Variant #0001026552 (NC_000015.9:g.98513893_98513896del, NM_183376.2:c.1120_1123del (ARRDC4))

Chromosome 15
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.98513893_98513896del
DNA change (hg38) -
Published as ARRDC4(NM_183376.3):c.1120_1123delAACT (p.N374Vfs*34)
ISCN -
DB-ID ARRDC4_000003
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-02-07 18:57:27 +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     
ARRDC4 NM_183376.2 ?/. - c.1120_1123del r.(?) p.(Asn374Valfs*34)


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