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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TGFBR1
(I72L)
Single nucleotide variant
(missense variant)
TGFBR1-related disorder
+4 more
GConflicting classifications of pathogenicity
TGFBR1
(E74D)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GUncertain significance
TGFBR1
Single nucleotide variant
(synonymous variant)
Loeys-Dietz syndrome
+2 more
GConflicting classifications of pathogenicity
TGFBR1
(V134M +1 more)
Single nucleotide variant
(missense variant +1 more)
Familial thoracic aortic aneurysm and aortic dissection
GUncertain significance
TGFBR1
(N160S +1 more)
Single nucleotide variant
(missense variant +1 more)
Loeys-Dietz syndrome 1
+3 more
GUncertain significance
TGFBR1
(S236F +2 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
TGFBR1
(R240C +2 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TGFBR1
(H283del +2 more)
Deletion
(inframe_deletion)
Loeys-Dietz syndrome 1
+2 more
GUncertain significance
TGFBR1
(H285R +2 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GUncertain significance
TGFBR1
(G312S +2 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic/Likely pathogenic
TGFBR1
(G312D +2 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+2 more
GUncertain significance
TGFBR1
Single nucleotide variant
(splice donor variant)
not provided
GUncertain significance
TGFBR1
(R482G +2 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
GPathogenic
TGFBR1
(R487W +2 more)
Single nucleotide variant
(missense variant)
not provided
+4 more
GPathogenic/Likely pathogenic
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