Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g38900 | A09 | 46630319 | C | T | upstream_gene_variant | MODIFIER | c.-3785C>T| |
S296 |
2 | BAA09g38900 | A09 | 46630647 | G | A | upstream_gene_variant | MODIFIER | c.-3457G>A| |
S79 S84 |
3 | BAA09g38900 | A09 | 46630864 | C | T | upstream_gene_variant | MODIFIER | c.-3240C>T| |
S206 S26 |
4 | BAA09g38900 | A09 | 46631310 | C | T | upstream_gene_variant | MODIFIER | c.-2794C>T| |
S247 |
5 | BAA09g38900 | A09 | 46631472 | C | T | upstream_gene_variant | MODIFIER | c.-2632C>T| |
S28 |
6 | BAA09g38900 | A09 | 46632021 | G | A | upstream_gene_variant | MODIFIER | c.-2083G>A| |
S47 |
7 | BAA09g38900 | A09 | 46632169 | G | A | upstream_gene_variant | MODIFIER | c.-1935G>A| |
S79 |
8 | BAA09g38900 | A09 | 46632779 | A | G | upstream_gene_variant | MODIFIER | c.-1325A>G| |
S268 |
9 | BAA09g38900 | A09 | 46633197 | C | T | upstream_gene_variant | MODIFIER | c.-907C>T| |
S109 |
10 | BAA09g38900 | A09 | 46633587 | C | T | upstream_gene_variant | MODIFIER | c.-517C>T| |
S208 S219 |
11 | BAA09g38900 | A09 | 46633626 | G | A | upstream_gene_variant | MODIFIER | c.-478G>A| |
S25 |
12 | BAA09g38900 | A09 | 46633860 | C | T | upstream_gene_variant | MODIFIER | c.-244C>T| |
S286 |
13 | BAA09g38900 | A09 | 46633960 | G | A | upstream_gene_variant | MODIFIER | c.-144G>A| |
S298 |
14 | BAA09g38900 | A09 | 46634191 | C | T | missense_variant | MODERATE | c.88C>T|p.Leu30Phe |
S208 S93 |
15 | BAA09g38900 | A09 | 46634375 | C | T | missense_variant | MODERATE | c.272C>T|p.Ser91Phe |
S171 |
16 | BAA09g38900 | A09 | 46634707 | G | A | missense_variant | MODERATE | c.604G>A|p.Gly202Ser |
S13 |
17 | BAA09g38900 | A09 | 46634913 | C | T | synonymous_variant | LOW | c.810C>T|p.Asn270Asn |
S204 |
18 | BAA09g38900 | A09 | 46636298 | C | T | missense_variant | MODERATE | c.1652C>T|p.Ser551Phe |
S171 |
19 | BAA09g38900 | A09 | 46641346 | G | A | downstream_gene_variant | MODIFIER | c.*4609G>A| |
S308 |
20 | BAA09g38900 | A09 | 46641507 | C | T | downstream_gene_variant | MODIFIER | c.*4770C>T| |
S30 S31 |