Variant #0000234363 (NC_000023.10:g.32361267T>A, NM_004006.2:c.5723A>T (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.32361267T>A
DNA change (hg38) g.32343150T>A
Published as DMD(NM_004006.3):c.5723A>T (p.D1908V), DMD(NM_004010.3):c.5354A>T (p.D1785V)
ISCN -
DB-ID DMD_000961 See all 11 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) 0.00022 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
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 ?/. 40 c.5723A>T r.(?) p.(Asp1908Val)


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