"PreventionGenetics, part of Exact Sciences"[submitter] AND "SEMA6B"[g - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2355486	NM_032108.4(SEMA6B):c.2593G>T (p.Ala865Ser)	SEMA6B (A865S)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GBenign/Likely benign
Select item 2629489	NM_032108.4(SEMA6B):c.2477C>T (p.Thr826Met)	SEMA6B (T826M)	Single nucleotide variant (missense variant)	SEMA6B-related disorder	GUncertain significance
Select item 3035133	NM_032108.4(SEMA6B):c.2289C>T (p.Pro763=)	SEMA6B	Single nucleotide variant (synonymous variant)	SEMA6B-related disorder	GLikely benign
Select item 2311730	NM_032108.4(SEMA6B):c.2284C>A (p.Pro762Thr)	SEMA6B (P762T)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 3045968	NM_032108.4(SEMA6B):c.2115G>T (p.Gly705=)	SEMA6B	Single nucleotide variant (synonymous variant)	SEMA6B-related disorder	GLikely benign
Select item 2349539	NM_032108.4(SEMA6B):c.2053A>G (p.Met685Val)	SEMA6B (M685V)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 2355485	NM_032108.4(SEMA6B):c.2011G>A (p.Gly671Ser)	SEMA6B (G671S)	Single nucleotide variant (missense variant)	SEMA6B-related disorder +1 more	GLikely benign
Select item 781379	NM_032108.4(SEMA6B):c.1979A>C (p.Gln660Pro)	SEMA6B (Q660P)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2326779	NM_032108.4(SEMA6B):c.1967A>G (p.Glu656Gly)	SEMA6B (E656G)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 3038541	NM_032108.4(SEMA6B):c.1923G>C (p.Ala641=)	SEMA6B	Single nucleotide variant (synonymous variant)	SEMA6B-related disorder	GLikely benign
Select item 3038336	NM_032108.4(SEMA6B):c.1833C>T (p.Ala611=)	SEMA6B	Single nucleotide variant (synonymous variant)	SEMA6B-related disorder	GLikely benign
Select item 3038213	NM_032108.4(SEMA6B):c.1644C>T (p.Pro548=)	SEMA6B	Single nucleotide variant (synonymous variant)	SEMA6B-related disorder	GLikely benign
Select item 3050554	NM_032108.4(SEMA6B):c.1551C>T (p.Cys517=)	SEMA6B	Single nucleotide variant (synonymous variant)	SEMA6B-related disorder	GLikely benign
Select item 3050277	NM_032108.4(SEMA6B):c.1223C>T (p.Ala408Val)	SEMA6B (A408V)	Single nucleotide variant (missense variant)	SEMA6B-related disorder	GLikely benign
Select item 3041412	NM_032108.4(SEMA6B):c.1140C>A (p.Ala380=)	SEMA6B	Single nucleotide variant (synonymous variant)	SEMA6B-related disorder	GLikely benign
Select item 3051633	NM_032108.4(SEMA6B):c.1092G>A (p.Pro364=)	SEMA6B	Single nucleotide variant (synonymous variant)	SEMA6B-related disorder	GLikely benign
Select item 2649077	NM_032108.4(SEMA6B):c.654C>T (p.Thr218=)	SEMA6B	Single nucleotide variant (synonymous variant)	SEMA6B-related disorder +1 more	GLikely benign
Select item 2636213	NM_032108.4(SEMA6B):c.541G>C (p.Ala181Pro)	SEMA6B (A181P)	Single nucleotide variant (missense variant)	SEMA6B-related disorder	GUncertain significance
Select item 735989	NM_032108.4(SEMA6B):c.507C>T (p.Ser169=)	SEMA6B	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 781380	NM_032108.4(SEMA6B):c.63G>A (p.Gly21=)	SEMA6B	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 781421	NM_032108.4(SEMA6B):c.48G>T (p.Leu16=)	SEMA6B	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 1237432	NM_032108.4(SEMA6B):c.39G>C (p.Leu13=)	SEMA6B	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign

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Items: 22