Variant #0000653818 (NC_000001.10:g.181620575C>A, NM_000721.3:c.1053C>A (CACNA1E))

Chromosome 1
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.181620575C>A
DNA change (hg38) g.181651439C>A
Published as CACNA1E(NM_001205293.2):c.1053C>A (p.S351=)
ISCN -
DB-ID CACNA1E_000025
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) 0.00121 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 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1E NM_000721.3 -?/. - c.1053C>A r.(?) p.(Ser351=)
CACNA1E NM_001205293.1 -?/. - c.1053C>A r.(?) p.(Ser351=)


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