Variant #0000907114 (NC_000012.11:g.(?_103232104)_(103234294_103237423)del, NM_000277.1:c.(1199+1_1200-1)_*849{0} (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.(?_103232104)_(103234294_103237423)del |
DNA change (hg38) |
g.(?_102838326)_(102840516_102843645)del |
Published as |
del ex12-13 c.1200-?_1359+?del |
ISCN |
- |
DB-ID |
PAH_000564 |
Variant remarks |
allelic phenotype value 0, variant associated with classic PKU |
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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