Variant #0000895450 (NC_000021.8:g.33043762A>T, NM_020706.2:c.3394T>A (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.33043762A>T
DNA change (hg38) -
Published as SCAF4(NM_020706.2):c.3394T>A (p.S1132T)
ISCN -
DB-ID SCAF4_000015 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) 2.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
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.*2871A>T r.(=) p.(=)
SCAF4 NM_020706.2 ?/. - c.3394T>A r.(?) p.(Ser1132Thr)


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