Variant #0000842048 (NC_000006.11:g.131900326A>T, ARG1(NM_000045.3):c.206A>T)

Individual ID 00404653
Chromosome 6
Allele Parent #1
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic (recessive)
DNA change (genomic) (Relative to hg19 / GRCh37) g.131900326A>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID ARG1_000083 See all 2 reported entries
Variant remarks -
Reference Mullane 2017, PubMed: Diez-Fernandez 2018
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARG1 NM_000045.3 +/. - c.206A>T r.(?) p.(Asn69Ile)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000405893 DNA SEQ - - ARG1 2 Johan den Dunnen