Variant #0000718949 (NC_000002.11:g.71892383C>T, NM_003494.3:c.5149C>T (DYSF))

Chromosome 2
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.71892383C>T
DNA change (hg38) -
Published as DYSF(NM_001130455.1):c.5152C>T (p.(Arg1718Trp)), DYSF(NM_001130981.1):c.5263C>T (p.R1755W), DYSF(NM_001130981.2):c.5263C>T (p.R1755W), DYSF(NM_003...)
ISCN -
DB-ID DYSF_000258 See all 9 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) 0.00053 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DYSF NM_003494.3 ?/. - c.5149C>T r.(?) p.(Arg1717Trp)


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