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Links from Gene

Items: 1 to 100 of 371

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZMYND11
Single nucleotide variant
(intron variant)
not specified
GLikely benign
ZMYND11
(R103H +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
LOC126860802, ZMYND11
(V261L +15 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ZMYND11
(D100E +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
ZMYND11
(D153Y +11 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC126860802, ZMYND11
(E275D +15 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ZMYND11
(N147fs +14 more)
Deletion
(frameshift variant +1 more)
See cases
+1 more
GPathogenic
ZMYND11
(A110S +13 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
ZMYND11
(Y107S +8 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC126860802, ZMYND11
(S287N +15 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ZMYND11
(W433R +15 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely pathogenic
ZMYND11
(D145N +11 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC126860802, ZMYND11
(C378Y +15 more)
Single nucleotide variant
(missense variant +1 more)
ZMYND11-related disorder
GUncertain significance
ZMYND11
Deletion
(nonsense +2 more)
ZMYND11-related disorder
GLikely pathogenic
LOC126860802, ZMYND11
(E376* +15 more)
Single nucleotide variant
(nonsense +1 more)
ZMYND11-related disorder
GLikely pathogenic
ZMYND11
Single nucleotide variant
(intron variant +1 more)
not provided
GUncertain significance
ZMYND11
(F154del +14 more)
Microsatellite
(inframe_deletion +1 more)
not provided
GLikely pathogenic
ZMYND11
(Q159* +14 more)
Single nucleotide variant
(nonsense +1 more)
not provided
GPathogenic
ZMYND11
Single nucleotide variant
(synonymous variant +2 more)
not provided
GUncertain significance
ZMYND11
Single nucleotide variant
(splice donor variant +1 more)
Inborn genetic diseases
GLikely pathogenic
ZMYND11
Duplication
(nonsense +1 more)
Inborn genetic diseases
GPathogenic
ZMYND11
Duplication
(inframe_insertion +1 more)
Inborn genetic diseases
GUncertain significance
ZMYND11
(L16P +3 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
ZMYND11
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
LOC126860802, ZMYND11
(G304S +15 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 30
GUncertain significance
ZMYND11
(R7I)
Single nucleotide variant
(missense variant +3 more)
not provided
GUncertain significance
ZMYND11
Duplication
not provided
GUncertain significance
ZMYND11
Duplication
not provided
GUncertain significance
ZMYND11
Duplication
not provided
GUncertain significance
DIP2C, ZMYND11
Duplication
not provided
GUncertain significance
ZMYND11
Deletion
not provided
GPathogenic
ZMYND11
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
LOC126860802, ZMYND11
(Q299* +15 more)
Single nucleotide variant
(nonsense +1 more)
Intellectual disability, autosomal dominant 30
GLikely pathogenic
ZMYND11
(R201Q +14 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 30
GUncertain significance
ZMYND11
(I103T +8 more)
Single nucleotide variant
(missense variant +2 more)
Intellectual disability, autosomal dominant 30
GUncertain significance
ZMYND11
(R160K +14 more)
Single nucleotide variant
(missense variant +1 more)
Intellectual disability, autosomal dominant 1
GUncertain significance
ZMYND11
(V206I +14 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZMYND11
(P128S +8 more)
Single nucleotide variant
(missense variant +2 more)
Inborn genetic diseases
GUncertain significance
ZMYND11
Single nucleotide variant
(intron variant)
Inborn genetic diseases
GLikely pathogenic
ADARB2, DIP2C
+6 more
Copy number loss
See cases
GPathogenic
LOC126860802, ZMYND11
(R338* +15 more)
Single nucleotide variant
(nonsense +1 more)
Intellectual disability, autosomal dominant 30
GPathogenic
ZMYND11
Copy number gain
not specified
GUncertain significance
ZMYND11
(C424R +15 more)
Single nucleotide variant
(missense variant +1 more)
ZMYND11-related disorder
GUncertain significance
ZMYND11
Single nucleotide variant
(synonymous variant +1 more)
ZMYND11-related disorder
GLikely benign
ZMYND11
(R213* +14 more)
Single nucleotide variant
(nonsense +1 more)
ZMYND11-related disorder
GLikely pathogenic
ZMYND11
(Y106fs +13 more)
Deletion
(frameshift variant +2 more)
Intellectual disability, autosomal dominant 30
GLikely pathogenic
ZMYND11
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ZMYND11
(R3H)
Single nucleotide variant
(missense variant +3 more)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
(P128A +8 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
LOC126860802, ZMYND11
Deletion
(intron variant)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
(D160E +8 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GBenign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LOC126860802, ZMYND11
(N319S +15 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
LOC126860802, ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
Insertion
(intron variant)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LOC126860802, ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LOC126860802, ZMYND11
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
(F236fs +14 more)
Insertion
(frameshift variant +1 more)
not provided
GPathogenic
LOC126860802, ZMYND11
(E372D +15 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
ZMYND11
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LOC126860802, ZMYND11
(N365K +15 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
ZMYND11
(H260Q +14 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
ZMYND11
Single nucleotide variant
(synonymous variant +2 more)
not provided
GLikely benign
ZMYND11
(H239Q +14 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
ZMYND11
(G29S +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GBenign
LOC126860802, ZMYND11
(D312H +15 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ZMYND11
Duplication
(splice donor variant)
not provided
GUncertain significance
ZMYND11
Single nucleotide variant
(synonymous variant +3 more)
not provided
GLikely benign
ZMYND11
(D170N +14 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
LOC126860802, ZMYND11
(L566V +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
ZMYND11
Duplication
(intron variant)
not provided
GLikely benign
ZMYND11
(C156S +13 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
LOC126860802, ZMYND11
Deletion
(intron variant)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
(E166Q +14 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
ZMYND11
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
LOC126860802, ZMYND11
(A492V +15 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ZMYND11
Single nucleotide variant
(intron variant)
not provided
GLikely benign
LOC126860802, ZMYND11
(D361H +15 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ZMYND11
(R103C +3 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
ZMYND11
Deletion
(intron variant)
not provided
GUncertain significance
ZMYND11
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
ZMYND11
(E145D +14 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
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