Variant #0000288814 (NC_000006.11:g.146755132G>A, GRM1(NM_001278064.1):c.2785G>A)

Chromosome 6
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.146755132G>A
DNA change (hg38) g.146433996G>A
Published as GRM1(NM_001278064.1):c.2785G>A (p.V929I)
ISCN -
DB-ID GRM1_000028
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) 0.01296 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GRM1 NM_000838.3 -/. - c.2785G>A r.(?) p.(Val929Ile)
GRM1 NM_001278064.1 -/. - c.2785G>A r.(?) p.(Val929Ile)