Variant #0001047557 (NC_000007.13:g.44268443del, NM_001220.4:c.1424del (CAMK2B))

Chromosome 7
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.44268443del
DNA change (hg38) -
Published as -
ISCN -
DB-ID CAMK2B_000037 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1562813271
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-08-28 12:17:01 +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     
CAMK2B NM_001220.4 +?/. - c.1424del r.(?) p.(Pro475ArgfsTer9)


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