Variant #0000252681 (NC_000021.8:g.33039629A>G, NM_020706.2:c.*4083T>C (SCAF4))

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.33039629A>G
DNA change (hg38) g.31667316A>G
Published as SOD1(NM_000454.4):c.298A>G (p.I100V)
ISCN -
DB-ID SOD1_000016
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) 1.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.298A>G r.(?) p.(Ile100Val)
SCAF4 NM_020706.2 ?/. - c.*4083T>C r.(=) p.(=)


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