Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g08080 | A09 | 4510236 | G | A | missense_variant | MODERATE | c.4397C>T|p.Ser1466Phe |
S61 |
2 | BAA09g08080 | A09 | 4510359 | C | T | missense_variant | MODERATE | c.4274G>A|p.Arg1425Lys |
S174 S27 |
3 | BAA09g08080 | A09 | 4510777 | G | A | stop_gained | HIGH | c.3856C>T|p.Gln1286* |
S308 |
4 | BAA09g08080 | A09 | 4510875 | C | T | missense_variant | MODERATE | c.3758G>A|p.Ser1253Asn |
S287 |
5 | BAA09g08080 | A09 | 4510918 | G | A | synonymous_variant | LOW | c.3715C>T|p.Leu1239Leu |
S144 |
6 | BAA09g08080 | A09 | 4511442 | G | A | missense_variant | MODERATE | c.3191C>T|p.Ser1064Phe |
S57 |
7 | BAA09g08080 | A09 | 4511682 | G | A | missense_variant | MODERATE | c.2951C>T|p.Thr984Ile |
S221 S60 |
8 | BAA09g08080 | A09 | 4512109 | C | T | missense_variant | MODERATE | c.2524G>A|p.Val842Ile |
S18 |
9 | BAA09g08080 | A09 | 4512586 | C | T | missense_variant | MODERATE | c.2047G>A|p.Glu683Lys |
S131 |
10 | BAA09g08080 | A09 | 4513120 | C | T | missense_variant | MODERATE | c.1513G>A|p.Asp505Asn |
S13 S168 S219 S278 S72 |
11 | BAA09g08080 | A09 | 4513152 | C | T | missense_variant | MODERATE | c.1481G>A|p.Gly494Asp |
S234 |
12 | BAA09g08080 | A09 | 4513380 | T | A | missense_variant | MODERATE | c.1253A>T|p.Asp418Val |
S287 |
13 | BAA09g08080 | A09 | 4513902 | C | T | missense_variant | MODERATE | c.731G>A|p.Arg244Lys |
S149 |
14 | BAA09g08080 | A09 | 4514019 | G | A | missense_variant | MODERATE | c.614C>T|p.Pro205Leu |
S162 |
15 | BAA09g08080 | A09 | 4514264 | C | T | missense_variant | MODERATE | c.461G>A|p.Arg154Lys |
S148 S210 |
16 | BAA09g08080 | A09 | 4519315 | C | T | upstream_gene_variant | MODIFIER | c.-4452G>A| |
S18 |