Variant #0000320438 (NC_000001.10:g.1447667A>G, NM_018188.3:c.19A>G (ATAD3A))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.1447667A>G
DNA change (hg38) g.1512287A>G
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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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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