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Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
GARIN1A
(G6V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GARIN1A
(I50F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GARIN1A
(I50V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GARIN1A
(E56V)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
GARIN1A
(G56R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GARIN1A
(W67R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GARIN1A
(V77M +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GARIN1A
(S74T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
GARIN1A
(R127Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(I131T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(R169H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(V76G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(L174V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(E123D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(V212M +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
GARIN1A
(A129V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(N237S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(C256Y +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(K165Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(P169S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(R267K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
GARIN1A
(L293V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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