Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26000 | A01 | 14350816 | G | A | upstream_gene_variant | MODIFIER | c.-4708G>A| |
S34 |
2 | BAA01g26000 | A01 | 14350954 | C | T | upstream_gene_variant | MODIFIER | c.-4570C>T| |
S153 |
3 | BAA01g26000 | A01 | 14351181 | C | T | upstream_gene_variant | MODIFIER | c.-4343C>T| |
S41 |
4 | BAA01g26000 | A01 | 14352170 | T | A | upstream_gene_variant | MODIFIER | c.-3354T>A| |
S165 S211 S227 |
5 | BAA01g26000 | A01 | 14353031 | C | T | upstream_gene_variant | MODIFIER | c.-2493C>T| |
S61 |
6 | BAA01g26000 | A01 | 14353118 | C | T | upstream_gene_variant | MODIFIER | c.-2406C>T| |
S73 S91 |
7 | BAA01g26000 | A01 | 14355154 | G | A | upstream_gene_variant | MODIFIER | c.-370G>A| |
S287 |
8 | BAA01g26000 | A01 | 14355631 | G | A | synonymous_variant | LOW | c.108G>A|p.Lys36Lys |
S6 |
9 | BAA01g26000 | A01 | 14355872 | C | T | synonymous_variant | LOW | c.349C>T|p.Leu117Leu |
S291 |
10 | BAA01g26000 | A01 | 14356027 | G | A | synonymous_variant | LOW | c.504G>A|p.Gln168Gln |
S32 |
11 | BAA01g26000 | A01 | 14356340 | G | A | intron_variant | MODIFIER | c.576-40G>A| |
S186 |
12 | BAA01g26000 | A01 | 14356426 | G | A | missense_variant | MODERATE | c.622G>A|p.Gly208Arg |
S301 S304 |
13 | BAA01g26000 | A01 | 14356574 | C | T | missense_variant | MODERATE | c.770C>T|p.Ala257Val |
S153 |
14 | BAA01g26000 | A01 | 14356617 | G | A | missense_variant | MODERATE | c.813G>A|p.Met271Ile |
S126 |
15 | BAA01g26000 | A01 | 14357502 | G | A | missense_variant | MODERATE | c.1204G>A|p.Glu402Lys |
S109 |
16 | BAA01g26000 | A01 | 14357956 | C | T | intron_variant | MODIFIER | c.1556+28C>T| |
S125 |
17 | BAA01g26000 | A01 | 14357975 | G | A | intron_variant | MODIFIER | c.1556+47G>A| |
S172 |
18 | BAA01g26000 | A01 | 14358251 | C | T | intron_variant | MODIFIER | c.1556+323C>T| |
S107 |
19 | BAA01g26000 | A01 | 14358686 | C | T | missense_variant | MODERATE | c.1636C>T|p.Pro546Ser |
S20 |
20 | BAA01g26000 | A01 | 14359569 | A | T | intron_variant | MODIFIER | c.1821+519A>T| |
S62 |
21 | BAA01g26000 | A01 | 14360389 | G | A | splice_region_variant&intron_variant | LOW | c.1963+5G>A| |
S32 |
22 | BAA01g26000 | A01 | 14360619 | C | T | missense_variant | MODERATE | c.2113C>T|p.Leu705Phe |
S99 |
23 | BAA01g26000 | A01 | 14361330 | G | A | missense_variant | MODERATE | c.2725G>A|p.Gly909Ser |
S60 |
24 | BAA01g26000 | A01 | 14361444 | C | T | stop_gained | HIGH | c.2839C>T|p.Gln947* |
S8 |
25 | BAA01g26000 | A01 | 14361837 | G | A | missense_variant | MODERATE | c.3232G>A|p.Glu1078Lys |
S33 |