Variant #0000001108 (NC_000002.11:g.219135278C>T, PNKD(NM_015488.4):c.20C>T)
| Individual ID |
00001108 |
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.219135278C>T |
| Reference |
Fink JK1, Rainer S, Wilkowski J, Jones SM, Kume A, Hedera P, Albin R, Mathay J, Girbach L, Varvil T, Otterud B, Leppert M.(1996) |
| DB-ID |
PNKD_000002 See all 2 reported entries |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
Retrieve |
| Owner |
Y Yang |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
Y Yang |

Variant on transcripts
Screenings
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