Variant #0000302891 (NC_000003.11:g.47043594_47043602del, NM_015175.2:c.4967_4975del (NBEAL2))

Chromosome 3
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.47043594_47043602del
DNA change (hg38) g.47002104_47002112del
Published as NBEAL2(NM_015175.2):c.4948_4956del (p.(Ala1653_Ala1655del)), NBEAL2(NM_015175.2):c.4967_4975delCAGCTGCAG (p.A1656_A1658del)
ISCN -
DB-ID NBEAL2_000007 See all 3 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NBEAL2 NM_015175.2 ?/. - c.4967_4975del r.(?) p.(Ala1656_Ala1658del)


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