Variant #0000272543 (NC_000002.11:g.152695783C>T, NM_000726.3:c.1413G>A (CACNB4))

Chromosome 2
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.152695783C>T
DNA change (hg38) g.151839269C>T
Published as CACNB4(NM_001330117.1):c.855G>A (p.R285=), CACNB4(NM_001330117.2):c.855G>A (p.R285=)
ISCN -
DB-ID CACNB4_000003 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) 0.00192 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:07:21 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNB4 NM_000726.3 -?/. - c.1413G>A r.(?) p.(Arg471=)


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