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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
EOMES, LOC129936390
(L146F)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GConflicting classifications of pathogenicity
EOMES, LOC129936390
Microsatellite
(inframe_insertion +1 more)
not specified
GLikely benign
EOMES, LOC129936390
Microsatellite
(inframe_insertion +1 more)
not specified
+1 more
GBenign/Likely benign
EOMES, LOC129936390
Insertion
(inframe_insertion +1 more)
not specified
GConflicting classifications of pathogenicity
EOMES, LOC129936390
(A120G)
Single nucleotide variant
(intron variant +1 more)
not specified
GBenign
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