Variant #0000272438 (NC_000019.9:g.13318710_13318712del, NM_001127221.1:c.*185_*187del (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.13318710_13318712del
DNA change (hg38) g.13207896_13207898del
Published as CACNA1A(NM_000068.3):c.*173_*175del (p.(=)), CACNA1A(NM_023035.2):c.6991_6993delCAG (p.Q2331del), CACNA1A(NM_023035.3):c.6991_6993delCAG (p.Q2331del)
ISCN -
DB-ID CACNA1A_000087 See all 4 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +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.*185_*187del - r.(=) p.(=) -
CACNA1A NM_023035.2 -/. - c.6991_6993del - r.(?) p.(Gln2331del) -


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