Variant #0000894622 (NC_000018.9:g.60036429G>A, NM_003839.3:c.1279G>A (TNFRSF11A))

Chromosome 18
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.60036429G>A
DNA change (hg38) -
Published as TNFRSF11A(NM_001278268.1):c.1237G>A (p.D413N), TNFRSF11A(NM_003839.2):c.1279G>A (p.D427N)
ISCN -
DB-ID TNFRSF11A_000022 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) 0.0008 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF11A NM_003839.3 -?/. - c.1279G>A r.(?) p.(Asp427Asn)


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