Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g39880 | A07 | 35632204 | C | T | upstream_gene_variant | MODIFIER | c.-4542C>T| |
S212 |
2 | BAA07g39880 | A07 | 35632724 | C | T | upstream_gene_variant | MODIFIER | c.-4022C>T| |
S262 |
3 | BAA07g39880 | A07 | 35633656 | C | T | upstream_gene_variant | MODIFIER | c.-3090C>T| |
S221 |
4 | BAA07g39880 | A07 | 35633759 | C | T | upstream_gene_variant | MODIFIER | c.-2987C>T| |
S177 |
5 | BAA07g39880 | A07 | 35634982 | C | T | upstream_gene_variant | MODIFIER | c.-1764C>T| |
S161 |
6 | BAA07g39880 | A07 | 35635025 | C | T | upstream_gene_variant | MODIFIER | c.-1721C>T| |
S68 |
7 | BAA07g39880 | A07 | 35635580 | C | T | upstream_gene_variant | MODIFIER | c.-1166C>T| |
S42 |
8 | BAA07g39880 | A07 | 35636950 | C | T | missense_variant | MODERATE | c.205C>T|p.Pro69Ser |
S207 |
9 | BAA07g39880 | A07 | 35637165 | G | A | synonymous_variant | LOW | c.420G>A|p.Glu140Glu |
S166 |
10 | BAA07g39880 | A07 | 35637196 | C | T | missense_variant | MODERATE | c.451C>T|p.Leu151Phe |
S275 |
11 | BAA07g39880 | A07 | 35637205 | G | A | missense_variant | MODERATE | c.460G>A|p.Val154Ile |
S143 |
12 | BAA07g39880 | A07 | 35638441 | G | A | missense_variant | MODERATE | c.920G>A|p.Ser307Asn |
S65 |
13 | BAA07g39880 | A07 | 35638480 | C | T | missense_variant | MODERATE | c.959C>T|p.Pro320Leu |
S59 |
14 | BAA07g39880 | A07 | 35638918 | C | T | missense_variant | MODERATE | c.1225C>T|p.Leu409Phe |
S252 |
15 | BAA07g39880 | A07 | 35639335 | G | A | missense_variant | MODERATE | c.1468G>A|p.Asp490Asn |
S295 |
16 | BAA07g39880 | A07 | 35639464 | G | A | missense_variant | MODERATE | c.1531G>A|p.Ala511Thr |
S226 |
17 | BAA07g39880 | A07 | 35641708 | C | T | downstream_gene_variant | MODIFIER | c.*2191C>T| |
S161 |