Variant #0000847866 (NC_000019.9:g.13135757_13135759del, NC_000019.9(NM_001365902.2):c.28-78_28-76del (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.13135757_13135759del
DNA change (hg38) g.13024943_13024945del
Published as -
ISCN -
DB-ID NFIX_000090
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1330009306
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-05-06 11:23:01 +02:00 (CEST)
Date last edited 2023-06-28 10:02:38 +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.28-78_28-76del r.(?) p.?


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