Table 2.
SNV statistics of 65 genome variants used in analysis
SNV | Counts (%) |
---|---|
Intronic variants: | 33 (53.23) |
UTR 3’ variants | 28 (84.84) |
UTR 5’ variants | 5 (15.16) |
Exonic variants: | 29 (46.77) |
Synonymous | 11 (37.93) |
Nonsynonymous | 17 (58.62) |
Stopgain | 1 (3.48) |