U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 50

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CYP7A1
Indel
(3 prime UTR variant)
not provided
GUncertain significance
CYP7A1
Single nucleotide variant
(3 prime UTR variant)
not provided
GUncertain significance
CYP7A1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CYP7A1
(R483W)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(I470T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CYP7A1
(L462V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(M461T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(E453K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(K431R)
Single nucleotide variant
(missense variant)
CYP7A1-related condition
+1 more
GConflicting classifications of pathogenicity
CYP7A1
(L413fs)
Deletion
(frameshift variant)
not provided
GUncertain significance
CYP7A1, LOC126860400
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CYP7A1, LOC126860400
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
CYP7A1, LOC126860400
(P398A)
Single nucleotide variant
(missense variant)
CYP7A1-related condition
+2 more
GConflicting classifications of pathogenicity
CYP7A1, LOC126860400
(G377S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1, LOC126860400
(R364Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CYP7A1, LOC126860400
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CYP7A1, LOC126860400
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
CYP7A1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CYP7A1
(G330S)
Single nucleotide variant
(missense variant)
CYP7A1-related condition
+1 more
GUncertain significance
CYP7A1
(E313K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
CYP7A1
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
CYP7A1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CYP7A1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CYP7A1
(L273P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(R260L)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(E255K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(R235Q)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(R195W)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(T193I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(W166*)
Single nucleotide variant
(nonsense)
not provided
GUncertain significance
CYP7A1
(A164T)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(E143K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CYP7A1
(P116S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(A108T)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
CYP7A1
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
CYP7A1
(A106E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign/Likely benign
CYP7A1
(C69F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(G64D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CYP7A1
(L53F)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
(A45S)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
CYP7A1
Single nucleotide variant
(synonymous variant)
CYP7A1-related condition
+1 more
GConflicting classifications of pathogenicity
CYP7A1
(N36K)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
CYP7A1, LOC110596866
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
CYP7A1, LOC110596866
(A13V)
Single nucleotide variant
(missense variant)
CYP7A1-related condition
+1 more
GConflicting classifications of pathogenicity
CYP7A1, LOC110596866
(G9R)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
Format
Items per page
Sort by
Choose Destination