Variant #0000876299 (NC_000005.9:g.178416063G>T, NM_000843.3:c.1227C>A (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.178416063G>T
DNA change (hg38) -
Published as Y409X
ISCN -
DB-ID GRM6_000150
Variant remarks -
Reference PubMed: O'Connor 2006
ClinVar ID -
dbSNP ID -
Origin Germline
Segregation -
Frequency -
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
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRM6 NM_000843.3 +?/. 6 c.1227C>A r.(?) p.(Tyr409*)


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