Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g19570 | A07 | 25232465 | C | T | upstream_gene_variant | MODIFIER | c.-4736C>T| |
S149 S170 |
2 | BAA07g19570 | A07 | 25234183 | G | A | upstream_gene_variant | MODIFIER | c.-3018G>A| |
S132 S137 S215 S89 |
3 | BAA07g19570 | A07 | 25234465 | G | A | upstream_gene_variant | MODIFIER | c.-2736G>A| |
S296 |
4 | BAA07g19570 | A07 | 25235151 | G | A | upstream_gene_variant | MODIFIER | c.-2050G>A| |
S171 |
5 | BAA07g19570 | A07 | 25235908 | C | T | upstream_gene_variant | MODIFIER | c.-1293C>T| |
S68 |
6 | BAA07g19570 | A07 | 25236479 | G | A | upstream_gene_variant | MODIFIER | c.-722G>A| |
S97 |
7 | BAA07g19570 | A07 | 25236964 | C | T | upstream_gene_variant | MODIFIER | c.-237C>T| |
S144 |
8 | BAA07g19570 | A07 | 25237126 | G | A | upstream_gene_variant | MODIFIER | c.-75G>A| |
S84 S93 |
9 | BAA07g19570 | A07 | 25237212 | C | T | synonymous_variant | LOW | c.12C>T|p.Ile4Ile |
S267 |
10 | BAA07g19570 | A07 | 25237706 | G | A | synonymous_variant | LOW | c.390G>A|p.Lys130Lys |
S251 |
11 | BAA07g19570 | A07 | 25238852 | G | A | synonymous_variant | LOW | c.1131G>A|p.Lys377Lys |
S96 |
12 | BAA07g19570 | A07 | 25239044 | G | A | intron_variant | MODIFIER | c.1176+147G>A| |
S180 |
13 | BAA07g19570 | A07 | 25239243 | G | A | intron_variant | MODIFIER | c.1177-38G>A| |
S276 |
14 | BAA07g19570 | A07 | 25239903 | G | A | missense_variant | MODERATE | c.1636G>A|p.Asp546Asn |
S282 |
15 | BAA07g19570 | A07 | 25240184 | C | T | splice_region_variant&intron_variant | LOW | c.1753+5C>T| |
S5 |
16 | BAA07g19570 | A07 | 25240208 | G | A | intron_variant | MODIFIER | c.1753+29G>A| |
S51 |
17 | BAA07g19570 | A07 | 25240518 | G | A | missense_variant | MODERATE | c.1985G>A|p.Ser662Asn |
S134 |
18 | BAA07g19570 | A07 | 25240524 | C | T | missense_variant | MODERATE | c.1991C>T|p.Ser664Leu |
S213 |
19 | BAA07g19570 | A07 | 25240813 | C | T | synonymous_variant | LOW | c.2280C>T|p.His760His |
S261 |
20 | BAA07g19570 | A07 | 25240940 | C | T | intron_variant | MODIFIER | c.2326-18C>T| |
S149 |
21 | BAA07g19570 | A07 | 25240977 | G | A | missense_variant | MODERATE | c.2345G>A|p.Gly782Glu |
S146 |
22 | BAA07g19570 | A07 | 25241443 | G | A | missense_variant | MODERATE | c.2723G>A|p.Gly908Glu |
S40 S49 |
23 | BAA07g19570 | A07 | 25242064 | C | T | synonymous_variant | LOW | c.2992C>T|p.Leu998Leu |
S62 |
24 | BAA07g19570 | A07 | 25242392 | C | T | intron_variant | MODIFIER | c.3153+51C>T| |
S173 |
25 | BAA07g19570 | A07 | 25242408 | G | A | intron_variant | MODIFIER | c.3154-37G>A| |
S296 |