Variant #0000791893 (NC_000002.11:g.71886163G>T, NM_003494.3:c.4794G>T (DYSF))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.71886163G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID DYSF_000170 See all 11 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs141704244
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 6.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2021-08-02 16:28:01 +02:00 (CEST)
Date last edited 2022-09-26 12:22:42 +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.4794G>T r.(?) p.(Lys1598Asn)


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