Variant #0000560430 (NC_000017.10:g.16843759A>C, NM_012452.2:c.512T>G (TNFRSF13B))

Chromosome 17
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.16843759A>C
DNA change (hg38) g.16940445A>C
Published as TNFRSF13B(NM_012452.2):c.512T>G (p.L171R), TNFRSF13B(NM_012452.3):c.512T>G (p.(Leu171Arg), p.L171R)
ISCN -
DB-ID TNFRSF13B_000013 See all 6 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) 9.0E-5 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 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF13B NM_012452.2 +?/. - c.512T>G r.(?) p.(Leu171Arg)


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