Variant #0000016420 (NC_000006.11:g.41130781C>A, NM_018965.2:c.40G>T (TREM2))

Chromosome 6
Allele Both (homozygous)
Affects function (as reported) Affects function
Affects function (by curator) Affects function
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.41130781C>A
DNA change (hg38) g.41163043C>A
Published as 40G>T, last position of exon 1: r.0 (Glu14Stp)
ISCN -
DB-ID TREM2_000001
Variant remarks 1 German PLOSL patient (hom)
Reference PubMed: Paloneva et al. 2003
ClinVar ID -
dbSNP ID -
Origin SUMMARY record
Segregation ?
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Anne Polvi
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Anne Polvi
Date created 2012-11-15 13:58:52 +01:00 (CET)
Date last edited 2017-05-05 18:33:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TREM2 NM_018965.2 +/+ 1 c.40G>T r.0 p.0


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