Variant #0001068497 (NC_000005.9:g.pter_(4500001_9800000)delins[NC_000016.9:g.(51381183_51385183)_qter)])
| Individual ID |
00472547 |
| Chromosome |
5 |
| 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_(4500001_9800000)delins[NC_000016.9:g.(51381183_51385183)_qter)] |
| DNA change (hg38) |
g.pter_(4400001_9900000)delins[NC_000016.10:g.(51347272_51351272)_qter)] |
| Published as |
- |
| ISCN |
t(5;16)(p15.3;q12.1) |
| DB-ID |
chr5_007769 |
| Variant remarks |
- |
| Reference |
PubMed: Marlin 1999 |
| 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 |
2026-02-23 16:04:57 +01:00 (CET) |
| Date last edited |
2026-02-23 16:06:57 +01:00 (CET) |
Variant on transcripts
Screenings
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