Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g06880 | A10 | 3684035 | C | T | upstream_gene_variant | MODIFIER | c.-2254C>T| |
S282 |
2 | BAA10g06880 | A10 | 3685386 | G | A | upstream_gene_variant | MODIFIER | c.-903G>A| |
S100 |
3 | BAA10g06880 | A10 | 3686321 | G | A | synonymous_variant | LOW | c.33G>A|p.Arg11Arg |
S12 |
4 | BAA10g06880 | A10 | 3686631 | C | T | missense_variant | MODERATE | c.245C>T|p.Pro82Leu |
S235 |
5 | BAA10g06880 | A10 | 3686794 | G | A | synonymous_variant | LOW | c.408G>A|p.Ala136Ala |
S86 |
6 | BAA10g06880 | A10 | 3686940 | G | A | missense_variant | MODERATE | c.461G>A|p.Cys154Tyr |
S276 |
7 | BAA10g06880 | A10 | 3687336 | C | T | missense_variant | MODERATE | c.857C>T|p.Thr286Ile |
S44 |
8 | BAA10g06880 | A10 | 3687410 | C | T | missense_variant | MODERATE | c.931C>T|p.Pro311Ser |
S79 S91 |
9 | BAA10g06880 | A10 | 3687456 | G | A | missense_variant | MODERATE | c.977G>A|p.Cys326Tyr |
S18 |
10 | BAA10g06880 | A10 | 3687819 | C | T | missense_variant | MODERATE | c.1250C>T|p.Pro417Leu |
S297 |
11 | BAA10g06880 | A10 | 3687862 | G | A | synonymous_variant | LOW | c.1293G>A|p.Ser431Ser |
S221 |
12 | BAA10g06880 | A10 | 3688179 | C | T | missense_variant | MODERATE | c.1610C>T|p.Ser537Phe |
S19 |
13 | BAA10g06880 | A10 | 3689128 | C | T | missense_variant | MODERATE | c.2060C>T|p.Ser687Phe |
S40 S49 |
14 | BAA10g06880 | A10 | 3689255 | G | A | synonymous_variant | LOW | c.2187G>A|p.Gly729Gly |
S57 |
15 | BAA10g06880 | A10 | 3690179 | G | A | missense_variant | MODERATE | c.2935G>A|p.Val979Ile |
S59 |
16 | BAA10g06880 | A10 | 3690200 | C | T | missense_variant | MODERATE | c.2956C>T|p.Pro986Ser |
S139 |
17 | BAA10g06880 | A10 | 3690358 | C | T | synonymous_variant | LOW | c.3114C>T|p.Ile1038Ile |
S235 |
18 | BAA10g06880 | A10 | 3690450 | G | A | splice_region_variant&intron_variant | LOW | c.3202+4G>A| |
S250 |