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Items: 54

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CERCAM
(N75S)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
CERCAM
(A15V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(V16G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(N57K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(N153S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R157W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(Q109E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(F119L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R131H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(F231L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(P155L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(V169I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(F170V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(S180A +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CERCAM
(R188H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(Y189C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(G201E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(E215Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(A216G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R222C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R300H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(H228L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(H228Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(K238R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(E321K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R251C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R255H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R256W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R334Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(A261T +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CERCAM
(L293V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R304C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(H317D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R409W +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R340H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R348Q +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(V451M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(V381M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(Y472C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(K486E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(L487V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(A411T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R416C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R494H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R495P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R495H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(E435K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(F449V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(F449S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(Q530H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(A465D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(G482S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R561C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CERCAM
(R561H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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