Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g04170 | A07 | 3391959 | C | T | downstream_gene_variant | MODIFIER | c.*2001G>A| |
S144 |
2 | BAA07g04170 | A07 | 3392117 | C | T | downstream_gene_variant | MODIFIER | c.*1843G>A| |
S267 |
3 | BAA07g04170 | A07 | 3392193 | C | T | downstream_gene_variant | MODIFIER | c.*1767G>A| |
S249 |
4 | BAA07g04170 | A07 | 3392346 | C | T | downstream_gene_variant | MODIFIER | c.*1614G>A| |
S173 |
5 | BAA07g04170 | A07 | 3393516 | C | T | downstream_gene_variant | MODIFIER | c.*444G>A| |
S12 |
6 | BAA07g04170 | A07 | 3394171 | C | T | missense_variant | MODERATE | c.1313G>A|p.Gly438Glu |
S249 |
7 | BAA07g04170 | A07 | 3394374 | G | A | synonymous_variant | LOW | c.1110C>T|p.Ser370Ser |
S257 |
8 | BAA07g04170 | A07 | 3394604 | C | T | missense_variant | MODERATE | c.880G>A|p.Ala294Thr |
S213 |
9 | BAA07g04170 | A07 | 3394619 | G | A | missense_variant | MODERATE | c.865C>T|p.Arg289Trp |
S98 |
10 | BAA07g04170 | A07 | 3395013 | G | A | synonymous_variant | LOW | c.471C>T|p.Leu157Leu |
S48 |
11 | BAA07g04170 | A07 | 3395165 | C | T | missense_variant | MODERATE | c.319G>A|p.Asp107Asn |
S165 |
12 | BAA07g04170 | A07 | 3395314 | G | A | missense_variant | MODERATE | c.170C>T|p.Thr57Ile |
S61 |
13 | BAA07g04170 | A07 | 3395444 | C | T | missense_variant | MODERATE | c.40G>A|p.Glu14Lys |
S207 |
14 | BAA07g04170 | A07 | 3397284 | G | A | upstream_gene_variant | MODIFIER | c.-1801C>T| |
S135 |
15 | BAA07g04170 | A07 | 3397312 | C | T | upstream_gene_variant | MODIFIER | c.-1829G>A| |
S189 |