Variant #0000502919 (NC_000001.10:g.1407281G>A, NM_031921.4:c.17G>A (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.1407281G>A
DNA change (hg38) g.1471901G>A
Published as ATAD3B(NM_031921.5):c.17G>A (p.G6D)
ISCN -
DB-ID ATAD3B_000008
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) 0.00021 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATAD3C NM_001039211.2 ?/. - c.*3371G>A r.(=) p.(=)
VWA1 NM_022834.4 ?/. - c.*32114G>A r.(=) p.(=)
ATAD3B NM_031921.4 ?/. - c.17G>A r.(?) p.(Gly6Asp)


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