Variant #0000001927 (NC_000012.12:g.14018777G>C, NM_000834.4:c.366C>G (GRIN2B))

Individual ID 00000412
Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg38 / GRCh38) g.14018777G>C
Published as -
Reference Zainal Abidin et al. (2015)
DB-ID GRIN2B_000001
dbSNP ID rs7301328
Frequency -
Variant remarks -
Average frequency (gnomAD v.2.1.1) 0.40768 View details
Owner Nur Aisyah Athirah
Database submission license Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 InternationalCreative Commons License
Created by Nur Aisyah Athirah
Date created 2021-02-15 15:25:07 +08:00 (CST)
Date last edited 2021-03-29 09:16:51 +08:00 (CST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Published as     

RNA change     

Protein     

Clinical classification     
GRIN2B NM_000834.4 +/. - c.366C>G - r.(=) (p.Pro122=) Benign
GRIN2B XM_011520629.2 +/. - c.366C>G - r.(=) p.(=) Benign
GRIN2B XM_017019219.2 +/. - c.366C>G - r.(=) p.(=) Benign



Screenings


AscendingScreening ID     

Template     

Technique     

Genes screened     

Variants found     

Owner     
0000000429 DNA MCA GRIN2B 1 Nur Aisyah Athirah