Variant #0000565233 (NC_000018.9:g.60052034A>G, NM_003839.3:c.1618A>G (TNFRSF11A))

Chromosome 18
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.60052034A>G
DNA change (hg38) g.62384801A>G
Published as TNFRSF11A(NM_001278268.1):c.1576A>G (p.M526V), TNFRSF11A(NM_003839.2):c.1618A>G (p.M540V), TNFRSF11A(NM_003839.4):c.1618A>G (p.M540V)
ISCN -
DB-ID TNFRSF11A_000016 See all 4 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) 0.00068 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF11A NM_003839.3 ?/. - c.1618A>G r.(?) p.(Met540Val)


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