U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 23

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PLCE1
(A76V)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 3
+3 more
GBenign/Likely benign
PLCE1
Single nucleotide variant
(synonymous variant)
Focal segmental glomerulosclerosis
+2 more
GConflicting classifications of pathogenicity
PLCE1
(T200I)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
PLCE1
Single nucleotide variant
(synonymous variant)
Nephrotic syndrome, type 3
+2 more
GBenign
PLCE1
Single nucleotide variant
(synonymous variant)
Nephrotic syndrome, type 3
+2 more
GBenign
PLCE1
(Y401H)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 3
+1 more
GUncertain significance
PLCE1
(T467I +1 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 3
+2 more
GUncertain significance
PLCE1
(S469T +1 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 3
+3 more
GBenign/Likely benign
PLCE1
(R499C +1 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 3
+1 more
GConflicting classifications of pathogenicity
PLCE1
(R548L +1 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 3
+3 more
GBenign
PLCE1
(A643S +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
PLCE1
(M370V +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
PLCE1
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GBenign/Likely benign
PLCE1
Single nucleotide variant
(synonymous variant)
Kidney disorder
+2 more
GConflicting classifications of pathogenicity
PLCE1
(S929T +1 more)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
PLCE1
(F691L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
PLCE1
Single nucleotide variant
(synonymous variant)
Nephrotic syndrome, type 3
+1 more
GConflicting classifications of pathogenicity
PLCE1
(S1173F +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
PLCE1
Single nucleotide variant
(synonymous variant)
Nephrotic syndrome, type 3
+2 more
GBenign
PLCE1, PLCE1-AS1
(N1270S +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Kidney disorder
+2 more
GBenign/Likely benign
PLCE1
(V1928I +2 more)
Single nucleotide variant
(missense variant)
Nephrotic syndrome, type 3
+1 more
GConflicting classifications of pathogenicity
NOC3L, PLCE1
(A2161T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NOC3L, PLCE1
(E2286del +2 more)
Microsatellite
(inframe_deletion)
Nephrotic syndrome, type 3
+2 more
GConflicting classifications of pathogenicity
Format
Items per page
Sort by
Choose Destination