Variant #0000222712 (NC_000006.11:g.(117996640_118029751dup), NM_138459.3:c.(-194_*1573dup) (NUS1))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Affects function |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.(117996640_118029751dup) |
| DNA change (hg38) |
- |
| Published as |
g.95751061_95751062ins[95751062_95751078;G;NM_138459.2:c.-194_*1573;AAAAAAAAAAAAAAAAA] |
| ISCN |
- |
| DB-ID |
NUS1_000001 |
| Variant remarks |
the additional copy of this sequence is inserted in SLC25A13 intron 16 on chromosome 7 |
| Reference |
PubMed: Tabata 2008, Journal: Tabata 2008 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
DUPLICATE record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2017-11-02 08:53:56 +01:00 (CET) |
| Date last edited |
2017-11-02 08:54:20 +01:00 (CET) |

Variant on transcripts
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