Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g16070 | A08 | 13411453 | C | T | missense_variant | MODERATE | c.1784G>A|p.Gly595Asp |
S185 |
2 | BAA08g16070 | A08 | 13411845 | C | T | missense_variant | MODERATE | c.1580G>A|p.Gly527Glu |
S271 |
3 | BAA08g16070 | A08 | 13411978 | C | T | missense_variant | MODERATE | c.1447G>A|p.Val483Ile |
S167 |
4 | BAA08g16070 | A08 | 13412022 | C | T | missense_variant | MODERATE | c.1403G>A|p.Ser468Asn |
S74 |
5 | BAA08g16070 | A08 | 13412116 | C | T | missense_variant | MODERATE | c.1309G>A|p.Val437Ile |
S178 |
6 | BAA08g16070 | A08 | 13412181 | G | A | missense_variant | MODERATE | c.1244C>T|p.Ala415Val |
S234 |
7 | BAA08g16070 | A08 | 13412245 | C | A | stop_gained | HIGH | c.1180G>T|p.Glu394* |
S244 |
8 | BAA08g16070 | A08 | 13412251 | G | A | missense_variant | MODERATE | c.1174C>T|p.Pro392Ser |
S174 S306 S308 |
9 | BAA08g16070 | A08 | 13413028 | C | T | synonymous_variant | LOW | c.591G>A|p.Ser197Ser |
S210 |
10 | BAA08g16070 | A08 | 13413111 | C | T | missense_variant | MODERATE | c.508G>A|p.Asp170Asn |
S293 |
11 | BAA08g16070 | A08 | 13414349 | G | A | upstream_gene_variant | MODIFIER | c.-222C>T| |
S260 |
12 | BAA08g16070 | A08 | 13416265 | C | T | upstream_gene_variant | MODIFIER | c.-2138G>A| |
S274 |
13 | BAA08g16070 | A08 | 13417750 | C | T | upstream_gene_variant | MODIFIER | c.-3623G>A| |
S6 |
14 | BAA08g16070 | A08 | 13417920 | T | A | upstream_gene_variant | MODIFIER | c.-3793A>T| |
S215 |
15 | BAA08g16070 | A08 | 13418014 | G | A | upstream_gene_variant | MODIFIER | c.-3887C>T| |
S125 |
16 | BAA08g16070 | A08 | 13418153 | G | A | upstream_gene_variant | MODIFIER | c.-4026C>T| |
S131 |
17 | BAA08g16070 | A08 | 13418222 | C | T | upstream_gene_variant | MODIFIER | c.-4095G>A| |
S104 S52 |
18 | BAA08g16070 | A08 | 13418270 | G | A | upstream_gene_variant | MODIFIER | c.-4143C>T| |
S69 |