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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
KLHL10, NT5C3B
(L28V)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
KLHL10
(A7V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KLHL10
(A25T)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
KLHL10
(T75A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
KLHL10
(Y152H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KLHL10
(E67K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KLHL10
(E155G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KLHL10
(E194D +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KLHL10
(R287C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KLHL10
(F299L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KLHL10
(Y365C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KLHL10
(A396V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
KLHL10
(V443A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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