Variant #0000016240 (NC_000019.9:g.36398422_36398423ins42, NM_003332.3:c.154_155ins42 (TYROBP))
Chromosome |
19 |
Allele |
Unknown |
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.36398422_36398423ins42 |
DNA change (hg38) |
- |
Published as |
154-155ins42nt, Ins of 14 aa |
ISCN |
- |
DB-ID |
TYROBP_000006 |
Variant remarks |
1 Scottish PLOSL family |
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 |
2012-11-13 16:18:18 +01:00 (CET) |
Date last edited |
2017-05-05 19:04:32 +02:00 (CEST) |

Variant on transcripts
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