Variant #0000055807 (NC_000001.10:g.(151446793_151485910)_qterdelins[NC_000022.10:(24792059_24798018)_qter])
| Individual ID |
00029718 |
| Chromosome |
1 |
| Allele |
Parent #1 |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(151446793_151485910)_qterdelins[NC_000022.10:(24792059_24798018)_qter] |
| DNA change (hg38) |
- |
| Published as |
hg18 g.(149713417_149752534)::(23122059_23128018) |
| ISCN |
46,XX,t(1;22)(q21;q12) |
| DB-ID |
chr1_000447 |
| Variant remarks |
- |
| Reference |
PubMed: Saadi 2011, Journal: Saadi 2011 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2015-01-31 22:35:05 +01:00 (CET) |
| Date last edited |
2020-05-10 14:35:44 +02:00 (CEST) |
Variant on transcripts
Screenings
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