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Items: 20

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DPT
(V201I)
Single nucleotide variant
(missense variant)
not provided
GBenign
DPT
Single nucleotide variant
(synonymous variant)
not provided
GBenign
DPT
(R182C)
Single nucleotide variant
(missense variant)
Progressive sensorineural hearing impairment
GPathogenic
DPT
(Y153C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DPT
(R134C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DPT
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DPT
(R126Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DPT
(E121K)
Single nucleotide variant
(missense variant)
not provided
GBenign
DPT
Single nucleotide variant
(synonymous variant)
not provided
GBenign
DPT
(S83I)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
DPT
(P81T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DPT
(S69T)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
DPT
(V59M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DPT
Single nucleotide variant
(synonymous variant)
not provided
GBenign
DPT
(R43Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DPT
(S34R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DPT
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
DPT
(Q29R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
DPT
(L3P)
Single nucleotide variant
(missense variant)
not provided
GBenign
DPT
(D2A)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
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