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Items: 14

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACAT2, AFDN
+549 more
Copy number loss
See cases
GPathogenic
PHF10, PSMB1
+77 more
Copy number loss
See cases
GPathogenic
C6orf120, DLL1
+54 more
Copy number loss
See cases
GPathogenic
TBP
Single nucleotide variant
(intron variant)
not provided
GBenign
LOC108663996, TBP
Microsatellite
(inframe_insertion)
not provided
GBenign
LOC108663996, TBP
(Q95del +1 more)
Deletion
(inframe_deletion)
not provided
+1 more
GBenign
TBP, LOC108663996
Single nucleotide variant
(synonymous variant)
not provided
+3 more
GBenign/Likely benign
LOC108663996, TBP
(Q77fs +1 more)
Deletion
(frameshift variant)
not provided
+1 more
GBenign
LOC108663996, TBP
Single nucleotide variant
(synonymous variant)
not provided
GConflicting classifications of pathogenicity
TBP
Single nucleotide variant
(intron variant)
not provided
GBenign
TBP
Single nucleotide variant
(intron variant)
not provided
GBenign
TBP
Single nucleotide variant
(synonymous variant)
not provided
GBenign
TBP
Single nucleotide variant
(intron variant)
not provided
GBenign
AFDN, C6orf118
+30 more
Copy number loss
See cases
GPathogenic
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