Variant #0000946956 (NC_000001.10:g.1374762G>A, NM_022834.4:c.933G>A (VWA1))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.1374762G>A
DNA change (hg38) -
Published as VWA1(NM_022834.5):c.933G>A (p.S311=)
ISCN -
DB-ID ATAD3C_000005
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) 0.00122 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-11-27 17:35:39 +01:00 (CET)
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.-11302G>A r.(?) p.(=)
VWA1 NM_022834.4 -/. - c.933G>A r.(?) p.(=)


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