Variant #0000174946 (NC_000006.11:g.131894454T>C, ARG1(NM_000045.3):c.32T>C)

Individual ID 00108470
Chromosome 6
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.131894454T>C
DNA change (hg38) g.131573314T>C
Published as -
ISCN -
DB-ID ARG1_000011 See all 7 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs28941474
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 +?/. 1 c.32T>C r.(?) p.(ile11Thr)



Screenings


AscendingScreening ID     

Template     

Technique     

Tissue     

Remarks     

Genes screened     

Variants found     

Owner     
0000108937 DNA SEQ - - ARG1 1 Johan den Dunnen