ClinVar for Gene (Select 27197) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3282449	NM_080817.5(GPR82):c.479G>T (p.Trp160Leu)	CASK, GPR82 (W160L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3282448	NM_080817.5(GPR82):c.968T>C (p.Leu323Pro)	GPR82, CASK (L323P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3245362	NC_000023.10:g.(?_41193506)_(41646556_?)dup	CASK, DDX3X +3 more	Duplication	Intellectual disability, CASK-related, X-linked	GUncertain significance
Select item 3245351	NC_000023.10:g.(?_41437573)_(41712500_?)dup	CASK, GPR34 +1 more	Duplication	Intellectual disability, CASK-related, X-linked	GLikely pathogenic
Select item 3245339	NC_000023.10:g.(?_41495811)_(41782241_?)dup	CASK, GPR34 +1 more	Duplication	Intellectual disability, CASK-related, X-linked	GUncertain significance
Select item 3245328	NC_000023.10:g.(?_41530661)_(41646556_?)del	CASK, GPR34 +1 more	Deletion	Intellectual disability, CASK-related, X-linked	GPathogenic
Select item 3242589	GRCh38/hg38 Xp22.33-q28(chrX:2757837-156030895)x2	LOC130068417, LOC130068418 +2599 more	Copy number gain	Klinefelter syndrome	GPathogenic
Select item 3101872	NM_080817.5(GPR82):c.928C>A (p.Leu310Ile)	CASK, GPR82 (L310I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101871	NM_080817.5(GPR82):c.876C>G (p.Asn292Lys)	CASK, GPR82 (N292K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101870	NM_080817.5(GPR82):c.691A>G (p.Ile231Val)	CASK, GPR82 (I231V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101869	NM_080817.5(GPR82):c.602T>C (p.Ile201Thr)	CASK, GPR82 (I201T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3101868	NM_080817.5(GPR82):c.517T>C (p.Tyr173His)	CASK, GPR82 (Y173H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101867	NM_080817.5(GPR82):c.443A>G (p.Gln148Arg)	CASK, GPR82 (Q148R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3062511	GRCh37/hg19 Xp22.33-11.1(chrX:168546-58364114)	ACE2, ACOT9 +314 more	Copy number loss	not specified	GPathogenic
Select item 3062502	GRCh37/hg19 Xp11.4(chrX:41483585-41636324)	CASK, GPR34 +1 more	Copy number loss	not specified	GUncertain significance
Select item 3062471	GRCh37/hg19 Xp22.33-11.21(chrX:168546-55653170)	ACE2, ACOT9 +305 more	Copy number loss	not specified	GPathogenic
Select item 2685708	GRCh37/hg19 Xp21.1-11.22(chrX:36355238-54106257)x1	CCDC22, CFP +155 more	Copy number loss	not provided	GPathogenic
Select item 2685701	GRCh37/hg19 Xp22.11-11.3(chrX:24633854-44236178)x1	XK, ARX +51 more	Copy number loss	not provided	GPathogenic
Select item 2685690	GRCh37/hg19 Xp22.33-11.22(chrX:2696762-53113314)x1	HDAC6, RGN +275 more	Copy number loss	not provided	GPathogenic
Select item 2660355	NM_001367721.1(CASK):c.429+11848A>G	CASK, GPR82	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2601026	NM_080817.5(GPR82):c.59T>C (p.Ile20Thr)	CASK, GPR82 (I20T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2579274	GRCh38/hg38 Xp11.4(chrX:41333187-42099271)x1	CASK, CASK-AS1 +20 more	Copy number loss	Syndromic X-linked intellectual disability Najm type +1 more	GPathogenic
Select item 2547308	NM_080817.5(GPR82):c.860T>C (p.Leu287Ser)	CASK, GPR82 (L287S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2506546	GRCh37/hg19 Xp22.33-q28(chrX:200855-155240074)	ABCB7, ABCD1 +818 more	Copy number gain	Klinefelter syndrome	GPathogenic
Select item 2423950	NC_000023.10:g.(?_39911362)_(41782241_?)del	ATP6AP2, BCOR +9 more	Deletion	Syndromic X-linked intellectual disability Hedera type	GUncertain significance
Select item 2423949	NC_000023.10:g.(?_39911362)_(41782241_?)dup	ATP6AP2, BCOR +9 more	Duplication	not provided	GUncertain significance
Select item 2423545	NC_000023.10:g.(?_40440318)_(41782241_?)dup	ATP6AP2, CASK +8 more	Duplication	not provided	GUncertain significance
Select item 2355677	NM_080817.5(GPR82):c.614T>C (p.Ile205Thr)	CASK, GPR82 (I205T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2337875	NM_080817.5(GPR82):c.397T>C (p.Cys133Arg)	CASK, GPR82 (C133R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314126	NM_080817.5(GPR82):c.100A>T (p.Thr34Ser)	CASK, GPR82 (T34S)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2251719	NM_080817.5(GPR82):c.949A>C (p.Lys317Gln)	CASK, GPR82 (K317Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1808692	GRCh37/hg19 Xp11.4-11.3(chrX:41350855-44616591)x0	CASK, EFHC2 +6 more	Copy number loss	not provided	GPathogenic
Select item 1808658	GRCh37/hg19 Xp11.4-11.22(chrX:39525562-52832596)x3	AKAP4, ARAF +126 more	Copy number gain	not provided	GPathogenic
Select item 1707442	GRCh37/hg19 Xp22.2-q28(chrX:11522765-155233731)x1	ABCB7, ABCD1 +790 more	Copy number loss	See cases	GPathogenic
Select item 1704345	GRCh37/hg19 Xp22.33-q28(chrX:61545-155226048)x2	ABCB7, ABCD1 +818 more	Copy number gain	Klinefelter syndrome	GPathogenic
Select item 1703583	GRCh37/hg19 Xp22.33-11.21(chrX:168546-57841304)	ACE2, ACOT9 +315 more	Copy number loss	Turner syndrome	GPathogenic
Select item 1703582	Single allele	ADGRG2, ACE2 +309 more	Complex	Turner syndrome	GPathogenic
Select item 1703581	GRCh37/hg19 Xp22.33-11.22(chrX:168546-52573789)	ACE2, ACOT9 +267 more	Copy number loss	Turner syndrome	GPathogenic
Select item 1703580	GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)	ABCB7, ABCD1 +819 more	Copy number loss	Turner syndrome	GPathogenic
Select item 1703579	GRCh37/hg19 Xp22.33-q28(chrX:1-155270560)	AKAP14, CT47A11 +819 more	Copy number gain	Hypotonia +2 more	GPathogenic
Select item 1676159	NM_080817.5(GPR82):c.399C>T (p.Cys133=)	CASK, GPR82	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 1341233	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	RADX, RAI2 +818 more	Copy number loss	not provided	GPathogenic
Select item 1341223	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x3	GPM6B, KLHL15 +818 more	Copy number gain	not provided	GPathogenic
Select item 1180551	GRCh37/hg19 Xp22.33-q28(chrX:60000-155234966)x1	KLHL34, KLHL4 +818 more	Copy number loss	not provided	GPathogenic
Select item 1047884	GRCh37/hg19 Xp11.4(chrX:41553564-41696352)	CASK, GPR34 +1 more	Copy number loss	Neurodevelopmental delay +1 more	GPathogenic
Select item 1047883	GRCh37/hg19 Xp11.4-11.3(chrX:39645568-44199000)	MPC1L, GPR82 +13 more	Copy number loss	Motor delay +2 more	GPathogenic
Select item 1047878	GRCh37/hg19 Xp11.4-11.3(chrX:41342834-43901936)	CASK, GPR34 +4 more	Copy number loss	Global developmental delay +1 more	GPathogenic
Select item 992647	GRCh37/hg19 Xp22.33-11.21(chrX:168546-56457794)x1	ACE2, ACOT9 +309 more	Copy number loss	not provided	GPathogenic
Select item 983193	GRCh37/hg19 Xp22.33-11.21(chrX:219609-55466476)x1	ACE2, ACOT9 +304 more	Copy number loss	See cases	GPathogenic
Select item 832451	NC_000023.11:g.(?_41520400)_(41923008_?)del	CASK, GPR34 +1 more	Deletion	Intellectual disability, CASK-related, X-linked	GPathogenic
Select item 816337	GRCh37/hg19 Xp21.1-11.3(chrX:32849282-43713387)x1	ATP6AP2, BCOR +32 more	Copy number loss	not provided	GPathogenic
Select item 816270	GRCh37/hg19 Xp22.33-11.21(chrX:539722-55509385)x1	ACE2, ACOT9 +305 more	Copy number loss	not provided	GPathogenic
Select item 813719	GRCh37/hg19 Xp11.4-11.3(chrX:41150139-43976458)	MAOB, DDX3X +6 more	Copy number loss	Microcephaly	GPathogenic
Select item 694513	46,Y,inv(X)(p21.1q13.3)	ABCB7, AKAP4 +268 more	Inversion	Elevated circulating creatine kinase concentration	GLikely pathogenic
Select item 688137	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1	ARHGAP36, ARHGAP4 +818 more	Copy number loss	not provided	GPathogenic
Select item 685565	GRCh37/hg19 Xp22.33-q11.1(chrX:168546-61877279)x1	RBBP7, RBM10 +316 more	Copy number loss	not provided	GPathogenic
Select item 685331	GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x4	BEX1, BEX2 +818 more	Copy number gain	not provided	GPathogenic
Select item 684962	GRCh37/hg19 Xp11.4-q21.32(chrX:40572613-92796528)x1	ABCB7, AKAP4 +281 more	Copy number loss	not provided	GPathogenic
Select item 638115	GRCh37/hg19 Xp22.33-11.22(chrX:60814-50519984)x1	ACE2, ACOT9 +257 more	Copy number loss	See cases	GPathogenic
Select item 635934	Single allele	SUPT20HL2, SYAP1 +177 more	Deletion	Neurodevelopmental disorder	GPathogenic
Select item 626291	Single allele	AKAP14, CCDC22 +733 more	Duplication	Syndromic X-linked intellectual disability Lubs type	GPathogenic
Select item 564772	GRCh37/hg19 Xp22.31-q21.31(chrX:7841947-90815333)x1,2	RPS6KA6, UPRT +413 more	Copy number gain	not provided	GPathogenic
Select item 564696	GRCh37/hg19 Xp22.33-11.23(chrX:168546-46908284)x1	ACE2, ACOT9 +170 more	Copy number loss	not provided	GPathogenic
Select item 564695	GRCh37/hg19 Xp22.33-11.3(chrX:168546-43248706)x1	ACE2, ACOT9 +154 more	Copy number loss	not provided	GPathogenic
Select item 545551	NC_000023.10:g.36649710_136649711del100000002insG	AMER1, AMMECR1 +541 more	Indel	Heterotaxy, visceral, 1, X-linked	GPathogenic
Select item 533692	NC_000023.10:g.(?_39911342)_(41782261_?)dup	ATP6AP2, BCOR +9 more	Duplication	Syndromic X-linked intellectual disability Hedera type +1 more	GUncertain significance
Select item 488014	Single allele	ARSF, CFAP47 +2632 more	Duplication	Autism +1 more	GPathogenic
Select item 445537	NM_080817.5(GPR82):c.678C>A (p.Ser226Arg)	CASK, GPR82 (S226R)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 443974	GRCh37/hg19 Xp22.33-q28(chrX:168547-155233731)	ABCB7, ABCD1 +818 more	Copy number gain	See cases	GPathogenic
Select item 443946	GRCh37/hg19 Xp22.33-q23(chrX:168547-112474026)x1	EIF1AX, EIF2S3 +539 more	Copy number loss	See cases	GPathogenic
Select item 443504	GRCh37/hg19 Xp21.2-q28(chrX:31088082-155233731)x1	PNMA5, PNMA6A +695 more	Copy number loss	See cases	GPathogenic
Select item 443322	GRCh37/hg19 Xp22.33-11.1(chrX:168546-58527164)x1	ACE2, ACOT9 +314 more	Copy number loss	See cases	GPathogenic
Select item 443028	GRCh37/hg19 Xp22.33-11.21(chrX:168546-54996659)x1	SYN1, SYP +294 more	Copy number loss	See cases	GPathogenic
Select item 442832	GRCh37/hg19 Xp21.1-q22.1(chrX:37521774-98488534)x1	ABCB7, AKAP4 +300 more	Copy number loss	See cases	GPathogenic
Select item 442724	GRCh37/hg19 Xp22.33-q28(chrX:168547-151304063)x1	AP1S2, APEX2 +731 more	Copy number loss	See cases	GPathogenic
Select item 442354	GRCh37/hg19 Xp22.33-q13.3(chrX:168546-74549686)	ABCB7, ACE2 +390 more	Copy number loss	See cases	GPathogenic
Select item 442224	GRCh37/hg19 Xp11.4-11.23(chrX:41150139-46528262)x1	CASK, CHST7 +17 more	Copy number loss	See cases	GPathogenic
Select item 442162	GRCh37/hg19 Xp22.33-11.21(chrX:168546-55240087)x1	AP1S2, APEX2 +300 more	Copy number loss	See cases	GPathogenic
Select item 442067	GRCh37/hg19 Xp22.33-11.21(chrX:168546-57504183)x1	ARSF, XAGE2 +312 more	Copy number loss	See cases	GPathogenic
Select item 441968	GRCh37/hg19 Xp22.33-11.21(chrX:168564-57413442)x1	AP1S2, APEX2 +312 more	Copy number loss	See cases	GPathogenic
Select item 441856	GRCh37/hg19 Xp22.33-11.21(chrX:168546-57683964)x1	WDR45, WNK3 +313 more	Copy number loss	See cases	GPathogenic
Select item 425520	GRCh37/hg19 Xp22.2-q25(chrX:11692290-121187337)x2	BEX4, BEX5 +566 more	Copy number gain	not provided	GUncertain significance
Select item 395718	GRCh37/hg19 Xp22.33-q28(chrX:70297-155246585)x1	TMLHE, TMSB15A +819 more	Copy number loss	See cases	GPathogenic
Select item 395687	GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792)	ABCB7, ABCD1 +819 more	Copy number loss	See cases	GPathogenic
Select item 395686	GRCh37/hg19 Xp22.33-q28(chrX:70297-155255792)x4	BEX1, BEX2 +819 more	Copy number gain	See cases	GPathogenic
Select item 395011	GRCh37/hg19 Xp11.4-11.3(chrX:40933552-45379179)x2	CASK, DDX3X +12 more	Copy number gain	See cases	GLikely pathogenic
Select item 394706	GRCh37/hg19 Xp22.33-q28(chrX:60701-155246225)x3	ABCB7, ABCD1 +819 more	Copy number gain	See cases	GPathogenic
Select item 394672	GRCh37/hg19 Xp22.33-q28(chrX:318707-155224707)x1	ABCB7, ADGRG2 +818 more	Copy number loss	See cases	GPathogenic
Select item 394013	GRCh37/hg19 Xp22.33-q28(chrX:71267-155255792)x1	ABCB7, ABCD1 +819 more	Copy number loss	See cases	GPathogenic
Select item 377016	NM_080817.5(GPR82):c.554G>A (p.Ser185Asn)	CASK, GPR82 (S185N)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 253652	GRCh37/hg19 Xp22.33-q28(chrX:71267-155246643)x3	ABCB7, ABCD1 +819 more	Copy number gain	See cases	GPathogenic
Select item 253624	GRCh37/hg19 Xp22.33-q28(chrX:60701-155246271)x3	TMEM255A, TMEM31 +819 more	Copy number gain	See cases	GPathogenic
Select item 253615	GRCh37/hg19 Xp22.33-11.21(chrX:70297-58066465)x3	ACE2, ACOT9 +316 more	Copy number gain	See cases	GPathogenic
Select item 253613	GRCh37/hg19 Xp22.2-q28(chrX:13147668-155250222)x3	ABCB7, ABCD1 +783 more	Copy number gain	See cases	GPathogenic
Select item 253602	GRCh37/hg19 Xp22.33-q28(chrX:176426-155236656)x3	ABCB7, ABCD1 +818 more	Copy number gain	See cases	GPathogenic
Select item 253583	GRCh37/hg19 Xp22.33-q28(chrX:225816-155234036)x2	PNMA3, PLP1 +818 more	Copy number gain	See cases	GPathogenic
Select item 253571	GRCh37/hg19 Xp22.33-11.21(chrX:70297-58066465)x1	ACE2, ACOT9 +316 more	Copy number loss	See cases	GPathogenic
Select item 253495	GRCh37/hg19 Xp22.33-q28(chrX:71267-155224766)x1	MAGEB4, MAGEB5 +818 more	Copy number loss	See cases	GPathogenic
Select item 253492	GRCh37/hg19 Xp22.33-q28(chrX:71267-155255839)x1	ABCB7, ABCD1 +819 more	Copy number loss	See cases	GPathogenic
Select item 253487	GRCh37/hg19 Xp22.33-q28(chrX:2707626-155250222)x2	RPS6KA3, RPS6KA6 +819 more	Copy number gain	See cases	GPathogenic

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