Variant #0000018009 (NC_000002.11:g.168108032G>A, NM_152381.5:c.10130G>A (XIRP2))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Effect unknown |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.168108032G>A |
| DNA change (hg38) |
g.167251522G>A |
| Published as |
- |
| ISCN |
- |
| DB-ID |
XIRP2_000001 See all 2 reported entries |
| Variant remarks |
variant marked as interesting (probably affects the function of the gene with phenotypic consequences) from an exome analysis. Please contact me. |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
1 |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.02121 View details |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2013-05-08 23:53:32 +02:00 (CEST) |
| Date last edited |
2022-10-13 06:49:36 +02:00 (CEST) |

Variant on transcripts
Screenings
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