Variant #0000905538 (NC_000002.11:g.71681133T>C, NM_003494.3:c.5T>C (DYSF))

Chromosome 2
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.71681133T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID DYSF_001406 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1243373795
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-12-02 11:29:01 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYSF NM_003494.3 +?/. - c.5T>C r.(?) p.(Leu2Pro)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.