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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NFE2L2
(R433H +5 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
NFE2L2
(T353I +5 more)
Single nucleotide variant
(missense variant)
not specified
Gnot provided
NFE2L2
(L293F +5 more)
Single nucleotide variant
(missense variant)
not provided
GBenign/Likely benign
NFE2L2
(P284S +5 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NFE2L2
(V252M +5 more)
Single nucleotide variant
(missense variant)
not provided
GBenign/Likely benign
NFE2L2
(L161V +5 more)
Single nucleotide variant
(missense variant)
not provided
GBenign
NFE2L2
Single nucleotide variant
(intron variant)
not provided
GBenign
NFE2L2
Single nucleotide variant
(intron variant)
not provided
GLikely benign
NFE2L2
Single nucleotide variant
(intron variant)
not provided
GBenign
NFE2L2
(G82V +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
NFE2L2
(R27Q +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GBenign
NFE2L2
(R27W +1 more)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
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