Variant #0000270569 (NC_000002.11:g.211527838_211527839del, NC_000002.11(NM_001122633.2):c.3946-9_3946-8del (CPS1))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.211527838_211527839del |
| DNA change (hg38) |
g.210663114_210663115del |
| Published as |
CPS1(NM_001122633.3):c.3928-9_3928-8delTT, CPS1(NM_001875.5):c.3928-9_3928-8delTT |
| ISCN |
- |
| DB-ID |
CPS1_000262 See all 2 reported entries |
| Variant remarks |
VKGL data sharing initiative Nederland |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
CLASSIFICATION record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
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