Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g02300 | A06 | 1400956 | G | A | downstream_gene_variant | MODIFIER | c.*1713C>T| |
S71 |
2 | BAA06g02300 | A06 | 1401226 | G | A | downstream_gene_variant | MODIFIER | c.*1443C>T| |
S135 |
3 | BAA06g02300 | A06 | 1401301 | C | T | downstream_gene_variant | MODIFIER | c.*1368G>A| |
S16 |
4 | BAA06g02300 | A06 | 1401561 | G | A | downstream_gene_variant | MODIFIER | c.*1108C>T| |
S249 |
5 | BAA06g02300 | A06 | 1401601 | C | T | downstream_gene_variant | MODIFIER | c.*1068G>A| |
S59 |
6 | BAA06g02300 | A06 | 1402574 | C | T | downstream_gene_variant | MODIFIER | c.*95G>A| |
S259 |
7 | BAA06g02300 | A06 | 1402579 | G | A | downstream_gene_variant | MODIFIER | c.*90C>T| |
S244 |
8 | BAA06g02300 | A06 | 1402590 | G | A | downstream_gene_variant | MODIFIER | c.*79C>T| |
S169 |
9 | BAA06g02300 | A06 | 1402813 | C | T | intron_variant | MODIFIER | c.682-19G>A| |
S62 |
10 | BAA06g02300 | A06 | 1403712 | G | A | missense_variant | MODERATE | c.299C>T|p.Pro100Leu |
S139 |
11 | BAA06g02300 | A06 | 1403744 | C | T | synonymous_variant | LOW | c.267G>A|p.Lys89Lys |
S245 |
12 | BAA06g02300 | A06 | 1403948 | C | T | missense_variant | MODERATE | c.145G>A|p.Glu49Lys |
S255 |
13 | BAA06g02300 | A06 | 1404206 | G | A | missense_variant | MODERATE | c.32C>T|p.Ser11Phe |
S84 S93 |
14 | BAA06g02300 | A06 | 1405041 | G | A | upstream_gene_variant | MODIFIER | c.-804C>T| |
S293 S294 |
15 | BAA06g02300 | A06 | 1405353 | G | A | upstream_gene_variant | MODIFIER | c.-1116C>T| |
S262 |
16 | BAA06g02300 | A06 | 1405624 | C | T | upstream_gene_variant | MODIFIER | c.-1387G>A| |
S148 S210 S30 |
17 | BAA06g02300 | A06 | 1408457 | C | T | upstream_gene_variant | MODIFIER | c.-4220G>A| |
S293 |