Variant #0000965743 (NC_000010.10:g.52569681_52569683del, NM_001198819.1:c.1642_1644del (A1CF))

Chromosome 10
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.52569681_52569683del
DNA change (hg38) -
Published as A1CF(NM_001198819.2):c.1642_1644delGCT (p.A548del)
ISCN -
DB-ID A1CF_000001
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 2024-02-26 20:06:56 +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     
A1CF NM_001198819.1 -/. - c.1642_1644del r.(?) p.(Ala548del)
A1CF NM_014576.3 -/. - c.1594_1596del r.(?) p.(Ala532del)


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