Variant #0000129161 (NC_000017.10:g.(pter_1512910)_(2312362_3300000)del)
| Individual ID |
00080119 |
| Chromosome |
17 |
| 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_1512910)_(2312362_3300000)del |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
arr[hg19] 17p13.3(1,512,910-2,312,362)x1 dn |
| DB-ID |
chr17_001692 |
| Variant remarks |
deletion affecting 20 RefSeq genes |
| Reference |
PubMed: Spengler 2012, PubMed: Fokstuen2013, for EUCID-SRS consortium |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
De novo |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
normal methylation H19/IGF2:IG-DMR, KCNQ1OT1:TSS-DMR |
| Average frequency (gnomAD v.2.1.1) |
Genomic location of variant could not be determined |
| Owner |
Zeynep Tümer |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Julia Lopez |
| Date created |
2016-09-01 17:30:25 +02:00 (CEST) |
| Date last edited |
2020-10-01 16:53:33 +02:00 (CEST) |
Variant on transcripts
Screenings
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