Variant #0000516668 (NC_000002.11:g.71797762G>A, NM_003494.3:c.3065G>A (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.71797762G>A
DNA change (hg38) g.71570632G>A
Published as DYSF(NM_001130455.1):c.3068G>A (p.(Arg1023Gln)), DYSF(NM_001130981.2):c.3116G>A (p.R1039Q)
ISCN -
DB-ID DYSF_000121 See all 14 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) 0.01849 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-05-09 15:51:19 +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.3065G>A r.(?) p.(Arg1022Gln)


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