Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA07g01290 | A07 | 902331 | C | T | downstream_gene_variant | MODIFIER | c.*3251G>A| |
S220 |
2 | BAA07g01290 | A07 | 902363 | G | A | downstream_gene_variant | MODIFIER | c.*3219C>T| |
S209 |
3 | BAA07g01290 | A07 | 902574 | G | A | downstream_gene_variant | MODIFIER | c.*3008C>T| |
S14 |
4 | BAA07g01290 | A07 | 902643 | C | T | downstream_gene_variant | MODIFIER | c.*2939G>A| |
S13 S140 S219 S278 S72 |
5 | BAA07g01290 | A07 | 903981 | A | G | downstream_gene_variant | MODIFIER | c.*1601T>C| |
S80 |
6 | BAA07g01290 | A07 | 905298 | C | T | downstream_gene_variant | MODIFIER | c.*284G>A| |
S138 |
7 | BAA07g01290 | A07 | 906780 | G | A | splice_region_variant&intron_variant | LOW | c.1182+7C>T| |
S143 |
8 | BAA07g01290 | A07 | 906829 | G | A | synonymous_variant | LOW | c.1140C>T|p.Leu380Leu |
S223 |
9 | BAA07g01290 | A07 | 906894 | G | A | intron_variant | MODIFIER | c.1128+26C>T| |
S157 S163 |
10 | BAA07g01290 | A07 | 906933 | C | T | missense_variant | MODERATE | c.1115G>A|p.Ser372Asn |
S70 |
11 | BAA07g01290 | A07 | 907184 | G | A | missense_variant | MODERATE | c.1003C>T|p.Leu335Phe |
S84 |
12 | BAA07g01290 | A07 | 911296 | C | T | upstream_gene_variant | MODIFIER | c.-1530G>A| |
S77 S82 |
13 | BAA07g01290 | A07 | 913318 | G | A | upstream_gene_variant | MODIFIER | c.-3552C>T| |
S106 |