"PreventionGenetics, part of Exact Sciences"[submitter] AND "LHX1"[gen - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3057142	NM_005568.5(LHX1):c.169C>A (p.Arg57=)	LHX1	Single nucleotide variant (synonymous variant)	LHX1-related disorder	GBenign
Select item 3044599	NM_005568.5(LHX1):c.171-5del	LHX1	Deletion (intron variant)	LHX1-related disorder	GLikely benign
Select item 3038454	NM_005568.5(LHX1):c.405G>A (p.Thr135=)	LHX1	Single nucleotide variant (synonymous variant)	LHX1-related disorder	GBenign
Select item 3038676	NM_005568.5(LHX1):c.416C>A (p.Pro139His)	LHX1 (P139H)	Single nucleotide variant (missense variant)	LHX1-related disorder	GBenign
Select item 3045827	NM_005568.5(LHX1):c.621C>T (p.Arg207=)	LHX1	Single nucleotide variant (synonymous variant)	LHX1-related disorder	GLikely benign
Select item 3056351	NM_005568.5(LHX1):c.1020G>A (p.Ala340=)	LHX1	Single nucleotide variant (synonymous variant)	LHX1-related disorder	GLikely benign
Select item 3039491	NM_005568.5(LHX1):c.1098C>T (p.His366=)	LHX1	Single nucleotide variant (synonymous variant)	LHX1-related disorder	GBenign
Select item 3055916	NM_005568.5(LHX1):c.1162G>T (p.Ala388Ser)	LHX1 (A388S)	Single nucleotide variant (missense variant)	LHX1-related disorder	GLikely benign
Select item 3046967	NM_005568.5(LHX1):c.1188C>T (p.His396=)	LHX1	Single nucleotide variant (synonymous variant)	LHX1-related disorder	GLikely benign
Select item 3039185	NM_005568.5(LHX1):c.1215G>A (p.Val405=)	LHX1	Single nucleotide variant (synonymous variant)	LHX1-related disorder	GLikely benign