Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g21340 | A10 | 18802215 | G | A | downstream_gene_variant | MODIFIER | c.*3592C>T| |
S178 |
2 | BAA10g21340 | A10 | 18802588 | G | A | downstream_gene_variant | MODIFIER | c.*3219C>T| |
S16 |
3 | BAA10g21340 | A10 | 18803113 | G | A | downstream_gene_variant | MODIFIER | c.*2694C>T| |
S251 |
4 | BAA10g21340 | A10 | 18803238 | C | T | downstream_gene_variant | MODIFIER | c.*2569G>A| |
S79 S91 |
5 | BAA10g21340 | A10 | 18804539 | C | T | downstream_gene_variant | MODIFIER | c.*1268G>A| |
S265 S27 S39 |
6 | BAA10g21340 | A10 | 18805676 | G | A | downstream_gene_variant | MODIFIER | c.*131C>T| |
S112 |
7 | BAA10g21340 | A10 | 18805746 | C | T | downstream_gene_variant | MODIFIER | c.*61G>A| |
S249 |
8 | BAA10g21340 | A10 | 18806197 | C | T | missense_variant | MODERATE | c.1278G>A|p.Met426Ile |
S25 |
9 | BAA10g21340 | A10 | 18806348 | C | T | missense_variant | MODERATE | c.1127G>A|p.Gly376Glu |
S199 |
10 | BAA10g21340 | A10 | 18807063 | G | A | missense_variant | MODERATE | c.412C>T|p.Pro138Ser |
S219 S72 |
11 | BAA10g21340 | A10 | 18809100 | G | A | upstream_gene_variant | MODIFIER | c.-1389C>T| |
S75 S81 |
12 | BAA10g21340 | A10 | 18809193 | G | A | upstream_gene_variant | MODIFIER | c.-1482C>T| |
S32 |
13 | BAA10g21340 | A10 | 18809418 | G | A | upstream_gene_variant | MODIFIER | c.-1707C>T| |
S245 |
14 | BAA10g21340 | A10 | 18811600 | C | T | upstream_gene_variant | MODIFIER | c.-3889G>A| |
S176 |
15 | BAA10g21340 | A10 | 18811925 | C | T | upstream_gene_variant | MODIFIER | c.-4214G>A| |
S76 |