Variant #0000001195 (NC_000008.10:g.42698200C>T, THAP1(NM_018105.2):c.38G>A)
| Individual ID |
00001195 |
| Chromosome |
8 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42698200C>T |
| Reference |
Erogullari A1, Hollstein R1, Seibler P2, Braunholz D1, Koschmidder E2, Depping R3, Eckhold J4, Lohnau T2, Gillessen-Kaesbach G5, Grünewald A2, Rakovic A2, Lohmann K6, Kaiser FJ1.(2014) |
| DB-ID |
THAP1_000016 |
| 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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