Variant #0000001362 (NC_000017.10:g.42427661T>C, GRN(NM_002087.2):c.415T>C)
| Individual ID |
00001362 |
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42427661T>C |
| Reference |
Bernardi L1, Tomaino C, Anfossi M, Gallo M, Geracitano S, Costanzo A, Colao R, Puccio G, Frangipane F, Curcio SA, Mirabelli M, Smirne N, Iapaolo D, Maletta RG, Bruni AC.(2009) |
| DB-ID |
GRN_000010 See all 4 reported entries |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00018 View details |
| 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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