Variant #0000983806 (NC_000020.10:g.43249649A>C, NC_000020.10(NM_000022.2):c.975+10T>G (ADA))

Chromosome 20
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.43249649A>C
DNA change (hg38) -
Published as ADA(NM_000022.2):c.975+10T>G, ADA(NM_000022.4):c.975+10T>G
ISCN -
DB-ID ADA_000047 See all 2 reported entries
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) 1.0E-5 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 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ADA NM_000022.2 -?/. - c.975+10T>G r.(=) p.(=)
PKIG NM_007066.3 -?/. - c.*2644A>C r.(=) p.(=)


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