Variant #0000288806 (NC_000006.11:g.146720218T>C, NM_001278064.1:c.2043T>C (GRM1))

Chromosome 6
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.146720218T>C
DNA change (hg38) g.146399082T>C
Published as GRM1(NM_001278064.1):c.2043T>C (p.R681=), GRM1(NM_001278065.1):c.2043T>C (p.R681=)
ISCN -
DB-ID GRM1_000019
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00066 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRM1 NM_000838.3 -?/. - c.2043T>C r.(?) p.(Arg681=)
GRM1 NM_001278064.1 -?/. - c.2043T>C r.(?) p.(Arg681=)


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