Variant #0000842006 (NC_000006.11:g.131902389C>A, ARG1(NM_000045.3):c.336C>A)

Individual ID 00404617
Chromosome 6
Allele Parent #2
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.131902389C>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID ARG1_000068
Variant remarks -
Reference PubMed: Diez-Fernandez 2018
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
Re-site -
VIP 0
Methylation -
Average frequency (gnomAD v.2.1.1) Variant not found in online data sets
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARG1 NM_000045.3 -?/. - c.336C>A r.(?) p.(Ala112=)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000405857 DNA SEQ - - ARG1 3 Johan den Dunnen