Variant #0000933342 (NC_000010.10:g.18429682del, NM_201596.2:c.17del (CACNB2))

Chromosome 10
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.18429682del
DNA change (hg38) -
Published as -
ISCN -
DB-ID CACNB2_000153
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs786205787
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-09-14 14:03:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNB2 NM_201596.2 ?/. - c.17del r.(?) p.(Met6SerfsTer21)


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