Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g41340 | A06 | 26891158 | C | T | synonymous_variant | LOW | c.2667G>A|p.Gln889Gln |
S5 |
2 | BAA06g41340 | A06 | 26891304 | C | T | missense_variant | MODERATE | c.2521G>A|p.Asp841Asn |
S244 |
3 | BAA06g41340 | A06 | 26893142 | G | A | missense_variant | MODERATE | c.1523C>T|p.Ser508Phe |
S9 |
4 | BAA06g41340 | A06 | 26893923 | C | T | missense_variant | MODERATE | c.1190G>A|p.Gly397Glu |
S46 |
5 | BAA06g41340 | A06 | 26894336 | C | T | missense_variant | MODERATE | c.1025G>A|p.Arg342Lys |
S155 |
6 | BAA06g41340 | A06 | 26895723 | C | T | intron_variant | MODIFIER | c.403-73G>A| |
S242 |
7 | BAA06g41340 | A06 | 26896657 | C | T | upstream_gene_variant | MODIFIER | c.-197G>A| |
S18 |
8 | BAA06g41340 | A06 | 26896981 | G | A | upstream_gene_variant | MODIFIER | c.-521C>T| |
S170 |
9 | BAA06g41340 | A06 | 26897047 | C | T | upstream_gene_variant | MODIFIER | c.-587G>A| |
S64 |
10 | BAA06g41340 | A06 | 26897248 | C | T | upstream_gene_variant | MODIFIER | c.-788G>A| |
S62 |
11 | BAA06g41340 | A06 | 26897442 | G | A | upstream_gene_variant | MODIFIER | c.-982C>T| |
S283 |
12 | BAA06g41340 | A06 | 26898651 | G | A | upstream_gene_variant | MODIFIER | c.-2191C>T| |
S107 |
13 | BAA06g41340 | A06 | 26898715 | C | T | upstream_gene_variant | MODIFIER | c.-2255G>A| |
S78 |
14 | BAA06g41340 | A06 | 26898794 | G | A | upstream_gene_variant | MODIFIER | c.-2334C>T| |
S146 |
15 | BAA06g41340 | A06 | 26900222 | G | A | upstream_gene_variant | MODIFIER | c.-3762C>T| |
S67 |
16 | BAA06g41340 | A06 | 26901431 | C | T | upstream_gene_variant | MODIFIER | c.-4971G>A| |
S179 |