Variant #0000234251 (NC_000023.10:g.31165400G>A, NM_004006.2:c.10789C>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 likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31165400G>A
DNA change (hg38) g.31147283G>A
Published as DMD(NM_000109.3):c.10765C>T (p.(Leu3589=)), DMD(NM_004006.3):c.10789C>T (p.L3597=), DMD(NM_004010.3):c.10420C>T (p.L3474=)
ISCN -
DB-ID DMD_001019 See all 15 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) 0.00477 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2017-11-28 14:29:49 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +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 -?/. 75 c.10789C>T r.(?) p.(Leu3597=)


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