Variant #0000185995 (NC_000023.10:g.?)
| Individual ID |
00115130 |
| Chromosome |
X |
| Allele |
Maternal (confirmed) |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.? |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
SHOX_000233 See all 19 reported entries |
| Variant remarks |
pseudoautosomal microdeletion involving SHOX, 1/5 patients |
| Reference |
PubMed: Zinn 2002, OMIM:var0003 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Germline |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Ralph Roeth |
| Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
| Created by |
Ralph Roeth |
| Date created |
2006-12-13 14:29:32 +01:00 (CET) |
| Date last edited |
2017-08-09 14:14:35 +02:00 (CEST) |
Variant on transcripts
Screenings
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