"Ambry Genetics"[submitter] AND "FSTL5"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2481295	NM_020116.5(FSTL5):c.2431A>T (p.Met811Leu)	FSTL5 (M801L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2278153	NM_020116.5(FSTL5):c.2391C>G (p.Asn797Lys)	FSTL5 (N796K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2599791	NM_020116.5(FSTL5):c.2258A>G (p.Gln753Arg)	FSTL5 (Q753R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2401167	NM_020116.5(FSTL5):c.2034G>A (p.Met678Ile)	FSTL5 (M677I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2514493	NM_020116.5(FSTL5):c.1902G>C (p.Met634Ile)	FSTL5 (M624I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2393371	NM_020116.5(FSTL5):c.1886T>C (p.Ile629Thr)	FSTL5 (I628T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2274016	NM_020116.5(FSTL5):c.1459G>C (p.Asp487His)	FSTL5 (D477H +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2252578	NM_020116.5(FSTL5):c.1415T>G (p.Phe472Cys)	FSTL5 (F462C +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2531973	NM_020116.5(FSTL5):c.1400C>T (p.Pro467Leu)	FSTL5 (P466L +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2385019	NM_020116.5(FSTL5):c.1300G>A (p.Ala434Thr)	FSTL5 (A433T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2265535	NM_020116.5(FSTL5):c.1214A>G (p.Tyr405Cys)	FSTL5 (Y404C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2462803	NM_020116.5(FSTL5):c.1097G>T (p.Gly366Val)	FSTL5 (G366V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2214306	NM_020116.5(FSTL5):c.1000A>G (p.Ile334Val)	FSTL5 (I334V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2373649	NM_020116.5(FSTL5):c.854A>G (p.Asn285Ser)	FSTL5 (N284S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2622733	NM_020116.5(FSTL5):c.799G>T (p.Val267Phe)	FSTL5 (V266F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2624407	NM_020116.5(FSTL5):c.638T>C (p.Leu213Pro)	FSTL5 (L213P +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2459273	NM_020116.5(FSTL5):c.608T>C (p.Val203Ala)	FSTL5 (V202A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2214662	NM_020116.5(FSTL5):c.589A>G (p.Ile197Val)	FSTL5 (I196V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2290552	NM_020116.5(FSTL5):c.550T>C (p.Phe184Leu)	FSTL5 (F183L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2372773	NM_020116.5(FSTL5):c.511G>A (p.Asp171Asn)	FSTL5 (D170N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2342816	NM_020116.5(FSTL5):c.422A>T (p.Lys141Met)	FSTL5 (K140M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2332248	NM_020116.5(FSTL5):c.367C>A (p.Gln123Lys)	FSTL5 (Q122K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2260298	NM_020116.5(FSTL5):c.350C>A (p.Ala117Asp)	FSTL5 (A116D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2467836	NM_020116.5(FSTL5):c.308C>A (p.Ser103Tyr)	FSTL5 (S102Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2373006	NM_020116.5(FSTL5):c.166A>G (p.Met56Val)	FSTL5 (M56V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2399824	NM_020116.5(FSTL5):c.130G>A (p.Glu44Lys)	FSTL5, LOC101928052 (E43K +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 26