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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TP53RK
(L200V)
Single nucleotide variant
(missense variant)
Galloway-Mowat syndrome 4
GUncertain significance
TP53RK
Single nucleotide variant
(synonymous variant)
Galloway-Mowat syndrome 4
+1 more
GLikely benign
TP53RK
(T145A)
Single nucleotide variant
(missense variant)
Galloway-Mowat syndrome 4
+1 more
GBenign/Likely benign
TP53RK
(M113V)
Single nucleotide variant
(missense variant)
Galloway-Mowat syndrome 4
GUncertain significance
LOC130065998, TP53RK
+1 more
(A6fs)
Microsatellite
(frameshift variant)
Galloway-Mowat syndrome 4
GUncertain significance
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