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Links from Gene

Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
INO80, INO80-AS1
(W1077C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
INO80, INO80-AS1
(R991W)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
INO80, INO80-AS1
Single nucleotide variant
(non-coding transcript variant +1 more)
INO80-related disorder
GLikely benign
INO80
(P575L)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
INO80, INO80-AS1
Single nucleotide variant
(intron variant)
not specified
GBenign
INO80, INO80-AS1
(P1091A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
INO80, INO80-AS1
(L1003F)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
INO80, INO80-AS1
(S997L)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
INO80, INO80-AS1
(R1029G)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
INO80, INO80-AS1
(Q986H)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
INO80, INO80-AS1
(F1069L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
INO80, INO80-AS1
(A1013G)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
GUncertain significance
INO80, INO80-AS1
(R1000C)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
GUncertain significance
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