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Items: 23

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PRLR
(A478T +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
PRLR
(V451L +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
PRLR
(G450R +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GLikely benign
PRLR
(G551R +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GLikely benign
PRLR
(E541D +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
PRLR
(G437R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
PRLR
(P424Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PRLR
(E384A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
PRLR
(A345T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PRLR
(N331S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
PRLR
(E299G +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PRLR
(M399T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PRLR
(S234R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PRLR
(Y314H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PRLR
(A295V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PRLR
(V163M +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
PRLR
(V256A +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
PRLR
(V136M +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
PRLR
(L102H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PRLR
(L95V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PRLR
(P153L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
PRLR
(I79V)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
PRLR
(R37H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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