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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
POLD1
(R5W)
Single nucleotide variant
(missense variant +1 more)
POLD1-related condition
+4 more
GConflicting classifications of pathogenicity
POLD1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+3 more
GBenign/Likely benign
POLD1
(A221S)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
POLD1
Single nucleotide variant
(synonymous variant +1 more)
POLD1-related condition
+4 more
GBenign/Likely benign
POLD1
(S605del +1 more)
Microsatellite
(inframe_deletion +1 more)
POLD1-related condition
+4 more
GPathogenic
POLD1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+3 more
GBenign/Likely benign
POLD1
(R1004C +1 more)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+2 more
GUncertain significance
POLD1
Single nucleotide variant
(synonymous variant +1 more)
not provided
+3 more
GBenign/Likely benign
POLD1
Single nucleotide variant
(synonymous variant +1 more)
not specified
+3 more
GConflicting classifications of pathogenicity
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