Variant #0000153935 (NC_000009.11:g.34637027C>G, NM_005866.2:c.412G>C (SIGMAR1))

Chromosome 9
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.34637027C>G
DNA change (hg38) g.34637030C>G
Published as -
ISCN -
DB-ID SIGMAR1_000002 See all 2 reported entries
Variant remarks expression cloning in different neuronal cells shows increased cell death, protein mislocalisation, impaired Ca2+ handling and induced p62 and LC3 aggregation
Reference PubMed: Gregianin 2016, Journal: Gregianin 2016
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2017-01-05 13:08:30 +01:00 (CET)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SIGMAR1 NM_005866.2 +/. 3 c.412G>C r.(?) p.Glu138Gln


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