Variant #0000721436 (NC_000007.13:g.33976901A>G, NM_133468.4:c.220A>G (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.33976901A>G
DNA change (hg38) -
Published as BMPER(NM_133468.4):c.220A>G (p.(Asn74Asp)), BMPER(NM_133468.5):c.220A>G (p.N74D)
ISCN -
DB-ID BMPER_000016 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) 0.00178 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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
BMPER NM_133468.4 -?/. - c.220A>G r.(?) p.(Asn74Asp)


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