Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g11710 | A08 | 10367284 | G | A | upstream_gene_variant | MODIFIER | c.-4000G>A| |
S20 |
2 | BAA08g11710 | A08 | 10369042 | G | A | upstream_gene_variant | MODIFIER | c.-2242G>A| |
S96 |
3 | BAA08g11710 | A08 | 10369339 | C | T | upstream_gene_variant | MODIFIER | c.-1945C>T| |
S251 |
4 | BAA08g11710 | A08 | 10369371 | C | T | upstream_gene_variant | MODIFIER | c.-1913C>T| |
S9 |
5 | BAA08g11710 | A08 | 10369385 | C | T | upstream_gene_variant | MODIFIER | c.-1899C>T| |
S277 |
6 | BAA08g11710 | A08 | 10369565 | C | T | upstream_gene_variant | MODIFIER | c.-1719C>T| |
S82 S92 |
7 | BAA08g11710 | A08 | 10371086 | G | A | upstream_gene_variant | MODIFIER | c.-198G>A| |
S199 |
8 | BAA08g11710 | A08 | 10371143 | G | A | upstream_gene_variant | MODIFIER | c.-141G>A| |
S274 |
9 | BAA08g11710 | A08 | 10371309 | G | A | missense_variant | MODERATE | c.26G>A|p.Arg9Lys |
S187 |
10 | BAA08g11710 | A08 | 10371536 | C | T | synonymous_variant | LOW | c.168C>T|p.Leu56Leu |
S262 |
11 | BAA08g11710 | A08 | 10374464 | C | T | downstream_gene_variant | MODIFIER | c.*2460C>T| |
S162 |
12 | BAA08g11710 | A08 | 10375376 | G | A | downstream_gene_variant | MODIFIER | c.*3372G>A| |
S186 |
13 | BAA08g11710 | A08 | 10375469 | G | A | downstream_gene_variant | MODIFIER | c.*3465G>A| |
S48 |
14 | BAA08g11710 | A08 | 10375473 | C | T | downstream_gene_variant | MODIFIER | c.*3469C>T| |
S52 |
15 | BAA08g11710 | A08 | 10376009 | G | A | downstream_gene_variant | MODIFIER | c.*4005G>A| |
S195 |
16 | BAA08g11710 | A08 | 10376375 | G | A | downstream_gene_variant | MODIFIER | c.*4371G>A| |
S81 S85 |
17 | BAA08g11710 | A08 | 10376700 | C | T | downstream_gene_variant | MODIFIER | c.*4696C>T| |
S176 |