U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 58

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ABLIM3, ACSL6
+1672 more
Copy number loss
See cases
GPathogenic
BRD8, C5orf15
+230 more
Copy number loss
See cases
GPathogenic
KDM3B, LOC129994737
(A31V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KDM3B, LOC129994737
(W47C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
KDM3B
(V89M)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(P104L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(T123I)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KDM3B
(P124A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(N165K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(A173V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(D243H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(R321L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(N351H)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(S492C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(N524K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(S531F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(S551Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(S588P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(N617S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(L621I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(G721E)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KDM3B
(E737K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(M842I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(N848D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(K861E)
Single nucleotide variant
not provided
+1 more
GConflicting classifications of pathogenicity
KDM3B
(R921W)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(R949*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
KDM3B
(V952I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(P974S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(E1075G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(P1100S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(G1142E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(T1159A)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GBenign
KDM3B
(A1168V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(S1201N)
Single nucleotide variant
(missense variant)
not provided
GBenign
KDM3B
(P1210L)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
KDM3B
(A1226T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(L1278W)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(S1291P)
Single nucleotide variant
(missense variant)
Developmental disorder
+1 more
GConflicting classifications of pathogenicity
KDM3B
(E1345G)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(Q1363R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(P1396S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(R1460W)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(D1461V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(K1471E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(R1517*)
Single nucleotide variant
(nonsense)
not provided
GPathogenic/Likely pathogenic
KDM3B
(S1525T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(Y1541C)
Single nucleotide variant
(missense variant)
not provided
GPathogenic
KDM3B
(Y1544C)
Single nucleotide variant
(missense variant)
Diets-Jongmans syndrome
+1 more
GPathogenic
KDM3B
(Y1617C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(H1648R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(V1668L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(D150N)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(S1133P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(S1455Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
KDM3B
(S1342T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
Format
Items per page
Sort by
Choose Destination