U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 86

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CUL7
Single nucleotide variant
(synonymous variant)
3M syndrome 1
+2 more
GBenign
CUL7
(F1694V +3 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
CUL7
(Y1646H +3 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
CUL7
(T1633M +3 more)
Single nucleotide variant
(missense variant)
3M syndrome 1
+2 more
GBenign
CUL7
(L1588I +3 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
CUL7
(R1573* +3 more)
Single nucleotide variant
(nonsense)
Inborn genetic diseases
+1 more
GPathogenic
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GConflicting classifications of pathogenicity
CUL7
(R1542Q +3 more)
Single nucleotide variant
(missense variant)
3-M syndrome
+3 more
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CUL7
(R1440* +2 more)
Single nucleotide variant
(nonsense)
3M syndrome 1
+2 more
GPathogenic
CUL7
(G1420S +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CUL7
(D1335H +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
3M syndrome 1
+2 more
GBenign/Likely benign
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CUL7
(G1257S +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
3M syndrome 1
+2 more
GConflicting classifications of pathogenicity
CUL7
(R1232Q +2 more)
Single nucleotide variant
(missense variant)
3M syndrome 1
+3 more
GBenign/Likely benign
CUL7
(A1204T +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(S1183I +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(R1164W +2 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
3M syndrome 1
+2 more
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CUL7
(E1033K +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(L1014R +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+3 more
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CUL7
(R962L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(R962Q +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CUL7
(K950* +1 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CUL7
(S930fs +1 more)
Deletion
(frameshift variant)
not provided
GPathogenic
CUL7
Duplication
(intron variant)
not provided
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GConflicting classifications of pathogenicity
CUL7
(T918M +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(R904* +1 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CUL7
(G883S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(R882Q +1 more)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
CUL7
(R882W +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(G872S +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
CUL7
(N868S +1 more)
Single nucleotide variant
(missense variant)
not specified
+3 more
GBenign/Likely benign
CUL7
(K862N +1 more)
Single nucleotide variant
(missense variant)
3M syndrome 1
+1 more
GUncertain significance
CUL7
(K855E +1 more)
Single nucleotide variant
(missense variant)
not specified
+4 more
GUncertain significance
CUL7
(S854fs +1 more)
Deletion
(frameshift variant)
not provided
GPathogenic
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CUL7
(G795E +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(R773Q +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CUL7
(R722* +1 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
not specified
+3 more
GConflicting classifications of pathogenicity
CUL7
(W704* +1 more)
Single nucleotide variant
(nonsense)
not provided
GPathogenic
CUL7
(P620L +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
CUL7-related condition
+1 more
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CUL7
(R550* +2 more)
Single nucleotide variant
(nonsense)
not provided
+1 more
GPathogenic
CUL7
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CUL7
(Q514H +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
CUL7
(R358H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(R356H +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CUL7
(A344T +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign/Likely benign
CUL7
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CUL7
(R312H +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
CUL7
(R312C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(M300fs +1 more)
Deletion
(frameshift variant)
not provided
GPathogenic
CUL7
Single nucleotide variant
(synonymous variant)
3M syndrome 1
+2 more
GConflicting classifications of pathogenicity
CUL7
(S262L +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CUL7
(R178L)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
CUL7
(L170W)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
CUL7
(S105F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CUL7
(R47C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(R46W)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CUL7
(R27C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CUL7
(E9Q)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
Format
Items per page
Sort by
Choose Destination