Variant #0000667041 (NC_000002.11:g.pter_85474807delins[NC_000011.9:pter_16035758])
| Individual ID |
00302556 |
| Chromosome |
2 |
| 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.pter_85474807delins[NC_000011.9:pter_16035758] |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
46,XY,t(2;11)(p11.2;p15.2) |
| DB-ID |
chr2_016758 |
| Variant remarks |
- |
| Reference |
PubMed: Tolchin 2020 |
| 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 |
2020-05-24 15:52:32 +02:00 (CEST) |
| Date last edited |
N/A |
Variant on transcripts
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