"PreventionGenetics, part of Exact Sciences"[submitter] AND "LIMK1"[ge - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 709429	NM_002314.4(LIMK1):c.292-8C>G	LIMK1	Single nucleotide variant (intron variant)	LIMK1-related disorder +1 more	GBenign
Select item 723302	NM_002314.4(LIMK1):c.549C>T (p.Asp183=)	LIMK1	Single nucleotide variant (synonymous variant)	LIMK1-related disorder +1 more	GLikely benign
Select item 3038729	NM_002314.4(LIMK1):c.687G>A (p.Thr229=)	LIMK1	Single nucleotide variant (synonymous variant)	LIMK1-related disorder	GLikely benign
Select item 707978	NM_002314.4(LIMK1):c.715-6C>A	LIMK1	Single nucleotide variant (intron variant)	LIMK1-related disorder +1 more	GLikely benign
Select item 3047192	NM_002314.4(LIMK1):c.732G>A (p.Gln244=)	LIMK1	Single nucleotide variant (synonymous variant)	LIMK1-related disorder	GLikely benign
Select item 712470	NM_002314.4(LIMK1):c.777C>G (p.His259Gln)	LIMK1 (H225Q +1 more)	Single nucleotide variant (missense variant)	LIMK1-related disorder +1 more	GBenign/Likely benign
Select item 726650	NM_002314.4(LIMK1):c.1080G>A (p.Glu360=)	LIMK1	Single nucleotide variant (synonymous variant)	LIMK1-related disorder +1 more	GBenign/Likely benign
Select item 711707	NM_002314.4(LIMK1):c.1265G>A (p.Arg422Gln)	LIMK1 (R422Q +1 more)	Single nucleotide variant (missense variant)	LIMK1-related disorder +1 more	GBenign/Likely benign
Select item 3044999	NM_002314.4(LIMK1):c.1446G>A (p.Ala482=)	LIMK1	Single nucleotide variant (synonymous variant)	LIMK1-related disorder	GLikely benign
Select item 3037439	NM_002314.4(LIMK1):c.1567+7G>A	LIMK1	Single nucleotide variant (intron variant)	LIMK1-related disorder	GBenign
Select item 734999	NM_002314.4(LIMK1):c.1611C>T (p.Ile537=)	LIMK1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 731523	NM_002314.4(LIMK1):c.1739T>A (p.Phe580Tyr)	LIMK1 (F546Y +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 3044233	NM_002314.4(LIMK1):c.*1G>A	LIMK1	Single nucleotide variant (3 prime UTR variant)	LIMK1-related disorder	GLikely benign