Variant #0000451269 (NC_000002.11:g.71827854G>A, NM_003494.3:c.3725G>A (DYSF))

Chromosome 2
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.71827854G>A
DNA change (hg38) g.71600724G>A
Published as -
ISCN -
DB-ID DYSF_000085 See all 12 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2303603
Origin Germline
Segregation -
Frequency 0.02
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00087 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2002-11-29 16:49:11 +01:00 (CET)
Date last edited 2019-01-20 16:48:47 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYSF NM_003494.3 -/. 34 c.3725G>A r.(?) p.(Arg1242His)


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