CDK11A[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2664871	GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3	A2ML1-AS2, A3GALT2 +2151 more	Copy number gain	Trisomy 12p	GPathogenic
Select item 58242	GRCh38/hg38 1p36.33-36.23(chr1:629025-8537745)x1	LOC121967050, LOC121967051 +520 more	Copy number loss	See cases	GPathogenic
Select item 58244	GRCh38/hg38 1p36.33-36.31(chr1:629044-7008678)x1	LOC129929262, LOC129929263 +458 more	Copy number loss	See cases	GPathogenic
Select item 58243	GRCh38/hg38 1p36.33-36.32(chr1:629044-3346226)x1	LOC129929093, LOC129929110 +282 more	Copy number loss	See cases	GPathogenic
Select item 151451	GRCh38/hg38 1p36.33-36.32(chr1:778698-4898439)x1	ACAP3, ACTRT2 +336 more	Copy number loss	See cases	GPathogenic
Select item 58036	GRCh38/hg38 1p36.33-36.32(chr1:792758-5006311)x3	LINC01786, LINC02593 +338 more	Copy number gain	See cases	GPathogenic
Select item 1684638	Single allele	TMEM240, TMEM88B +181 more	Deletion	Chromosome 1p36 deletion syndrome	GPathogenic
Select item 152849	GRCh38/hg38 1p36.33-36.32(chr1:821713-4225085)x1	LOC129929191, LOC129929192 +325 more	Copy number loss	See cases	GPathogenic
Select item 152807	GRCh38/hg38 1p36.33-36.32(chr1:821713-5099990)x1	ACAP3, ACTRT2 +337 more	Copy number loss	See cases	GPathogenic
Select item 152695	GRCh38/hg38 1p36.33-36.32(chr1:821713-2976123)x1	ACAP3, AGRN +254 more	Copy number loss	See cases	GPathogenic
Select item 152675	GRCh38/hg38 1p36.33-36.32(chr1:821713-2636393)x1	LOC129929104, LOC129929105 +249 more	Copy number loss	See cases	GPathogenic
Select item 152050	GRCh38/hg38 1p36.33-36.31(chr1:821713-5480263)x1	VWA1, WRAP73 +341 more	Copy number loss	See cases	GPathogenic
Select item 151110	GRCh38/hg38 1p36.33-36.32(chr1:821713-2554047)x1	ACAP3, AGRN +243 more	Copy number loss	See cases	GPathogenic
Select item 150995	GRCh38/hg38 1p36.33-36.32(chr1:821713-3438208)x1	ACAP3, ACTRT2 +275 more	Copy number loss	See cases	GPathogenic
Select item 149968	GRCh38/hg38 1p36.33-36.31(chr1:821713-7000838)x1	CEP104, CFAP74 +449 more	Copy number loss	See cases	GPathogenic
Select item 149171	GRCh38/hg38 1p36.33-36.32(chr1:821713-3569891)x1	ACAP3, ACTRT2 +284 more	Copy number loss	See cases	GPathogenic
Select item 149107	GRCh38/hg38 1p36.33-36.32(chr1:821713-3928354)x3	LOC129929084, LOC129929085 +320 more	Copy number gain	See cases	GLikely pathogenic
Select item 148916	GRCh38/hg38 1p36.33-36.32(chr1:821713-5239643)x1	ACAP3, ACTRT2 +337 more	Copy number loss	See cases	GPathogenic
Select item 148829	GRCh38/hg38 1p36.33-36.32(chr1:821713-2463016)x4	ACAP3, AGRN +238 more	Copy number gain	See cases	GUncertain significance
Select item 148825	GRCh38/hg38 1p36.33-36.32(chr1:821713-2463016)x1	ACAP3, AGRN +238 more	Copy number loss	See cases	GPathogenic
Select item 58245	GRCh38/hg38 1p36.33-36.32(chr1:821713-4155674)x1	ACAP3, ACTRT2 +325 more	Copy number loss	See cases	GPathogenic
Select item 58037	GRCh38/hg38 1p36.33-36.32(chr1:826553-4719105)x3	ACAP3, ACTRT2 +332 more	Copy number gain	See cases	GPathogenic
Select item 160923	GRCh38/hg38 1p36.33-36.32(chr1:844347-2627474)x1	ACAP3, AGRN +244 more	Copy number loss	See cases	GPathogenic
Select item 154642	GRCh38/hg38 1p36.33-36.23(chr1:844347-7870545)x1	PUSL1, RER1 +470 more	Copy number loss	See cases	GPathogenic
Select item 147521	GRCh38/hg38 1p36.33-36.22(chr1:844347-12470133)x1	ACAP3, ACOT7 +806 more	Copy number loss	See cases	GPathogenic
Select item 147354	GRCh38/hg38 1p36.33-36.23(chr1:844347-8171914)x1	LOC129929192, LOC129929193 +490 more	Copy number loss	See cases	GPathogenic
Select item 144707	GRCh38/hg38 1p36.33-36.32(chr1:844347-4398122)x1	ACAP3, ACTRT2 +325 more	Copy number loss	See cases	GPathogenic
Select item 144461	GRCh38/hg38 1p36.33-36.31(chr1:844347-6916587)x1	ACAP3, ACOT7 +441 more	Copy number loss	See cases	GPathogenic
Select item 58292	GRCh38/hg38 1p36.33(chr1:844347-2131805)x1	ACAP3, AGRN +205 more	Copy number loss	See cases	GPathogenic
Select item 58289	GRCh38/hg38 1p36.33-36.32(chr1:844347-4665295)x1	ACAP3, ACTRT2 +329 more	Copy number loss	See cases	GPathogenic
Select item 57440	GRCh38/hg38 1p36.33-36.31(chr1:844347-6477436)x1	ACAP3, ACOT7 +401 more	Copy number loss	See cases	GPathogenic
Select item 57218	GRCh38/hg38 1p36.33-36.32(chr1:844347-3712147)x1	ACAP3, ACTRT2 +292 more	Copy number loss	See cases	GPathogenic
Select item 57201	GRCh38/hg38 1p36.33-36.32(chr1:844347-3006252)x1	LOC129929161, LOC129929162 +252 more	Copy number loss	See cases	GPathogenic
Select item 57120	GRCh38/hg38 1p36.33-36.32(chr1:844347-2627474)x1	LOC129929114, LOC129929115 +244 more	Copy number loss	See cases	GPathogenic
Select item 57052	GRCh38/hg38 1p36.33-36.32(chr1:844347-3319395)x1	ACAP3, ACTRT2 +270 more	Copy number loss	See cases	GPathogenic
Select item 57049	GRCh38/hg38 1p36.33-36.31(chr1:844347-5682587)x1	LINC01786, LINC02593 +339 more	Copy number loss	See cases	GPathogenic
Select item 150566	GRCh38/hg38 1p36.33-36.31(chr1:844353-6477474)x1	LOC129929237, LOC129929238 +401 more	Copy number loss	See cases	GPathogenic
Select item 149739	GRCh38/hg38 1p36.33-36.32(chr1:844353-3153909)x1	ACAP3, ACTRT2 +260 more	Copy number loss	See cases	GPathogenic
Select item 145360	GRCh38/hg38 1p36.33-36.31(chr1:844353-5827192)x3	ACAP3, ACTRT2 +341 more	Copy number gain	See cases	GPathogenic
Select item 145356	GRCh38/hg38 1p36.33-36.32(chr1:844353-3487877)x1	ACAP3, ACTRT2 +274 more	Copy number loss	See cases	GPathogenic
Select item 144576	GRCh38/hg38 1p36.33-36.32(chr1:844353-2420916)x1	ACAP3, AGRN +234 more	Copy number loss	See cases	GPathogenic
Select item 58293	GRCh38/hg38 1p36.33-36.32(chr1:845437-2523513)x1	ACAP3, AGRN +237 more	Copy number loss	See cases	GPathogenic
Select item 58294	GRCh38/hg38 1p36.33-36.23(chr1:859215-8747647)x1	ACAP3, ACOT7 +519 more	Copy number loss	See cases	GPathogenic
Select item 58311	GRCh38/hg38 1p36.33-36.32(chr1:870177-4426613)x1	ACAP3, ACTRT2 +325 more	Copy number loss	See cases	GPathogenic
Select item 58316	GRCh38/hg38 1p36.33-36.32(chr1:872305-2642603)x1	ACAP3, AGRN +246 more	Copy number loss	See cases	GPathogenic
Select item 58315	GRCh38/hg38 1p36.33-36.32(chr1:872305-2642603)x3	ACAP3, AGRN +246 more	Copy number gain	See cases	GPathogenic
Select item 58314	GRCh38/hg38 1p36.33-36.32(chr1:872305-4133409)x1	ACAP3, ACTRT2 +320 more	Copy number loss	See cases	GPathogenic
Select item 58313	GRCh38/hg38 1p36.33-36.32(chr1:872305-3054463)x1	LOC126805582, LOC129388419 +253 more	Copy number loss	See cases	GPathogenic
Select item 58312	GRCh38/hg38 1p36.33(chr1:872305-2047715)x1	ACAP3, AGRN +198 more	Copy number loss	See cases	GPathogenic
Select item 147545	GRCh38/hg38 1p36.33-36.32(chr1:874379-4973261)x1	ACAP3, ACTRT2 +328 more	Copy number loss	See cases	GPathogenic
Select item 154584	GRCh38/hg38 1p36.33-36.23(chr1:898721-7811306)x1	LOC129929075, LOC129929076 +464 more	Copy number loss	See cases	GPathogenic
Select item 153078	GRCh38/hg38 1p36.33-36.22(chr1:902111-9556305)x1	ACAP3, ACOT7 +578 more	Copy number loss	See cases	GPathogenic
Select item 154687	GRCh38/hg38 1p36.33-36.32(chr1:911300-2963389)x1	ACAP3, AGRN +247 more	Copy number loss	See cases	GPathogenic
Select item 154548	GRCh38/hg38 1p36.33-36.22(chr1:911300-9329925)x1	LRRC47, MEGF6 +564 more	Copy number loss	See cases	GPathogenic
Select item 144176	GRCh38/hg38 1p36.33-36.32(chr1:911300-3614487)x3	ACAP3, ACTRT2 +277 more	Copy number gain	See cases	GPathogenic
Select item 153663	GRCh38/hg38 1p36.33-36.22(chr1:914086-9567122)x1	LOC129929302, LOC129929303 +577 more	Copy number loss	See cases	GPathogenic
Select item 153195	GRCh38/hg38 1p36.33-36.32(chr1:914086-3587042)x1	ACAP3, ACTRT2 +277 more	Copy number loss	See cases	GPathogenic
Select item 152333	GRCh38/hg38 1p36.33-36.32(chr1:914086-3305463)x1	ACAP3, ACTRT2 +264 more	Copy number loss	See cases	GPathogenic
Select item 152331	GRCh38/hg38 1p36.33-36.32(chr1:914086-2465738)x1	LOC129929169, LOC129929170 +231 more	Copy number loss	See cases	GPathogenic
Select item 145604	GRCh38/hg38 1p36.33(chr1:932163-1792271)x4	ACAP3, AGRN +168 more	Copy number gain	See cases	GLikely benign
Select item 144721	GRCh38/hg38 1p36.33(chr1:1013081-1722599)x1	ACAP3, AGRN +137 more	Copy number loss	See cases	GPathogenic
Select item 148305	GRCh38/hg38 1p36.33-36.32(chr1:1022094-4665295)x1	ACAP3, ACTRT2 +301 more	Copy number loss	See cases	GPathogenic
Select item 149947	GRCh38/hg38 1p36.33-36.32(chr1:1072906-2806838)x1	ACAP3, ANKRD65 +209 more	Copy number loss	See cases	GPathogenic
Select item 144807	GRCh38/hg38 1p36.33-36.32(chr1:1118636-4179080)x1	ACAP3, ACTRT2 +273 more	Copy number loss	See cases	GPathogenic
Select item 58318	GRCh38/hg38 1p36.33-36.31(chr1:1181847-5507243)x1	ACAP3, ACTRT2 +273 more	Copy number loss	See cases	GPathogenic
Select item 150863	GRCh38/hg38 1p36.33-36.32(chr1:1330915-3743546)x3	LOC129929178, LOC129929179 +195 more	Copy number gain	See cases	GUncertain significance
Select item 58319	GRCh38/hg38 1p36.33-36.32(chr1:1482278-3152536)x1	ACTRT2, ATAD3A +125 more	Copy number loss	See cases	GPathogenic
Select item 154682	GRCh38/hg38 1p36.33-36.32(chr1:1515661-2349832)x3	ATAD3A, CALML6 +84 more	Copy number gain	See cases	GUncertain significance
Select item 156723	NM_001110781.2(SLC35E2B):c.-40384_-148+4347del	SLC35E2A, SLC35E2B +4 more	Deletion	Large for gestational age	Gnot provided
Select item 156724	NM_182838.2(SLC35E2):c.733-162_*35907del	CDK11A, LOC129929146 +1 more	Deletion	Normal pregnancy	Gnot provided
Select item 3265407	NM_024011.4(CDK11A):c.2054T>C (p.Met685Thr)	CDK11A (M675T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2638052	NM_024011.4(CDK11A):c.2049C>T (p.Asp683=)	CDK11A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2638053	NM_024011.4(CDK11A):c.2047G>A (p.Asp683Asn)	CDK11A (D673N +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3141462	NM_024011.4(CDK11A):c.2046C>G (p.Phe682Leu)	CDK11A (F682L +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141461	NM_024011.4(CDK11A):c.2021G>C (p.Gly674Ala)	CDK11A (G673A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469375	NM_024011.4(CDK11A):c.2015G>A (p.Arg672His)	CDK11A (R675H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141459	NM_024011.4(CDK11A):c.2014C>T (p.Arg672Cys)	CDK11A (R675C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141458	NM_024011.4(CDK11A):c.2008C>T (p.Arg670Cys)	CDK11A (R669C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1810316	NM_024011.4(CDK11A):c.1927del (p.Ser643fs)	CDK11A (S633fs +3 more)	Deletion (frameshift variant +1 more)	not provided	Gnot provided
Select item 3141457	NM_024011.4(CDK11A):c.1853C>T (p.Thr618Ile)	CDK11A (T621I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3265410	NM_024011.4(CDK11A):c.1829G>C (p.Gly610Ala)	CDK11A (G600A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141456	NM_024011.4(CDK11A):c.1818G>C (p.Met606Ile)	CDK11A (M605I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337185	NM_024011.4(CDK11A):c.1771C>G (p.Pro591Ala)	CDK11A (P594A +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2251824	NM_024011.4(CDK11A):c.1768G>A (p.Ala590Thr)	CDK11A (A580T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2554715	NM_024011.4(CDK11A):c.1765C>T (p.Arg589Cys)	CDK11A (R588C +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2638054	NM_024011.4(CDK11A):c.1757A>T (p.Gln586Leu)	CDK11A (Q576L +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3265405	NM_024011.4(CDK11A):c.1739C>G (p.Thr580Ser)	CDK11A (T580S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2227540	NM_024011.4(CDK11A):c.1721C>A (p.Ser574Tyr)	CDK11A (S574Y +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2524988	NM_024011.4(CDK11A):c.1709G>A (p.Arg570Gln)	CDK11A (R569Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2468748	NM_024011.4(CDK11A):c.1700G>A (p.Gly567Glu)	CDK11A (G557E +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2638055	NM_024011.4(CDK11A):c.1698T>C (p.Phe566=)	CDK11A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2638056	NM_024011.4(CDK11A):c.1695T>C (p.Asp565=)	CDK11A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2638057	NM_024011.4(CDK11A):c.1671C>T (p.His557=)	CDK11A	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2479151	NM_024011.4(CDK11A):c.1637G>A (p.Arg546His)	CDK11A (R536H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206824	NM_024011.4(CDK11A):c.1618G>A (p.Asp540Asn)	CDK11A (D543N +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141454	NM_024011.4(CDK11A):c.1518C>A (p.His506Gln)	CDK11A (H496Q +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520986	NM_024011.4(CDK11A):c.1471G>A (p.Gly491Ser)	CDK11A (G481S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374706	NM_024011.4(CDK11A):c.1463T>C (p.Ile488Thr)	CDK11A (I488T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406348	NM_024011.4(CDK11A):c.1453G>A (p.Val485Ile)	CDK11A (V484I +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141453	NM_024011.4(CDK11A):c.1433A>G (p.Gln478Arg)	CDK11A (Q468R +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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