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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RTN4
(G251A +4 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
RTN4
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
RTN4
(Q755E +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
RTN4
(N735H +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
RTN4
(S920C +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
RTN4
(E693Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
RTN4
Single nucleotide variant
(synonymous variant +1 more)
not provided
GLikely benign
RTN4
(L608M +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GLikely benign
RTN4
Single nucleotide variant
(synonymous variant +1 more)
not provided
GBenign
RTN4
(T244M +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
RTN4
(S234N +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
ACYP2, CCDC88A
+8 more
Duplication
not provided
GUncertain significance
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