Variant #0000001846 (NC_000001.10:g.12062071G>T, MFN2(NM_014874.3):c.1071G>T)
| Individual ID |
00001846 |
| Chromosome |
1 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.12062071G>T |
| Reference |
Kijima K1, Numakura C, Izumino H, Umetsu K, Nezu A, Shiiki T, Ogawa M, Ishizaki Y, Kitamura T, Shozawa Y, Hayasaka K.(2005) |
| DB-ID |
MFN2_000017 |
| 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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