"Ambry Genetics"[submitter] AND "FSD1L"[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2526659	NM_001145313.3(FSD1L):c.25A>C (p.Lys9Gln)	FSD1L (K9Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391444	NM_001145313.3(FSD1L):c.71C>G (p.Ser24Cys)	FSD1L (S24C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097176	NM_001145313.3(FSD1L):c.82A>G (p.Ile28Val)	FSD1L (I28V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2271804	NM_001145313.3(FSD1L):c.101A>G (p.Asn34Ser)	FSD1L (N34S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302742	NM_001145313.3(FSD1L):c.152A>G (p.Asn51Ser)	FSD1L (N19S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280030	NM_001145313.3(FSD1L):c.281A>C (p.Lys94Thr)	FSD1L (K94T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291567	NM_001145313.3(FSD1L):c.285A>C (p.Glu95Asp)	FSD1L (E63D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350041	NM_001145313.3(FSD1L):c.293T>C (p.Ile98Thr)	FSD1L (I98T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463325	NM_001145313.3(FSD1L):c.308A>G (p.Gln103Arg)	FSD1L (Q71R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248151	NM_001145313.3(FSD1L):c.319C>T (p.Arg107Cys)	FSD1L (R107C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521764	NM_001145313.3(FSD1L):c.320G>A (p.Arg107His)	FSD1L (R107H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302875	NM_001145313.3(FSD1L):c.488G>A (p.Arg163His)	FSD1L (R163H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517214	NM_001145313.3(FSD1L):c.532A>G (p.Met178Val)	FSD1L (M146V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551840	NM_001145313.3(FSD1L):c.540T>G (p.Asp180Glu)	FSD1L (D148E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523145	NM_001145313.3(FSD1L):c.593A>G (p.Lys198Arg)	FSD1L (K198R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592149	NM_001145313.3(FSD1L):c.603G>T (p.Glu201Asp)	FSD1L (E201D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280028	NM_001145313.3(FSD1L):c.731G>A (p.Arg244His)	FSD1L (R244H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097175	NM_001145313.3(FSD1L):c.778A>G (p.Thr260Ala)	FSD1L (T260A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393894	NM_001145313.3(FSD1L):c.785A>G (p.Tyr262Cys)	FSD1L (Y230C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590985	NM_001145313.3(FSD1L):c.787A>G (p.Thr263Ala)	FSD1L (T231A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280029	NM_001145313.3(FSD1L):c.970C>T (p.Pro324Ser)	FSD1L (P292S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548426	NM_001145313.3(FSD1L):c.973A>C (p.Thr325Pro)	FSD1L (T325P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097177	NM_001145313.3(FSD1L):c.990A>C (p.Gln330His)	FSD1L (Q298H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313591	NM_001145313.3(FSD1L):c.994A>G (p.Ser332Gly)	FSD1L (S300G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461677	NM_001145313.3(FSD1L):c.1084G>A (p.Gly362Ser)	FSD1L (G341S +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456645	NM_001145313.3(FSD1L):c.1182T>A (p.Asp394Glu)	FSD1L (D373E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237397	NM_001145313.3(FSD1L):c.1585A>C (p.Thr529Pro)	FSD1L (T496P +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 27