Variant #0000234268 (NC_000023.10:g.32380996C>T, NM_004006.2:c.5234G>A (DMD))

Chromosome X
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.32380996C>T
DNA change (hg38) g.32362879C>T
Published as DMD(NM_004006.3):c.5234G>A (p.R1745H), DMD(NM_004010.3):c.4865G>A (p.R1622H)
ISCN -
DB-ID DMD_001039 See all 67 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) 0.52943 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2017-11-28 14:29:49 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMD NM_004006.2 -/. 37 c.5234G>A r.(?) p.(Arg1745His)


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