Variant #0000545143 (NC_000011.9:g.66333807G>A, NM_001104.3:c.*3143G>A (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.66333807G>A
DNA change (hg38) g.66566336G>A
Published as CTSF(NM_003793.3):c.676C>T (p.R226C), CTSF(NM_003793.4):c.676C>T (p.R226C)
ISCN -
DB-ID CTSF_000012 See all 3 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) 0.00292 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.*3143G>A r.(=) p.(=)
CTSF NM_003793.3 -?/. - c.676C>T r.(?) p.(Arg226Cys)


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