Variant #0000258979 (NC_000022.10:g.24837301T>C, NR_103546.1:n.5262T>C (SPECC1L-ADORA2A))

Chromosome 22
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.24837301T>C
DNA change (hg38) g.24441333T>C
Published as ADORA2A(NM_001278497.2):c.1083T>C (p.Y361=), ADORA2A-AS1(NR_028484.3):n.833+659A>G, SPECC1L-ADORA2A(NR_103546.1):n.5262T>C
ISCN -
DB-ID ADORA2A_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.54408 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADORA2A NM_000675.4 -/. - c.1083T>C r.(?) p.(Tyr361=)
ADORA2A-AS1 NR_028483.1 -/. - n.1011+659A>G r.(?) -
SPECC1L-ADORA2A NR_103546.1 -/. - n.5262T>C r.(?) -


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