Variant #0000620381 (NC_000001.10:g.1458925C>T, NM_018188.3:c.1085C>T (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.1458925C>T
DNA change (hg38) g.1523545C>T
Published as ATAD3A(NM_001170535.3):c.941C>T (p.(Ala314Val)), ATAD3A(NM_018188.5):c.1085C>T (p.A362V)
ISCN -
DB-ID ATAD3A_000040 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) 0.0004 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATAD3A NM_018188.3 ?/. - c.1085C>T r.(?) p.(Ala362Val)


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