Variant #0000236324 (NC_000004.11:g.147028554_qterdelins[NC_000023.10:pter_32567260inv])
| Individual ID |
00122471 |
| Chromosome |
4 |
| Allele |
Unknown |
| 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.147028554_qterdelins[NC_000023.10:pter_32567260inv] |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
46,X,t(X;4)(p21.2;q31.22) |
| DB-ID |
chr4_000578 |
| Variant remarks |
translocation, der4, includes deletion 147028556_147028561 |
| Reference |
PubMed: Giacalone 1992 |
| 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 |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2017-12-10 13:27:04 +01:00 (CET) |
| Date last edited |
2020-05-12 19:21:26 +02:00 (CEST) |
Variant on transcripts
Screenings
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