Variant #0000566276 (NC_000019.9:g.13616912C>T, NM_001127221.1:c.127G>A (CACNA1A))

Chromosome 19
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.13616912C>T
DNA change (hg38) g.13506098C>T
Published as CACNA1A(NM_000068.3):c.127G>A (p.(Gly43Arg))
ISCN -
DB-ID CACNA1A_000363
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 View details
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 2020-03-23 16:13:27 +01:00 (CET)
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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.127G>A - r.(?) p.(Gly43Arg) -
CACNA1A NM_023035.2 -?/. - c.127G>A - r.(?) p.(Gly43Arg) -


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