Variant #0000004398 (NC_000021.8:g.45194178G>A, CSTB(NM_000100.3):c.202C>T)
Individual ID |
00004398 |
Chromosome |
21 |
Allele |
Unknown |
Affects function (as reported) |
Not classified |
Affects function (by curator) |
Not classified |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.45194178G>A |
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_000002 See all 3 reported entries |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
4.0E-5 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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