Variant #0000984948 (NC_000017.10:g.16843692G>T, NM_012452.2:c.579C>A (TNFRSF13B))

Chromosome 17
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.16843692G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID TNFRSF13B_000034 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs72553885
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-04-29 13:28:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNFRSF13B NM_012452.2 +/. - c.579C>A r.(?) p.(Cys193Ter)


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