Variant #0000249908 (NC_000011.9:g.66331458A>G, NM_001104.3:c.*794A>G (ACTN3))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.66331458A>G
DNA change (hg38) g.66563987A>G
Published as CTSF(NM_003793.3):c.1401T>C (p.R467=), CTSF(NM_003793.4):c.1401T>C (p.R467=)
ISCN -
DB-ID CTSF_000004 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) 0.52057 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 2018-01-15 20:58:59 +01:00 (CET)
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.*794A>G r.(=) p.(=)
CTSF NM_003793.3 -/. - c.1401T>C r.(?) p.(Arg467=)


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