Variant #0000566273 (NC_000019.9:g.13482554C>T, NM_001127221.1:c.579G>A (CACNA1A))

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.13482554C>T
DNA change (hg38) g.13371740C>T
Published as CACNA1A(NM_000068.3):c.579G>A (p.(Thr193=)), CACNA1A(NM_023035.2):c.579G>A (p.T193=), CACNA1A(NM_023035.3):c.579G>A (p.T193=)
ISCN -
DB-ID CACNA1A_000003 See all 8 reported entries
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) 0.01033 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +02:00 (CEST)
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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.579G>A - r.(?) p.(Thr193=) -
CACNA1A NM_023035.2 -/. - c.579G>A - r.(?) p.(Thr193=) -


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