Variant #0001031166 (NC_000001.10:g.1403801A>C, NM_031921.4:c.-3464A>C (ATAD3B))

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.1403801A>C
DNA change (hg38) -
Published as ATAD3C(NM_001039211.3):c.1127A>C (p.(Glu376Ala))
ISCN -
DB-ID ATAD3B_000041
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) 1.0E-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     
ATAD3C NM_001039211.2 ?/. - c.1127A>C r.(?) p.(Glu376Ala)
VWA1 NM_022834.4 ?/. - c.*28634A>C r.(=) p.(=)
ATAD3B NM_031921.4 ?/. - c.-3464A>C r.(?) p.(=)


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