Variant #0000947961 (NC_000002.11:g.71827820C>T, NC_000002.11(NM_003494.3):c.3703-12C>T (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.71827820C>T
DNA change (hg38) -
Published as DYSF(NM_001130455.1):c.3706-12C>T (p.(=)), DYSF(NM_001130981.2):c.3754-12C>T
ISCN -
DB-ID DYSF_000392 See all 7 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) 0.00596 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2023-11-27 17:35:39 +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.3703-12C>T r.(=) p.(=)


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