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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBX15
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
TBX15
(M460R +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GBenign
TBX15
(M395I +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(M389V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX15
(R336K +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
TBX15
(R221H +1 more)
Single nucleotide variant
(missense variant)
Pelviscapular dysplasia
+3 more
GLikely benign
TBX15
(R221C +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
TBX15
Single nucleotide variant
(synonymous variant)
not provided
+2 more
GBenign/Likely benign
TBX15
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
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