Variant #0000896094 (NC_000023.10:g.31496398T>C, NM_004006.2:c.8762A>G (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.31496398T>C
DNA change (hg38) -
Published as DMD(NM_000109.3):c.8738A>G (p.(His2913Arg)), DMD(NM_004010.3):c.8393A>G (p.H2798R)
ISCN -
DB-ID DMD_001060 See all 33 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) 0.02578 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMD NM_004006.2 -/. - c.8762A>G r.(?) p.(His2921Arg)


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