Variant #0000576385 (NC_000023.10:g.49087015del, NM_005183.2:c.579del (CACNA1F))

Chromosome X
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.49087015del
DNA change (hg38) g.49230553del
Published as CACNA1F(NM_001256789.1):c.579delC (p.(Gly195fs)), CACNA1F(NM_005183.4):c.579delC (p.G195Efs*8)
ISCN -
DB-ID CACNA1F_000134 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) Retrieve
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 2024-08-28 13:16:32 +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.579del r.(?) p.(Gly195GlufsTer8)
CACNA1F NM_005183.2 +/. - c.579del r.(?) p.(Gly195GlufsTer8)
CCDC22 NM_014008.3 +/. - c.-5082del r.(?) p.(=)
FOXP3 NM_014009.3 +/. - c.*20781del r.(?) p.(=)


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