Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g14830 | A08 | 12549043 | G | A | downstream_gene_variant | MODIFIER | c.*2770C>T| |
S30 |
2 | BAA08g14830 | A08 | 12550381 | G | A | downstream_gene_variant | MODIFIER | c.*1432C>T| |
S179 |
3 | BAA08g14830 | A08 | 12555715 | C | T | intron_variant | MODIFIER | c.747-286G>A| |
S71 |
4 | BAA08g14830 | A08 | 12556186 | G | A | intron_variant | MODIFIER | c.747-757C>T| |
S37 |
5 | BAA08g14830 | A08 | 12556213 | G | A | intron_variant | MODIFIER | c.747-784C>T| |
S86 |
6 | BAA08g14830 | A08 | 12557736 | G | A | intron_variant | MODIFIER | c.746+831C>T| |
S94 |
7 | BAA08g14830 | A08 | 12557998 | C | T | intron_variant | MODIFIER | c.746+569G>A| |
S251 |
8 | BAA08g14830 | A08 | 12558705 | C | T | missense_variant | MODERATE | c.608G>A|p.Gly203Asp |
S201 |
9 | BAA08g14830 | A08 | 12558808 | G | A | stop_gained | HIGH | c.505C>T|p.Gln169* |
S128 |
10 | BAA08g14830 | A08 | 12559560 | C | T | missense_variant | MODERATE | c.104G>A|p.Cys35Tyr |
S270 |
11 | BAA08g14830 | A08 | 12561963 | G | A | upstream_gene_variant | MODIFIER | c.-2300C>T| |
S204 |
12 | BAA08g14830 | A08 | 12562245 | G | A | upstream_gene_variant | MODIFIER | c.-2582C>T| |
S19 |
13 | BAA08g14830 | A08 | 12562589 | C | T | upstream_gene_variant | MODIFIER | c.-2926G>A| |
S251 |
14 | BAA08g14830 | A08 | 12562702 | G | A | upstream_gene_variant | MODIFIER | c.-3039C>T| |
S200 |
15 | BAA08g14830 | A08 | 12563924 | T | A | upstream_gene_variant | MODIFIER | c.-4261A>T| |
S280 |
16 | BAA08g14830 | A08 | 12564311 | C | T | upstream_gene_variant | MODIFIER | c.-4648G>A| |
S247 |