Variant #0000656866 (NC_000011.9:g.66331443A>C, NM_001104.3:c.*779A>C (ACTN3))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.66331443A>C
DNA change (hg38) g.66563972A>C
Published as CTSF(NM_003793.4):c.1416T>G (p.C472W)
ISCN -
DB-ID CTSF_000029
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2020-03-23 16:13:27 +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.*779A>C r.(=) p.(=)
CTSF NM_003793.3 +?/. - c.1416T>G r.(?) p.(Cys472Trp)


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