Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g27790 | A07 | 29369481 | C | T | downstream_gene_variant | MODIFIER | c.*3491G>A| |
S123 |
2 | BAA07g27790 | A07 | 29369492 | G | A | downstream_gene_variant | MODIFIER | c.*3480C>T| |
S87 |
3 | BAA07g27790 | A07 | 29369997 | C | T | downstream_gene_variant | MODIFIER | c.*2975G>A| |
S245 |
4 | BAA07g27790 | A07 | 29371167 | G | A | downstream_gene_variant | MODIFIER | c.*1805C>T| |
S45 |
5 | BAA07g27790 | A07 | 29371619 | G | A | downstream_gene_variant | MODIFIER | c.*1353C>T| |
S163 |
6 | BAA07g27790 | A07 | 29373008 | G | A | synonymous_variant | LOW | c.1872C>T|p.Phe624Phe |
S278 |
7 | BAA07g27790 | A07 | 29373197 | C | T | splice_region_variant&synonymous_variant | LOW | c.1782G>A|p.Gln594Gln |
S66 |
8 | BAA07g27790 | A07 | 29375811 | C | T | missense_variant | MODERATE | c.802G>A|p.Ala268Thr |
S217 |
9 | BAA07g27790 | A07 | 29377187 | G | A | missense_variant | MODERATE | c.251C>T|p.Ala84Val |
S276 |
10 | BAA07g27790 | A07 | 29378073 | G | A | upstream_gene_variant | MODIFIER | c.-636C>T| |
S131 |
11 | BAA07g27790 | A07 | 29380293 | C | T | upstream_gene_variant | MODIFIER | c.-2856G>A| |
S126 |
12 | BAA07g27790 | A07 | 29380347 | G | A | upstream_gene_variant | MODIFIER | c.-2910C>T| |
S40 S49 |
13 | BAA07g27790 | A07 | 29380649 | G | A | upstream_gene_variant | MODIFIER | c.-3212C>T| |
S136 |
14 | BAA07g27790 | A07 | 29381175 | C | T | upstream_gene_variant | MODIFIER | c.-3738G>A| |
S122 |