Variant #0000612038 (NC_000009.11:g.140063765_140063766insTT, NM_007327.3:c.*1786_*1787insTT (GRIN1))

Chromosome 9
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.140063765_140063766insTT
DNA change (hg38) g.137169313_137169314insTT
Published as LRRC26(NM_001013653.2):c.630_631insAA (p.(Pro211AsnfsTer28))
ISCN -
DB-ID GRIN1_000053
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) 0.00023 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-26 13:07:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC26 NM_001013653.2 ?/. - c.630_631insAA r.(?) p.(Pro211AsnfsTer28)
GRIN1 NM_007327.3 ?/. - c.*1786_*1787insTT r.(=) p.(=)
TMEM210 XM_003846333.2 ?/. - c.*1661_*1662insAA r.(=) p.(=)


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