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Items: 11

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
COL10A1, NT5DC1
Insertion
(3 prime UTR variant +1 more)
not provided
+3 more
GBenign
COL10A1, NT5DC1
(M680T)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
COL10A1, NT5DC1
(D643N)
Single nucleotide variant
(missense variant +1 more)
not provided
GConflicting classifications of pathogenicity
COL10A1, NT5DC1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GConflicting classifications of pathogenicity
COL10A1, NT5DC1
(P339L)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
COL10A1, NT5DC1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GUncertain significance
COL10A1, NT5DC1
Single nucleotide variant
(synonymous variant +1 more)
not provided
GConflicting classifications of pathogenicity
COL10A1, NT5DC1
(S103*)
Single nucleotide variant
(nonsense +1 more)
not provided
GUncertain significance
COL10A1, NT5DC1
(S50R)
Single nucleotide variant
(missense variant +1 more)
COL10A1-related condition
+3 more
GBenign/Likely benign
COL10A1, NT5DC1
(R24*)
Single nucleotide variant
(nonsense +1 more)
not provided
GUncertain significance
COL10A1, NT5DC1
(L8W)
Single nucleotide variant
(missense variant +1 more)
not specified
+2 more
GBenign/Likely benign
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