Variant #0000620449 (NC_000001.10:g.181702831C>T, NM_000721.3:c.3207C>T (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.181702831C>T
DNA change (hg38) g.181733695C>T
Published as CACNA1E(NM_001205293.2):c.3207C>T (p.S1069=)
ISCN -
DB-ID CACNA1E_000028
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) 0.00182 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1E NM_000721.3 -?/. - c.3207C>T r.(?) p.(Ser1069=)
CACNA1E NM_001205293.1 -?/. - c.3207C>T r.(?) p.(Ser1069=)


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