Variant #0000163053 (NC_000002.11:g.55910954G>A, NM_033109.4:c.419C>T (PNPT1))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.55910954G>A |
DNA change (hg38) |
g.55683819G>A |
Published as |
g.55910954C>T |
ISCN |
- |
DB-ID |
PNPT1_000002 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Germline |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
2.0E-5 View details |
Owner |
Sanna Matilainen |
Database submission license |
No license selected |
Created by |
Sanna Matilainen |
Date created |
2017-02-10 15:27:25 +01:00 (CET) |
Date last edited |
2017-02-19 11:22:36 +01:00 (CET) |

Variant on transcripts
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