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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KNL1
(R43T)
Single nucleotide variant
(missense variant)
Primary Microcephaly, Recessive
+3 more
GBenign
KNL1
(T113A +1 more)
Single nucleotide variant
(missense variant)
Primary Microcephaly, Recessive
+3 more
GBenign
KNL1
Duplication
(intron variant)
Microcephaly 4, primary, autosomal recessive
+1 more
GBenign
KNL1
(A486S +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign
KNL1
(M598T +1 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GBenign
KNL1
Single nucleotide variant
(synonymous variant)
Primary Microcephaly, Recessive
+3 more
GBenign
KNL1
Single nucleotide variant
(synonymous variant)
Primary Microcephaly, Recessive
+3 more
GBenign
KNL1
(R910G +1 more)
Single nucleotide variant
(missense variant)
Microcephaly 4, primary, autosomal recessive
+2 more
GBenign
KNL1
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign
KNL1
Deletion
(intron variant)
Microcephaly 4, primary, autosomal recessive
+1 more
GBenign
KNL1
Single nucleotide variant
(intron variant)
Microcephaly 4, primary, autosomal recessive
+1 more
GBenign
KNL1
Single nucleotide variant
(intron variant)
Microcephaly 4, primary, autosomal recessive
+1 more
GBenign
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