Variant #0001032418 (NC_000002.11:g.152727089T>C, NM_000726.3:c.655A>G (CACNB4))

Chromosome 2
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.152727089T>C
DNA change (hg38) -
Published as CACNB4(NM_001330114.1):c.1A>G (p.M1?), CACNB4(NM_001330114.2):c.1A>G (p.(Met1?), p.M1?)
ISCN -
DB-ID CACNB4_000030 See all 3 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) 0.00051 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNB4 NM_000726.3 -/. - c.655A>G r.(?) p.(Met219Val)


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