Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g05130 | A10 | 2646610 | G | A | upstream_gene_variant | MODIFIER | c.-4773G>A| |
S125 |
2 | BAA10g05130 | A10 | 2647038 | G | A | upstream_gene_variant | MODIFIER | c.-4345G>A| |
S157 S163 |
3 | BAA10g05130 | A10 | 2647081 | C | T | upstream_gene_variant | MODIFIER | c.-4302C>T| |
S270 |
4 | BAA10g05130 | A10 | 2647415 | C | T | upstream_gene_variant | MODIFIER | c.-3968C>T| |
S143 |
5 | BAA10g05130 | A10 | 2647676 | G | A | upstream_gene_variant | MODIFIER | c.-3707G>A| |
S76 |
6 | BAA10g05130 | A10 | 2647701 | G | A | upstream_gene_variant | MODIFIER | c.-3682G>A| |
S45 |
7 | BAA10g05130 | A10 | 2647853 | C | T | upstream_gene_variant | MODIFIER | c.-3530C>T| |
S44 |
8 | BAA10g05130 | A10 | 2648011 | G | A | upstream_gene_variant | MODIFIER | c.-3372G>A| |
S9 |
9 | BAA10g05130 | A10 | 2648615 | G | A | upstream_gene_variant | MODIFIER | c.-2768G>A| |
S191 |
10 | BAA10g05130 | A10 | 2649203 | C | T | upstream_gene_variant | MODIFIER | c.-2180C>T| |
S194 |
11 | BAA10g05130 | A10 | 2649857 | C | T | upstream_gene_variant | MODIFIER | c.-1526C>T| |
S56 |
12 | BAA10g05130 | A10 | 2650049 | C | T | upstream_gene_variant | MODIFIER | c.-1334C>T| |
S155 S211 |
13 | BAA10g05130 | A10 | 2650659 | C | T | upstream_gene_variant | MODIFIER | c.-724C>T| |
S54 |
14 | BAA10g05130 | A10 | 2651235 | C | T | upstream_gene_variant | MODIFIER | c.-148C>T| |
S139 |
15 | BAA10g05130 | A10 | 2651569 | G | A | missense_variant | MODERATE | c.187G>A|p.Glu63Lys |
S228 |
16 | BAA10g05130 | A10 | 2651826 | C | T | synonymous_variant | LOW | c.444C>T|p.Ile148Ile |
S123 |
17 | BAA10g05130 | A10 | 2652298 | G | A | stop_gained | HIGH | c.519G>A|p.Trp173* |
S211 S227 |
18 | BAA10g05130 | A10 | 2653362 | C | T | missense_variant | MODERATE | c.1162C>T|p.Leu388Phe |
S232 |
19 | BAA10g05130 | A10 | 2654375 | C | A | missense_variant | MODERATE | c.1769C>A|p.Pro590His |
S306 S308 |
20 | BAA10g05130 | A10 | 2656996 | G | A | downstream_gene_variant | MODIFIER | c.*2237G>A| |
S284 |