Variant #0001005649 (NC_000021.8:g.33043939C>T, NM_000454.4:c.*3048C>T (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.33043939C>T
DNA change (hg38) -
Published as SCAF4(NM_020706.2):c.3217G>A (p.(Glu1073Lys))
ISCN -
DB-ID SOD1_000035
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SOD1 NM_000454.4 -?/. - c.*3048C>T r.(=) p.(=)
SCAF4 NM_020706.2 -?/. - c.3217G>A r.(?) p.(Glu1073Lys)


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