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Items: 48

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DHX16
(V940I +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(E995G +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(R475Q +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
DHX16
(R459C +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
DHX16
(R855W +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(R808H +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(R387C +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(I780F +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(T810M +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(P723A +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
DHX16
(T691I +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(L256M +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(L228P +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(R643H +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(S699N +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(V689M +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(I202V +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(V189L +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(R177C +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(R640W +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(R634C +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(A142T +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(R575C +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(R78S +2 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
DHX16
(A452G +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R337H +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R337C +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(L371F +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(F305V +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(E358Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R268C +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(Q266R +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(T235I +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R224Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R221W +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(K213T +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R204Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R204W +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R240L +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R151C +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(E146A +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(K152E +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R125Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R62C +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(D42G +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(R28W +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
DHX16
(D13E)
Single nucleotide variant
(5 prime UTR variant +2 more)
Inborn genetic diseases
GUncertain significance
DHX16
(E8Q)
Single nucleotide variant
(5 prime UTR variant +2 more)
Inborn genetic diseases
GUncertain significance
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