Variant #0000576387 (NC_000023.10:g.49087440C>T, NM_005183.2:c.393G>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.49087440C>T
DNA change (hg38) g.49230978C>T
Published as CACNA1F(NM_005183.3):c.393G>A (p.E131=), CACNA1F(NM_005183.4):c.393G>A (p.E131=)
ISCN -
DB-ID CACNA1F_000136 See all 2 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) 6.0E-5 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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CACNA1F NM_001256789.1 -/. - c.393G>A r.(?) p.(Glu131=)
CACNA1F NM_005183.2 -/. - c.393G>A r.(?) p.(Glu131=)
CCDC22 NM_014008.3 -/. - c.-4657C>T r.(?) p.(=)
FOXP3 NM_014009.3 -/. - c.*20355G>A r.(=) p.(=)


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