Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01580 | A08 | 1155040 | G | A | synonymous_variant | LOW | c.690C>T|p.His230His |
S103 |
2 | BAA08g01580 | A08 | 1155112 | C | T | synonymous_variant | LOW | c.618G>A|p.Glu206Glu |
S303 |
3 | BAA08g01580 | A08 | 1155315 | C | T | missense_variant | MODERATE | c.506G>A|p.Ser169Asn |
S267 |
4 | BAA08g01580 | A08 | 1155707 | G | A | intron_variant | MODIFIER | c.491+196C>T| |
S61 |
5 | BAA08g01580 | A08 | 1156082 | C | T | synonymous_variant | LOW | c.384G>A|p.Lys128Lys |
S1 S90 |
6 | BAA08g01580 | A08 | 1156240 | C | T | missense_variant | MODERATE | c.226G>A|p.Glu76Lys |
S48 |
7 | BAA08g01580 | A08 | 1156345 | C | T | missense_variant | MODERATE | c.121G>A|p.Glu41Lys |
S305 |
8 | BAA08g01580 | A08 | 1156679 | G | A | upstream_gene_variant | MODIFIER | c.-214C>T| |
S195 |
9 | BAA08g01580 | A08 | 1157034 | C | T | upstream_gene_variant | MODIFIER | c.-569G>A| |
S48 |
10 | BAA08g01580 | A08 | 1158259 | C | T | upstream_gene_variant | MODIFIER | c.-1794G>A| |
S293 |
11 | BAA08g01580 | A08 | 1158748 | C | T | upstream_gene_variant | MODIFIER | c.-2283G>A| |
S36 |
12 | BAA08g01580 | A08 | 1160786 | C | T | upstream_gene_variant | MODIFIER | c.-4321G>A| |
S163 |