LIMK1[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146075	GRCh38/hg38 7p22.3-q36.3(chr7:54185-159282390)x1	CUL1, CUX1 +4737 more	Copy number loss	See cases	GPathogenic
Select item 154461	GRCh38/hg38 7q11.21-11.23(chr7:62736364-75432710)x1	LOC129998564, LOC129998565 +351 more	Copy number loss	See cases	GPathogenic
Select item 154104	GRCh38/hg38 7q11.21-11.23(chr7:62977085-75415352)x3	ABHD11, ABHD11-AS1 +350 more	Copy number gain	See cases	GPathogenic
Select item 60237	GRCh38/hg38 7q11.22-11.23(chr7:69382353-77823832)x1	SPDYE12, SPDYE13 +330 more	Copy number loss	See cases	GPathogenic
Select item 57096	GRCh38/hg38 7q11.22-21.11(chr7:71225344-81735657)x1	ABHD11, ABHD11-AS1 +317 more	Copy number loss	See cases	GPathogenic
Select item 155387	GRCh38/hg38 7q11.22-21.11(chr7:72179092-79164071)	ABHD11, ABHD11-AS1 +285 more	Copy number gain	See cases	GLikely pathogenic
Select item 58217	GRCh38/hg38 7q11.22-11.23(chr7:72649515-75361855)x3	ABHD11, ABHD11-AS1 +162 more	Copy number gain	See cases	GPathogenic
Select item 58218	GRCh38/hg38 7q11.23(chr7:72768821-74869255)x3	ABHD11, ABHD11-AS1 +147 more	Copy number gain	See cases	GPathogenic
Select item 57313	GRCh38/hg38 7q11.23(chr7:72930548-74869255)x1	ABHD11, ABHD11-AS1 +141 more	Copy number loss	See cases	GPathogenic
Select item 147066	GRCh38/hg38 7q11.23(chr7:72938064-74779028)x3	ABHD11, ABHD11-AS1 +140 more	Copy number gain	See cases	GPathogenic
Select item 148663	GRCh38/hg38 7q11.23(chr7:73040501-75255046)x3	ABHD11, ABHD11-AS1 +148 more	Copy number gain	See cases	GPathogenic
Select item 146414	GRCh38/hg38 7q11.23(chr7:73040501-75255046)x3	ABHD11, ABHD11-AS1 +148 more	Copy number gain	See cases	GUncertain significance
Select item 59305	GRCh38/hg38 7q11.23(chr7:73096542-74727989)x1	ABHD11, ABHD11-AS1 +133 more	Copy number loss	See cases	GPathogenic
Select item 153242	GRCh38/hg38 7q11.23(chr7:73175475-74740268)x3	ABHD11, ABHD11-AS1 +132 more	Copy number gain	See cases	GPathogenic
Select item 152064	GRCh38/hg38 7q11.23(chr7:73192369-74883978)x3	ABHD11, ABHD11-AS1 +134 more	Copy number gain	See cases	GPathogenic
Select item 150322	GRCh38/hg38 7q11.23(chr7:73192369-74869255)x1	ABHD11, ABHD11-AS1 +134 more	Copy number loss	See cases	GPathogenic
Select item 149044	GRCh38/hg38 7q11.23(chr7:73192369-74779057)x1	ABHD11, ABHD11-AS1 +133 more	Copy number loss	See cases	GPathogenic
Select item 149043	GRCh38/hg38 7q11.23(chr7:73192369-74779057)x3	LOC129998592, LOC129998593 +133 more	Copy number gain	See cases	GPathogenic
Select item 2505469	Single allele	ABHD11, ABHD11-AS1 +132 more	Deletion	Williams syndrome	GPathogenic
Select item 2499666	GRCh38/hg38 7q11.23(chr7:73229597-74727852)	ABHD11, ABHD11-AS1 +131 more	Copy number loss	Williams syndrome	GPathogenic
Select item 3236844	GRCh38/hg38 7q11.23(chr7:73247356-74727974)x3	ABHD11, ABHD11-AS1 +130 more	Copy number gain	7q11.23 microduplication syndrome	GPathogenic
Select item 149310	GRCh38/hg38 7q11.23(chr7:73271690-74727989)x1	ABHD11, ABHD11-AS1 +130 more	Copy number loss	See cases	GPathogenic
Select item 155323	GRCh38/hg38 7q11.23(chr7:73280574-74728722)x3	LOC129998592, LOC129998593 +129 more	Copy number gain	See cases	GPathogenic
Select item 154347	GRCh38/hg38 7q11.23(chr7:73280574-74789341)x1	ABHD11, ABHD11-AS1 +131 more	Copy number loss	See cases	GPathogenic
Select item 153973	GRCh38/hg38 7q11.23(chr7:73280574-74727918)x1	ABHD11, ABHD11-AS1 +129 more	Copy number loss	See cases	GPathogenic
Select item 150236	GRCh38/hg38 7q11.23(chr7:73280574-74779057)x3	ABHD11, ABHD11-AS1 +131 more	Copy number gain	See cases	GPathogenic
Select item 149309	GRCh38/hg38 7q11.23(chr7:73280574-74727989)x3	ABHD11, ABHD11-AS1 +129 more	Copy number gain	See cases	GPathogenic
Select item 147170	GRCh38/hg38 7q11.23(chr7:73280574-74924007)x1	ABHD11, ABHD11-AS1 +133 more	Copy number loss	See cases	GPathogenic
Select item 59315	GRCh38/hg38 7q11.23(chr7:73280574-74723034)x1	ABHD11, ABHD11-AS1 +129 more	Copy number loss	See cases	GPathogenic
Select item 58238	GRCh38/hg38 7q11.23(chr7:73280574-74839100)x3	ABHD11, ABHD11-AS1 +132 more	Copy number gain	See cases	GPathogenic
Select item 58237	GRCh38/hg38 7q11.23(chr7:73280574-74725240)x3	ABHD11, ABHD11-AS1 +129 more	Copy number gain	See cases	GPathogenic
Select item 58219	GRCh38/hg38 7q11.23(chr7:73280574-74725240)x3	ABHD11, ABHD11-AS1 +129 more	Copy number gain	See cases	GPathogenic
Select item 154259	GRCh38/hg38 7q11.23(chr7:73286125-74732517)x3	DNAJC30, EIF4H +129 more	Copy number gain	See cases	GPathogenic
Select item 154824	GRCh38/hg38 7q11.23(chr7:73286412-74758583)x1	ABHD11, ABHD11-AS1 +130 more	Copy number loss	See cases	GPathogenic
Select item 151986	GRCh38/hg38 7q11.23(chr7:73286412-74779057)x1	ABHD11, ABHD11-AS1 +131 more	Copy number loss	See cases	GPathogenic
Select item 151015	GRCh38/hg38 7q11.23(chr7:73286412-74869255)x1	ABHD11, ABHD11-AS1 +132 more	Copy number loss	See cases	GPathogenic
Select item 149308	GRCh38/hg38 7q11.23(chr7:73286412-74727989)x1	ABHD11, ABHD11-AS1 +129 more	Copy number loss	See cases	GPathogenic
Select item 59319	GRCh38/hg38 7q11.23(chr7:73286412-74707848)x1	ABHD11, ABHD11-AS1 +129 more	Copy number loss	See cases	GPathogenic
Select item 59318	GRCh38/hg38 7q11.23(chr7:73286412-74725240)x1	ABHD11, ABHD11-AS1 +129 more	Copy number loss	See cases	GPathogenic
Select item 59317	GRCh38/hg38 7q11.23(chr7:73286412-74725240)x3	ABHD11, ABHD11-AS1 +129 more	Copy number gain	See cases	GPathogenic
Select item 59316	GRCh38/hg38 7q11.23(chr7:73286412-74723034)x1	EIF4H, ELN +129 more	Copy number loss	See cases	GPathogenic
Select item 154080	GRCh38/hg38 7q11.23(chr7:73286508-74727852)x1	ABHD11, ABHD11-AS1 +129 more	Copy number loss	See cases	GPathogenic
Select item 153978	GRCh38/hg38 7q11.23(chr7:73286522-74727156)x1	ABHD11, ABHD11-AS1 +129 more	Copy number loss	See cases	GPathogenic
Select item 3252027	NC_000007.14:g.(?_73303398)_(74735532_?)del	ABHD11, ABHD11-AS1 +130 more	Deletion	Williams syndrome	GLikely pathogenic
Select item 144925	GRCh38/hg38 7q11.23(chr7:73304255-74718954)x1	ABHD11, ABHD11-AS1 +129 more	Copy number loss	See cases	GPathogenic
Select item 2574138	NC_000007.14:g.73304277_74727414del	ABHD11, ABHD11-AS1 +129 more	Deletion	Williams syndrome	GPathogenic
Select item 155565	GRCh38/hg38 7q11.23(chr7:73304280-74727852)x1	ABHD11, ABHD11-AS1 +129 more	Copy number loss	See cases	GPathogenic
Select item 58239	GRCh38/hg38 7q11.23(chr7:73312575-74723034)x3	ABHD11, ABHD11-AS1 +128 more	Copy number gain	See cases	GPathogenic
Select item 147629	GRCh38/hg38 7q11.23(chr7:73312582-74725057)x1	LOC129998612, LOC129998613 +128 more	Copy number loss	See cases	GPathogenic
Select item 545349	Single allele	ABHD11, ABHD11-AS1 +128 more	Duplication	Schizophrenia	GPathogenic
Select item 545350	Single allele	ABHD11, ABHD11-AS1 +128 more	Duplication	Autism	GPathogenic
Select item 59321	GRCh38/hg38 7q11.23(chr7:73352104-74719154)x1	ABHD11, ABHD11-AS1 +127 more	Copy number loss	See cases	GPathogenic
Select item 59320	GRCh38/hg38 7q11.23(chr7:73352104-74719154)x3	EIF4H, ELN +127 more	Copy number gain	See cases	GPathogenic
Select item 146838	GRCh38/hg38 7q11.23(chr7:73352303-74924023)x1	LOC129998611, LOC129998612 +131 more	Copy number loss	See cases	GPathogenic
Select item 146807	GRCh38/hg38 7q11.23(chr7:73352303-74719008)x1	ABHD11, ABHD11-AS1 +127 more	Copy number loss	See cases	GPathogenic
Select item 146803	GRCh38/hg38 7q11.23(chr7:73352303-74719008)x3	ABHD11, ABHD11-AS1 +127 more	Copy number gain	See cases	GPathogenic
Select item 146774	GRCh38/hg38 7q11.23(chr7:73352303-74779051)x1	ABHD11, ABHD11-AS1 +129 more	Copy number loss	See cases	GPathogenic
Select item 160898	GRCh38/hg38 7q11.23(chr7:73352304-74719013)x1	ABHD11, ABHD11-AS1 +127 more	Copy number loss	See cases	GPathogenic
Select item 160823	GRCh38/hg38 7q11.23(chr7:73352304-74924037)x1	ABHD11, ABHD11-AS1 +131 more	Copy number loss	See cases	GPathogenic
Select item 160822	GRCh38/hg38 7q11.23(chr7:73352304-74719013)x3	ABHD11, ABHD11-AS1 +127 more	Copy number gain	See cases	GPathogenic
Select item 154623	GRCh38/hg38 7q11.23(chr7:73352304-75065728)x3	LOC129998621, LOC129998622 +134 more	Copy number gain	See cases	GPathogenic
Select item 144156	GRCh38/hg38 7q11.23(chr7:73352304-76722261)x1	LOC129998696, LOC129998697 +219 more	Copy number loss	See cases	GPathogenic
Select item 57316	GRCh38/hg38 7q11.23(chr7:73352304-74869255)x1	ABHD11, ABHD11-AS1 +130 more	Copy number loss	See cases	GPathogenic
Select item 33969	GRCh38/hg38 7q11.23(chr7:73352304-74924037)x1	ABHD11, ABHD11-AS1 +131 more	Copy number loss	See cases	GPathogenic
Select item 32643	GRCh38/hg38 7q11.23(chr7:73352304-74719013)x1	ABHD11, ABHD11-AS1 +127 more	Copy number loss	See cases	GPathogenic
Select item 32380	GRCh38/hg38 7q11.23(chr7:73352304-74719013)x3	ABHD11, ABHD11-AS1 +127 more	Copy number gain	See cases	GPathogenic
Select item 149956	GRCh38/hg38 7q11.23(chr7:73755813-74133404)x3	CLDN3, CLDN4 +22 more	Copy number gain	See cases	GUncertain significance
Select item 154350	GRCh38/hg38 7q11.23(chr7:73755831-74131326)x1	CLDN3, CLDN4 +22 more	Copy number loss	See cases	GPathogenic
Select item 60244	GRCh38/hg38 7q11.23-21.11(chr7:73873420-83988860)x1	APTR, CACNA2D1 +249 more	Copy number loss	See cases	GPathogenic
Select item 146296	GRCh38/hg38 7q11.23(chr7:74031409-74104712)x3	ELN, ELN-AS1 +7 more	Copy number gain	See cases	GLikely benign
Select item 59712	GRCh38/hg38 7q11.23(chr7:74035454-74133404)x3	LOC129998616, ELN +7 more	Copy number gain	See cases	GPathogenic
Select item 147810	GRCh38/hg38 7q11.23(chr7:74047652-74924037)x1	CLIP2, EIF4H +71 more	Copy number loss	See cases	GPathogenic
Select item 152805	GRCh38/hg38 7q11.23(chr7:74068087-75068321)x3	CASTOR2, CLIP2 +74 more	Copy number gain	See cases	GLikely benign
Select item 752326	NM_002314.4(LIMK1):c.60C>T (p.Ser20=)	LIMK1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2227142	NM_002314.4(LIMK1):c.70G>A (p.Val24Met)	LIMK1 (V24M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2483533	NM_002314.4(LIMK1):c.100G>C (p.Asp34His)	LIMK1 (D34H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3251243	NM_002314.4(LIMK1):c.127G>A (p.Ala43Thr)	LIMK1 (A43T)	Single nucleotide variant (missense variant)	See cases	GLikely pathogenic
Select item 719215	NM_002314.4(LIMK1):c.144C>T (p.Asp48=)	LIMK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 773740	NM_002314.4(LIMK1):c.180G>A (p.Ser60=)	LIMK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2335595	NM_002314.4(LIMK1):c.194A>G (p.Glu65Gly)	LIMK1 (E65G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781649	NM_002314.4(LIMK1):c.197A>C (p.Lys66Thr)	LIMK1 (K66T +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2396746	NM_002314.4(LIMK1):c.232G>A (p.Ala78Thr)	LIMK1 (A78T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290751	NM_002314.4(LIMK1):c.238T>C (p.Tyr80His)	LIMK1 (Y46H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394499	NM_002314.4(LIMK1):c.286G>A (p.Val96Ile)	LIMK1 (V62I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2657582	NM_002314.4(LIMK1):c.292-8C>T	LIMK1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 709429	NM_002314.4(LIMK1):c.292-8C>G	LIMK1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 782705	NM_002314.4(LIMK1):c.339G>A (p.Thr113=)	LIMK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2657583	NM_002314.4(LIMK1):c.384G>A (p.Glu128=)	LIMK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2467291	NM_002314.4(LIMK1):c.392A>G (p.Lys131Arg)	LIMK1 (K131R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118889	NM_002314.4(LIMK1):c.433C>G (p.Pro145Ala)	LIMK1 (P111A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 723302	NM_002314.4(LIMK1):c.549C>T (p.Asp183=)	LIMK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2317493	NM_002314.4(LIMK1):c.554C>A (p.Pro185Gln)	LIMK1 (P185Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2657584	NM_002314.4(LIMK1):c.567G>A (p.Pro189=)	LIMK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 773741	NM_002314.4(LIMK1):c.569G>C (p.Gly190Ala)	LIMK1 (G156A +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2454208	NM_002314.4(LIMK1):c.595G>A (p.Val199Ile)	LIMK1 (V165I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 797183	NM_002314.4(LIMK1):c.600C>A (p.Arg200=)	LIMK1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3118890	NM_002314.4(LIMK1):c.607G>C (p.Gly203Arg)	LIMK1 (G203R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 734703	NM_002314.4(LIMK1):c.608+10C>T	LIMK1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 719018	NM_002314.4(LIMK1):c.609-6C>A	LIMK1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 727303	NM_002314.4(LIMK1):c.620G>A (p.Gly207Asp)	LIMK1 (G173D +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign

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