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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TBX3
(Y620C +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX3
(S615A +1 more)
Single nucleotide variant
(missense variant)
TBX3-related condition
+2 more
GBenign/Likely benign
TBX3
(T557S +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX3
(A562V +1 more)
Single nucleotide variant
(missense variant)
TBX3-related condition
+2 more
GBenign/Likely benign
TBX3
(Q465H +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX3
(G373V +1 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TBX3
(M302V +1 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TBX3
Indel
(inframe_indel)
not provided
GUncertain significance
TBX3, TBX3-AS1
(V33L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
TBX3, TBX3-AS1
Single nucleotide variant
(synonymous variant)
TBX3-related condition
+1 more
GLikely benign
TBX3, TBX3-AS1
Single nucleotide variant
(synonymous variant)
Ulnar-mammary syndrome
+1 more
GBenign/Likely benign
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