Variant #0001031232 (NC_000001.10:g.1469412C>G, NM_018188.3:c.1865C>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.1469412C>G
DNA change (hg38) -
Published as ATAD3A(NM_001170535.3):c.1721C>G (p.(Ala574Gly))
ISCN -
DB-ID ATAD3A_000117
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) 4.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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     
TMEM240 NM_001114748.1 ?/. - c.*1327G>C r.(=) p.(=)
ATAD3A NM_001170535.3 ?/. - c.1721C>G r.(?) p.(Ala574Gly)
ATAD3A NM_018188.3 ?/. - c.1865C>G r.(?) p.(Ala622Gly)


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