C4310769[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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Search results

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 95474	NM_007214.5(SEC63):c.564C>T (p.Asn188=)	SEC63	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 769316	NM_007214.5(SEC63):c.340-6_340-4dup	SEC63	Duplication (intron variant)	Polycystic liver disease 2 +1 more	GBenign
Select item 403425	NM_007214.5(SEC63):c.340-7T>C	SEC63	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 354913	NM_007214.5(SEC63):c.340-9_340-7del	SEC63	Deletion (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 522188	NM_007214.5(SEC63):c.340-12_340-8del	SEC63	Deletion (intron variant)	Polycystic liver disease 2 +2 more	GBenign/Likely benign
Select item 403426	NM_007214.5(SEC63):c.340-8T>C	SEC63	Single nucleotide variant (intron variant)	not specified +2 more	GBenign/Likely benign
Select item 1332936	NM_007214.5(SEC63):c.340-10T>C	SEC63	Single nucleotide variant (intron variant)	Polycystic liver disease 2 +1 more	GBenign/Likely benign
Select item 1332937	NM_007214.5(SEC63):c.340-11T>C	SEC63	Single nucleotide variant (intron variant)	Polycystic liver disease 2 +1 more	GBenign/Likely benign
Select item 197286	NM_007214.5(SEC63):c.340-12_340-11del	SEC63	Deletion (intron variant)	not provided +3 more	GBenign/Likely benign
Select item 1332938	NM_007214.5(SEC63):c.340-12G>C	SEC63	Single nucleotide variant (intron variant)	Polycystic liver disease 2 +1 more	GBenign/Likely benign