Variant #0000855449 (NC_000019.9:g.13106668G>A, NM_001365902.2:c.17G>A (NFIX))

Chromosome 19
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.13106668G>A
DNA change (hg38) g.12995854G>A
Published as NFIX(NM_001365902.1):c.17G>A (p.C6Y)
ISCN -
DB-ID NFIX_000091
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.17G>A r.(?) p.(Cys6Tyr)
NFIX NM_002501.2 ?/. - c.17G>A r.(?) p.(Cys6Tyr)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.