ClinVar for Gene (Select 646023) - ClinVar

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Items: 63

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3273467	NM_000675.6(ADORA2A):c.1033G>C (p.Val345Leu)	ADORA2A, ADORA2A-AS1 +1 more (V345L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3273456	NM_000675.6(ADORA2A):c.443A>G (p.Gln148Arg)	ADORA2A, ADORA2A-AS1 +1 more (Q148R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3273446	NM_000675.6(ADORA2A):c.1018G>A (p.Gly340Ser)	ADORA2A, ADORA2A-AS1 +1 more (G340S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3090073	NM_000675.6(ADORA2A):c.919G>A (p.Val307Ile)	ADORA2A, ADORA2A-AS1 +1 more (V307I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3090070	NM_000675.6(ADORA2A):c.911G>A (p.Arg304His)	ADORA2A, ADORA2A-AS1 +1 more (R304H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3090064	NM_000675.6(ADORA2A):c.871C>T (p.Arg291Cys)	ADORA2A, ADORA2A-AS1 +1 more (R291C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3090062	NM_000675.6(ADORA2A):c.869A>T (p.Tyr290Phe)	ADORA2A, ADORA2A-AS1 +1 more (Y290F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3090022	NM_000675.6(ADORA2A):c.1072C>T (p.Pro358Ser)	ADORA2A, ADORA2A-AS1 +1 more (P358S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2622323	NM_000675.6(ADORA2A):c.1091G>T (p.Gly364Val)	ADORA2A, ADORA2A-AS1 +1 more (G364V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2620824	NM_000675.6(ADORA2A):c.352G>A (p.Gly118Ser)	ADORA2A, ADORA2A-AS1 +1 more (G118S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2603874	NM_000675.6(ADORA2A):c.887G>A (p.Arg296His)	ADORA2A, ADORA2A-AS1 +1 more (R296H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2557710	NM_000675.6(ADORA2A):c.148G>T (p.Ala50Ser)	ADORA2A, ADORA2A-AS1 +1 more (A50S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2546609	NM_000675.6(ADORA2A):c.203C>T (p.Thr68Ile)	ADORA2A, ADORA2A-AS1 +1 more (T68I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2496108	NM_000675.6(ADORA2A):c.391C>G (p.Leu131Val)	ADORA2A, ADORA2A-AS1 +1 more (L131V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2459042	NM_000675.6(ADORA2A):c.1169T>C (p.Leu390Pro)	ADORA2A, ADORA2A-AS1 +1 more (L390P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2379112	NM_000675.6(ADORA2A):c.424G>A (p.Gly142Ser)	ADORA2A, ADORA2A-AS1 +1 more (G142S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2372318	NM_000675.6(ADORA2A):c.478G>A (p.Gly160Arg)	ADORA2A, ADORA2A-AS1 +1 more (G160R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2327114	NM_000675.6(ADORA2A):c.1036T>C (p.Trp346Arg)	ADORA2A, ADORA2A-AS1 +1 more (W346R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2286427	NM_000675.6(ADORA2A):c.751A>T (p.Ile251Phe)	ADORA2A, ADORA2A-AS1 +1 more (I251F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2280611	NM_000675.6(ADORA2A):c.23T>C (p.Val8Ala)	ADORA2A, ADORA2A-AS1 +1 more (V8A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2252860	NM_000675.6(ADORA2A):c.587T>C (p.Val196Ala)	ADORA2A, ADORA2A-AS1 +1 more (V196A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2208066	NM_000675.6(ADORA2A):c.356C>T (p.Thr119Met)	ADORA2A, ADORA2A-AS1 +1 more (T119M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 782351	NM_000675.6(ADORA2A):c.432C>T (p.Asn144=)	ADORA2A, ADORA2A-AS1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 780634	NM_000675.6(ADORA2A):c.1044C>T (p.Asn348=)	ADORA2A, ADORA2A-AS1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 774536	NM_000675.6(ADORA2A):c.885C>T (p.Phe295=)	ADORA2A, ADORA2A-AS1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 769158	NM_000675.6(ADORA2A):c.711C>A (p.Ile237=)	ADORA2A, ADORA2A-AS1 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 769157	NM_000675.6(ADORA2A):c.439G>A (p.Gly147Ser)	ADORA2A, ADORA2A-AS1 +1 more (G147S)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 758935	NM_000675.6(ADORA2A):c.332+9G>A	SPECC1L-ADORA2A, ADORA2A +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 545275	Single allele	DDT, C22orf15 +78 more	Duplication	Schizophrenia	GLikely pathogenic
Select item 545274	Single allele	LRRC75B, MIF +78 more	Duplication	Schizophrenia	GLikely pathogenic
Select item 545272	Single allele	DDTL, DERL3 +164 more	Duplication	Schizophrenia	GLikely pathogenic
Select item 160934	GRCh38/hg38 22q11.23(chr22:23377984-24563859)x3	ADORA2A, ADORA2A-AS1 +74 more	Copy number gain	See cases	GUncertain significance
Select item 160821	GRCh38/hg38 22q11.22-11.23(chr22:22669543-24563859)x3	ADORA2A, ADORA2A-AS1 +160 more	Copy number gain	See cases	GUncertain significance
Select item 155683	GRCh38/hg38 22q11.22-11.23(chr22:22655333-24647020)x3	ADORA2A, ADORA2A-AS1 +163 more	Copy number gain	See cases	GUncertain significance
Select item 155560	GRCh38/hg38 22q11.23(chr22:23348201-24647020)x3	LOC130067120, LOC130067121 +76 more	Copy number gain	See cases	GUncertain significance
Select item 155495	GRCh38/hg38 22q11.23(chr22:23310399-24643051)x3	ADORA2A, ADORA2A-AS1 +81 more	Copy number gain	See cases	GLikely benign
Select item 155476	GRCh38/hg38 22q11.22-11.23(chr22:22920775-24606692)x3	ADORA2A, ADORA2A-AS1 +124 more	Copy number gain	See cases	GUncertain significance
Select item 154068	GRCh38/hg38 22q11.22-11.23(chr22:22655333-24630890)x3	ADORA2A, ADORA2A-AS1 +163 more	Copy number gain	See cases	GUncertain significance
Select item 153611	GRCh38/hg38 22q11.22-11.23(chr22:22655333-24663664)x3	ADORA2A, ADORA2A-AS1 +163 more	Copy number gain	See cases	GUncertain significance
Select item 153399	GRCh38/hg38 22q11.23(chr22:23308686-24647020)x3	ADORA2A, ADORA2A-AS1 +81 more	Copy number gain	See cases	GUncertain significance
Select item 150614	GRCh38/hg38 22q11.23(chr22:23311976-24669609)x3	ADORA2A, ADORA2A-AS1 +80 more	Copy number gain	See cases	GUncertain significance
Select item 149196	GRCh38/hg38 22q11.22-11.23(chr22:22660239-24596054)x3	ADORA2A, ADORA2A-AS1 +163 more	Copy number gain	See cases	GUncertain significance
Select item 149114	GRCh38/hg38 22q11.23-12.3(chr22:23279231-36247369)x3	LOC130067187, LOC130067188 +556 more	Copy number gain	See cases	GPathogenic
Select item 148933	GRCh38/hg38 22q11.23(chr22:23311976-24600238)x3	LOC130067094, LOC130067095 +80 more	Copy number gain	See cases	GUncertain significance
Select item 148861	GRCh38/hg38 22q11.21-12.3(chr22:20907226-37187347)x3	ADORA2A, ADORA2A-AS1 +823 more	Copy number gain	See cases	GPathogenic
Select item 148729	GRCh38/hg38 22q11.22-11.23(chr22:22660239-24600238)x3	ADORA2A, ADORA2A-AS1 +163 more	Copy number gain	See cases	GUncertain significance
Select item 148633	GRCh38/hg38 22q11.23(chr22:23311976-24644628)x3	ADORA2A, ADORA2A-AS1 +80 more	Copy number gain	See cases	GUncertain significance
Select item 148336	GRCh38/hg38 22q11.22-11.23(chr22:22660239-24644628)x3	ADORA2A, ADORA2A-AS1 +163 more	Copy number gain	See cases	GUncertain significance
Select item 148096	GRCh38/hg38 22q11.23(chr22:23804407-24669609)x3	ADORA2A, ADORA2A-AS1 +57 more	Copy number gain	See cases	GUncertain significance
Select item 146821	GRCh38/hg38 22q11.22-11.23(chr22:22669599-24670517)x3	DRICH1, FAM230I +162 more	Copy number gain	See cases	GUncertain significance
Select item 145336	GRCh38/hg38 22q11.1-13.33(chr22:16916743-50739785)x3	LOC130067403, LOC130067404 +2088 more	Copy number gain	See cases	GPathogenic
Select item 144164	GRCh38/hg38 22q11.1-13.33(chr22:16916608-50739836)x3	IL17RA, LINC01640 +2088 more	Copy number gain	See cases	GPathogenic
Select item 59346	GRCh38/hg38 22q11.23(chr22:23414627-24563859)x3	ADORA2A, ADORA2A-AS1 +74 more	Copy number gain	See cases	GUncertain significance
Select item 59343	GRCh38/hg38 22q11.23(chr22:23369950-24669609)x3	ADORA2A, ADORA2A-AS1 +76 more	Copy number gain	See cases	GUncertain significance
Select item 59342	GRCh38/hg38 22q11.23(chr22:23354221-24541945)x3	ADORA2A, ADORA2A-AS1 +70 more	Copy number gain	See cases	GUncertain significance
Select item 59341	GRCh38/hg38 22q11.23(chr22:23338443-24577664)x3	ADORA2A, ADORA2A-AS1 +74 more	Copy number gain	See cases	GUncertain significance
Select item 59340	GRCh38/hg38 22q11.23(chr22:23338443-24610403)x3	ADORA2A, ADORA2A-AS1 +76 more	Copy number gain	See cases	GUncertain significance
Select item 59331	GRCh38/hg38 22q11.23(chr22:23285152-24723136)x3	ADORA2A, ADORA2A-AS1 +84 more	Copy number gain	See cases	GUncertain significance
Select item 59330	GRCh38/hg38 22q11.22-11.23(chr22:22703701-24669609)x3	ADORA2A, ADORA2A-AS1 +157 more	Copy number gain	See cases	GUncertain significance
Select item 59329	GRCh38/hg38 22q11.22-11.23(chr22:22686122-24577664)x3	IGLV3-22, IGLV3-25 +160 more	Copy number gain	See cases	GUncertain significance
Select item 57132	GRCh38/hg38 22q11.21-12.3(chr22:18178957-31821193)x3	ADORA2A, ADORA2A-AS1 +798 more	Copy number gain	See cases	GPathogenic
Select item 33448	GRCh38/hg38 22q11.23(chr22:23377984-24563859)x3	ADORA2A, ADORA2A-AS1 +74 more	Copy number gain	See cases	GConflicting classifications of pathogenicity
Select item 33061	GRCh38/hg38 22q11.22-11.23(chr22:22669543-24563859)x3	ADORA2A, ADORA2A-AS1 +160 more	Copy number gain	See cases	GConflicting classifications of pathogenicity

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Items: 63