Variant #0000016428 (NC_000006.11:g.41127611T>C, NM_018965.2:c.401A>G (TREM2))

Chromosome 6
Allele Both (homozygous)
Affects function (as reported) Probably affects function
Affects function (by curator) Probably affects function
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.41127611T>C
DNA change (hg38) g.41159873T>C
Published as 401A→G
ISCN -
DB-ID TREM2_000009
Variant remarks 1 American PLOSL patient (hom)
Reference PubMed: Paloneva et al. 2002
ClinVar ID -
dbSNP ID rs28939079
Origin SUMMARY record
Segregation yes
Frequency 0/100 CON
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0 View details
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TREM2 NM_018965.2 +?/+? 3 c.401A>G r.(401a>g) p.(Asp134Gly)


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