Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38060 | A09 | 46095562 | G | A | upstream_gene_variant | MODIFIER | c.-2598G>A| |
S133 |
2 | BAA09g38060 | A09 | 46095823 | G | A | upstream_gene_variant | MODIFIER | c.-2337G>A| |
S165 S176 |
3 | BAA09g38060 | A09 | 46096168 | C | T | upstream_gene_variant | MODIFIER | c.-1992C>T| |
S224 |
4 | BAA09g38060 | A09 | 46096170 | G | A | upstream_gene_variant | MODIFIER | c.-1990G>A| |
S20 |
5 | BAA09g38060 | A09 | 46096774 | A | T | upstream_gene_variant | MODIFIER | c.-1386A>T| |
S259 |
6 | BAA09g38060 | A09 | 46098267 | C | T | intron_variant | MODIFIER | c.51+57C>T| |
S303 |
7 | BAA09g38060 | A09 | 46098936 | C | T | synonymous_variant | LOW | c.423C>T|p.Ile141Ile |
S80 |
8 | BAA09g38060 | A09 | 46099009 | G | A | missense_variant | MODERATE | c.496G>A|p.Ala166Thr |
S42 |
9 | BAA09g38060 | A09 | 46099433 | G | A | missense_variant | MODERATE | c.920G>A|p.Arg307Lys |
S203 |
10 | BAA09g38060 | A09 | 46099950 | C | T | synonymous_variant | LOW | c.1437C>T|p.Leu479Leu |
S277 |
11 | BAA09g38060 | A09 | 46101201 | G | A | missense_variant | MODERATE | c.1714G>A|p.Ala572Thr |
S98 |
12 | BAA09g38060 | A09 | 46101568 | G | A | missense_variant | MODERATE | c.2081G>A|p.Arg694Lys |
S128 |
13 | BAA09g38060 | A09 | 46101579 | C | T | stop_gained | HIGH | c.2092C>T|p.Gln698* |
S106 S123 |
14 | BAA09g38060 | A09 | 46101590 | G | A | synonymous_variant | LOW | c.2103G>A|p.Leu701Leu |
S273 |
15 | BAA09g38060 | A09 | 46101621 | C | T | stop_gained | HIGH | c.2134C>T|p.Gln712* |
S202 |
16 | BAA09g38060 | A09 | 46102005 | G | A | downstream_gene_variant | MODIFIER | c.*196G>A| |
S13 |