Variant #0000565227 (NC_000018.9:g.60029014A>G, NM_003839.3:c.718A>G (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.60029014A>G
DNA change (hg38) g.62361781A>G
Published as TNFRSF11A(NM_001270949.1):c.718A>G (p.(Lys240Glu)), TNFRSF11A(NM_001278268.1):c.676A>G (p.K226E), TNFRSF11A(NM_001278268.2):c.676A>G (p.K226E)
ISCN -
DB-ID TNFRSF11A_000019 See all 3 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) 0.00107 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF11A NM_003839.3 -?/. - c.718A>G r.(?) p.(Lys240Glu)


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