Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g11150 | A04 | 17091753 | T | C | downstream_gene_variant | MODIFIER | c.*1794A>G| |
S259 |
2 | BAA04g11150 | A04 | 17093923 | G | A | synonymous_variant | LOW | c.3213C>T|p.Ile1071Ile |
S201 |
3 | BAA04g11150 | A04 | 17094131 | G | A | missense_variant | MODERATE | c.3005C>T|p.Ala1002Val |
S273 |
4 | BAA04g11150 | A04 | 17094552 | C | T | synonymous_variant | LOW | c.2724G>A|p.Val908Val |
S189 |
5 | BAA04g11150 | A04 | 17094722 | C | T | missense_variant | MODERATE | c.2639G>A|p.Gly880Glu |
S294 |
6 | BAA04g11150 | A04 | 17094976 | G | A | synonymous_variant | LOW | c.2385C>T|p.Val795Val |
S245 |
7 | BAA04g11150 | A04 | 17098466 | C | T | missense_variant | MODERATE | c.1272G>A|p.Met424Ile |
S20 |
8 | BAA04g11150 | A04 | 17098667 | C | T | synonymous_variant | LOW | c.1149G>A|p.Ala383Ala |
S192 S239 |
9 | BAA04g11150 | A04 | 17098921 | C | T | missense_variant | MODERATE | c.1072G>A|p.Asp358Asn |
S276 |
10 | BAA04g11150 | A04 | 17099386 | C | T | missense_variant | MODERATE | c.814G>A|p.Asp272Asn |
S159 S299 |
11 | BAA04g11150 | A04 | 17099792 | C | T | synonymous_variant | LOW | c.534G>A|p.Glu178Glu |
S32 |
12 | BAA04g11150 | A04 | 17101290 | C | T | upstream_gene_variant | MODIFIER | c.-887G>A| |
S115 |
13 | BAA04g11150 | A04 | 17101297 | C | T | upstream_gene_variant | MODIFIER | c.-894G>A| |
S23 |
14 | BAA04g11150 | A04 | 17101388 | G | A | upstream_gene_variant | MODIFIER | c.-985C>T| |
S259 |
15 | BAA04g11150 | A04 | 17101664 | C | T | upstream_gene_variant | MODIFIER | c.-1261G>A| |
S294 |
16 | BAA04g11150 | A04 | 17102089 | C | T | upstream_gene_variant | MODIFIER | c.-1686G>A| |
S54 |
17 | BAA04g11150 | A04 | 17102939 | C | T | upstream_gene_variant | MODIFIER | c.-2536G>A| |
S137 |
18 | BAA04g11150 | A04 | 17104107 | G | A | upstream_gene_variant | MODIFIER | c.-3704C>T| |
S158 |
19 | BAA04g11150 | A04 | 17104801 | G | A | upstream_gene_variant | MODIFIER | c.-4398C>T| |
S261 |