Variant #0000911139 (NC_000001.10:g.78407895T>C, NC_000001.10(NM_144573.3):c.1659+2T>C (NEXN))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.78407895T>C
DNA change (hg38) -
Published as NEXN(NM_144573.4):c.1659+2T>C
ISCN -
DB-ID FUBP1_000026
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2023-01-11 15:44:22 +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     
FUBP1 NM_003902.3 +?/. - c.*6556A>G r.(=) p.(=)
NEXN NM_144573.3 +?/. - c.1659+2T>C r.spl? p.?


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