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Items: 8

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CLDN14, CLDN14-AS1
Single nucleotide variant
(3 prime UTR variant)
CLDN14-related condition
+3 more
GConflicting classifications of pathogenicity
CLDN14, CLDN14-AS1
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GConflicting classifications of pathogenicity
CLDN14, CLDN14-AS1
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign
CLDN14, CLDN14-AS1
(V136I)
Single nucleotide variant
(missense variant)
CLDN14-related condition
+1 more
GConflicting classifications of pathogenicity
CLDN14, CLDN14-AS1
(V134fs)
Deletion
(frameshift variant)
not provided
GLikely pathogenic
CLDN14, CLDN14-AS1
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GConflicting classifications of pathogenicity
CLDN14, CLDN14-AS1
Single nucleotide variant
(synonymous variant)
not specified
+2 more
GBenign/Likely benign
CLDN14, CLDN14-AS1
(T4M)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
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