Variant #0000314615 (NC_000018.9:g.60036669G>A, NM_003839.3:c.1519G>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.60036669G>A
DNA change (hg38) g.62369436G>A
Published as TNFRSF11A(NM_001278268.1):c.1477G>A (p.(Ala493Thr)), TNFRSF11A(NM_003839.2):c.1519G>A (p.A507T)
ISCN -
DB-ID TNFRSF11A_000015 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) 0.00637 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF11A NM_003839.3 -?/. - c.1519G>A r.(?) p.(Ala507Thr)


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