Variant #0000516670 (NC_000002.11:g.71801344_71801349dup, NM_003494.3:c.3191_3196dup (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.71801344_71801349dup
DNA change (hg38) g.71574214_71574219dup
Published as DYSF(NM_001130455.1):c.3194_3199dup (p.(Ala1065_Glu1066dup)), DYSF(NM_001130981.2):c.3242_3247dupCGGAGG (p.A1081_E1082dup)
ISCN -
DB-ID DYSF_000112 See all 32 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) Retrieve
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +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.3191_3196dup r.(?) p.(Ala1064_Glu1065dup)


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