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Links from Gene

Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ARHGEF28, LOC123497908
(M45V)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ARHGEF28
(C309Y +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ARHGEF28
Copy number gain
not provided
GUncertain significance
ARHGEF28
Copy number gain
not provided
GUncertain significance
ARHGEF28
Copy number loss
not specified
GUncertain significance
ARHGEF28
(K790R +2 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
ARHGEF28
Copy number loss
not provided
GUncertain significance
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