Variant #0000576389 (NC_000023.10:g.49088375G>T, NM_005183.2:c.40C>A (CACNA1F))

Chromosome X
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.49088375G>T
DNA change (hg38) g.49231913G>T
Published as CACNA1F(NM_005183.4):c.40C>A (p.P14T)
ISCN -
DB-ID CACNA1F_000137
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) 0.00017 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1F NM_001256789.1 ?/. - c.40C>A r.(?) p.(Pro14Thr)
CACNA1F NM_005183.2 ?/. - c.40C>A r.(?) p.(Pro14Thr)
CCDC22 NM_014008.3 ?/. - c.-3722G>T r.(?) p.(=)
FOXP3 NM_014009.3 ?/. - c.*19420C>A r.(=) p.(=)


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