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
|
|