Variant #0000659355 (NC_000023.10:g.49081230C>T, NM_005183.2:c.1903G>A (CACNA1F))

Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.49081230C>T
DNA change (hg38) g.49224768C>T
Published as CACNA1F(NM_001256789.1):c.1870G>A (p.(Val624Ile)), CACNA1F(NM_005183.3):c.1903G>A (p.V635I), CACNA1F(NM_005183.4):c.1903G>A (p.V635I)
ISCN -
DB-ID CACNA1F_000003 See all 9 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) 0.00212 View details
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 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1F NM_001256789.1 -/. - c.1870G>A r.(?) p.(Val624Ile)
CACNA1F NM_005183.2 -/. - c.1903G>A r.(?) p.(Val635Ile)


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