Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16580 | A01 | 8068465 | G | A | upstream_gene_variant | MODIFIER | c.-3802G>A| |
S172 S217 |
2 | BAA01g16580 | A01 | 8074421 | C | T | synonymous_variant | LOW | c.948C>T|p.Gly316Gly |
S18 |
3 | BAA01g16580 | A01 | 8075457 | G | A | missense_variant | MODERATE | c.1903G>A|p.Asp635Asn |
S246 |
4 | BAA01g16580 | A01 | 8075479 | C | T | missense_variant | MODERATE | c.1925C>T|p.Pro642Leu |
S46 |
5 | BAA01g16580 | A01 | 8075609 | G | A | missense_variant | MODERATE | c.1978G>A|p.Glu660Lys |
S72 S78 |
6 | BAA01g16580 | A01 | 8075921 | C | T | missense_variant | MODERATE | c.2290C>T|p.Arg764Cys |
S284 |
7 | BAA01g16580 | A01 | 8076017 | G | A | missense_variant | MODERATE | c.2386G>A|p.Ala796Thr |
S191 |
8 | BAA01g16580 | A01 | 8076138 | G | A | missense_variant | MODERATE | c.2507G>A|p.Arg836Lys |
S152 |
9 | BAA01g16580 | A01 | 8076666 | G | A | missense_variant | MODERATE | c.3035G>A|p.Ser1012Asn |
S257 |
10 | BAA01g16580 | A01 | 8076775 | G | A | synonymous_variant | LOW | c.3144G>A|p.Leu1048Leu |
S32 |
11 | BAA01g16580 | A01 | 8077403 | C | T | missense_variant | MODERATE | c.3772C>T|p.Pro1258Ser |
S53 |
12 | BAA01g16580 | A01 | 8077449 | G | A | missense_variant | MODERATE | c.3818G>A|p.Gly1273Glu |
S114 |
13 | BAA01g16580 | A01 | 8077716 | C | T | missense_variant | MODERATE | c.4085C>T|p.Thr1362Ile |
S4 |
14 | BAA01g16580 | A01 | 8077725 | G | A | missense_variant | MODERATE | c.4094G>A|p.Gly1365Glu |
S83 S88 |
15 | BAA01g16580 | A01 | 8081182 | C | T | downstream_gene_variant | MODIFIER | c.*3435C>T| |
S240 |
16 | BAA01g16580 | A01 | 8081233 | G | A | downstream_gene_variant | MODIFIER | c.*3486G>A| |
S28 |