Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g11480 | A07 | 20197216 | G | A | downstream_gene_variant | MODIFIER | c.*4282C>T| |
S83 |
2 | BAA07g11480 | A07 | 20197370 | C | T | downstream_gene_variant | MODIFIER | c.*4128G>A| |
S97 |
3 | BAA07g11480 | A07 | 20197636 | G | A | downstream_gene_variant | MODIFIER | c.*3862C>T| |
S158 |
4 | BAA07g11480 | A07 | 20198066 | G | A | downstream_gene_variant | MODIFIER | c.*3432C>T| |
S238 |
5 | BAA07g11480 | A07 | 20198420 | G | A | downstream_gene_variant | MODIFIER | c.*3078C>T| |
S204 |
6 | BAA07g11480 | A07 | 20198624 | G | A | downstream_gene_variant | MODIFIER | c.*2874C>T| |
S262 |
7 | BAA07g11480 | A07 | 20199030 | C | T | downstream_gene_variant | MODIFIER | c.*2468G>A| |
S107 |
8 | BAA07g11480 | A07 | 20199356 | C | T | downstream_gene_variant | MODIFIER | c.*2142G>A| |
S32 |
9 | BAA07g11480 | A07 | 20200571 | G | A | downstream_gene_variant | MODIFIER | c.*927C>T| |
S119 |
10 | BAA07g11480 | A07 | 20202391 | G | A | missense_variant | MODERATE | c.1226C>T|p.Thr409Ile |
S228 |
11 | BAA07g11480 | A07 | 20203373 | G | A | intron_variant | MODIFIER | c.399-155C>T| |
S183 |
12 | BAA07g11480 | A07 | 20203717 | C | T | splice_region_variant&intron_variant | LOW | c.297-7G>A| |
S221 |
13 | BAA07g11480 | A07 | 20207267 | G | A | upstream_gene_variant | MODIFIER | c.-3157C>T| |
S10 |
14 | BAA07g11480 | A07 | 20208017 | G | A | upstream_gene_variant | MODIFIER | c.-3907C>T| |
S280 |
15 | BAA07g11480 | A07 | 20208292 | G | A | upstream_gene_variant | MODIFIER | c.-4182C>T| |
S237 |
16 | BAA07g11480 | A07 | 20208847 | C | T | upstream_gene_variant | MODIFIER | c.-4737G>A| |
S34 |