Variant #0000876306 (NC_000005.9:g.178416288G>A, NM_000843.3:c.1131C>T (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.178416288G>A
DNA change (hg38) -
Published as c.1131C>T
ISCN -
DB-ID GRM6_000002 See all 4 reported entries
Variant remarks -
Reference PubMed: Xu 2009
ClinVar ID -
dbSNP ID rs2071246
Origin Germline
Segregation -
Frequency 87/96 patients with high myopia
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.72255 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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRM6 NM_000843.3 -?/. 5 c.1131C>T r.(=) p.(=)


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