Variant #0000539665 (NC_000010.10:g.18439809_18439810insTTTTTTTTTTTTTTTTTTTTTTTTTTTGT, NC_000010.10(NM_201596.2):c.121-3_121-2insTTTTTTTTTTTTTTTTTTTTTTTTTTTGT (CACNB2))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.18439809_18439810insTTTTTTTTTTTTTTTTTTTTTTTTTTTGT
DNA change (hg38) g.18150880_18150881insTTTTTTTTTTTTTTTTTTTTTTTTTTTGT
Published as CACNB2(NM_201571.4):c.37-2_37-1insTTTTTTTTTTTTTTTTTTTTTTTTTTGTT
ISCN -
DB-ID CACNB2_000100
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

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


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.