Variant #0000675939 (NC_000001.10:g.78408237T>A, NM_144573.3:c.1751T>A (NEXN))

Chromosome 1
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.78408237T>A
DNA change (hg38) -
Published as NEXN(NM_144573.3):c.1751T>A (p.F584Y)
ISCN -
DB-ID FUBP1_000018 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) 0 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FUBP1 NM_003902.3 ?/. - c.*6214A>T r.(=) p.(=)
NEXN NM_144573.3 ?/. - c.1751T>A r.(?) p.(Phe584Tyr)


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