Variant #0001035146 (NC_000005.9:g.179260100_179260101del, NM_003900.4:c.823_824del (SQSTM1))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.179260100_179260101del
DNA change (hg38) -
Published as SQSTM1(NM_003900.5):c.823_824del (p.(Ser275Phefs*17))
ISCN -
DB-ID SQSTM1_000034 See all 2 reported entries
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 2025-05-05 21:14:00 +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     
SQSTM1 NM_003900.4 +/. - c.823_824del r.(?) p.(Ser275Phefs*17)
MGAT4B NM_014275.4 +/. - c.-26514_-26513del r.(?) p.(=)
C5orf45 NM_016175.3 +/. - c.*4294_*4295del r.(=) p.(=)


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