| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 59051 | BAA01g31620 | A01 | 20682362 | C | T | upstream_gene_variant | MODIFIER | c.-7G>A| |
S42 |
| 59052 | BAA01g31630 | A01 | 20684913 | C | T | synonymous_variant | LOW | c.801C>T|p.Gly267Gly |
S100 |
| 59053 | BAA01g31620 | A01 | 20685719 | C | T | upstream_gene_variant | MODIFIER | c.-3364G>A| |
S155 S211 |
| 59054 | BAA01g31630 | A01 | 20687608 | G | A | downstream_gene_variant | MODIFIER | c.*2230G>A| |
S246 |
| 59055 | BAA01g31640 | A01 | 20688631 | C | T | upstream_gene_variant | MODIFIER | c.-4099C>T| |
S15 S2 S3 S34 S4 S6 |
| 59056 | BAA01g31640 | A01 | 20692051 | G | A | upstream_gene_variant | MODIFIER | c.-679G>A| |
S8 |
| 59057 | BAA01g31640 | A01 | 20692070 | G | A | upstream_gene_variant | MODIFIER | c.-660G>A| |
S262 |
| 59058 | BAA01g31640 | A01 | 20692245 | C | T | upstream_gene_variant | MODIFIER | c.-485C>T| |
S200 |
| 59059 | BAA01g31640 | A01 | 20693255 | C | T | missense_variant | MODERATE | c.526C>T|p.Leu176Phe |
S293 |
| 59060 | BAA01g31640 | A01 | 20693482 | G | A | missense_variant | MODERATE | c.753G>A|p.Met251Ile |
S260 |
| 59061 | BAA01g31640 | A01 | 20693650 | G | A | synonymous_variant | LOW | c.921G>A|p.Glu307Glu |
S61 |
| 59062 | BAA01g31640 | A01 | 20693772 | C | T | missense_variant | MODERATE | c.1043C>T|p.Pro348Leu |
S251 |
| 59063 | BAA01g31640 | A01 | 20693932 | G | A | synonymous_variant | LOW | c.1203G>A|p.Lys401Lys |
S221 |
| 59064 | BAA01g31640 | A01 | 20693955 | C | T | missense_variant | MODERATE | c.1226C>T|p.Ala409Val |
S10 |
| 59065 | BAA01g31650 | A01 | 20695268 | C | T | missense_variant | MODERATE | c.236C>T|p.Pro79Leu |
S167 |
| 59066 | BAA01g31650 | A01 | 20695449 | C | T | synonymous_variant | LOW | c.417C>T|p.Ile139Ile |
S20 |
| 59067 | BAA01g31650 | A01 | 20696179 | G | A | missense_variant | MODERATE | c.1147G>A|p.Asp383Asn |
S241 |
| 59068 | BAA01g31660 | A01 | 20696296 | C | T | upstream_gene_variant | MODIFIER | c.-498C>T| |
S136 |
| 59069 | BAA01g31660 | A01 | 20696312 | C | T | upstream_gene_variant | MODIFIER | c.-482C>T| |
S94 |
| 59070 | BAA01g31660 | A01 | 20696469 | C | T | upstream_gene_variant | MODIFIER | c.-325C>T| |
S267 |
| 59071 | BAA01g31640 | A01 | 20697035 | G | A | downstream_gene_variant | MODIFIER | c.*3052G>A| |
S1 S90 |
| 59072 | BAA01g31640 | A01 | 20697171 | C | T | downstream_gene_variant | MODIFIER | c.*3188C>T| |
S54 |
| 59073 | BAA01g31650 | A01 | 20699503 | G | A | downstream_gene_variant | MODIFIER | c.*3229G>A| |
S189 |
| 59074 | BAA01g31650 | A01 | 20699586 | C | T | downstream_gene_variant | MODIFIER | c.*3312C>T| |
S128 |
| 59075 | BAA01g31650 | A01 | 20700617 | C | T | downstream_gene_variant | MODIFIER | c.*4343C>T| |
S7 |