Variant #0000211248 (NC_000023.10:g.31138589T>C, NM_004006.2:c.*1447A>G (DMD))

Chromosome X
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.31138589T>C
DNA change (hg38) g.31120472T>C
Published as 11058+1447A>G
ISCN -
DB-ID DMD_000784 See all 8 reported entries
Variant remarks -
Reference {GenBankM18533}
ClinVar ID -
dbSNP ID rs3361
Origin Germline
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2009-12-12 19:01:36 +01:00 (CET)
Date last edited 2012-11-02 20:41:15 +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 ?/. 79 c.*1447A>G r.(?) p.(=)


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