Variant #0000000042 (NC_000017.10:g.42990798C>T, GFAP(NM_002055.4):c.619G>A)
| Individual ID |
00000042 |
| Chromosome |
17 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.42990798C>T |
| Reference |
Li R1, Johnson AB, Salomons G, Goldman JE, Naidu S, Quinlan R, Cree B, Ruyle SZ, Banwell B, D'Hooghe M, Siebert JR, Rolf CM, Cox H, Reddy A, GutiƩrrez-Solana LG, Collins A, Weller RO, Messing A, van der Knaap MS, Brenner M.(2005) |
| DB-ID |
GFAP_000048 |
| 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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