Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g03770 | A06 | 2132273 | G | A | intron_variant | MODIFIER | c.1722+56G>A| |
S206 S26 |
2 | BAA06g03770 | A06 | 2132409 | G | A | intron_variant | MODIFIER | c.1723-18G>A| |
S174 |
3 | BAA06g03770 | A06 | 2132586 | A | G | splice_region_variant&intron_variant | LOW | c.1875+7A>G| |
S125 |
4 | BAA06g03770 | A06 | 2133016 | C | T | intron_variant | MODIFIER | c.1876-11C>T| |
S75 S81 |
5 | BAA06g03770 | A06 | 2133326 | C | T | missense_variant | MODERATE | c.2086C>T|p.Pro696Ser |
S6 |
6 | BAA06g03770 | A06 | 2133865 | G | A | missense_variant | MODERATE | c.2266G>A|p.Ala756Thr |
S19 |
7 | BAA06g03770 | A06 | 2136342 | G | A | missense_variant | MODERATE | c.3206G>A|p.Arg1069Lys |
S212 |
8 | BAA06g03770 | A06 | 2137769 | C | T | intron_variant | MODIFIER | c.3574-211C>T| |
S165 S211 S227 |
9 | BAA06g03770 | A06 | 2138357 | C | T | splice_region_variant&intron_variant | LOW | c.3879+4C>T| |
S296 |
10 | BAA06g03770 | A06 | 2138838 | C | T | missense_variant | MODERATE | c.3938C>T|p.Ala1313Val |
S303 |
11 | BAA06g03770 | A06 | 2139328 | C | T | intron_variant | MODIFIER | c.4149-37C>T| |
S134 |
12 | BAA06g03770 | A06 | 2139723 | C | T | intron_variant | MODIFIER | c.4246+261C>T| |
S17 |
13 | BAA06g03770 | A06 | 2139828 | C | T | intron_variant | MODIFIER | c.4247-163C>T| |
S183 S198 |
14 | BAA06g03770 | A06 | 2140429 | G | A | intron_variant | MODIFIER | c.4531-39G>A| |
S144 |
15 | BAA06g03770 | A06 | 2141597 | C | T | intron_variant | MODIFIER | c.4918-13C>T| |
S142 |
16 | BAA06g03770 | A06 | 2143304 | G | A | splice_region_variant&intron_variant | LOW | c.5946+8G>A| |
S143 |
17 | BAA06g03770 | A06 | 2143614 | C | T | missense_variant | MODERATE | c.5956C>T|p.His1986Tyr |
S34 |
18 | BAA06g03770 | A06 | 2144343 | C | T | intron_variant | MODIFIER | c.6330+69C>T| |
S267 |
19 | BAA06g03770 | A06 | 2144914 | G | A | missense_variant | MODERATE | c.6653G>A|p.Arg2218Gln |
S191 |
20 | BAA06g03770 | A06 | 2145365 | G | A | splice_region_variant&intron_variant | LOW | c.6853-8G>A| |
S83 S88 |
21 | BAA06g03770 | A06 | 2145430 | G | A | missense_variant | MODERATE | c.6910G>A|p.Gly2304Arg |
S190 |
22 | BAA06g03770 | A06 | 2145626 | C | T | missense_variant | MODERATE | c.7106C>T|p.Ala2369Val |
S305 |