Variant #0000894793 (NC_000019.9:g.13189422C>G, NC_000019.9(NM_002501.2):c.956-5C>G (NFIX))

Chromosome 19
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.13189422C>G
DNA change (hg38) g.13078608C>G
Published as NFIX(NM_001271043.1):c.980-5C>G (p.?)
ISCN -
DB-ID NFIX_000093
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) 5.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NFIX NM_001365902.2 -?/. - c.956-5C>G r.spl? p.?
NFIX NM_002501.2 -?/. - c.956-5C>G r.spl? p.?


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