotide variant
(5 prime UTR variant)
not provided
+1 more
GConflicting classifications of pathogenicity
LAMC3
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
LAMC3
(R31L)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign
LAMC3
(Q49R)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
LAMC3
(H73Q)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
LAMC3
(R141H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LAMC3
(P174Q)
Indel
(missense variant)
not specified
+1 more
GBenign/Likely benign
LAMC3
(R340Q)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
LAMC3
Single nucleotide variant
(intron variant)
LAMC3-related condition
+2 more
GConflicting classifications of pathogenicity
LAMC3
(P522S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
LAMC3
Single nucleotide variant
(intron variant)
LAMC3-related condition
+2 more
GBenign/Likely benign
LAMC3
(G647R)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
LAMC3
(P689L)
Single nucleotide variant
(missense variant)
LAMC3-related condition
+4 more
GConflicting classifications of pathogenicity
LAMC3
(C810*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
LAMC3
(S813K)
Indel
(missense variant)
not specified
+1 more
GBenign/Likely benign
LAMC3
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GConflicting classifications of pathogenicity
LAMC3
Single nucleotide variant
(intron variant)
not specified
+1 more
GConflicting classifications of pathogenicity
LAMC3
(E1084Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
LAMC3
(A1116G)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
LAMC3
(E1127K)
Single nucleotide variant
(missense variant)
LAMC3-related condition
+3 more
GConflicting classifications of pathogenicity
LAMC3
(A1137P)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
LAMC3
(T1203S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
LAMC3
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
LAMC3
Single nucleotide variant
(intron variant)
not specified
+1 more
GBenign/Likely benign
LAMC3
Single nucleotide variant
(intron variant)
not provided
GConflicting classifications of pathogenicity
LAMC3
Single nucleotide variant
(synonymous variant)
LAMC3-related condition
+2 more
GBenign/Likely benign
LAMC3
Single nucleotide variant
(synonymous variant)
LAMC3-related condition
+2 more
GConflicting classifications of pathogenicity
LAMC3
(R1382S)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
LAMC3
(A1387V)
Single nucleotide variant
(missense variant)
LAMC3-related condition
+3 more
GConflicting classifications of pathogenicity
LAMC3
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
LAMC3
(E1569K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
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