Variant #0000539656 (NC_000010.10:g.18439809_18439810insTG, NC_000010.10(NM_201596.2):c.121-3_121-2insTG (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.18439809_18439810insTG
DNA change (hg38) g.18150880_18150881insTG
Published as CACNB2(NM_201571.4):c.37-3_37-2insTG
ISCN -
DB-ID CACNB2_000091
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 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     
CACNB2 NM_201596.2 -/. - c.121-3_121-2insTG r.spl? p.?


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