Variant #0000681703 (NC_000021.8:g.33036251_33036257del, NC_000021.8(NM_000454.4):c.169+52_169+58del (SOD1))

Chromosome 21
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.33036251_33036257del
DNA change (hg38) -
Published as SOD1(NM_000454.4):c.169+52_169+58delAACAGTA, SOD1(NM_000454.4):c.169+52_169+58delAACAGTA (p.?)
ISCN -
DB-ID SOD1_000021 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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOD1 NM_000454.4 -?/. - c.169+52_169+58del r.(=) p.(=)


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