Variant #0000211206 (NC_000023.10:g.32834621T>A, NM_004006.2:c.494A>T (DMD))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.32834621T>A
DNA change (hg38) g.32816504T>A
Published as -
ISCN -
DB-ID DMD_000547 See all 6 reported entries
Variant remarks protein isolated from expression cloning Sf9 insect cells; unchanged actin-binding affinity
Reference PubMed: Henderson 2010
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
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 2010-06-04 21:20:39 +02:00 (CEST)
Date last edited 2020-07-19 18:24:43 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DMD NM_004006.2 -?/. 6 c.494A>T r.(?) p.Asp165Val


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