Variant #0000837169 (NC_000002.11:g.71740914C>T, NM_003494.3:c.526C>T (DYSF))

Chromosome 2
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.71740914C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID DYSF_000264 See all 7 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1553521017
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2022-02-01 12:22:01 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYSF NM_003494.3 +/. - c.526C>T r.(?) p.(Gln176Ter)


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