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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BUB1B, LOC130056830
(V4M)
Single nucleotide variant
(missense variant)
BUB1B-related condition
+3 more
GLikely benign
BUB1B
(T40M)
Single nucleotide variant
(missense variant)
not provided
+4 more
GBenign/Likely benign
BUB1B
Single nucleotide variant
(synonymous variant)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
BUB1B, BUB1B-PAK6
(G929S)
Single nucleotide variant
(5 prime UTR variant +1 more)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
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