Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11820 | A09 | 6656557 | C | T | synonymous_variant | LOW | c.11463G>A|p.Glu3821Glu |
S273 |
2 | BAA09g11820 | A09 | 6656571 | C | T | missense_variant | MODERATE | c.11449G>A|p.Glu3817Lys |
S182 |
3 | BAA09g11820 | A09 | 6656654 | C | T | missense_variant&splice_region_variant | MODERATE | c.11443G>A|p.Glu3815Lys |
S208 S93 |
4 | BAA09g11820 | A09 | 6657268 | C | T | synonymous_variant | LOW | c.10920G>A|p.Lys3640Lys |
S161 |
5 | BAA09g11820 | A09 | 6657581 | G | A | intron_variant | MODIFIER | c.10683+57C>T| |
S276 |
6 | BAA09g11820 | A09 | 6657637 | C | T | splice_donor_variant&intron_variant | HIGH | c.10683+1G>A| |
S296 |
7 | BAA09g11820 | A09 | 6658101 | G | A | missense_variant | MODERATE | c.10313C>T|p.Pro3438Leu |
S167 |
8 | BAA09g11820 | A09 | 6658214 | C | T | synonymous_variant | LOW | c.10200G>A|p.Glu3400Glu |
S249 |
9 | BAA09g11820 | A09 | 6658429 | C | T | missense_variant | MODERATE | c.9985G>A|p.Glu3329Lys |
S132 S137 S215 |
10 | BAA09g11820 | A09 | 6658502 | G | A | intron_variant | MODIFIER | c.9972+34C>T| |
S221 |
11 | BAA09g11820 | A09 | 6658628 | G | A | synonymous_variant | LOW | c.9880C>T|p.Leu3294Leu |
S241 |
12 | BAA09g11820 | A09 | 6659116 | G | A | synonymous_variant | LOW | c.9471C>T|p.Ile3157Ile |
S274 |
13 | BAA09g11820 | A09 | 6659141 | G | A | missense_variant | MODERATE | c.9446C>T|p.Pro3149Leu |
S210 |
14 | BAA09g11820 | A09 | 6660457 | G | A | synonymous_variant | LOW | c.8376C>T|p.Leu2792Leu |
S166 |
15 | BAA09g11820 | A09 | 6660723 | C | T | missense_variant | MODERATE | c.8110G>A|p.Gly2704Arg |
S272 |
16 | BAA09g11820 | A09 | 6662051 | C | T | missense_variant | MODERATE | c.7063G>A|p.Val2355Met |
S6 |
17 | BAA09g11820 | A09 | 6663147 | G | A | synonymous_variant | LOW | c.6397C>T|p.Leu2133Leu |
S75 S81 |
18 | BAA09g11820 | A09 | 6664239 | C | T | intron_variant | MODIFIER | c.5617-120G>A| |
S173 |
19 | BAA09g11820 | A09 | 6665237 | G | A | missense_variant | MODERATE | c.5144C>T|p.Thr1715Ile |
S182 |
20 | BAA09g11820 | A09 | 6666031 | G | A | missense_variant | MODERATE | c.4579C>T|p.Leu1527Phe |
S44 |
21 | BAA09g11820 | A09 | 6666397 | C | T | missense_variant | MODERATE | c.4297G>A|p.Val1433Met |
S213 |
22 | BAA09g11820 | A09 | 6666742 | C | T | missense_variant | MODERATE | c.4083G>A|p.Met1361Ile |
S135 |
23 | BAA09g11820 | A09 | 6667516 | C | T | missense_variant | MODERATE | c.3400G>A|p.Val1134Ile |
S68 |
24 | BAA09g11820 | A09 | 6667826 | C | T | synonymous_variant | LOW | c.3090G>A|p.Lys1030Lys |
S296 |
25 | BAA09g11820 | A09 | 6668897 | G | A | missense_variant | MODERATE | c.2137C>T|p.Pro713Ser |
S144 |