Variant #0000876304 (NC_000005.9:g.178418606C>G, NC_000005.9(NM_000843.3):c.726-50G>C (GRM6))

Chromosome 5
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.178418606C>G
DNA change (hg38) -
Published as c.726-50g>c
ISCN -
DB-ID GRM6_000153
Variant remarks -
Reference PubMed: Xu 2009
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency 1/96 patients with high myopia
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
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 ?/. 2i c.726-50G>C r.spl? p.?


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