Variant #0000129082 (NC_000007.13:g.(54000001_58000000)_(147900000_qter)inv)
| Individual ID |
00080080 |
| Chromosome |
7 |
| Allele |
Maternal (confirmed) |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(54000001_58000000)_(147900000_qter)inv |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
46,XY,inv(7)(p11.2q36) dn |
| DB-ID |
chr7_000407 |
| Variant remarks |
inversion |
| Reference |
PubMed: Monk 2002, for EUCID-SRS consortium |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Zeynep Tümer |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2016-09-01 17:30:25 +02:00 (CEST) |
| Date last edited |
2020-10-01 16:53:33 +02:00 (CEST) |
Variant on transcripts
Screenings
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