"PreventionGenetics, part of Exact Sciences"[submitter] AND "LHX8"[gen - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2638883	NM_001256114.2(LHX8):c.1A>C (p.Met1Leu)	LHX8 (M11L +1 more)	Single nucleotide variant (missense variant +1 more)	LHX8-related condition +1 more	GBenign/Likely benign
Select item 3041330	NM_001256114.2(LHX8):c.75+9G>A	LHX8	Single nucleotide variant (intron variant)	LHX8-related condition	GLikely benign
Select item 787748	NM_001256114.2(LHX8):c.92C>T (p.Ala31Val)	LHX8 (A31V +1 more)	Single nucleotide variant (missense variant)	LHX8-related condition +1 more	GBenign
Select item 3051304	NM_001256114.2(LHX8):c.213G>A (p.Glu71=)	LHX8	Single nucleotide variant (synonymous variant)	LHX8-related condition	GLikely benign
Select item 787749	NM_001256114.2(LHX8):c.411C>T (p.Asp137=)	LHX8	Single nucleotide variant (synonymous variant)	LHX8-related condition +1 more	GBenign
Select item 3043391	NM_001256114.2(LHX8):c.606C>T (p.Ala202=)	LHX8	Single nucleotide variant (synonymous variant)	LHX8-related condition	GLikely benign
Select item 3044949	NM_001256114.2(LHX8):c.741A>G (p.Lys247=)	LHX8	Single nucleotide variant (synonymous variant)	LHX8-related condition	GLikely benign
Select item 782378	NM_001256114.2(LHX8):c.783G>T (p.Val261=)	LHX8	Single nucleotide variant (synonymous variant)	LHX8-related condition +1 more	GBenign
Select item 3059961	NM_001256114.2(LHX8):c.964+4G>C	LHX8	Single nucleotide variant (intron variant)	LHX8-related condition	GLikely benign