Variant #0000570497 (NC_000021.8:g.33040834A>G, NM_000454.4:c.408A>G (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.33040834A>G
DNA change (hg38) g.31668521A>G
Published as SOD1(NM_000454.5):c.408A>G (p.T136=)
ISCN -
DB-ID SCAF4_000009
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOD1 NM_000454.4 -?/. - c.408A>G r.(?) p.(Thr136=)
SCAF4 NM_020706.2 -?/. - c.*2878T>C r.(=) p.(=)


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