Variant #0000951553 (NC_000022.10:g.24717548A>T, NR_103546.1:n.908A>T (SPECC1L-ADORA2A))

Chromosome 22
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.24717548A>T
DNA change (hg38) -
Published as SPECC1L(NM_001145468.2):c.600A>T (p.(Leu200Phe))
ISCN -
DB-ID SPECC1L-ADORA2A_000013
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) 0.01045 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPECC1L-ADORA2A NR_103546.1 -?/. - n.908A>T r.(?) -


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