Table 2.
Variant no. | Contig | Cov | Position of variant | Nucl. change | Mut type | Exon | Intron | Within probe range (±80 bp) | MAF | Gene |
---|---|---|---|---|---|---|---|---|---|---|
1 | NW_018027618.1 | 10 | 81,300 | T → A | TV | + | + | 0.10 | ||
2 | NW_018028177.1 | 10 | 361,879 | G → A | TI | + | + | 0.10 | arhgap31 | |
3 | NW_018028334.1 | 10 | 259,900 | C → T | TI | + | + | 0.10 | ||
4 | NW_018028334.1 | 10 | 259,937 | A → G | TI | + | + | 0.10 | ||
5 | NW_018028334.1 | 10 | 259,952 | C → T | TI | + | + | 0.10 | ||
6 | NW_018030239.1 | 10 | 300,687 | A → G | TI | + | + | 0.10 | ||
7 | NW_018030239.1 | 10 | 300,695 | A → T | TI | + | + | 0.10 | ||
8 | NW_018031751.1 | 10 | 272,654 | AGTTTCTGT → AGT | DEL | + | + | 0.30 | ||
9 | NW_018031751.1 | 10 | 272,838 | G → T | TV | + | + | 0.10 | ||
10 | NW_018032444.1 | 10 | 219,962 | T → C | TI | + | + | 0.10 | ||
11 | NW_018033032.1 | 10 | 57,538 | C → T | TI | + | + | 0.10 | ||
12 | NW_018034852.1 | 10 | 57,766 | A → G | TI | – | 0.10 | |||
13 | NW_018035951.1 | 10 | 70,329 | C → T | TI | + | + | 0.10 | ||
14 | NW_018048269.1 | 10 | 39,955 | A → G | TI | + | + | 0.10 | ||
15 | NW_018049874.1 | 64 | 2,967 | A → G | TI | – | 0.05 | |||
16 | NW_018055946.1 | 26 | 795,896 | T → C | TI | + | – | 0.23 | ||
17 | NW_018055946.1 | 28 | 795,897 | A → G | TI | + | – | 0.21 | ||
18 | NW_018056210.1 | 10 | 348,679 | A → G | TI | + | + | 0.10 | ||
19 | NW_018061029.1 | 10 | 213,227 | A → G | TI | + | + | 0.10 | ||
20 | NW_018067024.1 | 10 | 123,091 | C → G | TV | + | + | 0.10 | ||
21 | NW_018071985.1 | 10 | 326,258 | T → A | TV | + | + | 0.10 | ||
22 | NW_018071985.1 | 10 | 326,259 | G → C | TV | + | + | 0.10 |
Mut type: type of mutation, either transition (TI), transversion (TV) or deletion (DEL). Exon: variant occurs in exonic region (+). Intron: variant occurs in intronic region (+).
Abbreviations: Cov, coverage; MAF, minor allele frequency.