Variant #0000531904 (NC_000007.13:g.34125622C>T, NM_133468.4:c.1663C>T (BMPER))

Chromosome 7
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.34125622C>T
DNA change (hg38) g.34086010C>T
Published as BMPER(NM_133468.4):c.1663C>T (p.(Arg555Trp)), BMPER(NM_133468.5):c.1663C>T (p.R555W)
ISCN -
DB-ID BMPER_000009 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) 0.00516 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMPER NM_133468.4 -?/. - c.1663C>T r.(?) p.(Arg555Trp)


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