Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g06980 | A04 | 4664766 | C | T | downstream_gene_variant | MODIFIER | c.*1142G>A| |
S216 |
2 | BAA04g06980 | A04 | 4665338 | G | A | downstream_gene_variant | MODIFIER | c.*570C>T| |
S88 |
3 | BAA04g06980 | A04 | 4666216 | G | A | missense_variant | MODERATE | c.1324C>T|p.His442Tyr |
S125 |
4 | BAA04g06980 | A04 | 4666963 | C | T | missense_variant | MODERATE | c.577G>A|p.Asp193Asn |
S167 |
5 | BAA04g06980 | A04 | 4667352 | G | A | intron_variant | MODIFIER | c.322-134C>T| |
S17 |
6 | BAA04g06980 | A04 | 4667639 | G | A | intron_variant | MODIFIER | c.322-421C>T| |
S262 |
7 | BAA04g06980 | A04 | 4667751 | G | A | intron_variant | MODIFIER | c.322-533C>T| |
S138 |
8 | BAA04g06980 | A04 | 4668343 | G | A | intron_variant | MODIFIER | c.322-1125C>T| |
S40 S49 |
9 | BAA04g06980 | A04 | 4668437 | C | T | intron_variant | MODIFIER | c.322-1219G>A| |
S192 |
10 | BAA04g06980 | A04 | 4669046 | C | T | intron_variant | MODIFIER | c.321+803G>A| |
S302 |
11 | BAA04g06980 | A04 | 4669734 | C | T | intron_variant | MODIFIER | c.321+115G>A| |
S68 |
12 | BAA04g06980 | A04 | 4670680 | G | A | upstream_gene_variant | MODIFIER | c.-511C>T| |
S210 |
13 | BAA04g06980 | A04 | 4670901 | G | A | upstream_gene_variant | MODIFIER | c.-732C>T| |
S53 |
14 | BAA04g06980 | A04 | 4670941 | G | A | upstream_gene_variant | MODIFIER | c.-772C>T| |
S236 |
15 | BAA04g06980 | A04 | 4671143 | A | T | upstream_gene_variant | MODIFIER | c.-974T>A| |
S35 |
16 | BAA04g06980 | A04 | 4671767 | C | T | upstream_gene_variant | MODIFIER | c.-1598G>A| |
S296 |
17 | BAA04g06980 | A04 | 4671827 | G | A | upstream_gene_variant | MODIFIER | c.-1658C>T| |
S166 |
18 | BAA04g06980 | A04 | 4672803 | G | A | upstream_gene_variant | MODIFIER | c.-2634C>T| |
S245 |
19 | BAA04g06980 | A04 | 4673589 | G | A | upstream_gene_variant | MODIFIER | c.-3420C>T| |
S266 |
20 | BAA04g06980 | A04 | 4673723 | G | A | upstream_gene_variant | MODIFIER | c.-3554C>T| |
S36 |