Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g28320 | A07 | 29583473 | C | T | upstream_gene_variant | MODIFIER | c.-1836C>T| |
S88 |
2 | BAA07g28320 | A07 | 29584472 | G | A | upstream_gene_variant | MODIFIER | c.-837G>A| |
S92 |
3 | BAA07g28320 | A07 | 29585585 | C | T | missense_variant | MODERATE | c.152C>T|p.Ala51Val |
S37 |
4 | BAA07g28320 | A07 | 29585990 | G | A | missense_variant | MODERATE | c.485G>A|p.Gly162Glu |
S172 |
5 | BAA07g28320 | A07 | 29587135 | G | A | missense_variant | MODERATE | c.1564G>A|p.Glu522Lys |
S157 |
6 | BAA07g28320 | A07 | 29587198 | G | A | missense_variant | MODERATE | c.1627G>A|p.Gly543Arg |
S296 |
7 | BAA07g28320 | A07 | 29587619 | C | T | missense_variant | MODERATE | c.2048C>T|p.Thr683Ile |
S162 |
8 | BAA07g28320 | A07 | 29587672 | G | A | missense_variant | MODERATE | c.2101G>A|p.Asp701Asn |
S269 |
9 | BAA07g28320 | A07 | 29587828 | C | T | missense_variant | MODERATE | c.2257C>T|p.Arg753Trp |
S233 |
10 | BAA07g28320 | A07 | 29587957 | G | A | missense_variant | MODERATE | c.2386G>A|p.Gly796Ser |
S15 S3 |
11 | BAA07g28320 | A07 | 29588237 | G | A | missense_variant | MODERATE | c.2666G>A|p.Gly889Asp |
S13 |
12 | BAA07g28320 | A07 | 29588703 | C | T | synonymous_variant | LOW | c.3132C>T|p.Leu1044Leu |
S261 |
13 | BAA07g28320 | A07 | 29588815 | G | A | missense_variant | MODERATE | c.3244G>A|p.Asp1082Asn |
S48 |
14 | BAA07g28320 | A07 | 29589161 | G | A | missense_variant | MODERATE | c.3521G>A|p.Gly1174Glu |
S95 |
15 | BAA07g28320 | A07 | 29589414 | G | A | synonymous_variant | LOW | c.3774G>A|p.Arg1258Arg |
S80 |
16 | BAA07g28320 | A07 | 29589728 | C | T | missense_variant | MODERATE | c.4088C>T|p.Pro1363Leu |
S35 |