Variant #0000951492 (NC_000021.8:g.33038826_33038828del, NM_000454.4:c.234_236del (SOD1))

Chromosome 21
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.33038826_33038828del
DNA change (hg38) -
Published as SOD1(NM_000454.4):c.234_236delAGA (p.E79del)
ISCN -
DB-ID SOD1_000030
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOD1 NM_000454.4 ?/. - c.234_236del r.(?) p.(Glu79del)
SCAF4 NM_020706.2 ?/. - c.*4886_*4888del r.(=) p.(=)


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