Variant #0000678623 (NC_000009.11:g.140069431G>A, NM_007327.3:c.*7452G>A (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.140069431G>A
DNA change (hg38) -
Published as ANAPC2(NM_013366.4):c.2432C>T (p.S811L)
ISCN -
DB-ID ANAPC2_000004
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
LRRC26 NM_001013653.2 ?/. - c.-5036C>T r.(?) p.(=)
SSNA1 NM_003731.2 ?/. - c.-13748G>A r.(?) p.(=)
GRIN1 NM_007327.3 ?/. - c.*7452G>A r.(=) p.(=)
ANAPC2 NM_013366.3 ?/. - c.2432C>T r.(?) p.(Ser811Leu)
TMEM210 XM_003846333.2 ?/. - c.-2952C>T r.(?) p.(=)


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