Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g21220 | A09 | 13230057 | C | T | downstream_gene_variant | MODIFIER | c.*3988G>A| |
S284 |
2 | BAA09g21220 | A09 | 13232358 | G | A | downstream_gene_variant | MODIFIER | c.*1687C>T| |
S23 |
3 | BAA09g21220 | A09 | 13233015 | G | A | downstream_gene_variant | MODIFIER | c.*1030C>T| |
S78 S83 |
4 | BAA09g21220 | A09 | 13233086 | C | T | downstream_gene_variant | MODIFIER | c.*959G>A| |
S216 |
5 | BAA09g21220 | A09 | 13233688 | C | T | downstream_gene_variant | MODIFIER | c.*357G>A| |
S179 |
6 | BAA09g21220 | A09 | 13234839 | C | T | intron_variant | MODIFIER | c.4138-31G>A| |
S296 |
7 | BAA09g21220 | A09 | 13235417 | G | A | intron_variant | MODIFIER | c.3840+9C>T| |
S4 |
8 | BAA09g21220 | A09 | 13235565 | G | A | missense_variant | MODERATE | c.3701C>T|p.Ala1234Val |
S162 |
9 | BAA09g21220 | A09 | 13235618 | G | A | synonymous_variant | LOW | c.3648C>T|p.Arg1216Arg |
S157 |
10 | BAA09g21220 | A09 | 13235946 | C | T | synonymous_variant | LOW | c.3465G>A|p.Gln1155Gln |
S174 S216 |
11 | BAA09g21220 | A09 | 13236007 | C | T | missense_variant | MODERATE | c.3404G>A|p.Cys1135Tyr |
S18 |
12 | BAA09g21220 | A09 | 13236243 | G | A | missense_variant | MODERATE | c.3257C>T|p.Ala1086Val |
S249 |
13 | BAA09g21220 | A09 | 13236684 | G | A | missense_variant | MODERATE | c.3053C>T|p.Thr1018Ile |
S184 |
14 | BAA09g21220 | A09 | 13237062 | C | T | missense_variant | MODERATE | c.2746G>A|p.Glu916Lys |
S15 |
15 | BAA09g21220 | A09 | 13237069 | G | A | synonymous_variant | LOW | c.2739C>T|p.Asp913Asp |
S47 |
16 | BAA09g21220 | A09 | 13237136 | G | A | intron_variant | MODIFIER | c.2733+32C>T| |
S249 |
17 | BAA09g21220 | A09 | 13237508 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.2515-1G>A| |
S168 |
18 | BAA09g21220 | A09 | 13237807 | C | T | synonymous_variant | LOW | c.2370G>A|p.Gln790Gln |
S28 |
19 | BAA09g21220 | A09 | 13238313 | C | T | intron_variant | MODIFIER | c.2069+26G>A| |
S270 |
20 | BAA09g21220 | A09 | 13238511 | G | A | intron_variant | MODIFIER | c.1959+29C>T| |
S38 |
21 | BAA09g21220 | A09 | 13238877 | G | A | synonymous_variant | LOW | c.1695C>T|p.Asn565Asn |
S262 |
22 | BAA09g21220 | A09 | 13240323 | G | A | missense_variant | MODERATE | c.1175C>T|p.Ala392Val |
S40 S49 |
23 | BAA09g21220 | A09 | 13240576 | C | T | missense_variant | MODERATE | c.1009G>A|p.Gly337Arg |
S232 |
24 | BAA09g21220 | A09 | 13240776 | C | T | missense_variant | MODERATE | c.871G>A|p.Asp291Asn |
S133 |
25 | BAA09g21220 | A09 | 13241442 | C | T | missense_variant | MODERATE | c.571G>A|p.Val191Met |
S37 |