Variant #0000305332 (NC_000001.10:g.144930746T>C, NM_022359.5:c.*21451A>G (PDE4DIP))
| Chromosome |
1 |
| 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.144930746T>C |
| DNA change (hg38) |
g.148953729T>G |
| Published as |
PDE4DIP(NM_001002811.2):c.963A>G (p.G321=) |
| ISCN |
- |
| DB-ID |
PDE4DIP_000010 |
| 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_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2018-01-15 20:58:59 +01:00 (CET) |
| Date last edited |
2025-03-10 00:20:11 +01:00 (CET) |

Variant on transcripts
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