Variant #0000174964 (NC_000006.11:g.131904532G>C, ARG1(NM_000045.3):c.703G>C)

Individual ID 00108481
Chromosome 6
Allele Maternal (confirmed)
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.131904532G>C
DNA change (hg38) g.131583392G>C
Published as -
ISCN -
DB-ID ARG1_000009 See all 4 reported entries
Variant remarks -
Reference PubMed: Uchino 1992, OMIM:var0006
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 +/. 7 c.703G>C r.(?) p.(Gly235Arg)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000108948 DNA SEQ - - ARG1 2 Johan den Dunnen