Variant #0000923246 (NC_000001.10:g.78407833A>G, NM_144573.3:c.1599A>G (NEXN))

Chromosome 1
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.78407833A>G
DNA change (hg38) -
Published as NEXN(NM_144573.3):c.1599A>G (p.E533=)
ISCN -
DB-ID FUBP1_000028
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 2023-04-16 21:50:28 +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     
FUBP1 NM_003902.3 -?/. - c.*6618T>C r.(=) p.(=)
NEXN NM_144573.3 -?/. - c.1599A>G r.(?) p.(Glu533=)


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