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
SEMA3F
(L2F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SEMA3F
(A4T)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
SEMA3F
(S19F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SEMA3F
(P27L)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
SEMA3F
(R31Q)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
SEMA3F
(V32I)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
SEMA3F
(T42I)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
SEMA3F
(F47Y)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
SEMA3F
(F47L)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
SEMA3F
(R68C)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
SEMA3F
(R68H)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
SEMA3F
(V3M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(V77M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(D16N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(V119I +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
SEMA3F
(Q123R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(R127Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(A151D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(A153T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SEMA3F
(A161V)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
SEMA3F
(R165C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SEMA3F
(G172S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SEMA3F
(L187V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(Y149H +2 more)
Single nucleotide variant
(missense variant)
SEMA3F-related disorder
+1 more
GUncertain significance
SEMA3F
(D273N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(N363S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(R351Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(R420Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(I435V +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
SEMA3F
(Q470K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(R446H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(R456C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(D468N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(M523I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(L433H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(V534M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(R476H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(A479V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(R497S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(R500H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(N505S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(V610L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(R641Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(R648Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(T659R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(G698A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(R600W +2 more)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism
+1 more
GUncertain significance
SEMA3F
(A602T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(V603I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SEMA3F
(P715L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
Format
Items per page
Sort by
Choose Destination