Variant #0000514265 (NC_000002.11:g.21233102_21233104del, NM_000384.2:c.6639_6641del (APOB))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.21233102_21233104del
DNA change (hg38) g.21010230_21010232del
Published as APOB(NM_000384.2):c.6639_6641delTGA (p.D2213del), APOB(NM_000384.3):c.6639_6641delTGA (p.D2213del)
ISCN -
DB-ID APOB_000802 See all 9 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
APOB NM_000384.2 ?/. - c.6639_6641del r.(?) p.(Asp2213del)


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