Variant #0001005648 (NC_000021.8:g.33040869G>C, NM_020706.2:c.*2843C>G (SCAF4))

Chromosome 21
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.33040869G>C
DNA change (hg38) -
Published as SOD1(NM_000454.4):c.443G>C (p.G148A)
ISCN -
DB-ID SOD1_000034
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 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.443G>C r.(?) p.(Gly148Ala)
SCAF4 NM_020706.2 +?/. - c.*2843C>G r.(=) p.(=)


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