Variant #0000576379 (NC_000023.10:g.49083552C>T, NM_005183.2:c.1156G>A (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.49083552C>T
DNA change (hg38) g.49227090C>T
Published as CACNA1F(NM_005183.4):c.1156G>A (p.G386R)
ISCN -
DB-ID CACNA1F_000129 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) 3.0E-5 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 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.1156G>A r.(?) p.(Gly386Arg)
CACNA1F NM_005183.2 -?/. - c.1156G>A r.(?) p.(Gly386Arg)


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