Variant #0000971149 (NC_000023.10:g.49087325T>A, NM_005183.2:c.508A>T (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.49087325T>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID CACNA1F_000514
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-02-26 20:06:56 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1F NM_001256789.1 ?/. - c.508A>T r.(?) p.(Ile170Phe)
CACNA1F NM_005183.2 ?/. - c.508A>T r.(?) p.(Ile170Phe)
CCDC22 NM_014008.3 ?/. - c.-4772T>A r.(?) p.(=)
FOXP3 NM_014009.3 ?/. - c.*20470A>T r.(=) p.(=)


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