Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g03960 | A07 | 3247815 | C | T | upstream_gene_variant | MODIFIER | c.-4707C>T| |
S27 |
2 | BAA07g03960 | A07 | 3249561 | C | T | upstream_gene_variant | MODIFIER | c.-2961C>T| |
S281 |
3 | BAA07g03960 | A07 | 3250566 | G | A | upstream_gene_variant | MODIFIER | c.-1956G>A| |
S216 |
4 | BAA07g03960 | A07 | 3250741 | G | A | upstream_gene_variant | MODIFIER | c.-1781G>A| |
S203 |
5 | BAA07g03960 | A07 | 3251427 | C | T | upstream_gene_variant | MODIFIER | c.-1095C>T| |
S167 |
6 | BAA07g03960 | A07 | 3251485 | C | T | upstream_gene_variant | MODIFIER | c.-1037C>T| |
S195 |
7 | BAA07g03960 | A07 | 3251898 | G | A | upstream_gene_variant | MODIFIER | c.-624G>A| |
S234 |
8 | BAA07g03960 | A07 | 3252784 | G | A | missense_variant | MODERATE | c.263G>A|p.Ser88Asn |
S246 |
9 | BAA07g03960 | A07 | 3253643 | G | A | synonymous_variant | LOW | c.1122G>A|p.Thr374Thr |
S171 |
10 | BAA07g03960 | A07 | 3253731 | G | A | missense_variant | MODERATE | c.1210G>A|p.Glu404Lys |
S205 |
11 | BAA07g03960 | A07 | 3254277 | G | A | missense_variant | MODERATE | c.1756G>A|p.Val586Ile |
S235 |
12 | BAA07g03960 | A07 | 3254335 | C | T | missense_variant | MODERATE | c.1814C>T|p.Ser605Phe |
S197 |
13 | BAA07g03960 | A07 | 3254553 | G | A | missense_variant | MODERATE | c.2032G>A|p.Gly678Ser |
S298 |
14 | BAA07g03960 | A07 | 3255225 | C | T | missense_variant | MODERATE | c.2704C>T|p.Leu902Phe |
S34 |