"KCCC/NGS Laboratory, Kuwait Cancer Control Center"[submitter] AND "EL - ClinVar - NCBI

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Search results

Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 415251	NM_018127.7(ELAC2):c.2457G>A (p.Gln819=)	ELAC2	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 2 +1 more	GLikely benign
Select item 220685	NM_018127.7(ELAC2):c.2376G>A (p.Ala792=)	ELAC2	Single nucleotide variant (synonymous variant)	Prostate cancer, hereditary, 2 +2 more	GLikely benign
Select item 381413	NM_018127.7(ELAC2):c.2130C>T (p.Ser710=)	ELAC2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign
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 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 241270	NM_018127.7(ELAC2):c.1479G>C (p.Pro493=)	ELAC2	Single nucleotide variant (synonymous variant)	not provided +3 more	GBenign
Select item 380508	NM_018127.7(ELAC2):c.1389C>T (p.Tyr463=)	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 380183	NM_018127.7(ELAC2):c.798-20G>T	ELAC2	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 2 +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 241279	NM_018127.7(ELAC2):c.368-4T>A	ELAC2	Single nucleotide variant (intron variant)	not provided +3 more	GBenign/Likely benign
Select item 379967	NM_018127.7(ELAC2):c.297-11T>C	ELAC2	Single nucleotide variant (intron variant)	Prostate cancer, hereditary, 2 +3 more	GBenign
Select item 382955	NM_018127.7(ELAC2):c.174G>A (p.Val58=)	ELAC2	Single nucleotide variant (synonymous variant)	Combined oxidative phosphorylation defect type 17 +2 more	GBenign
Select item 241272	NM_018127.7(ELAC2):c.155C>T (p.Ser52Phe)	ELAC2 (S52F)	Single nucleotide variant (missense variant)	Combined oxidative phosphorylation defect type 17 +2 more	GLikely benign