Variant #0001024676 (NC_000002.11:g.71825884G>T, NC_000002.11(NM_003494.3):c.3702+9G>T (DYSF))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.71825884G>T
DNA change (hg38) -
Published as DYSF(NM_001130455.1):c.3705+9G>T (p.(=)), DYSF(NM_001130981.1):c.3753+9G>T, DYSF(NM_001130981.2):c.3753+9G>T
ISCN -
DB-ID DYSF_000488 See all 6 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) 0.00058 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2025-02-07 18:57:27 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYSF NM_003494.3 -?/. - c.3702+9G>T r.(=) p.(=)


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