Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g67270 | A09 | 61040780 | C | T | upstream_gene_variant | MODIFIER | c.-3866C>T| |
S287 |
2 | BAA09g67270 | A09 | 61043066 | G | A | upstream_gene_variant | MODIFIER | c.-1580G>A| |
S233 |
3 | BAA09g67270 | A09 | 61044040 | C | T | upstream_gene_variant | MODIFIER | c.-606C>T| |
S153 S213 |
4 | BAA09g67270 | A09 | 61044710 | C | T | missense_variant | MODERATE | c.65C>T|p.Ser22Phe |
S192 |
5 | BAA09g67270 | A09 | 61046285 | C | A | intron_variant | MODIFIER | c.658+36C>A| |
S4 |
6 | BAA09g67270 | A09 | 61046436 | G | A | intron_variant | MODIFIER | c.685+46G>A| |
S181 |
7 | BAA09g67270 | A09 | 61047241 | G | A | intron_variant | MODIFIER | c.875-46G>A| |
S190 |
8 | BAA09g67270 | A09 | 61047262 | C | T | intron_variant | MODIFIER | c.875-25C>T| |
S192 |
9 | BAA09g67270 | A09 | 61048386 | G | A | intron_variant | MODIFIER | c.1341+37G>A| |
S40 S49 |
10 | BAA09g67270 | A09 | 61048429 | G | A | intron_variant | MODIFIER | c.1342-24G>A| |
S79 S84 |
11 | BAA09g67270 | A09 | 61049395 | G | A | intron_variant | MODIFIER | c.1769-94G>A| |
S288 |
12 | BAA09g67270 | A09 | 61049558 | G | A | intron_variant | MODIFIER | c.1822+16G>A| |
S84 S93 |
13 | BAA09g67270 | A09 | 61049666 | C | T | missense_variant | MODERATE | c.1855C>T|p.Arg619Cys |
S27 |
14 | BAA09g67270 | A09 | 61050820 | C | T | downstream_gene_variant | MODIFIER | c.*43C>T| |
S33 |
15 | BAA09g67270 | A09 | 61051679 | G | A | downstream_gene_variant | MODIFIER | c.*902G>A| |
S197 S45 |
16 | BAA09g67270 | A09 | 61051859 | C | T | downstream_gene_variant | MODIFIER | c.*1082C>T| |
S171 |
17 | BAA09g67270 | A09 | 61052879 | G | A | downstream_gene_variant | MODIFIER | c.*2102G>A| |
S170 |
18 | BAA09g67270 | A09 | 61053883 | C | T | downstream_gene_variant | MODIFIER | c.*3106C>T| |
S308 |
19 | BAA09g67270 | A09 | 61054417 | G | A | downstream_gene_variant | MODIFIER | c.*3640G>A| |
S88 |