"PreventionGenetics, part of Exact Sciences"[submitter] AND "SEMA7A"[g - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3059310	NM_003612.5(SEMA7A):c.1944C>T (p.Ala648=)	SEMA7A	Single nucleotide variant (synonymous variant)	SEMA7A-related disorder	GBenign
Select item 3060979	NM_003612.5(SEMA7A):c.1545A>G (p.Gln515=)	SEMA7A	Single nucleotide variant (synonymous variant)	SEMA7A-related disorder	GBenign
Select item 3042116	NM_003612.5(SEMA7A):c.1491C>T (p.Gly497=)	SEMA7A	Single nucleotide variant (synonymous variant)	SEMA7A-related disorder	GBenign
Select item 3059177	NM_003612.5(SEMA7A):c.1239C>T (p.Val413=)	SEMA7A	Single nucleotide variant (synonymous variant)	SEMA7A-related disorder	GBenign
Select item 3033564	NM_003612.5(SEMA7A):c.1095+7G>A	SEMA7A	Single nucleotide variant (intron variant)	SEMA7A-related disorder	GBenign
Select item 3042393	NM_003612.5(SEMA7A):c.525C>T (p.Asp175=)	SEMA7A	Single nucleotide variant (synonymous variant)	SEMA7A-related disorder	GLikely benign
Select item 3059494	NM_003612.5(SEMA7A):c.507C>T (p.Tyr169=)	SEMA7A	Single nucleotide variant (synonymous variant)	SEMA7A-related disorder	GBenign
Select item 3056538	NM_003612.5(SEMA7A):c.378C>T (p.Cys126=)	SEMA7A	Single nucleotide variant (synonymous variant +1 more)	SEMA7A-related disorder	GBenign
Select item 3052608	NM_003612.5(SEMA7A):c.339C>T (p.Ile113=)	SEMA7A	Single nucleotide variant (5 prime UTR variant +2 more)	SEMA7A-related disorder	GLikely benign
Select item 3049304	NM_003612.5(SEMA7A):c.168C>G (p.Ala56=)	LOC130057537, SEMA7A	Single nucleotide variant (synonymous variant)	SEMA7A-related disorder	GLikely benign
Select item 3047754	NM_003612.5(SEMA7A):c.144A>T (p.Leu48=)	LOC130057537, SEMA7A	Single nucleotide variant (synonymous variant)	SEMA7A-related disorder	GLikely benign