Variant #0000990223 (NC_000001.10:g.1447667A>G, NM_018188.3:c.19A>G (ATAD3A))

Chromosome 1
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.1447667A>G
DNA change (hg38) -
Published as ATAD3A(NM_001170535.1):c.19A>G (p.(Ile7Val))
ISCN -
DB-ID ATAD3A_000002 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) Retrieve
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-08-28 13:07:21 +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     
ATAD3A NM_018188.3 -?/. - c.19A>G r.(?) p.(Ile7Val)
ATAD3B NM_031921.4 -?/. - c.*16470A>G r.(=) p.(=)


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