Variant #0000876301 (NC_000005.9:g.178421961delinsA, NC_000005.9(NM_000843.3):c.67-82delCAGGCGGGCCTGGCGCinsT (GRM6))

Chromosome 5
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.178421961delinsA
DNA change (hg38) -
Published as c.67-82delCAGGCGGGCCTGGCGCinsT
ISCN -
DB-ID GRM6_000156
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 +?/. 1 c.67-82delCAGGCGGGCCTGGCGCinsT r.spl? p.?


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