Variant #0000539647 (NC_000010.10:g.18439799_18439809del, NC_000010.10(NM_201596.2):c.121-13_121-3del (CACNB2))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18439799_18439809del
DNA change (hg38) g.18150870_18150880del
Published as CACNB2(NM_201571.4):c.37-13_37-3delTTTTTTTTTTT
ISCN -
DB-ID CACNB2_000083
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_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-26 13:44:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNB2 NM_201596.2 -/. - c.121-13_121-3del r.spl? p.?


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