U.S. flag

An official website of the United States government

Display optionsSort by LocationDownload
Format
Items per page
Sort by
Choose Destination

Search results

Items: 64

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
E4F1
(A15T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(A29V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(D53E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(R62H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(R84Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(P86L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
E4F1
(A98G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(G101D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(Q102R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(A124V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(S126P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(S132N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(A134T)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
E4F1
(S135P)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
E4F1
(V146D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(A152V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(P163L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(G170R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(L173F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(R230C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(R258W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(R278C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(A292T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(E313Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(E313V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(T317A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(P354S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(R384L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(A406G)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
E4F1
(A464S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(C468F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(K480N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(R487P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(R489C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(R489H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(R490H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(D495N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(L499F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(H505R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(P546L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(R554C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(R387Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(A408T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(R595L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(V432L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(E611G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
E4F1
(T445M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(S633P +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(V635M +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(V458A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(A637D +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(E645Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
E4F1
(A471E +1 more)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GUncertain significance
E4F1
(A651V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(I483F +1 more)
Single nucleotide variant
(synonymous variant +1 more)
not specified
GUncertain significance
E4F1
(S643P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
E4F1
(V513M +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
E4F1
(E697K +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
E4F1
(A700V +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
E4F1
(M725V +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
E4F1
(A551S +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
E4F1
(E556K +1 more)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
Display optionsSort by LocationDownload
Format
Items per page
Sort by
Choose Destination