Variant #0000438429 (NC_000003.11:g.[NC_000012.11:52312101_qter]delins[G;pter_48252146inv])
| Individual ID |
00207502 |
| Chromosome |
3 |
| 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.[NC_000012.11:52312101_qter]delins[G;pter_48252146inv] |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
t(12,3)(q13,p21) |
| DB-ID |
chr3_004452 |
| Variant remarks |
other translocation not described |
| Reference |
PubMed: Wooderchak-Donahue 2018 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
DUPLICATE record |
| 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 |
2018-11-23 17:41:00 +01:00 (CET) |
| Date last edited |
2020-05-12 19:21:26 +02:00 (CEST) |
Variant on transcripts
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