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Links from Gene

Items: 10

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MROH8, RPN2
Single nucleotide variant
(synonymous variant +1 more)
Congenital disorder of glycosylation
GLikely benign
MROH8, RPN2
(R48G)
Single nucleotide variant
(missense variant +2 more)
Congenital disorder of glycosylation
GUncertain significance
MROH8, RPN2
Insertion
(nonsense +1 more)
Congenital disorder of glycosylation
GLikely benign
MROH8, RPN2
(G36fs)
Insertion
(frameshift variant +1 more)
Congenital disorder of glycosylation
GLikely benign
MROH8, RPN2
(L38fs)
Insertion
(frameshift variant +1 more)
Congenital disorder of glycosylation
GLikely benign
MROH8, RPN2
(A33fs)
Insertion
(intron variant +1 more)
Congenital disorder of glycosylation
GLikely benign
MROH8, RPN2
(Q44K)
Single nucleotide variant
(missense variant +1 more)
Congenital disorder of glycosylation
GLikely benign
RPN2, MROH8
(I40fs)
Insertion
(frameshift variant +1 more)
Congenital disorder of glycosylation
GLikely benign
MROH8, RPN2
Insertion
(nonsense +1 more)
Congenital disorder of glycosylation
GLikely benign
MROH8, RPN2
(H51fs)
Duplication
(frameshift variant +2 more)
not specified
GBenign
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