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Items: 15

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASGR1
(R235L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(C230F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(D204Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(E191K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(I166M +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ASGR1
(V153I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(D186E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(H122Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(V117L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(P116S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(Q129R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(L91F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(S25Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASGR1
(P28S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ASGR1
(Q6E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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