Related gene-specific medical variations for Gene (Select 11167) - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3280103	NM_007085.5(FSTL1):c.761T>A (p.Val254Asp)	FSTL1, LRRC58-DT (V254D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280102	NM_007085.5(FSTL1):c.341A>G (p.Tyr114Cys)	FSTL1, LRRC58-DT (Y114C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280101	NM_007085.5(FSTL1):c.242G>A (p.Arg81Gln)	FSTL1, LRRC58-DT (R81Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280100	NM_007085.5(FSTL1):c.424G>A (p.Gly142Ser)	FSTL1, LRRC58-DT (G142S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097335	NM_007085.5(FSTL1):c.623A>C (p.Asn208Thr)	FSTL1, LRRC58-DT (N208T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097334	NM_007085.5(FSTL1):c.604A>G (p.Ile202Val)	FSTL1, LRRC58-DT (I202V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097332	NM_007085.5(FSTL1):c.352C>T (p.Arg118Cys)	FSTL1, LRRC58-DT (R118C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097331	NM_007085.5(FSTL1):c.283G>A (p.Asp95Asn)	FSTL1, LRRC58-DT (D95N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097330	NM_007085.5(FSTL1):c.190C>G (p.Pro64Ala)	FSTL1, LRRC58-DT (P64A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594877	NM_007085.5(FSTL1):c.781G>A (p.Val261Ile)	FSTL1, LRRC58-DT (V261I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540475	NM_007085.5(FSTL1):c.115G>A (p.Gly39Ser)	FSTL1, LRRC58-DT (G39S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514390	NM_007085.5(FSTL1):c.745G>A (p.Asp249Asn)	FSTL1, LRRC58-DT (D249N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481185	NM_007085.5(FSTL1):c.905G>C (p.Arg302Thr)	FSTL1, LRRC58-DT (R302T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470117	NM_007085.5(FSTL1):c.797C>T (p.Thr266Ile)	FSTL1, LRRC58-DT (T266I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404892	NM_007085.5(FSTL1):c.652T>A (p.Phe218Ile)	FSTL1, LRRC58-DT (F218I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377633	NM_007085.5(FSTL1):c.408T>G (p.Asp136Glu)	FSTL1, LRRC58-DT (D136E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362124	NM_007085.5(FSTL1):c.367C>T (p.Arg123Cys)	FSTL1, LRRC58-DT (R123C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359693	NM_007085.5(FSTL1):c.865G>C (p.Glu289Gln)	FSTL1, LRRC58-DT (E289Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333839	NM_007085.5(FSTL1):c.676T>G (p.Phe226Val)	FSTL1, LRRC58-DT (F226V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329672	NM_007085.5(FSTL1):c.119G>A (p.Arg40Gln)	FSTL1, LRRC58-DT (R40Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325967	NM_007085.5(FSTL1):c.157C>G (p.Leu53Val)	FSTL1, LRRC58-DT (L53V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317047	NM_007085.5(FSTL1):c.742G>A (p.Val248Met)	FSTL1, LRRC58-DT (V248M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226319	NM_007085.5(FSTL1):c.821G>C (p.Gly274Ala)	FSTL1, LRRC58-DT (G274A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213960	NM_007085.5(FSTL1):c.542T>C (p.Ile181Thr)	FSTL1, LRRC58-DT (I181T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 784017	NM_007085.5(FSTL1):c.804C>T (p.Asp268=)	FSTL1, LRRC58-DT	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign

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Links from Gene

Items: 25