Variant #0000876302 (NC_000005.9:g.178421770T>G, NM_000843.3:c.176A>C (GRM6))

Chromosome 5
Allele Unknown
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.178421770T>G
DNA change (hg38) -
Published as c.176A>C
ISCN -
DB-ID GRM6_000033 See all 3 reported entries
Variant remarks -
Reference PubMed: Xu 2009
ClinVar ID -
dbSNP ID rs2645329
Origin Germline
Segregation -
Frequency 76/96 patients with high myopia
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.54981 View details
Owner LOVD
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by Julia Lopez
Date created 2022-08-15 15:41:08 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRM6 NM_000843.3 -?/. 1 c.176A>C r.(?) p.(Gln59Pro)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.