"PreventionGenetics, part of Exact Sciences"[submitter] AND "LFNG"[gen - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2657231	NM_002304.3(LFNG):c.27G>T (p.Ala9=)	LFNG	Single nucleotide variant (synonymous variant +1 more)	LFNG-related disorder +1 more	GLikely benign
Select item 1165699	NM_001040167.2(LFNG):c.75C>T (p.Thr25=)	LFNG, LOC129997823	Single nucleotide variant (synonymous variant +1 more)	Spondylocostal dysostosis 3, autosomal recessive +1 more	GBenign
Select item 1080361	NM_001040167.2(LFNG):c.480G>A (p.Thr160=)	LFNG	Single nucleotide variant (synonymous variant)	LFNG-related disorder +1 more	GLikely benign
Select item 257265	NM_001040167.2(LFNG):c.481+3G>A	LFNG	Single nucleotide variant (intron variant)	Spondylocostal dysostosis 3, autosomal recessive +1 more	GBenign
Select item 257266	NM_001040167.2(LFNG):c.482-4A>G	LFNG	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 916354	NM_001040167.2(LFNG):c.546C>T (p.Ala182=)	LFNG	Single nucleotide variant (synonymous variant)	Spondylocostal dysostosis 3, autosomal recessive +2 more	GLikely benign
Select item 257267	NM_001040167.2(LFNG):c.612C>T (p.Tyr204=)	LFNG	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign/Likely benign
Select item 800232	NM_001040167.2(LFNG):c.667G>A (p.Val223Ile)	LFNG (V223I +2 more)	Single nucleotide variant (missense variant)	Spondylocostal dysostosis 3, autosomal recessive +1 more	GLikely benign
Select item 257268	NM_001040167.2(LFNG):c.672C>T (p.Tyr224=)	LFNG	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 534226	NM_001040167.2(LFNG):c.723C>T (p.Ser241=)	LFNG	Single nucleotide variant (synonymous variant)	LFNG-related disorder +1 more	GLikely benign
Select item 257269	NM_001040167.2(LFNG):c.736-36C>T	LFNG	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 2059942	NM_001040167.2(LFNG):c.765C>T (p.Gly255=)	LFNG	Single nucleotide variant (synonymous variant)	Spondylocostal dysostosis 3, autosomal recessive +1 more	GLikely benign
Select item 287728	NM_001040167.2(LFNG):c.774C>T (p.Gly258=)	LFNG	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 257270	NM_001040167.2(LFNG):c.822-38C>T	LFNG	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 3042280	NM_001040167.2(LFNG):c.897C>T (p.Ala299=)	LFNG	Single nucleotide variant (synonymous variant)	LFNG-related disorder	GLikely benign
Select item 257271	NM_001040167.2(LFNG):c.972G>A (p.Ser324=)	LFNG	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 2722414	NM_001040167.2(LFNG):c.981C>T (p.His327=)	LFNG	Single nucleotide variant (synonymous variant)	Spondylocostal dysostosis 3, autosomal recessive +1 more	GLikely benign
Select item 257272	NM_001040167.2(LFNG):c.988-37G>A	LFNG	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 257264	NM_001040167.2(LFNG):c.1002C>T (p.Tyr334=)	LFNG	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign