Variant #0000804033 (NC_000009.11:g.140917855_140917860del, NM_000718.3:c.2660_2665del (CACNA1B))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.140917855_140917860del
DNA change (hg38) -
Published as CACNA1B(NM_000718.3):c.2660_2665delGGCCGC (p.R887_P888del)
ISCN -
DB-ID CACNA1B_000091
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +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     
CACNA1B NM_000718.3 ?/. - c.2660_2665del r.(?) p.(Arg887_Pro888del)


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