HSPA4L[gene] and "single gene"[properties] - ClinVar

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Items: 43

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2457436	NM_014278.4(HSPA4L):c.173C>T (p.Thr58Met)	HSPA4L (T58M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 711912	NM_014278.4(HSPA4L):c.177C>T (p.Asn59=)	HSPA4L	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2568068	NM_014278.4(HSPA4L):c.179T>C (p.Val60Ala)	HSPA4L (V34A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327841	NM_014278.4(HSPA4L):c.252G>T (p.Arg84Ser)	HSPA4L (R115S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327842	NM_014278.4(HSPA4L):c.253A>T (p.Ile85Phe)	HSPA4L (I116F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107332	NM_014278.4(HSPA4L):c.272T>C (p.Leu91Pro)	HSPA4L (L91P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334813	NM_014278.4(HSPA4L):c.293G>C (p.Ser98Thr)	HSPA4L (S129T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370662	NM_014278.4(HSPA4L):c.311G>A (p.Arg104Gln)	HSPA4L (R135Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2552267	NM_014278.4(HSPA4L):c.319G>C (p.Glu107Gln)	HSPA4L (E107Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512810	NM_014278.4(HSPA4L):c.340A>G (p.Ile114Val)	HSPA4L (I114V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319525	NM_014278.4(HSPA4L):c.415G>C (p.Asp139His)	HSPA4L (D170H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2655089	NM_014278.4(HSPA4L):c.539C>T (p.Ala180Val)	HSPA4L (A139V +3 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2322432	NM_014278.4(HSPA4L):c.579G>T (p.Glu193Asp)	HSPA4L (E193D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599169	NM_014278.4(HSPA4L):c.583C>G (p.Pro195Ala)	HSPA4L (P195A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107333	NM_014278.4(HSPA4L):c.794G>A (p.Arg265His)	HSPA4L (R224H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107323	NM_014278.4(HSPA4L):c.1066A>G (p.Lys356Glu)	HSPA4L (K356E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484027	NM_014278.4(HSPA4L):c.1238G>A (p.Gly413Glu)	HSPA4L (G387E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281122	NM_014278.4(HSPA4L):c.1274C>T (p.Pro425Leu)	HSPA4L (P384L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615566	NM_014278.4(HSPA4L):c.1342A>C (p.Asn448His)	HSPA4L (N479H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617944	NM_014278.4(HSPA4L):c.1402T>A (p.Phe468Ile)	HSPA4L (F468I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299431	NM_014278.4(HSPA4L):c.1482C>A (p.Ser494Arg)	HSPA4L (S453R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2655090	NM_014278.4(HSPA4L):c.1515C>T (p.Gly505=)	HSPA4L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2226724	NM_014278.4(HSPA4L):c.1516G>C (p.Asp506His)	HSPA4L (D465H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107324	NM_014278.4(HSPA4L):c.1577T>C (p.Met526Thr)	HSPA4L (M526T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291522	NM_014278.4(HSPA4L):c.1648A>G (p.Ile550Val)	HSPA4L (I581V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374548	NM_014278.4(HSPA4L):c.1685C>T (p.Ser562Leu)	HSPA4L (S562L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107326	NM_014278.4(HSPA4L):c.1737T>G (p.Ser579Arg)	HSPA4L (S538R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387477	NM_014278.4(HSPA4L):c.1757G>A (p.Ser586Asn)	HSPA4L (S617N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107327	NM_014278.4(HSPA4L):c.1821G>A (p.Met607Ile)	HSPA4L (M581I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471662	NM_014278.4(HSPA4L):c.1898A>T (p.Asp633Val)	HSPA4L (D592V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362749	NM_014278.4(HSPA4L):c.2017G>A (p.Val673Ile)	HSPA4L (V673I +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3107328	NM_014278.4(HSPA4L):c.2038G>A (p.Glu680Lys)	HSPA4L (E654K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 771363	NM_014278.4(HSPA4L):c.2052C>T (p.Tyr684=)	HSPA4L	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2358042	NM_014278.4(HSPA4L):c.2138T>C (p.Met713Thr)	HSPA4L (M687T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530130	NM_014278.4(HSPA4L):c.2151A>C (p.Glu717Asp)	HSPA4L (E717D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107329	NM_014278.4(HSPA4L):c.2185C>G (p.Leu729Val)	HSPA4L (L688V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522384	NM_014278.4(HSPA4L):c.2216A>C (p.Lys739Thr)	HSPA4L (K698T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545358	NM_014278.4(HSPA4L):c.2219G>A (p.Cys740Tyr)	HSPA4L (C714Y +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2469570	NM_014278.4(HSPA4L):c.2237G>A (p.Ser746Asn)	HSPA4L (S705N +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2207325	NM_014278.4(HSPA4L):c.2345G>A (p.Cys782Tyr)	HSPA4L (C741Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2655091	NM_014278.4(HSPA4L):c.2421T>C (p.Asn807=)	HSPA4L	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3107330	NM_014278.4(HSPA4L):c.2423G>A (p.Gly808Asp)	HSPA4L (G782D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3107331	NM_014278.4(HSPA4L):c.2429T>C (p.Met810Thr)	HSPA4L (M769T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 43