Variant #0000994957 (NC_000005.9:g.179251013G>A, NM_003900.4:c.457G>A (SQSTM1))

Chromosome 5
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.179251013G>A
DNA change (hg38) -
Published as SQSTM1(NM_001142298.2):c.205G>A (p.V69I), SQSTM1(NM_003900.4):c.457G>A (p.(Val153Ile)), SQSTM1(NM_003900.5):c.457G>A (p.V153I)
ISCN -
DB-ID C5orf45_000005 See all 3 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) 0.00027 View details
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 13:16:32 +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.457G>A r.(?) p.(Val153Ile)
MGAT4B NM_014275.4 -?/. - c.-17430C>T r.(?) p.(=)
C5orf45 NM_016175.3 -?/. - c.*13378C>T r.(=) p.(=)


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