SCML2[gene] and "single gene"[properties] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2520012	NM_006089.3(SCML2):c.1724G>A (p.Arg575Gln)	SCML2 (R575Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2271861	NM_006089.3(SCML2):c.1444A>G (p.Lys482Glu)	SCML2 (K482E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341924	NM_006089.3(SCML2):c.1370A>G (p.Gln457Arg)	SCML2 (Q457R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485753	NM_006089.3(SCML2):c.1296T>G (p.His432Gln)	SCML2 (H432Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2660099	NM_006089.3(SCML2):c.1266G>A (p.Val422=)	SCML2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3158480	NM_006089.3(SCML2):c.1244C>G (p.Pro415Arg)	SCML2 (P415R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316489	NM_006089.3(SCML2):c.1217C>G (p.Thr406Ser)	SCML2 (T406S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3158479	NM_006089.3(SCML2):c.1160C>G (p.Pro387Arg)	SCML2 (P387R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316490	NM_006089.3(SCML2):c.1147T>C (p.Phe383Leu)	SCML2 (F383L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317246	NM_006089.3(SCML2):c.1016G>A (p.Gly339Asp)	SCML2 (G339D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2615276	NM_006089.3(SCML2):c.1012C>T (p.Arg338Cys)	SCML2 (R338C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316487	NM_006089.3(SCML2):c.967A>G (p.Ile323Val)	SCML2 (I323V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3316488	NM_006089.3(SCML2):c.857T>G (p.Ile286Ser)	SCML2 (I286S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3158483	NM_006089.3(SCML2):c.803C>T (p.Pro268Leu)	SCML2 (P268L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554815	NM_006089.3(SCML2):c.800C>T (p.Ser267Phe)	SCML2 (S267F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2380439	NM_006089.3(SCML2):c.775G>A (p.Glu259Lys)	SCML2 (E259K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2603406	NM_006089.3(SCML2):c.614C>T (p.Thr205Ile)	SCML2 (T205I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492944	NM_006089.3(SCML2):c.596G>A (p.Gly199Glu)	SCML2 (G199E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3158481	NM_006089.3(SCML2):c.227A>G (p.Asn76Ser)	SCML2 (N76S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3158482	NM_006089.3(SCML2):c.59C>T (p.Thr20Ile)	SCML2 (T20I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 20