Variant #0001047230 (NC_000003.11:g.52610513T>C, NC_000003.11(NM_018313.4):c.3616+44A>G (PBRM1))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.52610513T>C |
| DNA change (hg38) |
- |
| Published as |
- |
| ISCN |
- |
| DB-ID |
PBRM1_000010 |
| Variant remarks |
- |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs2028220 |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.04355 View details |
| Owner |
MobiDetails |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
MobiDetails |
| Date created |
2025-08-07 12:33:01 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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