Variant #0000894801 (NC_000019.9:g.13319693A>G, NM_001127222.2:c.6657T>C (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.13319693A>G
DNA change (hg38) -
Published as CACNA1A(NM_000068.3):c.6675delinsC (p.(His2225=)), CACNA1A(NM_023035.2):c.6675T>C (p.H2225=), CACNA1A(NM_023035.3):c.6675T>C (p.H2225=)
ISCN -
DB-ID CACNA1A_000046 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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.6660T>C - r.(?) p.(His2220=) -
CACNA1A NM_001127222.2 -/. - c.6657T>C - r.(?) p.(=) -


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