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Items: 23

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HMOX2
(E67K +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
HMOX2
(R101W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(R101Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(E36G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(A80G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
Single nucleotide variant
(synonymous variant)
not provided
GBenign
HMOX2
(A108V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(K100M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(Q132R +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
HMOX2
(R210C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(D160N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(S133L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(K169N +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(Y283C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(I204L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(I204M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(N206H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(A294P +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(P320S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(E271K +2 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
HMOX2
(D244G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(C253S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
HMOX2
(Y286C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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