ELOVL7[gene] and "single gene"[properties] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3088486	NM_024930.3(ELOVL7):c.827G>A (p.Cys276Tyr)	ELOVL7 (C276Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088485	NM_024930.3(ELOVL7):c.791G>A (p.Gly264Asp)	ELOVL7 (G264D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312036	NM_024930.3(ELOVL7):c.698A>T (p.Tyr233Phe)	ELOVL7 (Y146F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275232	NM_024930.3(ELOVL7):c.688G>A (p.Asp230Asn)	ELOVL7 (D143N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088484	NM_024930.3(ELOVL7):c.671A>G (p.Gln224Arg)	ELOVL7 (Q137R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275231	NM_024930.3(ELOVL7):c.665T>G (p.Ile222Arg)	ELOVL7 (I222R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511782	NM_024930.3(ELOVL7):c.637G>T (p.Val213Phe)	ELOVL7 (V126F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205056	NM_024930.3(ELOVL7):c.617A>G (p.Tyr206Cys)	ELOVL7 (Y119C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275229	NM_024930.3(ELOVL7):c.572C>A (p.Ser191Tyr)	ELOVL7 (S178Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258551	NM_024930.3(ELOVL7):c.542A>C (p.His181Pro)	ELOVL7 (H94P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088483	NM_024930.3(ELOVL7):c.440A>G (p.His147Arg)	ELOVL7 (H134R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286428	NM_024930.3(ELOVL7):c.410G>A (p.Arg137His)	ELOVL7 (R124H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283549	NM_024930.3(ELOVL7):c.388G>C (p.Asp130His)	ELOVL7 (D117H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088482	NM_024930.3(ELOVL7):c.317G>A (p.Arg106Gln)	ELOVL7 (R106Q +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2303642	NM_024930.3(ELOVL7):c.303T>G (p.Ile101Met)	ELOVL7 (I14M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273226	NM_024930.3(ELOVL7):c.271T>C (p.Trp91Arg)	ELOVL7 (W78R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288481	NM_024930.3(ELOVL7):c.209C>T (p.Thr70Met)	ELOVL7 (T70M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3088481	NM_024930.3(ELOVL7):c.142G>T (p.Val48Phe)	ELOVL7 (V48F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3088480	NM_024930.3(ELOVL7):c.131A>G (p.Tyr44Cys)	ELOVL7 (Y44C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2655478	NM_024930.3(ELOVL7):c.-85-3412G>A	ELOVL7	Single nucleotide variant (intron variant)	not provided	GLikely benign

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Items: 20