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Items: 7

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
THRB
(P453T +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GPathogenic
THRB
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
LOC126806630, THRB
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GBenign
THRB
Single nucleotide variant
(intron variant)
not provided
GConflicting classifications of pathogenicity
THRB
(R23*)
Single nucleotide variant
(nonsense +1 more)
not provided
GPathogenic
THRB
(K18Q)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
THRB
(M1V)
Single nucleotide variant
(missense variant +2 more)
not provided
GUncertain significance
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