Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g16500 | A06 | 8201970 | T | A | downstream_gene_variant | MODIFIER | c.*4807A>T| |
S197 |
2 | BAA06g16500 | A06 | 8206812 | C | T | missense_variant | MODERATE | c.2812G>A|p.Gly938Arg |
S293 |
3 | BAA06g16500 | A06 | 8207377 | G | A | missense_variant | MODERATE | c.2405C>T|p.Thr802Ile |
S219 |
4 | BAA06g16500 | A06 | 8207489 | G | A | missense_variant | MODERATE | c.2293C>T|p.Leu765Phe |
S25 |
5 | BAA06g16500 | A06 | 8208546 | G | A | synonymous_variant | LOW | c.1236C>T|p.Ile412Ile |
S191 |
6 | BAA06g16500 | A06 | 8209212 | C | T | synonymous_variant | LOW | c.570G>A|p.Glu190Glu |
S195 |
7 | BAA06g16500 | A06 | 8209476 | C | T | stop_gained | HIGH | c.306G>A|p.Trp102* |
S247 |
8 | BAA06g16500 | A06 | 8211705 | C | T | upstream_gene_variant | MODIFIER | c.-1748G>A| |
S4 |
9 | BAA06g16500 | A06 | 8211899 | G | A | upstream_gene_variant | MODIFIER | c.-1942C>T| |
S146 |
10 | BAA06g16500 | A06 | 8212708 | G | A | upstream_gene_variant | MODIFIER | c.-2751C>T| |
S100 |
11 | BAA06g16500 | A06 | 8213352 | G | A | upstream_gene_variant | MODIFIER | c.-3395C>T| |
S249 |
12 | BAA06g16500 | A06 | 8213402 | G | A | upstream_gene_variant | MODIFIER | c.-3445C>T| |
S182 |