Variant #0001006273 (NC_000023.10:g.100093318G>A, NM_007052.4:c.*5623C>T (NOX1))

Chromosome X
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.100093318G>A
DNA change (hg38) -
Published as CSTF2(NM_001325.2):c.1702G>A (p.(Glu568Lys))
ISCN -
DB-ID NOX1_000053
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     
CSTF2 NM_001325.2 ?/. - c.1702G>A r.(?) p.(Glu568Lys)
NOX1 NM_007052.4 ?/. - c.*5623C>T r.(=) p.(=)


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