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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CAMKV
(A444T +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
CAMKV
(P431L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CAMKV
(A425S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CAMKV
(E409D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CAMKV
(T407I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CAMKV
(T391I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CAMKV
(A355T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CAMKV
(R384C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CAMKV
Single nucleotide variant
(intron variant)
not provided
GBenign
CAMKV
Single nucleotide variant
(synonymous variant)
not provided
GBenign
CAMKV
(R196Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CAMKV
(Q195H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CAMKV
(R58Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
CAMKV
Single nucleotide variant
(synonymous variant)
not provided
GBenign
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