Variant #0000990916 (NC_000001.10:g.228284834_228284835del, NM_001658.3:c.19_20del (ARF1))

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.228284834_228284835del
DNA change (hg38) -
Published as ARF1(NM_001658.3):c.19_20delAA (p.(Asn7fs))
ISCN -
DB-ID C1orf35_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:07:21 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARF1 NM_001658.3 ?/. - c.19_20del r.(?) p.(Asn7Profs*31)
C1orf35 NM_024319.2 ?/. - c.*3997_*3998del r.(=) p.(=)


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