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Links from Gene

Items: 24

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PHF11, SETDB2-PHF11
(S286L +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(G223A +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(K178N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(A561V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(I26T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
Single nucleotide variant
(3 prime UTR variant +1 more)
PHF11-related disorder
GBenign
PHF11, SETDB2-PHF11
Single nucleotide variant
(synonymous variant +1 more)
PHF11-related disorder
GBenign
PHF11, SETDB2-PHF11
Duplication
(splice acceptor variant)
PHF11-related disorder
GLikely benign
PHF11, SETDB2-PHF11
Single nucleotide variant
(synonymous variant +1 more)
PHF11-related disorder
GLikely benign
LOC130009778, PHF11
+1 more
Microsatellite
(5 prime UTR variant +2 more)
not provided
GBenign
PHF11, SETDB2-PHF11
(E233K +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(K60N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(D85V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(E154K +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(S286T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(M1V +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(Q167P +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(E2D +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(Y193N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(G223R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(S586N +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
PHF11, SETDB2-PHF11
(P677S +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(P677T +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PHF11, SETDB2-PHF11
(S273P +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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