Variant #0000659360 (NC_000023.10:g.49087047C>A, NM_005183.2:c.546G>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.49087047C>A
DNA change (hg38) g.49230585C>A
Published as CACNA1F(NM_005183.3):c.546G>T (p.Q182H)
ISCN -
DB-ID CACNA1F_000157
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.546G>T r.(?) p.(Gln182His)
CACNA1F NM_005183.2 -?/. - c.546G>T r.(?) p.(Gln182His)
CCDC22 NM_014008.3 -?/. - c.-5050C>A r.(?) p.(=)
FOXP3 NM_014009.3 -?/. - c.*20748G>T r.(=) p.(=)


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