Variant #0001013337 (NC_000001.10:g.61872228_61872229insT, NC_000001.10(NM_001134673.3):c.1255-6_1255-5insT (NFIA))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.61872228_61872229insT
DNA change (hg38) -
Published as NFIA(NM_001145512.1):c.1390-6_1390-5insT, NFIA(NM_005595.5):c.1255-6_1255-5insT
ISCN -
DB-ID NFIA_000009 See all 2 reported entries
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-10-29 20:49:11 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NFIA NM_001134673.3 -/. - c.1255-6_1255-5insT r.spl? p.?


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