Variant #0000894818 (NC_000019.9:g.13470592G>A, NM_001127221.1:c.806C>T (CACNA1A))

Chromosome 19
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.13470592G>A
DNA change (hg38) -
Published as CACNA1A(NM_001127222.2):c.806C>T (p.P269L)
ISCN -
DB-ID CACNA1A_000479
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     

P-domain     
CACNA1A NM_001127221.1 ?/. - c.806C>T - r.(?) p.(Pro269Leu) -
CACNA1A NM_023035.2 ?/. - c.806C>T - r.(?) p.(Pro269Leu) -


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