Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g14570 | A07 | 22135879 | G | A | downstream_gene_variant | MODIFIER | c.*2720C>T| |
S186 |
2 | BAA07g14570 | A07 | 22136150 | A | T | downstream_gene_variant | MODIFIER | c.*2449T>A| |
S87 |
3 | BAA07g14570 | A07 | 22136808 | G | A | downstream_gene_variant | MODIFIER | c.*1791C>T| |
S296 |
4 | BAA07g14570 | A07 | 22137343 | C | T | downstream_gene_variant | MODIFIER | c.*1256G>A| |
S301 S304 |
5 | BAA07g14570 | A07 | 22137367 | C | T | downstream_gene_variant | MODIFIER | c.*1232G>A| |
S47 |
6 | BAA07g14570 | A07 | 22137775 | G | A | downstream_gene_variant | MODIFIER | c.*824C>T| |
S185 |
7 | BAA07g14570 | A07 | 22138458 | G | A | downstream_gene_variant | MODIFIER | c.*141C>T| |
S71 |
8 | BAA07g14570 | A07 | 22138958 | G | A | missense_variant | MODERATE | c.182C>T|p.Thr61Ile |
S53 |
9 | BAA07g14570 | A07 | 22138963 | C | T | synonymous_variant | LOW | c.177G>A|p.Gly59Gly |
S252 |
10 | BAA07g14570 | A07 | 22139069 | C | T | intron_variant | MODIFIER | c.148-77G>A| |
S153 |
11 | BAA07g14570 | A07 | 22139552 | G | A | upstream_gene_variant | MODIFIER | c.-102C>T| |
S219 |
12 | BAA07g14570 | A07 | 22141190 | C | T | upstream_gene_variant | MODIFIER | c.-1740G>A| |
S4 |
13 | BAA07g14570 | A07 | 22141647 | G | A | upstream_gene_variant | MODIFIER | c.-2197C>T| |
S203 |
14 | BAA07g14570 | A07 | 22143264 | C | T | upstream_gene_variant | MODIFIER | c.-3814G>A| |
S301 |
15 | BAA07g14570 | A07 | 22143303 | C | T | upstream_gene_variant | MODIFIER | c.-3853G>A| |
S58 |
16 | BAA07g14570 | A07 | 22144100 | C | T | upstream_gene_variant | MODIFIER | c.-4650G>A| |
S243 |
17 | BAA07g14570 | A07 | 22144192 | C | T | upstream_gene_variant | MODIFIER | c.-4742G>A| |
S250 |