Variant #0001006818 (NC_000023.10:g.49088375G>A, NM_005183.2:c.40C>T (CACNA1F))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49088375G>A
DNA change (hg38) -
Published as CACNA1F(NM_001256789.1):c.40C>T (p.(Pro14Ser))
ISCN -
DB-ID CACNA1F_000528
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) 2.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1F NM_001256789.1 -?/. - c.40C>T r.(?) p.(Pro14Ser)
CACNA1F NM_005183.2 -?/. - c.40C>T r.(?) p.(Pro14Ser)
CCDC22 NM_014008.3 -?/. - c.-3722G>A r.(?) p.(=)
FOXP3 NM_014009.3 -?/. - c.*19420C>T r.(=) p.(=)


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