Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g20420 | A04 | 23525222 | C | T | missense_variant | MODERATE | c.3517G>A|p.Glu1173Lys |
S53 |
2 | BAA04g20420 | A04 | 23526677 | G | A | intron_variant | MODIFIER | c.2842-18C>T| |
S94 |
3 | BAA04g20420 | A04 | 23526949 | G | A | intron_variant | MODIFIER | c.2692-24C>T| |
S59 |
4 | BAA04g20420 | A04 | 23527354 | C | T | intron_variant | MODIFIER | c.2476-47G>A| |
S167 |
5 | BAA04g20420 | A04 | 23527470 | G | A | synonymous_variant | LOW | c.2415C>T|p.Ser805Ser |
S67 |
6 | BAA04g20420 | A04 | 23527998 | G | A | missense_variant | MODERATE | c.2192C>T|p.Ser731Phe |
S201 |
7 | BAA04g20420 | A04 | 23528122 | G | A | synonymous_variant | LOW | c.2068C>T|p.Leu690Leu |
S12 |
8 | BAA04g20420 | A04 | 23528151 | G | A | missense_variant | MODERATE | c.2039C>T|p.Ala680Val |
S295 |
9 | BAA04g20420 | A04 | 23528682 | C | T | missense_variant | MODERATE | c.1774G>A|p.Asp592Asn |
S243 S299 |
10 | BAA04g20420 | A04 | 23528778 | C | T | missense_variant&splice_region_variant | MODERATE | c.1678G>A|p.Asp560Asn |
S279 |
11 | BAA04g20420 | A04 | 23530435 | C | T | intron_variant | MODIFIER | c.930+16G>A| |
S169 |
12 | BAA04g20420 | A04 | 23531498 | C | T | intron_variant | MODIFIER | c.357+39G>A| |
S95 |
13 | BAA04g20420 | A04 | 23532689 | A | G | missense_variant | MODERATE | c.62T>C|p.Met21Thr |
S231 |
14 | BAA04g20420 | A04 | 23532935 | G | A | upstream_gene_variant | MODIFIER | c.-185C>T| |
S52 |
15 | BAA04g20420 | A04 | 23534092 | C | T | upstream_gene_variant | MODIFIER | c.-1342G>A| |
S299 |
16 | BAA04g20420 | A04 | 23534115 | C | T | upstream_gene_variant | MODIFIER | c.-1365G>A| |
S163 |
17 | BAA04g20420 | A04 | 23535105 | C | T | upstream_gene_variant | MODIFIER | c.-2355G>A| |
S32 |
18 | BAA04g20420 | A04 | 23535621 | G | A | upstream_gene_variant | MODIFIER | c.-2871C>T| |
S259 |
19 | BAA04g20420 | A04 | 23536743 | G | A | upstream_gene_variant | MODIFIER | c.-3993C>T| |
S170 |