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Items: 20

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RHBDL2
(F378S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(Y285S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(I251V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
RHBDL2
(P239L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(G276R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(R261T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(R238H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(R158C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(V145A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(I191S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(P109S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(G104S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(L101M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(A164T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(E56K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(E28A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(E103D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(M89L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(H5R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
RHBDL2
(V84A +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
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