Variant #0000612398 (NC_000010.10:g.18787304G>A, NM_201596.2:c.354G>A (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.18787304G>A
DNA change (hg38) g.18498375G>A
Published as CACNB2(NM_000724.3):c.189G>A (p.A63=), CACNB2(NM_000724.4):c.189G>A (p.A63=)
ISCN -
DB-ID CACNB2_000105 See all 2 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) 0.00112 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-26 13:44:15 +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.354G>A r.(?) p.(Ala118=)


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