Variant #0000990239 (NC_000001.10:g.1460671C>T, NM_018188.3:c.1410C>T (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.1460671C>T
DNA change (hg38) -
Published as ATAD3A(NM_001170535.3):c.1266C>T (p.T422=)
ISCN -
DB-ID ATAD3A_000105
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) 0.00048 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATAD3A NM_001170535.3 -?/. - c.1266C>T r.(?) p.(Thr422=)
ATAD3A NM_018188.3 -?/. - c.1410C>T r.(?) p.(=)


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