"PreventionGenetics, part of Exact Sciences"[submitter] AND "LENG8"[ge - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3045293	NM_052925.4(LENG8):c.102C>T (p.His34=)	LENG8	Single nucleotide variant (synonymous variant)	LENG8-related disorder	GLikely benign
Select item 3049713	NM_052925.4(LENG8):c.255G>C (p.Gln85His)	LENG8 (Q67H +1 more)	Single nucleotide variant (missense variant)	LENG8-related disorder	GBenign
Select item 3049835	NM_052925.4(LENG8):c.594C>T (p.Pro198=)	LENG8	Single nucleotide variant (synonymous variant)	LENG8-related disorder	GLikely benign
Select item 3035905	NM_052925.4(LENG8):c.973C>T (p.Leu325=)	LENG8	Single nucleotide variant (synonymous variant)	LENG8-related disorder	GLikely benign
Select item 3045258	NM_052925.4(LENG8):c.1023G>A (p.Pro341=)	LENG8	Single nucleotide variant (synonymous variant)	LENG8-related disorder	GLikely benign
Select item 3052389	NM_052925.4(LENG8):c.1288C>T (p.Arg430Cys)	LENG8 (R393C +2 more)	Single nucleotide variant (missense variant)	LENG8-related disorder	GBenign
Select item 3047313	NM_052925.4(LENG8):c.1392C>T (p.Gly464=)	LENG8	Single nucleotide variant (synonymous variant)	LENG8-related disorder	GLikely benign
Select item 2650450	NM_052925.4(LENG8):c.1458G>A (p.Ala486=)	LENG8	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3056840	NM_052925.4(LENG8):c.1669A>G (p.Ile557Val)	LENG8 (I520V +2 more)	Single nucleotide variant (missense variant)	LENG8-related disorder	GBenign
Select item 3037173	NM_052925.4(LENG8):c.1732-9C>T	LENG8	Single nucleotide variant (intron variant)	LENG8-related disorder	GBenign
Select item 3047873	NM_052925.4(LENG8):c.1791G>A (p.Ala597=)	LENG8	Single nucleotide variant (synonymous variant)	LENG8-related disorder	GLikely benign
Select item 3037344	NM_052925.4(LENG8):c.1848C>T (p.Arg616=)	LENG8	Single nucleotide variant (synonymous variant)	LENG8-related disorder	GLikely benign
Select item 3037782	NM_052925.4(LENG8):c.1890C>T (p.Ile630=)	LENG8	Single nucleotide variant (synonymous variant)	LENG8-related disorder	GBenign
Select item 3038368	NM_052925.4(LENG8):c.1935G>A (p.Thr645=)	LENG8	Single nucleotide variant (synonymous variant)	LENG8-related disorder	GLikely benign
Select item 3049268	NM_052925.4(LENG8):c.2250T>A (p.Pro750=)	LENG8	Single nucleotide variant (3 prime UTR variant +1 more)	LENG8-related disorder	GLikely benign