Related gene-specific medical variations for Gene (Select 752) - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3095837	NM_005892.4(FMNL1):c.1576C>T (p.Pro526Ser)	FMNL1, FMNL1-AS1 (P526S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3095836	NM_005892.4(FMNL1):c.1067A>G (p.Asp356Gly)	FMNL1, FMNL1-AS1 (D356G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2615025	NM_005892.4(FMNL1):c.902G>C (p.Gly301Ala)	FMNL1, FMNL1-AS1 (G301A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2595784	NM_005892.4(FMNL1):c.1556C>T (p.Pro519Leu)	FMNL1, FMNL1-AS1 (P519L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2589060	NM_005892.4(FMNL1):c.1226C>T (p.Ala409Val)	FMNL1, FMNL1-AS1 (A409V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550327	NM_005892.4(FMNL1):c.908A>C (p.Gln303Pro)	FMNL1, FMNL1-AS1 (Q303P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468937	NM_005892.4(FMNL1):c.1358T>C (p.Met453Thr)	FMNL1, FMNL1-AS1 (M453T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361222	NM_005892.4(FMNL1):c.940C>T (p.Arg314Trp)	FMNL1, FMNL1-AS1 (R314W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344926	NM_005892.4(FMNL1):c.1534A>G (p.Ser512Gly)	FMNL1, FMNL1-AS1 (S512G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308496	NM_005892.4(FMNL1):c.965T>A (p.Phe322Tyr)	FMNL1, FMNL1-AS1 (F322Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237151	NM_005892.4(FMNL1):c.1568C>T (p.Thr523Ile)	FMNL1, FMNL1-AS1 (T523I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236657	NM_005892.4(FMNL1):c.1487G>T (p.Gly496Val)	FMNL1, FMNL1-AS1 (G496V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216887	NM_005892.4(FMNL1):c.1567A>C (p.Thr523Pro)	FMNL1, FMNL1-AS1 (T523P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775325	NM_005892.4(FMNL1):c.895-3C>T	FMNL1, FMNL1-AS1	Single nucleotide variant (intron variant)	not provided	GBenign