Variant #0000728989 (NC_000023.10:g.49088195A>G, NM_005183.2:c.220T>C (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.49088195A>G
DNA change (hg38) -
Published as CACNA1F(NM_005183.4):c.220T>C (p.C74R)
ISCN -
DB-ID CACNA1F_000011 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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +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.220T>C r.(?) p.(Cys74Arg)
CACNA1F NM_005183.2 ?/. - c.220T>C r.(?) p.(Cys74Arg)
CCDC22 NM_014008.3 ?/. - c.-3902A>G r.(?) p.(=)
FOXP3 NM_014009.3 ?/. - c.*19600T>C r.(=) p.(=)


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