Variant #0000907150 (NC_000012.11:g.(103249111_103260373)_(103260442_103271239)del, NC_000012.11(NM_000277.1):c.(441+1_442-1)_(509+1_510-1)del (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.(103249111_103260373)_(103260442_103271239)del |
DNA change (hg38) |
g.(102855333_102866595)_(102866664_102877461)del |
Published as |
del ex5 442-?_509 + ?del, 443_509+1del |
ISCN |
- |
DB-ID |
PAH_000450 See all 4 reported entries |
Variant remarks |
- |
Reference |
PubMed: Hillert 2020, data copied from the BIOPKU database, 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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