Variant #0000545139 (NC_000011.9:g.66332132A>G, NM_001104.3:c.*1468A>G (ACTN3))

Chromosome 11
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.66332132A>G
DNA change (hg38) g.66564661A>G
Published as CTSF(NM_003793.4):c.1231-13T>C
ISCN -
DB-ID CTSF_000021
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) 0.00073 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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     
ACTN3 NM_001104.3 -?/. - c.*1468A>G r.(=) p.(=)
CTSF NM_003793.3 -?/. - c.1231-13T>C r.(=) p.(=)


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