Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g37050 | A09 | 45204610 | C | T | missense_variant | MODERATE | c.2884G>A|p.Ala962Thr |
S142 |
2 | BAA09g37050 | A09 | 45204616 | C | T | missense_variant | MODERATE | c.2878G>A|p.Val960Ile |
S155 S211 |
3 | BAA09g37050 | A09 | 45206627 | G | A | synonymous_variant | LOW | c.1767C>T|p.Asp589Asp |
S266 |
4 | BAA09g37050 | A09 | 45207151 | G | A | missense_variant | MODERATE | c.1342C>T|p.Leu448Phe |
S37 |
5 | BAA09g37050 | A09 | 45207206 | C | T | missense_variant | MODERATE | c.1287G>A|p.Met429Ile |
S135 |
6 | BAA09g37050 | A09 | 45207233 | G | A | synonymous_variant | LOW | c.1260C>T|p.Asp420Asp |
S88 |
7 | BAA09g37050 | A09 | 45207653 | G | A | intron_variant | MODIFIER | c.911-71C>T| |
S173 |
8 | BAA09g37050 | A09 | 45208360 | C | T | missense_variant | MODERATE | c.306G>A|p.Met102Ile |
S247 |
9 | BAA09g37050 | A09 | 45208450 | G | A | synonymous_variant | LOW | c.216C>T|p.Leu72Leu |
S181 |
10 | BAA09g37050 | A09 | 45209566 | G | A | upstream_gene_variant | MODIFIER | c.-901C>T| |
S13 |
11 | BAA09g37050 | A09 | 45209713 | C | T | upstream_gene_variant | MODIFIER | c.-1048G>A| |
S32 |
12 | BAA09g37050 | A09 | 45210381 | T | C | upstream_gene_variant | MODIFIER | c.-1716A>G| |
S72 |
13 | BAA09g37050 | A09 | 45211610 | C | T | upstream_gene_variant | MODIFIER | c.-2945G>A| |
S210 |
14 | BAA09g37050 | A09 | 45212417 | G | A | upstream_gene_variant | MODIFIER | c.-3752C>T| |
S42 |