Variant #0000016425 (NC_000006.11:g.41129125del, NM_018965.2:c.269del (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.41129125del |
| DNA change (hg38) |
g.41161387del |
| Published as |
267delG |
| ISCN |
- |
| DB-ID |
TREM2_000006 |
| Variant remarks |
1 French (Turkish) PLOSL family (hom) |
| Reference |
PubMed: Klünemann et al. 2005 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
SUMMARY record |
| Segregation |
yes |
| 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 International |
| Created by |
Anne Polvi |
| Date created |
2012-11-15 13:58:52 +01:00 (CET) |
| Date last edited |
2020-06-19 11:49:50 +02:00 (CEST) |

Variant on transcripts
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