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Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MCPH1
Single nucleotide variant
(synonymous variant +1 more)
Microcephaly 1, primary, autosomal recessive
+2 more
GBenign
MCPH1
(R137S +2 more)
Single nucleotide variant
(missense variant +2 more)
not provided
+1 more
GBenign
MCPH1
(R304I +3 more)
Single nucleotide variant
(missense variant +1 more)
Microcephaly 1, primary, autosomal recessive
+2 more
GBenign
MCPH1
(D314H +3 more)
Single nucleotide variant
(missense variant +1 more)
Microcephaly 1, primary, autosomal recessive
+2 more
GBenign
MCPH1
(D392G +3 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GBenign
MCPH1, MCPH1-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
Microcephaly 1, primary, autosomal recessive
+2 more
GBenign
MCPH1, MCPH1-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
Microcephaly 1, primary, autosomal recessive
+2 more
GBenign
MCPH1, MCPH1-AS1
(A761V +1 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Microcephaly 1, primary, autosomal recessive
+2 more
GBenign
MCPH1, MCPH1-AS1
Single nucleotide variant
(synonymous variant)
Microcephaly 1, primary, autosomal recessive
+2 more
GBenign
MCPH1, MCPH1-AS1
(P828S +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
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