Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g31070 | A06 | 21159568 | C | T | upstream_gene_variant | MODIFIER | c.-4934C>T| |
S205 |
2 | BAA06g31070 | A06 | 21159785 | C | T | upstream_gene_variant | MODIFIER | c.-4717C>T| |
S18 |
3 | BAA06g31070 | A06 | 21160603 | C | T | upstream_gene_variant | MODIFIER | c.-3899C>T| |
S6 |
4 | BAA06g31070 | A06 | 21161511 | G | A | upstream_gene_variant | MODIFIER | c.-2991G>A| |
S79 |
5 | BAA06g31070 | A06 | 21161565 | C | T | upstream_gene_variant | MODIFIER | c.-2937C>T| |
S247 |
6 | BAA06g31070 | A06 | 21162402 | A | T | upstream_gene_variant | MODIFIER | c.-2100A>T| |
S213 |
7 | BAA06g31070 | A06 | 21162546 | C | T | upstream_gene_variant | MODIFIER | c.-1956C>T| |
S153 |
8 | BAA06g31070 | A06 | 21163455 | C | T | upstream_gene_variant | MODIFIER | c.-1047C>T| |
S15 S180 S3 S38 |
9 | BAA06g31070 | A06 | 21163741 | C | T | upstream_gene_variant | MODIFIER | c.-761C>T| |
S150 |
10 | BAA06g31070 | A06 | 21164061 | C | T | upstream_gene_variant | MODIFIER | c.-441C>T| |
S172 S217 |
11 | BAA06g31070 | A06 | 21164758 | C | T | missense_variant | MODERATE | c.257C>T|p.Ser86Phe |
S196 |
12 | BAA06g31070 | A06 | 21165855 | C | T | downstream_gene_variant | MODIFIER | c.*841C>T| |
S107 |
13 | BAA06g31070 | A06 | 21166603 | G | A | downstream_gene_variant | MODIFIER | c.*1589G>A| |
S139 |
14 | BAA06g31070 | A06 | 21168128 | G | A | downstream_gene_variant | MODIFIER | c.*3114G>A| |
S149 |
15 | BAA06g31070 | A06 | 21168196 | C | T | downstream_gene_variant | MODIFIER | c.*3182C>T| |
S278 |
16 | BAA06g31070 | A06 | 21168868 | G | A | downstream_gene_variant | MODIFIER | c.*3854G>A| |
S219 S72 |
17 | BAA06g31070 | A06 | 21168869 | C | T | downstream_gene_variant | MODIFIER | c.*3855C>T| |
S178 |
18 | BAA06g31070 | A06 | 21169140 | G | A | downstream_gene_variant | MODIFIER | c.*4126G>A| |
S162 |
19 | BAA06g31070 | A06 | 21169156 | G | A | downstream_gene_variant | MODIFIER | c.*4142G>A| |
S262 |