Variant #0000002299 (NC_000023.11:g.31478221T>C, NM_004009.3:c.8810A>G (DMD))

Individual ID 00000507
Chromosome X
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.31478221T>C
Published as -
Reference Abdul Qawee Rani et al.(2013)dbSNP
DB-ID DMD_000003
dbSNP ID rs1800280
Frequency 1/35
Variant remarks -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-03-14 10:17:22 +08:00 (CST)
Date last edited 2021-09-05 15:19:02 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
DMD NM_004009.3 -/. 59 c.8810A>G - r.(?) p.(Glu2937Gly) ClinVar



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000554 DNA MLPA DMD 1 Nur Aisyah Athirah