Variant #0000618166 (NC_000020.10:g.43249693T>C, NM_000022.2:c.941A>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.43249693T>C
DNA change (hg38) g.44621052T>C
Published as ADA(NM_000022.2):c.941A>G (p.D314G)
ISCN -
DB-ID ADA_000048
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) 8.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +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     
ADA NM_000022.2 -?/. - c.941A>G r.(?) p.(Asp314Gly)
PKIG NM_007066.3 -?/. - c.*2688T>C r.(=) p.(=)


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