Variant #0000272505 (NC_000023.10:g.49086730C>A, NM_005183.2:c.769G>T (CACNA1F))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49086730C>A
DNA change (hg38) g.49230268C>A
Published as CACNA1F(NM_005183.3):c.769G>T (p.E257*)
ISCN -
DB-ID CACNA1F_000077
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 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1F NM_001256789.1 +/. - c.769G>T r.(?) p.(Glu257Ter)
CACNA1F NM_005183.2 +/. - c.769G>T r.(?) p.(Glu257Ter)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.