Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g05200 | A06 | 2928875 | C | T | synonymous_variant | LOW | c.40C>T|p.Leu14Leu |
S159 S243 |
2 | BAA06g05200 | A06 | 2929129 | C | T | missense_variant | MODERATE | c.109C>T|p.Leu37Phe |
S208 S93 |
3 | BAA06g05200 | A06 | 2931027 | G | A | missense_variant | MODERATE | c.596G>A|p.Gly199Asp |
S186 |
4 | BAA06g05200 | A06 | 2932560 | G | A | missense_variant | MODERATE | c.1093G>A|p.Asp365Asn |
S64 |
5 | BAA06g05200 | A06 | 2932564 | G | A | missense_variant | MODERATE | c.1097G>A|p.Arg366Lys |
S202 |
6 | BAA06g05200 | A06 | 2933469 | G | A | missense_variant | MODERATE | c.1528G>A|p.Gly510Arg |
S155 S211 |
7 | BAA06g05200 | A06 | 2933774 | G | A | synonymous_variant | LOW | c.1704G>A|p.Lys568Lys |
S183 S198 S246 |
8 | BAA06g05200 | A06 | 2934104 | G | A | intron_variant | MODIFIER | c.1798-213G>A| |
S291 |
9 | BAA06g05200 | A06 | 2934322 | G | A | stop_gained | HIGH | c.1803G>A|p.Trp601* |
S61 |
10 | BAA06g05200 | A06 | 2934392 | G | A | missense_variant | MODERATE | c.1873G>A|p.Glu625Lys |
S267 |
11 | BAA06g05200 | A06 | 2934451 | G | A | intron_variant | MODIFIER | c.1893+39G>A| |
S100 |
12 | BAA06g05200 | A06 | 2935156 | C | T | synonymous_variant | LOW | c.2157C>T|p.Phe719Phe |
S13 |
13 | BAA06g05200 | A06 | 2936134 | G | A | intron_variant | MODIFIER | c.2739+90G>A| |
S202 |
14 | BAA06g05200 | A06 | 2937098 | G | A | intron_variant | MODIFIER | c.3045+198G>A| |
S68 |
15 | BAA06g05200 | A06 | 2937187 | G | A | intron_variant | MODIFIER | c.3046-178G>A| |
S67 |
16 | BAA06g05200 | A06 | 2937461 | C | T | missense_variant | MODERATE | c.3142C>T|p.Pro1048Ser |
S266 |
17 | BAA06g05200 | A06 | 2937623 | G | A | missense_variant | MODERATE | c.3304G>A|p.Asp1102Asn |
S169 |
18 | BAA06g05200 | A06 | 2937866 | G | A | intron_variant | MODIFIER | c.3525+22G>A| |
S243 S299 |
19 | BAA06g05200 | A06 | 2937997 | G | A | missense_variant | MODERATE | c.3590G>A|p.Gly1197Asp |
S32 |
20 | BAA06g05200 | A06 | 2938337 | G | A | intron_variant | MODIFIER | c.3846+84G>A| |
S297 |
21 | BAA06g05200 | A06 | 2938713 | C | T | synonymous_variant | LOW | c.4005C>T|p.Gly1335Gly |
S240 |
22 | BAA06g05200 | A06 | 2940099 | C | T | missense_variant | MODERATE | c.4724C>T|p.Thr1575Ile |
S103 |
23 | BAA06g05200 | A06 | 2940379 | C | T | missense_variant | MODERATE | c.4900C>T|p.Pro1634Ser |
S171 |
24 | BAA06g05200 | A06 | 2941029 | G | A | intron_variant | MODIFIER | c.5478+72G>A| |
S117 |
25 | BAA06g05200 | A06 | 2941114 | C | T | intron_variant | MODIFIER | c.5479-29C>T| |
S63 |