Variant #0000248747 (NC_000022.10:g.24717850A>G, NR_103546.1:n.1210= (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.24717850A>G
DNA change (hg38) g.24321882=
Published as SPECC1L(NM_015330.6):c.902A>G (p.D301G), SPECC1L-ADORA2A(NR_103546.1):n.1210A>G
ISCN -
DB-ID SPECC1L_000009
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) 0.99995 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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPECC1L NM_015330.3 -/. - c.902A>G r.(?) p.(Asp301Gly)
SPECC1L-ADORA2A NR_103546.1 -/. - n.1210= r.(=) -


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