Variant #0000882745 (NC_000001.10:g.1375124_1375130del, NM_022834.4:c.1295_1301del (VWA1))

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.1375124_1375130del
DNA change (hg38) -
Published as VWA1(NM_022834.5):c.1295_1301delTGCCCCG (p.V432Afs*105)
ISCN -
DB-ID ATAD3C_000002
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2022-11-01 13:01:21 +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.-10940_-10934del r.(?) p.(=)
VWA1 NM_022834.4 ?/. - c.1295_1301del r.(?) p.(Val432Alafs*105)


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