"Genome-Nilou Lab"[submitter] AND "ELAC2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 380022	NM_018127.7(ELAC2):c.1893A>G (p.Thr631=)	ELAC2	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 2 +3 more	GBenign
Select item 1182888	NM_018127.7(ELAC2):c.1808+26G>C	ELAC2	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 379971	NM_018127.7(ELAC2):c.1560A>G (p.Thr520=)	ELAC2	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 2 +3 more	GBenign
Select item 379970	NM_018127.7(ELAC2):c.1305-8T>C	ELAC2	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 2 +3 more	GBenign
Select item 379969	NM_018127.7(ELAC2):c.1304+17A>T	ELAC2	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 2 +3 more	GBenign
Select item 379968	NM_018127.7(ELAC2):c.1218+15C>T	ELAC2	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 2 +3 more	GBenign
Select item 5055	NM_018127.7(ELAC2):c.650C>T (p.Ser217Leu)	ELAC2 (S217L)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GBenign
Select item 380021	NM_018127.7(ELAC2):c.491-14T>C	ELAC2	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 2 +3 more	GBenign
Select item 379967	NM_018127.7(ELAC2):c.297-11T>C	ELAC2	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 2 +3 more	GBenign

ClinVar