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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126806176, SUPT7L
(S260T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126806176, SUPT7L
(G387D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126806176, SUPT7L
(M372V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126806176, SUPT7L
(S353A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
LOC126806176, SUPT7L
(E216G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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