Variant #0000907182 (NC_000012.11:g.103248408_103256238del, NC_000012.11(NM_000277.1):c.509+4140_706+510del (PAH))
| Chromosome |
12 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic (recessive) |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.103248408_103256238del |
| DNA change (hg38) |
g.102854630_102862460del |
| Published as |
del ex6, c.509+4140_706+510del7831 |
| ISCN |
- |
| DB-ID |
PAH_000338 See all 12 reported entries |
| Variant remarks |
- |
| Reference |
PubMed: Hillert 2020, data copied from the BIOPKU database |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Johan den Dunnen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Johan den Dunnen |
| Date created |
2022-12-06 18:01:45 +01:00 (CET) |
| Date last edited |
2024-02-13 15:01:42 +01:00 (CET) |

Variant on transcripts
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