Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10650 | A10 | 12424029 | C | A | downstream_gene_variant | MODIFIER | c.*4424G>T| |
S298 |
2 | BAA10g10650 | A10 | 12424486 | C | T | downstream_gene_variant | MODIFIER | c.*3967G>A| |
S42 |
3 | BAA10g10650 | A10 | 12425465 | C | T | downstream_gene_variant | MODIFIER | c.*2988G>A| |
S99 |
4 | BAA10g10650 | A10 | 12428200 | G | A | downstream_gene_variant | MODIFIER | c.*253C>T| |
S293 |
5 | BAA10g10650 | A10 | 12428300 | C | T | downstream_gene_variant | MODIFIER | c.*153G>A| |
S135 |
6 | BAA10g10650 | A10 | 12428401 | G | A | downstream_gene_variant | MODIFIER | c.*52C>T| |
S13 |
7 | BAA10g10650 | A10 | 12428407 | G | A | downstream_gene_variant | MODIFIER | c.*46C>T| |
S226 |
8 | BAA10g10650 | A10 | 12428695 | C | T | missense_variant | MODERATE | c.1114G>A|p.Val372Ile |
S236 |
9 | BAA10g10650 | A10 | 12429753 | G | A | missense_variant | MODERATE | c.427C>T|p.Pro143Ser |
S112 |
10 | BAA10g10650 | A10 | 12431725 | G | A | upstream_gene_variant | MODIFIER | c.-1484C>T| |
S178 |
11 | BAA10g10650 | A10 | 12432058 | C | T | upstream_gene_variant | MODIFIER | c.-1817G>A| |
S191 |
12 | BAA10g10650 | A10 | 12432115 | C | T | upstream_gene_variant | MODIFIER | c.-1874G>A| |
S270 |
13 | BAA10g10650 | A10 | 12432622 | G | A | upstream_gene_variant | MODIFIER | c.-2381C>T| |
S245 |
14 | BAA10g10650 | A10 | 12432734 | C | T | upstream_gene_variant | MODIFIER | c.-2493G>A| |
S256 |
15 | BAA10g10650 | A10 | 12432822 | G | A | upstream_gene_variant | MODIFIER | c.-2581C>T| |
S182 |
16 | BAA10g10650 | A10 | 12432976 | C | T | upstream_gene_variant | MODIFIER | c.-2735G>A| |
S115 |
17 | BAA10g10650 | A10 | 12433692 | C | T | upstream_gene_variant | MODIFIER | c.-3451G>A| |
S196 |
18 | BAA10g10650 | A10 | 12433891 | C | T | upstream_gene_variant | MODIFIER | c.-3650G>A| |
S42 |
19 | BAA10g10650 | A10 | 12434413 | G | A | upstream_gene_variant | MODIFIER | c.-4172C>T| |
S13 |
20 | BAA10g10650 | A10 | 12434677 | C | T | upstream_gene_variant | MODIFIER | c.-4436G>A| |
S149 |