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Items: 22

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
UQCC1
(E229Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(N282K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(P251H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(M236R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(M194L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(D260G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(H218Y +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(N168S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(G157A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(G157E +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(A211T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
UQCC1
(A142S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
UQCC1
(K198R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
UQCC1
(L129Q +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
UQCC1
(Q116R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(R166W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(E98K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
UQCC1
(K75M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
UQCC1
(R51Q)
Single nucleotide variant
(missense variant +1 more)
not provided
GBenign
UQCC1
(A37S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(V5L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
UQCC1
(A2E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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