Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g03190 | A04 | 1932966 | G | A | missense_variant | MODERATE | c.4207C>T|p.Pro1403Ser |
S169 |
2 | BAA04g03190 | A04 | 1934158 | G | A | splice_region_variant&intron_variant | LOW | c.3507+7C>T| |
S167 |
3 | BAA04g03190 | A04 | 1936226 | G | A | stop_gained | HIGH | c.2155C>T|p.Gln719* |
S188 |
4 | BAA04g03190 | A04 | 1937873 | G | A | intron_variant | MODIFIER | c.1167+50C>T| |
S153 S213 |
5 | BAA04g03190 | A04 | 1938368 | G | A | intron_variant | MODIFIER | c.856-11C>T| |
S188 |
6 | BAA04g03190 | A04 | 1938844 | C | T | missense_variant | MODERATE | c.448G>A|p.Asp150Asn |
S279 |
7 | BAA04g03190 | A04 | 1939300 | G | A | intron_variant | MODIFIER | c.128-46C>T| |
S146 |
8 | BAA04g03190 | A04 | 1939339 | C | T | intron_variant | MODIFIER | c.127+16G>A| |
S302 |
9 | BAA04g03190 | A04 | 1939369 | G | A | missense_variant | MODERATE | c.113C>T|p.Thr38Ile |
S217 |
10 | BAA04g03190 | A04 | 1939759 | C | T | upstream_gene_variant | MODIFIER | c.-192G>A| |
S185 |
11 | BAA04g03190 | A04 | 1942100 | A | T | upstream_gene_variant | MODIFIER | c.-2533T>A| |
S74 |
12 | BAA04g03190 | A04 | 1942212 | G | A | upstream_gene_variant | MODIFIER | c.-2645C>T| |
S161 |
13 | BAA04g03190 | A04 | 1942427 | C | T | upstream_gene_variant | MODIFIER | c.-2860G>A| |
S25 |
14 | BAA04g03190 | A04 | 1942454 | C | T | upstream_gene_variant | MODIFIER | c.-2887G>A| |
S257 |
15 | BAA04g03190 | A04 | 1942985 | G | A | upstream_gene_variant | MODIFIER | c.-3418C>T| |
S167 |
16 | BAA04g03190 | A04 | 1943948 | G | A | upstream_gene_variant | MODIFIER | c.-4381C>T| |
S126 |