Variant #0000687929 (NC_000001.10:g.161599831G>T, NC_000001.10(NM_000570.4):c.62-6C>A (FCGR3B))

Chromosome 1
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.161599831G>T
DNA change (hg38) -
Published as FCGR3B(NM_000570.4):c.62-6C>A (p.(=)), FCGR3B(NM_001271036.1):c.11-6C>A
ISCN -
DB-ID FCGR3B_000010 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) 0.00048 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 2020-09-15 15:50:26 +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     
FCGR3B NM_000570.4 -?/. - c.62-6C>A r.(=) p.(=)


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