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Links from Gene

Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC130067822, SELENOO
(A57P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067822, SELENOO
(P29S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067822, SELENOO
(A2V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067822, SELENOO
(G9E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067822, SELENOO
(G9R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067822, SELENOO
(L8V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067822, SELENOO
(A70V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067822, SELENOO
(R43P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067822, SELENOO
(M38V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC130067822, SELENOO
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
LOC130067822, SELENOO
(A54S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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