U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CCDC88A
(K1853E +3 more)
Single nucleotide variant
(missense variant)
CCDC88A-related disorder
+1 more
GBenign
CCDC88A
Deletion
(intron variant)
CCDC88A-related disorder
+1 more
GBenign/Likely benign
CCDC88A
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
CCDC88A
(L1473V +2 more)
Single nucleotide variant
(missense variant)
CCDC88A-related disorder
+1 more
GBenign
CCDC88A
Single nucleotide variant
(synonymous variant)
CCDC88A-related disorder
+1 more
GBenign/Likely benign
CCDC88A
(R882H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GLikely benign
CCDC88A
Single nucleotide variant
(synonymous variant)
not provided
+1 more
GLikely benign
CCDC88A
(N512D)
Single nucleotide variant
(missense variant)
CCDC88A-related disorder
+1 more
GLikely benign
CCDC88A
Single nucleotide variant
(synonymous variant)
CCDC88A-related disorder
+1 more
GLikely benign
CCDC88A
Single nucleotide variant
(intron variant)
not provided
+2 more
GBenign/Likely benign
CCDC88A
Single nucleotide variant
(synonymous variant)
CCDC88A-related disorder
+1 more
GBenign
CCDC88A
Single nucleotide variant
(synonymous variant)
CCDC88A-related disorder
+1 more
GLikely benign
Format
Items per page
Sort by
Choose Destination