Variant #0000269893 (NC_000011.9:g.2400660_2400661del, CD81(NM_004356.3):c.66+1815_66+1816del)

Chromosome 11
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.2400660_2400661del
DNA change (hg38) g.2379430_2379431del
Published as CD81(NM_004356.3):c.66+1815_66+1816delAG
ISCN -
DB-ID CD81_000003
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CD81 NM_004356.3 -?/. - c.66+1815_66+1816del r.(=) p.(=)