Variant #0001018736 (NC_000005.9:g.(130600001_149800000)_qterdelins[NC_000023.10:g.(138000001_147100000)_qter])
| Individual ID |
00458185 |
| Chromosome |
5 |
| Allele |
Unknown |
| 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.(130600001_149800000)_qterdelins[NC_000023.10:g.(138000001_147100000)_qter] |
| DNA change (hg38) |
g.(131200001_150400000)_qterdelins[NC_000023.11:g.(138900001_148000000)_qter] |
| Published as |
- |
| ISCN |
46,XX,t(X;5)(q27;q31-q32) |
| DB-ID |
chr5_007321 |
| Variant remarks |
- |
| Reference |
PubMed: Mossman 1983 |
| 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 |
2024-12-07 19:38:47 +01:00 (CET) |
| Date last edited |
N/A |
Variant on transcripts
Screenings
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