Variant #0001052429 (NC_000006.11:g.83898330C>T, NC_000006.11(NM_015599.2):c.389+3G>A (PGM3))
| Chromosome |
6 |
| 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.83898330C>T |
| DNA change (hg38) |
- |
| Published as |
PGM3(NM_001199917.2):c.473+3G>A, PGM3(NM_001367287.1):c.473+3G>A, PGM3(NM_015599.3):c.389+3G>A |
| ISCN |
- |
| DB-ID |
PGM3_000001 See all 3 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) |
0.00036 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2025-11-01 13:22:20 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
|