SFT2D1[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2332685	NM_145169.3(SFT2D1):c.461G>A (p.Cys154Tyr)	SFT2D1 (C154Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160941	NM_145169.3(SFT2D1):c.407C>G (p.Thr136Ser)	SFT2D1 (T136S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351737	NM_145169.3(SFT2D1):c.373G>C (p.Val125Leu)	SFT2D1 (V125L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2233802	NM_145169.3(SFT2D1):c.218T>C (p.Leu73Pro)	SFT2D1 (L73P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262966	NM_145169.3(SFT2D1):c.212G>A (p.Gly71Asp)	SFT2D1 (G71D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2322521	NM_145169.3(SFT2D1):c.211G>A (p.Gly71Ser)	SFT2D1 (G71S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2245037	NM_145169.3(SFT2D1):c.179G>T (p.Gly60Val)	SFT2D1 (G60V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160939	NM_145169.3(SFT2D1):c.133G>A (p.Val45Ile)	SFT2D1 (V45I)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3317875	NM_145169.3(SFT2D1):c.14G>A (p.Arg5Gln)	SFT2D1 (R5Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3160938	NM_145169.3(SFT2D1):c.10C>A (p.Leu4Met)	SFT2D1 (L4M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance