Variant #0000004397 (NC_000021.8:g.45194641C>G, CSTB(NM_000100.3):c.67-1G>C)
| Individual ID |
00004397 |
| Chromosome |
21 |
| Allele |
Unknown |
| Affects function (as reported) |
Not classified |
| Affects function (by curator) |
Not classified |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45194641C>G |
| Reference |
Pennacchio LA1, Lehesjoki AE, Stone NE, Willour VL, Virtaneva K, Miao J, D'Amato E, Ramirez L, Faham M, Koskiniemi M, Warrington JA, Norio R, de la (1996) |
| DB-ID |
CSTB_000001 |
| Frequency |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00015 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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