Variant #0001010082 (NC_000005.9:g.7883859T>C, NC_000005.9(NM_002454.2):c.903+469T>C (MTRR))

Chromosome 5
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.7883859T>C
DNA change (hg38) g.7883746T>C
Published as -
ISCN -
DB-ID MTRR_000069 See all 8 reported entries
Variant remarks expression cloning beta globin mini-gene splicing construct; variant suggested to create a new exonic splicing enhancer (ESE)
Reference PubMed: Homolova 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 2024-09-27 16:11:54 +02:00 (CEST)
Date last edited 2024-09-27 18:50:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MTRR NM_002454.2 +/. 6i c.903+469T>C r.903_904ins[903+447_903+468;c;903+470_903+586] p.Asn302GlyfsTer61


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