Variant #0000659361 (NC_000023.10:g.49088170C>T, NM_005183.2:c.245G>A (CACNA1F))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49088170C>T
DNA change (hg38) g.49231708C>T
Published as -
ISCN -
DB-ID CACNA1F_000158 See all 7 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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2020-03-23 16:13:27 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1F NM_001256789.1 +?/. - c.245G>A r.(?) p.(Arg82Gln)
CACNA1F NM_005183.2 +?/. - c.245G>A r.(?) p.(Arg82Gln)
CCDC22 NM_014008.3 +?/. - c.-3927C>T r.(?) p.(=)
FOXP3 NM_014009.3 +?/. - c.*19625G>A r.(=) p.(=)


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