Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g13250 | A08 | 11499223 | G | A | upstream_gene_variant | MODIFIER | c.-4573G>A| |
S42 |
2 | BAA08g13250 | A08 | 11500664 | G | A | upstream_gene_variant | MODIFIER | c.-3132G>A| |
S100 |
3 | BAA08g13250 | A08 | 11500760 | C | T | upstream_gene_variant | MODIFIER | c.-3036C>T| |
S80 |
4 | BAA08g13250 | A08 | 11500776 | C | T | upstream_gene_variant | MODIFIER | c.-3020C>T| |
S7 |
5 | BAA08g13250 | A08 | 11501311 | C | T | upstream_gene_variant | MODIFIER | c.-2485C>T| |
S251 |
6 | BAA08g13250 | A08 | 11501626 | G | A | upstream_gene_variant | MODIFIER | c.-2170G>A| |
S243 S299 |
7 | BAA08g13250 | A08 | 11502013 | C | T | upstream_gene_variant | MODIFIER | c.-1783C>T| |
S225 |
8 | BAA08g13250 | A08 | 11502377 | G | A | upstream_gene_variant | MODIFIER | c.-1419G>A| |
S308 |
9 | BAA08g13250 | A08 | 11502932 | C | T | upstream_gene_variant | MODIFIER | c.-864C>T| |
S171 |
10 | BAA08g13250 | A08 | 11504296 | G | A | missense_variant | MODERATE | c.501G>A|p.Met167Ile |
S249 |
11 | BAA08g13250 | A08 | 11505070 | G | A | missense_variant | MODERATE | c.1028G>A|p.Gly343Glu |
S257 |
12 | BAA08g13250 | A08 | 11505389 | C | T | downstream_gene_variant | MODIFIER | c.*66C>T| |
S284 |
13 | BAA08g13250 | A08 | 11506619 | C | T | downstream_gene_variant | MODIFIER | c.*1296C>T| |
S139 |
14 | BAA08g13250 | A08 | 11507011 | C | T | downstream_gene_variant | MODIFIER | c.*1688C>T| |
S86 |
15 | BAA08g13250 | A08 | 11507299 | C | T | downstream_gene_variant | MODIFIER | c.*1976C>T| |
S166 |
16 | BAA08g13250 | A08 | 11507396 | G | A | downstream_gene_variant | MODIFIER | c.*2073G>A| |
S221 |
17 | BAA08g13250 | A08 | 11508103 | G | A | downstream_gene_variant | MODIFIER | c.*2780G>A| |
S161 |
18 | BAA08g13250 | A08 | 11508271 | C | T | downstream_gene_variant | MODIFIER | c.*2948C>T| |
S143 |
19 | BAA08g13250 | A08 | 11509686 | G | A | downstream_gene_variant | MODIFIER | c.*4363G>A| |
S193 |