Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g32250 | A01 | 21166414 | C | T | missense_variant | MODERATE | c.2776G>A|p.Asp926Asn |
S132 S137 S215 S89 |
2 | BAA01g32250 | A01 | 21166476 | C | T | missense_variant | MODERATE | c.2714G>A|p.Arg905Lys |
S19 |
3 | BAA01g32250 | A01 | 21168434 | G | A | intron_variant | MODIFIER | c.1963+34C>T| |
S308 |
4 | BAA01g32250 | A01 | 21169599 | C | T | missense_variant | MODERATE | c.1519G>A|p.Glu507Lys |
S186 |
5 | BAA01g32250 | A01 | 21169662 | G | A | missense_variant | MODERATE | c.1456C>T|p.Pro486Ser |
S97 |
6 | BAA01g32250 | A01 | 21170190 | G | A | intron_variant | MODIFIER | c.1395+98C>T| |
S280 |
7 | BAA01g32250 | A01 | 21170206 | C | T | intron_variant | MODIFIER | c.1395+82G>A| |
S23 |
8 | BAA01g32250 | A01 | 21170369 | C | T | synonymous_variant | LOW | c.1314G>A|p.Gln438Gln |
S182 |
9 | BAA01g32250 | A01 | 21170429 | C | T | synonymous_variant | LOW | c.1254G>A|p.Lys418Lys |
S167 |
10 | BAA01g32250 | A01 | 21171738 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.602-1G>A| |
S107 |
11 | BAA01g32250 | A01 | 21172728 | C | T | missense_variant | MODERATE | c.151G>A|p.Ala51Thr |
S128 |
12 | BAA01g32250 | A01 | 21172799 | G | A | missense_variant | MODERATE | c.80C>T|p.Thr27Ile |
S268 |
13 | BAA01g32250 | A01 | 21172884 | G | A | upstream_gene_variant | MODIFIER | c.-6C>T| |
S121 |
14 | BAA01g32250 | A01 | 21174850 | T | A | upstream_gene_variant | MODIFIER | c.-1972A>T| |
S134 S179 S193 |
15 | BAA01g32250 | A01 | 21176743 | C | T | upstream_gene_variant | MODIFIER | c.-3865G>A| |
S242 |
16 | BAA01g32250 | A01 | 21177363 | C | T | upstream_gene_variant | MODIFIER | c.-4485G>A| |
S192 |
17 | BAA01g32250 | A01 | 21177785 | G | A | upstream_gene_variant | MODIFIER | c.-4907C>T| |
S259 |