Variant #0000572088 (NC_000022.10:g.40059721_40059725del, NC_000022.10(NM_001003406.1):c.3369-2_3371del (CACNA1I))

Chromosome 22
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.40059721_40059725del
DNA change (hg38) g.39663716_39663720del
Published as CACNA1I(NM_001003406.1):c.3369-2_3371del (p.?)
ISCN -
DB-ID CACNA1I_000008
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-07-17 13:34:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1I NM_001003406.1 -?/. - c.3369-2_3371del r.spl? p.?


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