Variant #0000174968 (NC_000006.11:g.131904532G>C, ARG1(NM_000045.3):c.703G>C)

Chromosome 6
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.131904532G>C
DNA change (hg38) g.131583392G>C
Published as -
ISCN -
DB-ID ARG1_000009 See all 4 reported entries
Variant remarks E.coli expression cloning yields less then 0.01 protein activity
Reference PubMed: Uchino 1995
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
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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)