Variant #0000315711 (NC_000005.9:g.179260099G>C, NM_003900.4:c.822G>C (SQSTM1))

Chromosome 5
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.179260099G>C
DNA change (hg38) g.179833099G>C
Published as SQSTM1(NM_003900.5):c.822G>C (p.E274D)
ISCN -
DB-ID SQSTM1_000019 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) 0.01789 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-02-08 18:36:18 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SQSTM1 NM_003900.4 -/. - c.822G>C r.(?) p.(Glu274Asp)
MGAT4B NM_014275.4 -/. - c.-26516C>G r.(?) p.(=)
C5orf45 NM_016175.3 -/. - c.*4292C>G r.(=) p.(=)


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