Variant #0000999390 (NC_000011.9:g.66625678A>G, NC_000011.9(NM_001040716.1):c.1369-4824T>C (PC))

Chromosome 11
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.66625678A>G
DNA change (hg38) -
Published as LRFN4(NM_024036.4):c.463A>G (p.(Asn155Asp))
ISCN -
DB-ID PC_000035
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) 0 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 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PC NM_001040716.1 ?/. - c.1369-4824T>C r.(=) p.(=)
LRFN4 NM_024036.4 ?/. - c.463A>G r.(?) p.(Asn155Asp)


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