Related gene-specific medical variations for Gene (Select 135) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Links from Gene

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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	ADORA2A, ADORA2A-AS1 +1 more	Single nucleotide variant (intron variant)	not provided	GLikely benign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Links from Gene

Items: 25