Variant #0000855450 (NC_000019.9:g.13135961G>A, NM_002501.2:c.154G>A (NFIX))

Chromosome 19
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.13135961G>A
DNA change (hg38) g.13025147G>A
Published as -
ISCN -
DB-ID NFIX_000092
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited 2023-06-28 10:02:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NFIX NM_001365902.2 +?/. - c.154G>A r.(?) p.(Glu52Lys)
NFIX NM_002501.2 +?/. - c.154G>A r.(?) p.(Glu52Lys)


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