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Items: 13

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TGFBR2
(V258D +8 more)
Single nucleotide variant
(missense variant)
Loeys-Dietz syndrome
GUncertain significance
TGFBR2
(G351D +8 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GLikely pathogenic
TGFBR2
(H360D +8 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TGFBR2
(R378S +8 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TGFBR2
(L386F +8 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
TGFBR2
(D405E +8 more)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
TGFBR2
(P406L +8 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GUncertain significance
TGFBR2
Duplication
(inframe_indel +1 more)
not provided
GUncertain significance
TGFBR2
(A426V +8 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
GUncertain significance
TGFBR2
(C461Y +8 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+1 more
GLikely pathogenic
TGFBR2
(R495* +10 more)
Single nucleotide variant
(nonsense)
not provided
+5 more
GPathogenic
TGFBR2
(D524N +10 more)
Single nucleotide variant
(missense variant)
not provided
+3 more
GPathogenic/Likely pathogenic
TGFBR2
(R528C +10 more)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+4 more
GPathogenic
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